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Australian New Crops Info 2016
Supported by the Rural Industries Research and Development Corporation

Listing of Interesting Plants of the World:

Ascobolus immersus

 

 

This species name was not found in The Plant List

 

This species has no synonyms in The Plant List

 

No common names have been found

 

 

Trends (five databases) 1901-2013:
[Number of papers mentioning Ascobolus immersus: 680]

 

Ascobolus immersus.jpg

 

Popularity of Ascobolus immersus over time
[Left-hand Plot: Plot of numbers of papers mentioning Ascobolus immersus (histogram and left hand axis scale of left-hand plot) and line of best fit, 1901 to 2013 (equation and % variation accounted for in box); Right-hand Plot: Plot of a proportional micro index, derived from numbers of papers mentioning Ascobolus immersus as a proportion (scaled by multiplying by one million) of the approximate total number of papers available in databases for that year (frequency polygon and left-hand axis scale of right-hand plot) and line of best fit, 1901 to 2013 (equation and % variation accounted for in box)] 

[For larger charts showing the numbers of papers that have mentioned this species over years, select this link; there are links to come back from there]

 

Keywords

[Total number of keywords included in the papers that mentioned this species: 898]

 

fungi (28), DNA methylation (15), Gene silencing (10), chromatin (8), DNA (8), plants (8), Recombination (8), genetic recombination (7), plant breeding (7), plant genetics (7), Recombinant DNA (7), Ascomycota (6), Linear plasmid (6), Meiosis (6), methylation (6), neurospora (6), botany (5), Plant Science and Plant Products (5), Repeat-induced point mutation (5), DNA methyltransferase (4), epigenetics (4), Filamentous fungus (4), Gene conversion (4), gene expression (4), Mitochondria (4), Terminal protein (4), alleles (3), antibiotics (3), Argentinean high-altitude wetlands (3), ascobolus immersus (3), Ascospore (3), Biomechanics (3), BOX-PCR (3), carbapenems (3), Cell differentiation (3), Cell wall composition (3), cephabacins (3), cephalosporins (3), cephamycins (3), chromosome marker (3), chromosomes (3), clavams (3), clavulanic acid (3), DNA polymerase (3), DNA polymerase type B (3), DNA repair (3), genome evolution (3), homoserine O-transacetylase (3), Meiotic recombination (3), Micrococcus (3), monobactams (3), Neurospora crassa (3), nocardicins (3), nucleotide sequence (3), penicillins (3), plasmids (3), Protein glycosylation (3), RecA (3), Repair (3), RIP (3), segregation (3), Silencing of pmt genes (3), Transcription (3), Trichoderma reesei (3), Turgor pressure (3), Ustilago maydis (3), Xiphophorus maculatus (3), 5-Methylcytosine (2), AFLPs (2), Aging (2), arabidopsis (2), Argentinean high-altitude lakes (2), ascobolus (2), Ascomycete (2), ascospores (2), Ascus development (2), Ballistospore (2), cancer (2), Crossover (2), cytosine (2), Dinophyceae (2), Dinucleotide frequency distribution (2), Directional transition mutations (2), Dispersal (2), Encystment (2), epialleles (2), epigenetic (2), filamentous fungi (2), fungal transformation (2), genome (2), Genomic imprinting (2), GFP (2), Gymnodinium catenatum (2), Histone H1 (2), Intraclonal genetic variation (2), intron (2), Karyotyping (2), Life cycle (2), linear DNA replication (2), linear plasmids (2).....

 

[If all keywords are not here (as indicated by .....), they can be accessed from this link; there are links to come back from there]

 

 

Most likely scope for crop use/product (%):
[Please note: When there are only a few papers mentioning a species, care should be taken with the interpretation of these crop use/product results; as well, a mention may relate to the use of a species, or the context in which it grows, rather than a product]

 

genetics (77.05), boundary (4.49), hemiparasite (3.66), model (3.09), weed (1.57), medicinal (1.53), timber (1.42), fruit (1.29), pesticide (0.72), starch (0.55).....

 

[To see the full list of crop use/product outcomes, from searching abstracts of the papers that have mentioned this species, select this link; details of the analysis process have also been included; there are links to come back from there]

 

 

Recent mentions of this species in the literature:
[since 2012, with links to abstracts; The references from 1901-2013 which have been used for the trend, keyword and crop use/product analyses below, are listed below these references]

 

Catoni M, Griffiths J, Becker C, Zabet NR, Bayon C, Dapp M, Lieberman-Lazarovich M, Weigel D and Paszkowski J (2017) DNA sequence properties that predict susceptibility to epiallelic switching. The EMBO Journal, n/a-n/a. http://dx.doi.org/10.15252/embj.201695602

Catoni M, Griffiths J, Becker C, Zabet NR, Bayon C, Dapp M, Lieberman-Lazarovich M, Weigel D and Paszkowski J (2017) DNA sequence properties that predict susceptibility to epiallelic switching. EMBO J., embj.201695602. http://EMBOJ.embopress.org/cgi/content/abstract/embj.201695602v1

Selker E (2017) Repeat Induced Point Mutation. In Reference Module in Life Sciences. (Ed.^(Eds  pp. (Elsevier). http://www.sciencedirect.com/science/article/pii/B9780128096338070345

Izzo A and Schneider R (2016) The role of linker histone H1 modifications in the regulation of gene expression and chromatin dynamics. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms 1859, 486-495. http://www.sciencedirect.com/science/article/pii/S1874939915001893

Money NP (2016) Chapter 3 - Spore Production, Discharge, and Dispersal. In The Fungi (Third Edition). (Ed.^(Eds  pp. 67-97. (Academic Press: Boston). http://www.sciencedirect.com/science/article/pii/B9780123820341000037

Robert T, Vrielynck N, Mézard C, de Massy B and Grelon M (2016) A new light on the meiotic DSB catalytic complex. Seminars in Cell & Developmental Biology 54, 165-176. http://www.sciencedirect.com/science/article/pii/S1084952116300659

Rogers E, Correa R, Barreto B, Bravo Núñez MA, Minnick PJ, Vera Cruz D, Xia J, Hastings PJ and Rosenberg SM (2016) Double-Strand-Break Repair, Mutagenesis, and Stress. In Stress and Environmental Regulation of Gene Expression and Adaptation in Bacteria. (Ed.^(Eds  pp. 185-195. (John Wiley & Sons, Inc.). http://dx.doi.org/10.1002/9781119004813.ch15

Seymour M, Ji L, Santos AM, Kamei M, Sasaki T, Basenko EY, Schmitz RJ, Zhang X and Lewis ZA (2016) Histone H1 Limits DNA Methylation in Neurospora crassa. g3 6, 1879-1889. http://www.g3journal.org/cgi/content/abstract/6/7/1879

van Asperen EN, Kirby JR and Hunt CO (2016) The effect of preparation methods on dung fungal spores: Implications for recognition of megafaunal populations. Review of Palaeobotany and Palynology 229, 1-8. http://www.sciencedirect.com/science/article/pii/S0034666715300543

Zickler D and Espagne E (2016) Sordaria, a model system to uncover links between meiotic pairing and recombination. Seminars in Cell & Developmental Biology 54, 149-157. http://www.sciencedirect.com/science/article/pii/S1084952116300544

Kahl G (2015) Methylation induced premeiotically (MIP). In The Dictionary of Genomics, Transcriptomics and Proteomics. (Ed.^(Eds  pp. (Wiley-VCH Verlag GmbH & Co. KGaA). http://dx.doi.org/10.1002/9783527678679.dg07414

Kahl G (2015) HAT superfamily. In The Dictionary of Genomics, Transcriptomics and Proteomics. (Ed.^(Eds  pp. (Wiley-VCH Verlag GmbH & Co. KGaA). http://dx.doi.org/10.1002/9783527678679.dg05381

Martienssen R and Moazed D (2015) RNAi and Heterochromatin Assembly. Cold Spring Harb Perspect Biol 7, a019323-. http://cshperspectives.cshlp.org/cgi/content/abstract/7/8/a019323

Yelina NE, Lambing C, Hardcastle TJ, Zhao X, Santos B and Henderson IR (2015) DNA methylation epigenetically silences crossover hot spots and controls chromosomal domains of meiotic recombination in Arabidopsis. Genes & Dev. 29, 2183-2202. http://genesdev.cshlp.org/cgi/content/abstract/29/20/2183

Zickler D and Kleckner N (2015) Recombination, Pairing, and Synapsis of Homologs during Meiosis. Cold Spring Harb Perspect Biol 7, a016626-. http://cshperspectives.cshlp.org/cgi/content/abstract/7/6/a016626

Dong C-B, Mao J-F, Suo Y-J, Shi L, Wang J, Zhang P-D and Kang X-Y (2014) A strategy for characterization of persistent heteroduplex DNA in higher plants. The Plant Journal 80, 282-291. http://dx.doi.org/10.1111/tpj.12631

Dooner HK and He L (2014) Polarized gene conversion at the bz locus of maize. PNAS 111, 13918-13923. http://www.pnas.org/cgi/content/abstract/111/38/13918

Grandaubert J, Balesdent M-H and Rouxel T (2014) Chapter Three - Evolutionary and Adaptive Role of Transposable Elements in Fungal Genomes. In Advances in Botanical Research. (Ed.^(Eds Francis MM) pp. 79-107. (Academic Press). http://www.sciencedirect.com/science/article/pii/B9780123979407000033

Heil CSS (2014) No Detectable Effect of the DNA Methyltransferase DNMT2 on Drosophila Meiotic Recombination. g3 4, 2095-2100. http://www.g3journal.org/cgi/content/abstract/4/11/2095

Payen T, Murat C and Bonito G (2014) Chapter Seven - Truffle Phylogenomics: New Insights into Truffle Evolution and Truffle Life Cycle. In Advances in Botanical Research. (Ed.^(Eds Francis MM) pp. 211-234. (Academic Press). http://www.sciencedirect.com/science/article/pii/B9780123979407000070

Trail F and Seminara A (2014) The mechanism of ascus firing – Merging biophysical and mycological viewpoints. Fungal Biology Reviews 28, 70-76. http://www.sciencedirect.com/science/article/pii/S1749461314000189

(2013) Subject Index. In Brenners Encyclopedia of Genetics (Second Edition). (Ed.^(Eds Editors-in-Chief: Stanley M and Kelly H) pp. 403-598. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B978012374984009015X

(2013) Authors. In Brenners Encyclopedia of Genetics (Second Edition). (Ed.^(Eds Editors-in-Chief: Stanley M and Kelly H) pp. 1-8. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123749840090161

(2013) Index. In The Ecological Genomics of Fungi. (Ed.^(Eds  pp. 371-384. (John Wiley & Sons, Inc). http://dx.doi.org/10.1002/9781118735893.index

Aramayo R and Selker EU (2013) Neurospora crassa, a Model System for Epigenetics Research. Cold Spring Harb Perspect Biol 5, a017921-. http://cshperspectives.cshlp.org/cgi/content/abstract/5/10/a017921

Casadesús J and Noyer-Weidner M (2013) Epigenetics. In Brenners Encyclopedia of Genetics (Second Edition). (Ed.^(Eds Editors-in-Chief: Stanley M and Kelly H) pp. 500-503. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123749840004800

Casadesús J and Noyer-Weidner M (2013) Epigenetics A2 - Maloy, Stanley. In Brenners Encyclopedia of Genetics (Second Edition). (Ed.^(Eds Hughes K) pp. 500-503. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123749840004800

Fritz JA, Seminara A, Roper M, Pringle A and Brenner MP (2013) A natural O-ring optimizes the dispersal of fungal spores. J R Soc Interface 10, 20130187-. http://rsif.royalsocietypublishing.org/cgi/content/abstract/10/85/20130187

Ikeda K-i, Van Vu B, Kadotani N, Tanaka M, Murata T, Shiina K, Chuma I, Tosa Y and Nakayashiki H (2013) Is the Fungus Magnaporthe Losing DNA Methylation? Genetics 195, 845-855. http://www.genetics.org/cgi/content/abstract/195/3/845

Murat C, Payen T, Petitpierre D and Labbé J (2013) Repeated Elements in Filamentous Fungi with a Focus on Wood-Decay Fungi. In The Ecological Genomics of Fungi. (Ed.^(Eds  pp. 21-40. (John Wiley & Sons, Inc). http://dx.doi.org/10.1002/9781118735893.ch2

Sanchez-Moran E (2013) Genomics and Chromatin Packaging. In Annual Plant Reviews. (Ed.^(Eds  pp. 123-156. (John Wiley & Sons Ltd). http://dx.doi.org/10.1002/9781118472507.ch5

Selker E (2013) Repeat Induced Point Mutation. In Brenners Encyclopedia of Genetics (Second Edition). (Ed.^(Eds Editors-in-Chief: Stanley M and Kelly H) pp. 148-149. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123749840016946

Selker E (2013) Repeat Induced Point Mutation A2 - Maloy, Stanley. In Brenners Encyclopedia of Genetics (Second Edition). (Ed.^(Eds Hughes K) pp. 148-149. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123749840016946

Smith DR and Keeling PJ (2013) Gene Conversion Shapes Linear Mitochondrial Genome Architecture. Genome Biol Evol 5, 905-912. http://gbe.oxfordjournals.org/cgi/content/abstract/5/5/905

Vu BV, Pham KTM and Nakayashiki H (2013) Substrate-Induced Transcriptional Activation of the MoCel7C Cellulase Gene Is Associated with Methylation of Histone H3 at Lysine 4 in the Rice Blast Fungus Magnaporthe oryzae. Appl. Envir. Microbiol. 79, 6823-6832. http://aem.asm.org/cgi/content/abstract/79/21/6823

Wang X, Darwiche S and Heitman J (2013) Sex-Induced Silencing Operates During Opposite-Sex and Unisexual Reproduction in Cryptococcus neoformans. Genetics 193, 1163-1174. http://www.genetics.org/cgi/content/abstract/193/4/1163

Zemach A, Kim MY, Hsieh P-H, Coleman-Derr D, Eshed-Williams L, Thao K, Harmer Stacey L and Zilberman D (2013) The Arabidopsis Nucleosome Remodeler DDM1 Allows DNA Methyltransferases to Access H1-Containing Heterochromatin. Cell 153, 193-205. http://www.sciencedirect.com/science/article/pii/S0092867413002225

Bowring FJ, Yeadon PJ and Catcheside DEA (2012) Use of fluorescent protein to analyse recombination at three loci in Neurospora crassa. Fungal Genetics and Biology 49, 619-625. http://www.sciencedirect.com/science/article/pii/S1087184512001004

Kowalski A and Pałyga J (2012) Linker histone subtypes and their allelic variants. Cell Biology International 36, 981-996. http://dx.doi.org/10.1042/CBI20120133

Kumar TKA, Healy R, Spatafora JW, Blackwell M and McLaughlin DJ (2012) Orbilia ultrastructure, character evolution and phylogeny of Pezizomycotina. Mycologia 104, 462-476. http://www.mycologia.org/cgi/content/abstract/104/2/462

Satwika D, Klassen R and Meinhardt F (2012) Repeated capture of a cytoplasmic linear plasmid by the host nucleus in Debaryomyces hansenii. Yeast 29, 145-154. http://dx.doi.org/10.1002/yea.2893

 

 

References 1901-2013 (and links to abstracts):
[Number of papers mentioning Ascobolus immersus: 680; Any undated papers have been included at the end]

 

 

Anonymous (2013) Subject Index. In ‘Brenner’s Encyclopedia of Genetics (Second Edition)’. (Eds M Editors-in-Chief: Stanley and H Kelly) pp. 403-598. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B978012374984009015X

Anonymous (2013) Authors. In ‘Brenner’s Encyclopedia of Genetics (Second Edition)’. (Eds M Editors-in-Chief: Stanley and H Kelly) pp. 1-8. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123749840090161

Casadesús J, Noyer-Weidner M (2013) Epigenetics. In ‘Brenner’s Encyclopedia of Genetics (Second Edition)’. (Eds M Editors-in-Chief: Stanley and H Kelly) pp. 500-3. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123749840004800

Sanchez-Moran E (2013) Genomics and Chromatin Packaging. In ‘Annual Plant Reviews’ pp. 123-56. (John Wiley & Sons Ltd). http://dx.doi.org/10.1002/9781118472507.ch5

Selker E (2013) Repeat Induced Point Mutation. In ‘Brenner’s Encyclopedia of Genetics (Second Edition)’. (Eds M Editors-in-Chief: Stanley and H Kelly) pp. 148-9. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123749840016946

Smith DR, Keeling PJ (2013) Gene Conversion Shapes Linear Mitochondrial Genome Architecture. Genome Biol Evol 5, 905-12. http://gbe.oxfordjournals.org/cgi/content/abstract/5/5/905

Wang X, Darwiche S, Heitman J (2013) Sex-Induced Silencing Operates During Opposite-Sex and Unisexual Reproduction in Cryptococcus neoformans. Genetics 193, 1163-74. http://www.genetics.org/cgi/content/abstract/193/4/1163

Zemach A, Kim MY, Hsieh P-H, Coleman-Derr D, Eshed-Williams L, Thao K, Harmer Stacey L, Zilberman D (2013) The Arabidopsis Nucleosome Remodeler DDM1 Allows DNA Methyltransferases to Access H1-Containing Heterochromatin. Cell 153, 193-205. http://www.sciencedirect.com/science/article/pii/S0092867413002225

Bowring FJ, Yeadon PJ, Catcheside DEA (2012) Use of fluorescent protein to analyse recombination at three loci in Neurospora crassa. Fungal Genetics and Biology 49, 619-25. http://www.sciencedirect.com/science/article/pii/S1087184512001004

Kowalski A, Pałyga J (2012) Linker histone subtypes and their allelic variants. Cell Biology International 36, 981-96. http://dx.doi.org/10.1042/CBI20120133

Kumar TKA, Healy R, Spatafora JW, Blackwell M, McLaughlin DJ (2012) Orbilia ultrastructure, character evolution and phylogeny of Pezizomycotina. Mycologia 104, 462-76. http://www.mycologia.org/cgi/content/abstract/104/2/462

Satwika D, Klassen R, Meinhardt F (2012) Repeated capture of a cytoplasmic linear plasmid by the host nucleus in Debaryomyces hansenii. Yeast 29, 145-54. http://dx.doi.org/10.1002/yea.2893

Anonymous (2011) Index. In ‘Handbook of Epigenetics’. (Ed. T Trygve) pp. 617-24. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123757098000551

Górka-Nieć W, Kania A, Perlińska-Lenart U, Smoleńska-Sym G, Palamarczyk G, Kruszewska JS (2011) Integration of additional copies of Trichoderma reesei gene encoding protein O-mannosyltransferase I results in a decrease of the enzyme activity and alteration of cell wall composition. Fungal Biology 115, 124-32. http://www.sciencedirect.com/science/article/pii/S1878614610001820

Holliday R (2011) The recombination, repair and modification of DNA. DNA Repair 10, 993-9. http://www.sciencedirect.com/science/article/pii/S1568786411000887

John Clutterbuck A (2011) Genomic evidence of repeat-induced point mutation (RIP) in filamentous ascomycetes. Fungal Genetics and Biology 48, 306-26. http://www.sciencedirect.com/science/article/pii/S1087184510001799

Kashiwagi K, Nimura K, Ura K, Kaneda Y (2011) DNA methyltransferase 3b preferentially associates with condensed chromatin. Nucleic Acids Res. 39, 874-88. http://nar.oxfordjournals.org/cgi/content/abstract/39/3/874

Malagnac F, Silar P (2011) Chapter 13 - Epigenetics of Eukaryotic Microbes. In ‘Handbook of Epigenetics’. (Ed. T Trygve) pp. 185-201. (Academic Press: San Diego). http://www.sciencedirect.com/science/article/pii/B9780123757098000137

Nakayashiki H (2011) The Trickster in the genome: contribution and control of transposable elements. Genes to Cells 16, 827-41. http://dx.doi.org/10.1111/j.1365-2443.2011.01533.x

Pardo CE, Carr IM, Hoffman CJ, Darst RP, Markham AF, Bonthron DT, Kladde MP (2011) MethylViewer: computational analysis and editing for bisulfite sequencing and methyltransferase accessibility protocol for individual templates (MAPit) projects. Nucleic Acids Res. 39, e5-. http://nar.oxfordjournals.org/cgi/content/abstract/39/1/e5

Anonymous (2010) Authors. In ‘Encyclopedia of Genetics’. (Eds B Editors-in-Chief:  Sydney and HM Jeffrey) pp. 1-41. (Academic Press: New York). http://www.sciencedirect.com/science/article/pii/B9780122270802091006

Dib JR, Wagenknecht M, Hill RT, Farías ME, Meinhardt F (2010) First report of linear megaplasmids in the genus Micrococcus. Plasmid 63, 40-5. http://www.sciencedirect.com/science/article/pii/S0147619X09001176

Dib JR, Wagenknecht M, Hill RT, Farías ME, Meinhardt F (2010) Novel linear megaplasmid from Brevibacterium sp. isolated from extreme environment. Journal of Basic Microbiology 50, 280-4. http://dx.doi.org/10.1002/jobm.200900332

Figueroa RI, Rengefors K, Bravo I, Bensch S (2010) From homothally to heterothally: Mating preferences and genetic variation within clones of the dinoflagellate Gymnodinium catenatum. Deep Sea Research Part II: Topical Studies in Oceanography 57, 190-8. http://www.sciencedirect.com/science/article/pii/S0967064509003142

Fischer MWF, Stolze-Rybczynski JL, Davis DJ, Cui Y, Money NP (2010) Solving the aerodynamics of fungal flight: how air viscosity slows spore motion. Fungal Biology 114, 943-8. http://www.sciencedirect.com/science/article/pii/S187861461000142X

Kothe GO, Kitamura M, Masutani M, Selker EU, Inoue H (2010) PARP is involved in replicative aging in Neurospora crassa. Fungal Genetics and Biology 47, 297-309. http://www.sciencedirect.com/science/article/pii/S1087184509002230

Oide S, Liu J, Yun S-H, Wu D, Michev A, Choi MY, Horwitz BA, Turgeon BG (2010) Histidine Kinase Two-Component Response Regulator Proteins Regulate Reproductive Development, Virulence, and Stress Responses of the Fungal Cereal Pathogens Cochliobolus heterostrophus and Gibberella zeae. Eukaryot. Cell 9, 1867-80. http://ec.asm.org/cgi/content/abstract/9/12/1867

Roper M, Seminara A, Bandi MM, Cobb A, Dillard HR, Pringle A (2010) Dispersal of fungal spores on a cooperatively generated wind. PNAS 107, 17474-9. http://www.pnas.org/cgi/content/abstract/107/41/17474

Stahl FW, Foss HM (2010) A Two-Pathway Analysis of Meiotic Crossing Over and Gene Conversion in Saccharomyces cerevisiae. Genetics 186, 515-36. http://www.genetics.org/cgi/content/abstract/186/2/515

Uppalapati SR, Young CA, Marek SM, Mysore KS (2010) Phymatotrichum (cotton) root rot caused by Phymatotrichopsis omnivora: retrospects and prospects. Molecular Plant Pathology 11, 325-34. http://dx.doi.org/10.1111/j.1364-3703.2010.00616.x

Zemach A, Zilberman D (2010) Evolution of Eukaryotic DNA Methylation and the Pursuit of Safer Sex. Current Biology 20, R780-R5. http://www.sciencedirect.com/science/article/pii/S0960982210008663

Zhou Q, Braasch I, Froschauer A, Böhne A, Schultheis C, Schartl M, Volff J-N (2010) A novel marker for the platyfish (Xiphophorus maculatus) W chromosome is derived from a Polinton transposon. Journal of Genetics and Genomics 37, 181-8. http://www.sciencedirect.com/science/article/pii/S1673852709600369

Liras P, MartÍn JF, Editor-in-Chief:  Moselio S (2009) β-Lactam Antibiotics. In ‘Encyclopedia of Microbiology (Third Edition)’ pp. 274-89. (Academic Press: Oxford). http://www.sciencedirect.com/science/article/pii/B9780123739445000390

Liras P, Martín JF (2009) β-Lactam Antibiotics. In ‘Encyclopedia of Microbiology (Third Edition)’. (Ed. S Editor-in-Chief:  Moselio) pp. 274-89. (Academic Press: Oxford). http://www.sciencedirect.com/science/article/pii/B9780123739445000390

Liras P, Martín JF, Moselio S (2009) [beta]-Lactam Antibiotics. In ‘Encyclopedia of Microbiology’ pp. 274-89. (Academic Press: Oxford). http://www.sciencedirect.com/science/article/pii/B9780123739445000390

Pomraning KR, Smith KM, Freitag M (2009) Genome-wide high throughput analysis of DNA methylation in eukaryotes. Methods 47, 142-50. http://www.sciencedirect.com/science/article/pii/S1046202308001825

Singh PK, Iyer SV, Ramakrishnan M, Kasbekar DP (2009) Chromosome segment duplications in Neurospora crassa: barren crosses beget fertile science. BioEssays 31, 209-19. http://dx.doi.org/10.1002/bies.200800098

Arnaise S, Zickler D, Bourdais A, Dequard-Chablat M, Debuchy R (2008) Mutations in mating-type genes greatly decrease repeat-induced point mutation process in the fungus Podospora anserina. Fungal Genetics and Biology 45, 207-20. http://www.sciencedirect.com/science/article/pii/S1087184507001661

Brosch G, Loidl P, Graessle S (2008) Histone modifications and chromatin dynamics: a focus on filamentous fungi. FEMS Microbiology Reviews 32, 409-39. http://dx.doi.org/10.1111/j.1574-6976.2007.00100.x

Ferandon C, Chatel SEK, Castandet B, Castroviejo M, Barroso G (2008) The Agrocybe aegerita mitochondrial genome contains two inverted repeats of the nad4 gene arisen by duplication on both sides of a linear plasmid integration site. Fungal Genetics and Biology 45, 292-301. http://www.sciencedirect.com/science/article/pii/S1087184507001934

Gac ML, Giraud T (2008) Existence of a pattern of reproductive character displacement in Homobasidiomycota but not in Ascomycota. Journal of Evolutionary Biology 21, 761-72. http://dx.doi.org/10.1111/j.1420-9101.2008.01511.x

Godde JS, Ura K (2008) Cracking the Enigmatic Linker Histone Code. J. Biochem. 143, 287-93. http://jb.oxfordjournals.org/cgi/content/abstract/143/3/287

Hallen HE, Trail F (2008) The L-Type Calcium Ion Channel Cch1 Affects Ascospore Discharge and Mycelial Growth in the Filamentous Fungus Gibberella zeae (Anamorph Fusarium graminearum). Eukaryot. Cell 7, 415-24. http://ec.asm.org/cgi/content/abstract/7/2/415

Handa H (2008) Linear plasmids in plant mitochondria: Peaceful coexistences or malicious invasions. Mitochondrion 8, 15-25. http://www.sciencedirect.com/science/article/pii/S1567724907002449

Happel N, Doenecke D, Sekeri-Pataryas KE, Sourlingas TG (2008) H1 histone subtype constitution and phosphorylation state of the ageing cell system of human peripheral blood lymphocytes. Experimental Gerontology 43, 184-99. http://www.sciencedirect.com/science/article/pii/S0531556507002768

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Nagylaki T, Petes TD (1982) INTRACHROMOSOMAL GENE CONVERSION AND THE MAINTENANCE OF SEQUENCE HOMOGENEITY AMONG REPEATED GENES. Genetics 100, 315-37. http://www.genetics.org/cgi/content/abstract/100/2/315

Shcherbakov VP, Plugina LA, Kudryashova EA, Efremova OI, Sizova ST, Toompuu OG (1982) MARKER-DEPENDENT RECOMBINATION IN T4 BACTERIOPHAGE. I. OUTLINE OF THE PHENOMENON AND EVIDENCE SUGGESTING A MISMATCH REPAIR MECHANISM. Genetics 102, 615-25. http://www.genetics.org/cgi/content/abstract/102/4/615

Stahl FW, Stahl MM, Young L, Kobayashi I (1982) CHI-STIMULATED RECOMBINATION BETWEEN PHAGE lambda AND THE PLASMID lambdadv. Genetics 102, 599-613. http://www.genetics.org/cgi/content/abstract/102/4/599

Bellemere A, Melendez-Howell L, Nicolas A, Rossignol JL (1981) Comparative ultrastructural study of the development of ascospores in the wild line and in mutants with “belted” or “albino” ascospores of Ascobolus immersus Pers. ex Fr.. Etude ultrastructurale comparative du developpement des ascospores chea la lignee sauvage et chez des mutants a ascospores “ceinturees” ou “albinos”. Cryptogamie; mycologie., 4.

Catcheside DEA (1981) GENES IN NEUROSPORA THAT SUPPRESS RECOMBINATION WHEN THEY ARE HETEROZYGOUS. Genetics 98, 55-76. http://www.genetics.org/cgi/content/abstract/98/1/55

Decaris B (1981) Intragenic location of an unstable insertion element within gene b5 of the fungus Ascobolus immersus. MGG, molecular and general genetics. 184, 434-9.

Decaris B, Francou F, Kouassi A, Lefort C, Rizet G (1981) Genetic Instability in Ascobolus Immersus: Modalities of Back-mutations, Intragenic Mapping of Unstable Sites, and Unstable Insertion. Preliminary Biochemical Data. Cold Spring Harb Symp Quant Biol 45, 509-17. http://symposium.cshlp.org/cgi/content/abstract/45/0/509

Delange AM (1981) THE MUTATION SK(ad-3A) CANCELS THE DOMINANCE OF ad-3A+ OVER ad-3A IN THE ASCUS OF NEUROSPORA. Genetics 97, 237-46. http://www.genetics.org/cgi/content/abstract/97/2/237

Ellis DH (1981) Ultrastructure of thermophilic fungi: II. Ascus and ascospore development in Thermoascus aurantiacus. Transactions of the British Mycological Society 76, 467-78. http://www.sciencedirect.com/science/article/pii/S0007153681800757

Francou F (1981) Isolation and characterization of a linear DNA molecule in the fungus Ascobolus immersus. MGG, molecular and general genetics. 184, 440-4.

Hamza H, Haedens V, Mekki-Berrada A, Rossignol JL (1981) Hybrid DNA formation during meiotic recombination. PNAS 78, 7648-51. http://www.pnas.org/cgi/content/abstract/78/12/7648

Heath IB, G.H. Bourne JFDaKWJ (1981) Nucleus-Associated Organelles in Fungi. In ‘International Review of Cytology’ pp. 191-221. (Academic Press). http://www.sciencedirect.com/science/article/pii/S0074769608623232

Holden M (1981) The slide collection. Bulletin of the British Mycological Society 15, 9-18. http://www.sciencedirect.com/science/article/pii/S0007152881800302

NICOLAS A, ARNAISE S, HAEDENS V, ROSSIGNOL JL (1981) Ascospore Mutants and Genetic Map of Ascobolus immersus Stock 28. Microbiology 125, 257-72. http://mic.sgmjournals.org/cgi/content/abstract/125/2/257

Potter H, Dressler D (1981) Genome Fusion. Cold Spring Harb Symp Quant Biol 45, 371-83. http://symposium.cshlp.org/cgi/content/abstract/45/0/371

Radding CM, Shibata T, DasGupta C, Cunningham RP, Osber L (1981) Kinetics and Topology of Homologous Pairing Promoted by Escherichia coli recA-gene Protein. Cold Spring Harb Symp Quant Biol 45, 385-90. http://symposium.cshlp.org/cgi/content/abstract/45/0/385

Clark MC (1980) Non-lichenized discomycetes recorded in Britain in recent years. Bulletin of the British Mycological Society 14, 24-56. http://www.sciencedirect.com/science/article/pii/S0007152880800344

DasGupta C, Shibata T, Cunningham RP, Radding CM (1980) The topology of homologous pairing promoted by RecA protein. Cell 22, 437-46. http://www.sciencedirect.com/science/article/pii/0092867480903542

Eckardt F, Teh S-J, Haynes RH (1980) HETERODUPLEX REPAIR AS AN INTERMEDIATE STEP OF UV MUTAGENESIS IN YEAST. Genetics 95, 63-80. http://www.genetics.org/cgi/content/abstract/95/1/63

Jeng RS, Hubbes M (1980) Ultrastructure of Ceratocystis ulmi.1 II. Ascogenous system and ascosporogenesis. European Journal of Forest Pathology 10, 104-16. http://dx.doi.org/10.1111/j.1439-0329.1980.tb00015.x

Kalogeropoulos A, Rossignol JL (1980) Evidence for independent mismatch corrections along the same hybrid DNA tract during meiotic recombination in Ascobolus. Heredity. 45, 263-70.

Rossignol JL, Haedens V (1980) Relationship between asymmetrical and symmetrical hybrid DNA formation during meiotic recombination. Current genetics. 1, 185-91.

Anonymous (1979) Author index. Transactions of the British Mycological Society 41-47, 1-49. http://www.sciencedirect.com/science/article/pii/S0007153679800273

Decaris B, Lefont C, Francou F, Rizet G (1979) Unstable ascospore color mutants of Ascobolus immersus. II. Determinism and possible mechanisms of gene instability. Molecular and general genetics, 2.

Fogel S, Mortimer R, Lusnak K, Tavares F (1979) Meiotic Gene Conversion: A Signal of the Basic Recombination Event in Yeast. Cold Spring Harb Symp Quant Biol 43, 1325-41. http://symposium.cshlp.org/cgi/content/abstract/43/0/1325

Harrower KM, Nagy LA (1979) Effects of nutrients and water stress on growth and sporulation of coprophilous fungi. Transactions of the British Mycological Society 72, 459-62. http://www.sciencedirect.com/science/article/pii/S0007153679801540

Holliday R, Pukkila PJ, Dickson JM, Spanos A, Murray V (1979) Relationships between the Correction of Mismatched Bases in DNA and Mutability. Cold Spring Harb Symp Quant Biol 43, 1317-23. http://symposium.cshlp.org/cgi/content/abstract/43/0/1317

Lamb BC, Ghikas A (1979) THE INTERGRADATION, GENETIC INTERCHANGEABILITY AND INTERPRETATION OF GENE CONVERSION SPECTRUM TYPES. Genetics 92, 49-65. http://www.genetics.org/cgi/content/abstract/92/1/49

Leblon G (1979) INTRAGENIC SUPPRESSION AT THE b2 LOCUS IN ASCOBOLUS IMMERSUS. II. CHARACTERISTICS OF THE MUTATIONS IN GROUPS A AND E. Genetics 92, 1093-106. http://www.genetics.org/cgi/content/abstract/92/4/1093

Leblon G, Rossignol JL (1979) The interaction during recombination between closely linked allelic frameshift mutant sites in Ascobolus immersus. II. A and B type mutant sites. Heredity. 42, 337-52.

Nagy LA, Harrower KM (1979) Analysis of two southern hemisphere coprophilous fungus successions. Transactions of the British Mycological Society 72, 69-74. http://www.sciencedirect.com/science/article/pii/S0007153679800091

Nicolas A (1979) Variation of gene conversion and intragenic recombination frequencies in the genome of Ascobolus immersus. Mol Gen Genet 176, 129-38.

Radding CM (1979) The Mechanism of Conversion of Deletions and Insertions. Cold Spring Harb Symp Quant Biol 43, 1315-6. http://symposium.cshlp.org/cgi/content/abstract/43/0/1315

Rapp P (1979) An atlas of cellular oscillators. J. Exp. Biol. 81, 281-306. http://jeb.biologists.org

Rizet G, Lefort C, Decaris B, Francou F, Kouassi A (1979) Unstable ascospore color mutants of Ascobolus immersus. III. Mapping, temporal occurrences and modalities of back-mutations of 34 new unstable mutants. Molecular and general genetics., 3.

Rossignol JL, Paquette N (1979) Disparity of gene conversion in frameshift mutants located in locus b2 of Ascobolus immersus. Proceedings 76, 2871-5.

Rossignol J-L, Paquette N (1979) Disparity of gene conversion in frameshift mutants located in locus b2 of Ascobolus immersus. PNAS 76, 2871-5. http://www.pnas.org/cgi/content/abstract/76/6/2871

Rossignol J-L, Paquette N, Nicolas A (1979) Aberrant 4:4 Asci, Disparity in the Direction of Conversion, and Frequencies of Conversion in Ascobolus immersus. Cold Spring Harb Symp Quant Biol 43, 1343-52. http://symposium.cshlp.org/cgi/content/abstract/43/0/1343

Simola LK, LÖNnroth K (1979) The Effect of Some Protein and Non-Protein Amino Acids on the Growth of Cladosporium herbarum and Trichothecium roseum. Physiologia Plantarum 46, 381-7. http://dx.doi.org/10.1111/j.1399-3054.1979.tb02636.x

Decaris B, Francou F, Lefort C, Rizet G (1978) Unstable ascospore color mutants of Ascobolus immersus. i. temporal occurrence and modalities of back mutations.  162, 1.

Kitani Y (1978) ABSENCE OF INTERFERENCE IN ASSOCIATION WITH GENE CONVERSION IN SORDARIA FIMICOLA, AND PRESENCE OF INTERFERENCE IN ASSOCIATION WITH ORDINARY RECOMBINATION. Genetics 89, 467-97. http://www.genetics.org/cgi/content/abstract/89/3/467

Lamb BC, Helmi S (1978) A new type of genetic control of gene conversion, from Ascobolus immersus. Genetical research. 32, 1.

Leblon G, Paquette N (1978) INTRAGENIC SUPPRESSION AT THE b2 LOCUS IN ASCOBOLUS IMMERSUS. I. IDENTIFICATION OF THREE DISTINCT GROUPS OF SUPPRESSION. Genetics 90, 475-88. http://www.genetics.org/cgi/content/abstract/90/3/475

Morpurgo G, Volterra L (1978) Index of Authors

THE NATURE OF MITOTIC INTRAGENIC RECOMBINATION IN ASPERGILLUS NIDULANS. Microbiology 1978, 81-157. http://mic.sgmjournals.org

http://www.genetics.org

Paquette N (1978) Detection of aberrant 4:4 asci in Ascobolus immersus. Canadian journal of genetics and cytology 20, 1.

Paquette N, Rossignol JL (1978) Gene conversion spectrum of 15 mutants giving post meiotic segregation in the b2 locus of Ascobolus immersus.  163, 3.

Rossignol JL, Haedens V (1978) The interaction during recombination between closely linked allelic frameshift mutant sites in Ascobolus immersus I. a (or B) and C type mutant sites. Heredity : 40, 3.

Stadler DR, Kariya B (1978) Index of Authors

INTRAGENIC RECOMBINATION AT THE mtr LOCUS OF NEUROSPORA WITH SEGREGATION AT AN UNSELECTED SITE. Microbiology 1978, 1-79. http://mic.sgmjournals.org

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Wickramaratne MRT, Lamb BC (1978) The estimation of conversion parameters and the control of conversion in Ascobolus immersus.  159, 1.

Bull AT, Trinci APJ, Tempest AHRaDW (1977) The Physiology and Metabolic Control of Fungal Growth. In ‘Advances in Microbial Physiology’ pp. 1-84. (Academic Press). http://www.sciencedirect.com/science/article/pii/S0065291108603148

Ghikas A, Lamb BC (1977) The detection, in unordered octads, of 6+:2m and 2+:6m ratios with postmeiotic segregation, and of aberrant 4:4s, and their use in corresponding site interference studies. Genetical research. 29, 3.

Holden M (1977) The slide collection. Bulletin of the British Mycological Society 11, 18-23. http://www.sciencedirect.com/science/article/pii/S0007152877800242

Lamb B (1977) The use of gene conversion to study synaptinemal complex structure and molecular details of chromatid pairing in meiosis. Mol Gen Genet 157, 31-7.

Lamb BC (1977) The use of gene conversion to study synaptinemal complex structure and molecular details of chromatid pairing in meiosis.  157, 1.

Storms R, Hastings PJ (1977) A fine structure analysis of meiotic pairing in Chlamydomonas reinhardi. Experimental Cell Research 104, 39-46. http://www.sciencedirect.com/science/article/pii/0014482777900660

Clarke CH, Johnston AWB (1976) Intragenic mutational spectra and hot spots. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 36, 147-63. http://www.sciencedirect.com/science/article/pii/0027510776900038

Dicaprio L, Hastings PJ (1976) GENE CONVERSION AND INTRAGENIC RECOMBINATION AT AT THE SUP6 LOCUS AND THE SURROUNDING REGION IN SACCHAROMYCES CEREVISIAE. Genetics 84, 697-721. http://www.genetics.org/cgi/content/abstract/84/4/697

Gutz H, Leslie JF (1976) GENE CONVERSION: A HITHERTO OVERLOOKED PARAMETER IN POPULATION GENETICS. Genetics 83, 861-6. http://www.genetics.org/cgi/content/abstract/83/4/861

Hackett CJ, Chen KC (1976) Ultrastructure of developing ascospores in Sordaria brevicollis. J. Bacteriol. 126, 883-94. http://jb.asm.org/cgi/content/abstract/126/2/883

Heywood P, Magee PT (1976) Meiosis in protists. Some structural and physiological aspects of meiosis in algae, fungi, and protozoa. Microbiol. Mol. Biol. Rev. 40, 190-240. http://mmbr.asm.org

KlaŠTerskÁ I (1976) A new look on the role of the diffuse stage in problems of plant and animal meiosis. Hereditas 82, 193-203. http://dx.doi.org/10.1111/j.1601-5223.1976.tb01557.x

Kubai DF, G.H. Bourne JFDaKWJ (1976) The Evolution of the Mitotic Spindle. In ‘International Review of Cytology’ pp. 167-227. (Academic Press). http://www.sciencedirect.com/science/article/pii/S0074769608600698

Mekki-Berrada A, Rossignol J, Paquette N (1976) [High frequency reversion of a spontaneous mutant in Ascobolus immersus]. C R Acad Sci Hebd Seances Acad Sci D 283, 971-4.

Mekki-Berrada A, Rossignol JL, Paquette N (1976) High frequency reversion of a spontaneous mutant in Ascobolus immersus. Haute frequence de reversion d’un mutant spontane chez Ascobolus immersus. Comptes rendus hebdomadaires des seances. Serie D. Sciences naturelles 283, 8.

Tyson K, Griffiths DA (1976) Developmental morphology and fine strucutre of Placoasterella baileyi: II. Ascus and ascospore development. Transactions of the British Mycological Society 66, 263-79. http://www.sciencedirect.com/science/article/pii/S0007153676800538

Anonymous (1975) Author index. Transactions of the British Mycological Society 65, 571-3. http://www.sciencedirect.com/science/article/pii/S0007153675800672

Hamelin C, Cousineau G (1975) [Differences in RNA related to the intersterility of wild type strains of Ascobolus immersus (author’s transl)]. Experientia 31, 920-1.

Hamelin C, Cousineau G (1975) Differences in RNA content related to mating type in Ascobolus immersus. Experientia 31, 638-9.

Hamelin C, Cousineau GH (1975) Differences in RNA content related to mating type in Ascobolus immersus. Experientia 31, 6.

Hamelin C, Cousineau GH (1975) Differences in RNA related to the intersterility of wild type strains of Ascobolus immersus. Relation entre le contenu en ARN et l’intersterilite de souches sauvages d’Ascobolus immersus. Experientia 31, 8.

Koltin Y, Stamberg J, Ronen R (1975) Meiosis as a source of spontaneous mutations in Schizophyllum commune. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 27, 319-25. http://www.sciencedirect.com/science/article/pii/0027510775902882

Lewis LA (1975) Effect of visible light on the partial synchronization of meiosis in Ascobolus immersus. Transactions of the British Mycological Society 65, 148-52, IN30. http://www.sciencedirect.com/science/article/pii/S0007153675801951

Lindgren DAG (1975) Sensitivity of premeiotic and meiotic stages to spontaneous and induced mutations in barley and maize. Hereditas 79, 227-37. http://dx.doi.org/10.1111/j.1601-5223.1975.tb01479.x

Meselson MS, Radding CM (1975) A general model for genetic recombination. PNAS 72, 358-61. http://www.pnas.org/cgi/content/abstract/72/1/358

Moore CW, Sherman F (1975) ROLE OF DNA SEQUENCES IN GENETIC RECOMBINATION IN THE ISO-1-CYTOCHROME c GENE OF YEAST. I. DISCREPANCIES BETWEEN PHYSICAL DISTANCES AND GENETIC DISTANCES DETERMINED BY FIVE MAPPING PROCEDURES. Genetics 79, 397-418. http://www.genetics.org/cgi/content/abstract/79/3/397

Nelson OE (1975) THE WAXY LOCUS IN MAIZE III. EFFECT OF STRUCTURAL HETEROZYGOSITY ON INTRAGENIC RECOMBINATION AND FLANKING MARKER ASSORTMENT. Genetics 79, 31-44. http://www.genetics.org/cgi/content/abstract/79/1/31

Reid DA (1975) Rozites caperatus (Pers. Ex Fr.) Karst. in Southern England. Transactions of the British Mycological Society 65, 146-8. http://www.sciencedirect.com/science/article/pii/S000715367580194X

Anonymous (1974) Author index. Transactions of the British Mycological Society 63, 635-8. http://www.sciencedirect.com/science/article/pii/S0007153674801270

Girard J, Rossignol JL (1974) THE SUPPRESSION OF GENE CONVERSION AND INTRAGENIC CROSSING OVER IN ASCOBOLUS IMMERSUS: EVIDENCE FOR MODIFIERS ACTING IN THE HETEROZYGOUS STATE. Genetics 76, 221-43. http://www.genetics.org/cgi/content/abstract/76/2/221

Hamelin C, Cousineau G (1974) RNA variants in ascobolus immersus. Rev Can Biol 33, 249-54.

Hamelin C, Cousineau G (1974) Characterization of RNA populations in Ascobolus immersus, Sordaria Fimicola and Podospora anserina. Rev Can Biol 33, 243-7.

Hamelin C, Cousineau G (1974) A comparative study of the production of RNA by round spore mutations in Ascobolus immersus. Can J Genet Cytol 16, 39-48.

Hamelin C, Cousineau GH (1974) Characterization of RNA populations in Ascobolus immersus, Sordaria fimicola and Podospora anserina. Revue canadienne de biologie 33, 4.

Hamelin C, Cousineau GH (1974) A comarative study of the production of RNA by round spore mutations in Ascobolus immersus. Canadian journal of genetics and cytology 16, 1.

Holliday R (1974) MOLECULAR ASPECTS OF GENETIC EXCHANGE AND GENE CONVERSION. Genetics 78, 273-87. http://www.genetics.org

Lamb B, Wickramaratne M (1974) Corresponding-site interference, synaptinemal complex structure, and 8+:0m and 7+:1m octads from wild-type x mutant crosses of Ascobolus immersus. J Chem Soc Perkin 1 1, 113-24.

Lewis LA, Decaris B (1974) The induction of apothecial formation in Ascobolus immersus by a spermatization technique. Transactions of the British Mycological Society 63, 197-9. http://www.sciencedirect.com/science/article/pii/S0007153674801567

O’DONNELL KL, TAI W, BENEKE ES (1974) Nuclear Behaviour and Spindle-pole Bodies During Ascosporogenesis in Peziza quelepidotia. Microbiology 81, 303-14. http://mic.sgmjournals.org/cgi/content/abstract/81/2/303

Pearson V (1974) Virulence and cellulolytic enzyme activity of isolates of Gaeumannomyces graminis. Transactions of the British Mycological Society 63, 199-202. http://www.sciencedirect.com/science/article/pii/S0007153674801579

Rosazza JP (1974) Biotransformations and Fermentations. Science 183, 1217-8. http://www.sciencemag.org

Skalka A, Weissbach A, Bartl P (1974) Genetic Recombination: Genetic, Physical, and Biochemical Aspects. Science 183, 1218-9. http://www.sciencemag.org

Whitehouse HLK (1974) ADVANCES IN RECOMBINATION RESEARCH. Genetics 78, 237-45. http://www.genetics.org

Lamb BC, Wickramaratne MRT (1973) Corresponding-site interference, synaptinemal complex structure, and 8+:0m and 7 + :1m octads from wild-type x mutant crosses of Ascobolus immersus. Genetical research. 22, 1.

Leblon G, Rossignol J (1973) Mechanism of gene conversion in Ascobolus immersus. 3. The interaction of heteroallelas in the conversion process. Mol Gen Genet 122, 165-82.

Singh N, Webster J (1973) Antagonism between stilbella erythrocephala and other coprophilous fungi. Transactions of the British Mycological Society 61, 487-95, IN3. http://www.sciencedirect.com/science/article/pii/S0007153673801184

Sobell HM, Caspari EW (1973) Symmetry in Protein-Nucleic Acid Interaction and Its Genetic Implications. In ‘Advances in Genetics’ pp. 411-90. (Academic Press). http://www.sciencedirect.com/science/article/pii/S0065266008601753

Alloway JM, Wilson IM (1972) Fine structure of spore degeneration in Podospora arizonensis. Transactions of the British Mycological Society 58, 231-6, IN8-IN10. http://www.sciencedirect.com/science/article/pii/S0007153672801529

Bareyre MJ, Nguyen Van H (1972) Nuclear interactions and growth rhythms of Ascobolus immersus Pers. Interactions nucleaires et rythmes de croissance chez l’Ascobolus immersus Pers. July/Sept 13, 3.

Hopwood DA, Ribbons JRNaDW (1972) Chapter II Genetic Analysis in Micro-organisms. In ‘Methods in Microbiology’ pp. 29-158. (Academic Press). http://www.sciencedirect.com/science/article/pii/S0580951708706287

Leblon G (1972) Mechanism of gene conversion in Ascobolus immersus. II. The relationships between the genetic alterations in b 1 or b 2 mutants and their conversion spectrum. Mol Gen Genet 116, 322-35.

Leblon G (1972) Mechanism of gene conversion in Ascobolus immersus. I. Existence of a correlation between the origin of mutants induced by different mutagens and their conversion spectrum.  115, 1.

Paszewski A, Prazmo W (1972) [Intragenic recombination in eukaryots in the light of studies of the fungus Ascobolus immersus. Intragenic and intergenic recombination]. Postepy Hig Med Dosw 26, 685-703.

Richardson MJ (1972) Coprophilous ascomycetes on different dung types. Transactions of the British Mycological Society 58, 37-48. http://www.sciencedirect.com/science/article/pii/S000715367280069X

Rossingnol JL, Leblon G (1972) Are there two distinct processes leading to genic conversion? Existe-t-il deux processus distincts aboutissant a la conversion genique. Dec 275, 25.

Sobell HM (1972) Molecular Mechanism for Genetic Recombination. PNAS 69, 2483-7. http://www.pnas.org/cgi/content/abstract/69/9/2483

Bourret JA, Lincoln RG, Carpenter BH (1971) Modification of the Period of a Noncircadian Rhythm in Nectria cinnabarina. Plant Physiology 47, 682-4. http://www.plantphysiol.org/cgi/content/abstract/47/5/682

Chovnick A, Ballantyne GH, Holm DG (1971) STUDIES ON GENE CONVERSION AND ITS RELATIONSHIP TO LINKED EXCHANGE IN DROSOPHILA MELANOGASTER. Genetics 69, 179-209. http://www.genetics.org

Gutz H (1971) SITE SPECIFIC INDUCTION OF GENE CONVERSION IN SCHIZOSACCHAROMYCES POMBE. Genetics 69, 317-37. http://www.genetics.org

KlÁŠTerskÁ I (1971) New phenomena during meiosis in the genus Rosa. Hereditas 67, 55-63. http://dx.doi.org/10.1111/j.1601-5223.1971.tb02358.x

Makarewicz A (1971) Colorless facultative mutants of Ascobolus immersus.  12, 3.

Paszewski A, Prazmo W, Jaszczuk E (1971) Multiple recombinational events within the 84W locus of Ascobolus immersus. Genet Res 18, 199-214.

Stadler DR, Towe AM (1971) EVIDENCE FOR MEIOTIC RECOMBINATION IN ASCOBOLUS INVOLVING ONLY ONE MEMBER OF A TETRAD. Genetics 68, 401-13. http://www.genetics.org

Anonymous (1970) ADDENDUM. Biological Reviews 45, 313-5. http://dx.doi.org/10.1111/j.1469-185X.1970.tb01634.x

Adondi G, Heslot H (1970) Étude des conversions mitotoques au niveau du géne ad-9 de Schizosaccharomyces pombe. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 9, 41-58. http://www.sciencedirect.com/science/article/pii/0027510770900692

Bandiera M, Morpurgo G, Volterra L (1970) “Barriers” in intragenic mitotic crossing-over. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 9, 213-7. http://www.sciencedirect.com/science/article/pii/002751077090059X

Baranowska H (1970) Intragenic recombination pattern within the 164 locus of Ascobolus immersus in the presence of outside markers. Genet Res 16, 185-206.

Chovnick A, Ballantyne GH, Baillie DL, Holm DG (1970) GENE CONVERSION IN HIGHER ORGANISMS: HALF-TETRAD ANALYSIS OF RECOMBINATION WITHIN THE ROSY CISTRON OF DROSOPHILA MELANOGASTER. Genetics 66, 315-29. http://www.genetics.org

Greenhalgh GN, Griffiths HB (1970) The ascus vesicle. Transactions of the British Mycological Society 54, 489-92, IN13. http://www.sciencedirect.com/science/article/pii/S000715367080167X

Laane MM (1970) Nuclear behaviour during meiosis and ascus formation in Penicillium striatum. Hereditas 65, 133-57. http://dx.doi.org/10.1111/j.1601-5223.1970.tb02311.x

Leblon G (1970) On the existence of a correlation between a mutagenic agent and the spectrum of mutations induced in Ascobolus immersus. Sur l’existence d’une correlation entre l’agent mutagene et le spectre de conversions des mutants induits chez l’Ascobolus immersus. July 271, 2.

Pant DC, Tewari VP (1970) Korfiella, a new genus of sarcoscyphaceae. Transactions of the British Mycological Society 54, 492-5, IN14. http://www.sciencedirect.com/science/article/pii/S0007153670801681

Ribbons JRNaDW (1970) Subject Index. In ‘Methods in Microbiology’ pp. 473-505. (Academic Press). http://www.sciencedirect.com/science/article/pii/S0580951708705476

Stadler DR, Towe AM, Rossignol J-L (1970) INTRAGENIC RECOMBINATION OF ASCOSPORE COLOR MUTANTS IN ASCOBOLUS AND ITS RELATIONSHIP TO THE SEGREGATION OF OUTSIDE MARKERS. Genetics 66, 429-47. http://www.genetics.org

Webster J (1970) Presidential address: Coprophilous fungi. Transactions of the British Mycological Society 54, IN1, 161-80. http://www.sciencedirect.com/science/article/pii/S0007153670800304

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Wildenberg J (1970) THE RELATION OF MITOTIC RECOMBINATION TO DNA REPLICATION IN YEAST PEDIGREES. Genetics 66, 291-304. http://www.genetics.org

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