Experts and Doctors on y chromosome in Paris, Île de France, France

Summary

Locale: Paris, Île de France, France
Topic: y chromosome

Top Publications

  1. Mitchell M, Simon D, Affara N, Ferguson Smith M, Avner P, Bishop C. Localization of murine X and autosomal sequences homologous to the human Y located testis-determining region. Genetics. 1989;121:803-9 pubmed
    ..Comparative mapping indicates that in man these genes lie in separate conserved DNA segments. ..
  2. Roberts C, Weith A, Passage E, Michot J, Mattei M, Bishop C. Molecular and cytogenetic evidence for the location of Tdy and Hya on the mouse Y chromosome short arm. Proc Natl Acad Sci U S A. 1988;85:6446-9 pubmed
    ..Based on these results, we propose a model for the generation of the original Sxr region and the Sxr' and Sxr719 variants. ..
  3. Hassanin A, An J, Ropiquet A, Nguyen T, Couloux A. Combining multiple autosomal introns for studying shallow phylogeny and taxonomy of Laurasiatherian mammals: Application to the tribe Bovini (Cetartiodactyla, Bovidae). Mol Phylogenet Evol. 2013;66:766-75 pubmed publisher
    ..We compared our molecular dating estimates to the fossil record in order to propose a biogeographic scenario for the evolution of Bovini during the Neogene. ..
  4. Slim R, Levilliers J, Ludecke H, Claussen U, Nguyen V, Gough N, et al. A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivation. Genomics. 1993;16:26-33 pubmed
    ..This gene is transcribed from the Y chromosome and from the active and inactive X chromosomes. This gene thus escapes X-inactivation as predicted for genes belonging to the pseudoautosomal region. ..
  5. Dutrillaux A, Dutrillaux B. Evolution of the Sex Chromosomes in Beetles. I. The Loss of the Y Chromosome. Cytogenet Genome Res. 2017;152:97-104 pubmed publisher
    ..In conclusion, following Y chromosome loss, various strategies using nucleolar proteins have been developed to facilitate the migration of the unique X at meiotic anaphase I. ..
  6. Cocquet J, Ellis P, Mahadevaiah S, Affara N, Vaiman D, Burgoyne P. A genetic basis for a postmeiotic X versus Y chromosome intragenomic conflict in the mouse. PLoS Genet. 2012;8:e1002900 pubmed publisher
    ..It also provides a biological basis for the concept that intragenomic conflict is an important evolutionary force which impacts on gene expression, genome structure, and speciation...
  7. Dutrillaux A, Mercier J, Dutrillaux B. X-Y-autosome translocation, chromosome compaction, NOR expression and heterochromatin insulation in the Scarabaeid beetle Dynastes hercules hercules. Cytogenet Genome Res. 2007;116:305-10 pubmed
  8. Morey C, Navarro P, Debrand E, Avner P, Rougeulle C, Clerc P. The region 3' to Xist mediates X chromosome counting and H3 Lys-4 dimethylation within the Xist gene. EMBO J. 2004;23:594-604 pubmed
    ..Our results raise the possibility that H3 Lys-4 dimethylation within Xist may be functionally implicated in the counting process...
  9. Belin V, Cusin V, Viot G, Girlich D, Toutain A, Moncla A, et al. SHOX mutations in dyschondrosteosis (Leri-Weill syndrome). Nat Genet. 1998;19:67-9 pubmed
    ..Here, we report large-scale deletions (in seven families) and a nonsense mutation (in one family) of SHOX in patients with DCS and show that Langer mesomelic dwarfism results from homozygous mutations at the DCS locus. ..

More Information

Publications17

  1. Veitia R, Ion A, Barbaux S, Jobling M, Souleyreau N, Ennis K, et al. Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype. Hum Genet. 1997;99:648-52 pubmed
    ..In addition, two Y-specific polymorphisms were found 5' to the SRY gene, and a sequence variant was identified 3' to the SRY polyadenylation site. No duplications of the DSS region in 20 of these patients were detected. ..
  2. Calenda A, Allenet B, Escalier D, Bach J, Garchon H. The meiosis-specific Xmr gene product is homologous to the lymphocyte Xlr protein and is a component of the XY body. EMBO J. 1994;13:100-9 pubmed
    ..The Xmr protein provides a new tool for the investigation of sex chromosome behaviour during meiosis in mammals. ..
  3. Leroy P, Seboun E, Mattei M, Fellous M, Bishop C. Testis-specific transcripts detected by a human Y-DNA-derived probe. Development. 1987;101 Suppl:177-83 pubmed
    ..This cDNA, designated PL10, detects a mRNA of approximately 4 kb which is highly expressed in mouse testis, but not in male or female mouse liver. The gene corresponding to this cDNA is also well conserved among vertebrates. ..
  4. Bishop C, Roberts C, Michot J, Nagamine C, Winking H, Guenet J, et al. The use of specific DNA probes to analyse the Sxr mutation in the mouse. Development. 1987;101 Suppl:167-75 pubmed
    ..Finally, using an Sxr-specific probe we can define multiple Y-chromosome haplotypes in the mouse showing that the region is evolving very rapidly. ..
  5. Siffroi J, Le Bourhis C, Krausz C, Barbaux S, Quintana Murci L, Kanafani S, et al. Sex chromosome mosaicism in males carrying Y chromosome long arm deletions. Hum Reprod. 2000;15:2559-62 pubmed
    ..Moreover, two isodicentric Y chromosomes, classified as normal by cytogenetic methods, were detected. Therefore, Yq microdeletions may be associated with Y chromosomal instability leading to the formation of 45,XO cell lines...
  6. Pailhoux E, Vigier B, Chaffaux S, Servel N, Taourit S, Furet J, et al. A 11.7-kb deletion triggers intersexuality and polledness in goats. Nat Genet. 2001;29:453-8 pubmed publisher
    ..These two genes are located 20 and 200 kb telomeric from the deletion, respectively...
  7. Comptour A, Moretti C, Serrentino M, Auer J, Ialy Radio C, Ward M, et al. SSTY proteins co-localize with the post-meiotic sex chromatin and interact with regulators of its expression. FEBS J. 2014;281:1571-84 pubmed publisher
    ..As Slx/Slxl1 and Sly genes have been shown to be involved in the XY intra-genomic conflict, which affects the offspring sex ratio, Ssty may constitute another player in this conflict...
  8. del Castillo I, Cohen Salmon M, Blanchard S, Lutfalla G, Petit C. Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome. Nat Genet. 1992;2:305-10 pubmed