12
results
for author:"Carrel L."
in Literature Citations
| Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus. Li N., Carrel L. Proc. Natl. Acad. Sci. U.S.A. 105:17055-17060(2008) · Mapped (7) |
| The DNA sequence of the human X chromosome. Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al. Nature 434:325-337(2005) · UniProtKB (1,199) |
| An adjacent pair of human NUDT genes on chromosome X are preferentially expressed in testis and encode two new isoforms of diphosphoinositol polyphosphate phosphohydrolase. Hidaka K., Caffrey J.J., Hua L., Zhang T., Falck J.R., Nickel G.C., Carrel L., Barnes L.D., Shears S.B. J. Biol. Chem. 277:32730-32738(2002) · UniProtKB (2) |
| A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda. Tiller G.E., Hannig V.L., Dozier D., Carrel L., Trevarthen K.C., Wilcox W.R., Mundlos S., Haines J.L., Gedeon A.K., Gecz J. Am. J. Hum. Genet. 68:1398-1407(2001) · Mapped (1) |
| The UTX gene escapes X inactivation in mice and humans. Greenfield A., Carrel L., Pennisi D., Phillippe C., Quaderi N., Siggers P., Steiner K., Tam P.P.L., Monaco A.P., Willard H.F. et al. Hum. Mol. Genet. 7:737-742(1998) · UniProtKB (1) · Mapped (11) |
| The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Zotto L.D., Quaderi N.A., Elliott R., Lingerfelter P.A., Carrel L., Valsecchi V., Montini E., Yen C.-H., Chapman V., Kalcheva I. et al. Hum. Mol. Genet. 7:489-499(1998) · UniProtKB (1) · Mapped (3) |
| Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene. Carrel L., Hunt P.A., Willard H.F. Hum. Mol. Genet. 5:1361-1366(1996) · Mapped (6) |
| X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. Carrel L., Clemson C.M., Dunn J.M., Miller A.P., Hunt P.A., Lawrence J.B., Willard H.F. Hum. Mol. Genet. 5:391-401(1996) · Mapped (7) |
| A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status. Coleman M.P., Ambrose H.J., Carrel L., Nemeth A.H., Willard H.F., Davies K.E. Genomics 31:135-138(1996) · UniProtKB (1) |
| Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies. Greig G.M., Sharp C.B., Carrel L., Willard H.F. Hum. Mol. Genet. 2:1611-1618(1993) · UniProtKB (2) |
| A novel transmembrane transporter encoded by the XPCT gene in Xq13.2. Lafreniere R.G., Carrel L., Willard H.F. Hum. Mol. Genet. 3:1133-1140(1994) · UniProtKB (1) |
| The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation. Sultana R., Adler D.A., Edelhoff S., Carrel L., Lee K.H., Chapman V.C., Willard H.F., Disteche C.M. Hum. Mol. Genet. 4:257-263(1995) · Mapped (21) |
