| A genetic basis for a postmeiotic X versus Y chromosome intragenomic conflict in the mouse. Cocquet J., Ellis P.J., Mahadevaiah S.K., Affara N.A., Vaiman D., Burgoyne P.S.
PLoS Genet. 8:e1002900-e1002900(2012) · Mapped (3) |
| Deficiency in the multicopy Sycp3-like X-linked genes Slx and Slxl1 causes major defects in spermatid differentiation. Cocquet J., Ellis P.J., Yamauchi Y., Riel J.M., Karacs T.P., Rattigan A., Ojarikre O.A., Affara N.A., Ward M.A., Burgoyne P.S.
Mol. Biol. Cell 21:3497-3505(2010) · Mapped (2) |
| The human RPS4 paralogue on Yq11.223 encodes a structurally conserved ribosomal protein and is preferentially expressed during spermatogenesis. Lopes A.M., Miguel R.N., Sargent C.A., Ellis P.J., Amorim A., Affara N.A.
BMC Mol. Biol. 11:33-33(2010) · Mapped (1) |
| Transcriptional profiling of luteinizing hormone receptor-deficient mice before and after testosterone treatment provides insight into the hormonal control of postnatal testicular development and Leydig cell differentiation. Griffin D.K., Ellis P.J., Dunmore B., Bauer J., Abel M.H., Affara N.A.
Biol. Reprod. 82:1139-1150(2010) · Mapped (1) |
| The multicopy gene Sly represses the sex chromosomes in the male mouse germline after meiosis. Cocquet J., Ellis P.J., Yamauchi Y., Mahadevaiah S.K., Affara N.A., Ward M.A., Burgoyne P.S.
PLoS Biol. 7:e1000244-e1000244(2009) · Mapped (4) |
| Hypogonadal mouse, a model to study the effects of the endogenous lack of gonadotropins on apoptosis. Chausiaux O.E., Abel M.H., Baxter F.O., Khaled W.T., Ellis P.J., Charlton H.M., Affara N.A.
Biol. Reprod. 78:77-90(2008) · Mapped (3) |
| Gene expression study in the juvenile mouse testis: identification of stage-specific molecular pathways during spermatogenesis. Clemente E.J., Furlong R.A., Loveland K.L., Affara N.A.
Mamm. Genome 17:956-975(2006) · Mapped (7) |
| Identification of novel Y chromosome encoded transcripts by testis transcriptome analysis of mice with deletions of the Y chromosome long arm. Toure A., Clemente E.J., Ellis P., Mahadevaiah S.K., Ojarikre O.A., Ball P.A., Reynard L., Loveland K.L., Burgoyne P.S., Affara N.A.
Genome Biol. 6:R102-R102(2005) · Mapped (4) |
| A comparative analysis of the pig, mouse, and human PCDHX genes. Blanco-Arias P., Sargent C.A., Affara N.A.
Mamm. Genome 15:296-306(2004) · UniProtKB (1) · Mapped (13) |
| Protocadherin X (PCDHX) and Y (PCDHY) genes; multiple mRNA isoforms encoding variant signal peptides and cytoplasmic domains. Blanco-Arias P., Sargent C.A., Affara N.A.
Mamm. Genome 15:41-52(2004) · UniProtKB (13) |
| Usp9y (ubiquitin-specific protease 9 gene on the Y) is associated with a functional promoter and encodes an intact open reading frame homologous to Usp9x that is under selective constraint. Hall N.M., Brown G.M., Furlong R.A., Sargent C.A., Mitchell M., Rocha D., Affara N.A.
Mamm. Genome 14:437-447(2003) · Mapped (11) |
| A mapping and evolutionary study of porcine sex chromosome genes. Quilter C.R., Blott S.C., Mileham A.J., Affara N.A., Sargent C.A., Griffin D.K.
Mamm. Genome 13:588-594(2002) · Mapped (3) |
| The human-specific Yp11.2/Xq21.3 homology block encodes a potentially functional testis-specific TGIF-like retroposon. Blanco-Arias P., Sargent C.A., Affara N.A.
Mamm. Genome 13:463-468(2002) · UniProtKB (2) |
| A novel poly(A)-binding protein gene (PABPC5) maps to an X-specific subinterval in the Xq21.3/Yp11.2 homology block of the human sex chromosomes. Blanco P., Sargent C.A., Boucher C.A., Howell G., Ross M., Affara N.A.
Genomics 74:1-11(2001) · UniProtKB (10) · Mapped (1) |
| Comparative sequence analysis of the VHL tumor suppressor gene. Woodward E.R., Buchberger A., Clifford S.C., Hurst L.D., Affara N.A., Maher E.R.
Genomics 65:253-265(2000) · Mapped (2) |
| Five cases of isolated glycerol kinase deficiency, including two families: failure to find genotype:phenotype correlation. Sargent C.A., Kidd A., Moore S., Dean J., Besley G.T.N., Affara N.A.
J. Med. Genet. 37:434-441(2000) · UniProtKB (1) |
| Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolution. Ehrmann I.E., Ellis P.S., Mazeyrat S., Duthie S., Brockdorff N., Mattei M.-G., Gavin M.A., Affara N.A., Brown G.M., Simpson E. et al.
Hum. Mol. Genet. 7:1725-1737(1998) · UniProtKB (3) · Mapped (35) |
| The mouse Y chromosome interval necessary for spermatogonial proliferation is gene dense with syntenic homology to the human AZFa region. Mazeyrat S., Saut N., Sargent C.A., Grimmond S., Longepied G., Ehrmann I.E., Ellis P.S., Greenfield A., Affara N.A., Mitchell M.J.
Hum. Mol. Genet. 7:1713-1724(1998) · UniProtKB (2) · Mapped (27) |
| A potential human axonemal dynein heavy-chain gene maps to 17q25. Milisav I., Affara N.A.
Mamm. Genome 9:404-407(1998) · UniProtKB (1) |
| Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene. Brown G.M., Furlong R.A., Sargent C.A., Erickson R.P., Longepied G., Mitchell M., Jones M.H., Hargreave T.B., Cooke H.J., Affara N.A.
Hum. Mol. Genet. 7:97-107(1998) · UniProtKB (1) · Mapped (15) |
| Mapping, sequence, and expression analysis of the human fertilin beta gene (FTNB). Burkin H.R., Burkin D.J., Davey P.M., Griffin D.K., Affara N.A.
Genomics 40:190-192(1997) · UniProtKB (1) |
| Germline mutations in the von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Zbar B., Kishida T., Chen F., Schmidt L., Maher E.R., Richards F.M., Crossey P.A., Webster A.R., Affara N.A., Ferguson-Smith M.A. et al.
Hum. Mutat. 8:348-357(1996) · UniProtKB (1) |
| The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2. Jones M.H., Furlong R.A., Burkin H., Chalmers I.J., Brown G.M., Khwaja O., Affara N.A.
Hum. Mol. Genet. 5:1695-1701(1996) · UniProtKB (2) |
| Characterization of a novel human dynein-related gene that is specifically expressed in testis. Milisav I., Jones M.H., Affara N.A.
Mamm. Genome 7:667-672(1996) · UniProtKB (1) |
| Characterization of a kinesin-related gene ATSV, within the tuberous sclerosis locus (TSC1) candidate region on chromosome 9q34. Furlong R.A., Zhou C.Y., Ferguson-Smith M.A., Affara N.A.
Genomics 33:421-429(1996) · UniProtKB (1) |
