22 results for author:"Ferguson-Smith M.A." in Literature citations
Results Customize
› Repeat search in UniProtKB (51)
| Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1. Goudie D.R., D'Alessandro M., Merriman B., Lee H., Szeverenyi I., Avery S., O'Connor B.D., Nelson S.F., Coats S.E., Stewart A. et al. |
| Chromosome mapping of H1 histone and 5S rRNA gene clusters in three species of Astyanax (Teleostei, Characiformes). Hashimoto D.T., Ferguson-Smith M.A., Rens W., Foresti F., Porto-Foresti F. Cytogenet. Genome Res. 134:64-71(2011) · UniProtKB (3) |
| Geographic patterns of inversion polymorphisms in a wild African rodent, Mastomys erythroleucus. Dobigny G., Catalan J., Gauthier P., O'Brien P.C., Brouat C., Ba K., Tatard C., Ferguson-Smith M.A., Duplantier J.M., Granjon L. et al. Heredity (Edinb) 104:378-386(2010) · UniProtKB (25) |
| Sex determination in platypus and echidna: autosomal location of SOX3 confirms the absence of SRY from monotremes. Wallis M.C., Waters P.D., Delbridge M.L., Kirby P.J., Pask A.J., Grutzner F., Rens W., Ferguson-Smith M.A., Graves J.A. Chromosome Res. 15:949-959(2007) · UniProtKB (1) |
| Emergence of complex rearrangements at translocation breakpoints in a transgenic mouse; implications for mechanisms involved in the formation of chromosome rearrangements. Kasai F., Yoshihara M., Matsukuma S., O'Brien P., Ferguson-Smith M.A. Cytogenet. Genome Res. 119:83-90(2007) · UniProtKB (2) · Mapped (17) |
| Mapping platypus SOX genes; autosomal location of SOX9 excludes it from sex determining role. Wallis M.C., Delbridge M.L., Pask A.J., Alsop A.E., Grutzner F., O'Brien P.C., Rens W., Ferguson-Smith M.A., Graves J.A. Cytogenet. Genome Res. 116:232-234(2007) · UniProtKB (2) |
| Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome. Borg I., Freude K., Kubart S., Hoffmann K., Menzel C., Laccone F., Firth H., Ferguson-Smith M.A., Tommerup N., Ropers H.H. et al. Eur. J. Hum. Genet. 13:921-927(2005) · Mapped (12) |
| In the platypus a meiotic chain of ten sex chromosomes shares genes with the bird Z and mammal X chromosomes. Grutzner F., Rens W., Tsend-Ayush E., El-Mogharbel N., O'Brien P.C., Jones R.C., Ferguson-Smith M.A., Marshall Graves J.A. Nature 432:913-917(2004) · UniProtKB (2) |
| Disruption of the neuronal PAS3 gene in a family affected with schizophrenia. Kamnasaran D., Muir W.J., Ferguson-Smith M.A., Cox D.W. J. Med. Genet. 40:325-332(2003) · UniProtKB (1) |
| Comparative mapping of human Chromosome 14q11.2-q13 genes with mouse homologous gene regions. Kamnasaran D., O'Brien P.C., Ferguson-Smith M.A., Cox D.W. Mamm. Genome 11:993-999(2000) · Mapped (7) |
| Use of flow-sorted canine chromosomes in the assignment of canine linkage, radiation hybrid, and syntenic groups to chromosomes: refinement and verification of the comparative chromosome map for dog and human. Sargan D.R., Yang F., Squire M., Milne B.S., O'Brien P.C., Ferguson-Smith M.A. Genomics 69:182-195(2000) · Mapped (7) |
| 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) |
| 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) |
| Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue. Sargent C.A., Affara N.A., Bentley E., Pelmear A., Bailey D.M.D., Davey P., Dow D., Leversha M., Aplin H., Besley G.T.N. et al. Hum. Mol. Genet. 2:97-106(1993) · UniProtKB (1) · Mapped (1) |
| Identification of the von Hippel-Lindau disease tumor suppressor gene. Latif F., Tory K., Gnarra J., Yao M., Duh F.-M., Orcutt M.L., Stackhouse T., Kuzmin I., Modi W., Geil L. et al. Science 260:1317-1320(1993) · UniProtKB (1) |
| Duplicated KOX zinc finger gene clusters flank the centromere of human chromosome 10: evidence for a pericentric inversion during primate evolution. Tunnacliffe A., Liu L., Moore J.K., Leversha M.A., Jackson M.S., Ferguson-Smith M.A., Thiesen H.-J., Ponder B.A. Nucleic Acids Res. 21:1409-1417(1993) · UniProtKB (4) |
| Analysis of the SRY gene in 22 sex-reversed XY females identifies four new point mutations in the conserved DNA binding domain. Affara N.A., Chalmers I.J., Ferguson-Smith M.A. Hum. Mol. Genet. 2:785-789(1993) · UniProtKB (1) |
| The glycerol kinase gene family: structure of the Xp gene, and related intronless retroposons. Sargent C.A., Young C., Marsh S., Ferguson-Smith M.A., Affara N.A. Hum. Mol. Genet. 3:1317-1324(1994) · UniProtKB (3) |
| Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. Crossey P.A., Richards F.M., Foster K., Green J.S., Prowse A., Latif F., Lerman M.I., Zbar B., Affara N.A., Ferguson-Smith M.A. et al. Hum. Mol. Genet. 3:1303-1308(1994) · UniProtKB (1) |
| Evidence for distinguishable transcripts of the putative testis determining gene (ZFY) and mapping of homologous cDNA sequences to chromosomes X,Y and 9. Affara N.A., Chambers D., O'Brien J., Habeebu S.S.M., Kalaitsidaki M., Bishop C.E., Ferguson-Smith M.A. Nucleic Acids Res. 17:2987-2999(1989) · UniProtKB (1) |
| Comparison of ZFY and ZFX gene structure and analysis of alternative 3' untranslated regions of ZFY. North M., Sargent C., O'Brien J., Taylor K., Wolfe J., Affara N.A., Ferguson-Smith M.A. Nucleic Acids Res. 19:2579-2586(1991) · UniProtKB (2) |
| The X-Y homologous gene amelogenin maps to the short arms of both the X and Y chromosomes and is highly conserved in primates. Bailey D.M., Affara N.A., Ferguson-Smith M.A. Genomics 14:203-205(1992) · Mapped (3) |