-
1
-
-
0029278906
-
The origin and function of the mammalian Y chromosome and Y-borne genes - An evolving understanding
-
Graves, J.A.M. (1995) The origin and function of the mammalian Y chromosome and Y-borne genes - an evolving understanding. BioEssays, 17, 311-320.
-
(1995)
BioEssays
, vol.17
, pp. 311-320
-
-
Graves, J.A.M.1
-
2
-
-
84995840997
-
A syndrome of infantilism, congenital webbed neck, and cubitus valgus
-
Turner, H.H. (1938) A syndrome of infantilism, congenital webbed neck, and cubitus valgus. Endocrinology, 23, 566-574.
-
(1938)
Endocrinology
, vol.23
, pp. 566-574
-
-
Turner, H.H.1
-
3
-
-
0029021639
-
Turner syndrome and female sex chromosome aberrations: Deduction of the principal factors involved in the development of clinical features
-
Ogata, T. and Matsuo, N. (1995) Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features. Hum. Genet., 95, 607-629.
-
(1995)
Hum. Genet.
, vol.95
, pp. 607-629
-
-
Ogata, T.1
Matsuo, N.2
-
5
-
-
0022370034
-
Perinatal oocyte loss in XO mice and its implications for the aetiology of gonadal dysgenesis in XO women
-
Burgoyne, P.S. and Baker T.G. (1985) Perinatal oocyte loss in XO mice and its implications for the aetiology of gonadal dysgenesis in XO women. J. Reprod. Fertil., 75, 633-645.
-
(1985)
J. Reprod. Fertil.
, vol.75
, pp. 633-645
-
-
Burgoyne, P.S.1
Baker, T.G.2
-
6
-
-
0025732099
-
Survival of XO mouse fetuses: Effect of parental origin of the X chromosome or uterine environment
-
Hunt, P.A. (1991) Survival of XO mouse fetuses: effect of parental origin of the X chromosome or uterine environment. Development, 111, 1137-1141.
-
(1991)
Development
, vol.111
, pp. 1137-1141
-
-
Hunt, P.A.1
-
7
-
-
76549210828
-
Karyotype-phenotype correlations in gonadal dysgenesis and their bearing on the pathogenesis of malformations
-
Ferguson-Smith, M.A. (1965) Karyotype-phenotype correlations in gonadal dysgenesis and their bearing on the pathogenesis of malformations. J. Med. Genet., 2, 142-155.
-
(1965)
J. Med. Genet.
, vol.2
, pp. 142-155
-
-
Ferguson-Smith, M.A.1
-
8
-
-
0027475040
-
Turner syndrome: The case of the missing sex chromosome
-
Zinn, A.R., Page, D.C. and Fisher, E.M.C. (1993) Turner syndrome: the case of the missing sex chromosome. Trends Genet., 9, 90-93.
-
(1993)
Trends Genet.
, vol.9
, pp. 90-93
-
-
Zinn, A.R.1
Page, D.C.2
Fisher, E.M.C.3
-
9
-
-
0030952221
-
Expression of genes from the human active and inactive X chromosomes
-
Brown, C.J., Carrel, L. and Willard, H.F. (1997) Expression of genes from the human active and inactive X chromosomes. Am. J. Hum. Genet., 60, 1333-1343.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1333-1343
-
-
Brown, C.J.1
Carrel, L.2
Willard, H.F.3
-
10
-
-
0028264422
-
A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human
-
Agulnik, A.I., Mitchell, M.J., Mattei, M.-G., Borsani, G., Avner, P.A., Lerner, J.L. and Bishop C.E. (1994) A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human. Hum. Mol. Genet., 3, 879-884.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 879-884
-
-
Agulnik, A.I.1
Mitchell, M.J.2
Mattei, M.-G.3
Borsani, G.4
Avner, P.A.5
Lerner, J.L.6
Bishop, C.E.7
-
11
-
-
0028145743
-
The murine Xe169 gene escapes X-inactivation like its human homologue
-
Wu, J., Salido, E.C., Yen, P.H., Mohandas, T.K., Heng, H.H., Tsui, L.C., Park, J., Chapman, V.M. and Shapiro, L.J. (1994) The murine XE169 gene escapes X-inactivation like its human homologue. Nature Genet., 7, 491-496.
-
(1994)
Nature Genet.
, vol.7
, pp. 491-496
-
-
Wu, J.1
Salido, E.C.2
Yen, P.H.3
Mohandas, T.K.4
Heng, H.H.5
Tsui, L.C.6
Park, J.7
Chapman, V.M.8
Shapiro, L.J.9
-
12
-
-
0030137347
-
Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts)
-
Salido, E.C., Li, X.M., Yen, P.M., Martin, N., Mohandas, T.K. and Shapiro, L.J. (1996) Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts). Nature Genet., 13, 83-86.
-
(1996)
Nature Genet.
, vol.13
, pp. 83-86
-
-
Salido, E.C.1
Li, X.M.2
Yen, P.M.3
Martin, N.4
Mohandas, T.K.5
Shapiro, L.J.6
-
13
-
-
0025881630
-
X-chromosome inactivation may explain the difference in viability of XO humans and mice
-
Ashworth, A., Rastan, S., Lovell-Badge, R. and Kay, G. (1991) X-chromosome inactivation may explain the difference in viability of XO humans and mice. Nature, 351, 406-408.
-
(1991)
Nature
, vol.351
, pp. 406-408
-
-
Ashworth, A.1
Rastan, S.2
Lovell-Badge, R.3
Kay, G.4
-
14
-
-
0029658730
-
An H-YDb epitope is encoded by a novel mouse Y chromosome gene
-
Greenfield, A.J., Scott, D., Pennisi, D., Ehrmann, I., Ellis, P., Cooper, L., Simpson, E. and Koopman, P. (1996) An H-YDb epitope is encoded by a novel mouse Y chromosome gene. Nature Genet., 14, 474-478.
-
(1996)
Nature Genet.
, vol.14
, pp. 474-478
-
-
Greenfield, A.J.1
Scott, D.2
Pennisi, D.3
Ehrmann, I.4
Ellis, P.5
Cooper, L.6
Simpson, E.7
Koopman, P.8
-
15
-
-
0028843868
-
The tetratricopeptide repeals of Ssn6 interact with the homeodomain of α2
-
Smith, R.L., Redd, M.J. and Johnson, AD. (1995) The tetratricopeptide repeals of Ssn6 interact with the homeodomain of α2. Genes Dev., 9, 2903-2910.
-
(1995)
Genes Dev.
, vol.9
, pp. 2903-2910
-
-
Smith, R.L.1
Redd, M.J.2
Johnson, A.D.3
-
16
-
-
0030725069
-
Functional coherence of the human Y chromosome
-
Lahn, B.T. and Page, D.C. (1997) Functional coherence of the human Y chromosome. Science, 278, 675-680.
-
(1997)
Science
, vol.278
, pp. 675-680
-
-
Lahn, B.T.1
Page, D.C.2
-
17
-
-
0024118949
-
Molecular and genetic mapping of the mouse mdx locus
-
Cavanna, J.S., Coulton, G., Morgan, J.E., Brockdorff, N., Forrest, S.M., Davies, K.E. and Brown, S.D.M. (1988) Molecular and genetic mapping of the mouse mdx locus. Genomics, 3, 337-341.
-
(1988)
Genomics
, vol.3
, pp. 337-341
-
-
Cavanna, J.S.1
Coulton, G.2
Morgan, J.E.3
Brockdorff, N.4
Forrest, S.M.5
Davies, K.E.6
Brown, S.D.M.7
-
18
-
-
0025831142
-
A candidate spermatogenesis gene on the mouse Y chromosome is homologous to ubiquitin-activating enzyme E1
-
Kay, G.F., Ashworth, A., Penny, G.D., Dunlop, M., Swift, S., Brockdorff, N. and Rastan, S. (1991) A candidate spermatogenesis gene on the mouse Y chromosome is homologous to ubiquitin-activating enzyme E1. Nature, 354, 486-489.
-
(1991)
Nature
, vol.354
, pp. 486-489
-
-
Kay, G.F.1
Ashworth, A.2
Penny, G.D.3
Dunlop, M.4
Swift, S.5
Brockdorff, N.6
Rastan, S.7
-
19
-
-
0030633934
-
Mouse X chromosome
-
Boyd, Y., Herman, G.E., Avner, P., Disteche, C.M., Adler, D., Reed, V. and Blair, H.J. (1997) Mouse X chromosome. Mammalian Genome, 7, 313-326.
-
(1997)
Mammalian Genome
, vol.7
, pp. 313-326
-
-
Boyd, Y.1
Herman, G.E.2
Avner, P.3
Disteche, C.M.4
Adler, D.5
Reed, V.6
Blair, H.J.7
-
20
-
-
0026571899
-
Ssn6-Tupl is a general repressor of transcription in yeast
-
Keleher, C.A., Redd, M.J., Schultz, J., Carlson, M. and Johnson, A.D. (1992) Ssn6-Tupl is a general repressor of transcription in yeast. Cell, 68, 709-719.
-
(1992)
Cell
, vol.68
, pp. 709-719
-
-
Keleher, C.A.1
Redd, M.J.2
Schultz, J.3
Carlson, M.4
Johnson, A.D.5
-
21
-
-
0025918417
-
Physical mapping of 60 DNA markers in the p21.1→q21.3 region of the human X chromosome
-
Lafreniere, R.G., Brown, C.J., Powers, V.E., Carrel, L., Davies, K.E., Barker, D.F. and Willard, H.F. (1991) Physical mapping of 60 DNA markers in the p21.1→q21.3 region of the human X chromosome. Genomics, 11, 352-363.
-
(1991)
Genomics
, vol.11
, pp. 352-363
-
-
Lafreniere, R.G.1
Brown, C.J.2
Powers, V.E.3
Carrel, L.4
Davies, K.E.5
Barker, D.F.6
Willard, H.F.7
-
22
-
-
0002345846
-
-
Davies, K.E. and Tilghman, S.M. (eds), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Lchrach, H., Drmanac, R., Hoheisel, J.D., Larin, Z., Lennon, G., Monaco, A.P. et al. (1991) In Davies, K.E. and Tilghman, S.M. (eds), Genome Analysis, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, Vol. 1, pp. 39-81.
-
(1991)
Genome Analysis
, vol.1
, pp. 39-81
-
-
Lchrach, H.1
Drmanac, R.2
Hoheisel, J.D.3
Larin, Z.4
Lennon, G.5
Monaco, A.P.6
-
23
-
-
0026345290
-
Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: Their potential use as reference libraries
-
Nizetic, D., Zehetner, G., Monaco, A.P., Gellen, L., Young, B.D. and Lehrach, H. (1991) Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries. Proc. Natl Acad. Sci. USA, 88, 3233-3237.
-
(1991)
Proc. Natl Acad. Sci. USA
, vol.88
, pp. 3233-3237
-
-
Nizetic, D.1
Zehetner, G.2
Monaco, A.P.3
Gellen, L.4
Young, B.D.5
Lehrach, H.6
-
24
-
-
0026726412
-
The human Y chromosome: Overlapping DNA clones spanning the euchromatic region
-
Foote, S., Vollrath, D., Hilton, A. and Page, D.C. (1992) The human Y chromosome: overlapping DNA clones spanning the euchromatic region. Science, 258, 60-66.
-
(1992)
Science
, vol.258
, pp. 60-66
-
-
Foote, S.1
Vollrath, D.2
Hilton, A.3
Page, D.C.4
-
25
-
-
0007272350
-
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
-
Vogt, P.H., Edelmann, A., Kirsch, S., Henegariu, O., Hirschmann, P., Kiesewetter, F. et al. (1996) Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Hum. Mol. Genet., 5, 933-943.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 933-943
-
-
Vogt, P.H.1
Edelmann, A.2
Kirsch, S.3
Henegariu, O.4
Hirschmann, P.5
Kiesewetter, F.6
-
26
-
-
0029167051
-
Chromosomal localisation of a Y specific growth gene
-
Ogata, T., Tomita, K., Hida, A., Matsuo, N., Nakahori, Y. and Nakagome, Y. (1995) Chromosomal localisation of a Y specific growth gene. J. Med. Genet., 32, 572-575.
-
(1995)
J. Med. Genet.
, vol.32
, pp. 572-575
-
-
Ogata, T.1
Tomita, K.2
Hida, A.3
Matsuo, N.4
Nakahori, Y.5
Nakagome, Y.6
-
27
-
-
0019128555
-
Primary and secondary non-random X chromosome inactivation in early female mouse embryos carrying Searle's translocation T(X;16) 16H
-
Takagi, N. (1980) Primary and secondary non-random X chromosome inactivation in early female mouse embryos carrying Searle's translocation T(X;16) 16H. Chromosoma, 81, 439-459.
-
(1980)
Chromosoma
, vol.81
, pp. 439-459
-
-
Takagi, N.1
-
28
-
-
0030049766
-
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. and Willard, H.F. (1996) X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. Hum. Mol. Genet., 5, 391-401.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 391-401
-
-
Carrel, L.1
Clemson, C.M.2
Dunn, J.M.3
Miller, A.P.4
Hunt, P.A.5
Lawrence, J.B.6
Willard, H.F.7
-
29
-
-
0029791177
-
Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene
-
Carrel, L., Hunt, P.A. and Willard, H.F. (1996) Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene. Hum. Mol. Genet., 5, 1361-1366.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1361-1366
-
-
Carrel, L.1
Hunt, P.A.2
Willard, H.F.3
-
30
-
-
0027860527
-
Epigenetic and chromosomal control of gene expression: Molecular and genetic analysis of X chromosome inactivation
-
Willard, H.F., Brown, C.J., Carrel, L., Hendrich, B. and Miller, A.P. (1993) Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation. Cold Spring Harbor Symp. Quant. Biol., 58, 315-322.
-
(1993)
Cold Spring Harbor Symp. Quant. Biol.
, vol.58
, pp. 315-322
-
-
Willard, H.F.1
Brown, C.J.2
Carrel, L.3
Hendrich, B.4
Miller, A.P.5
-
31
-
-
0029811589
-
The mouse Smcx gene exhibits developmental and tissue-specific variation in degree of escape from X inactivation
-
Sheardown, S., Norris, D., Fisher, A. and Brockdorff, N. (1996) The mouse Smcx gene exhibits developmental and tissue-specific variation in degree of escape from X inactivation. Hum. Mol. Genet., 5, 1355-1360.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1355-1360
-
-
Sheardown, S.1
Norris, D.2
Fisher, A.3
Brockdorff, N.4
-
32
-
-
0028833226
-
Escape from X inactivation in human and mouse
-
Disteche, C.M. (1995) Escape from X inactivation in human and mouse. Trends Genet., 11, 17-22.
-
(1995)
Trends Genet.
, vol.11
, pp. 17-22
-
-
Disteche, C.M.1
-
33
-
-
0030940217
-
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
-
Rao, E., Weiss, B., Fukami, M., Rump, A., Niesler, B., Mertz, A. et al. (1997) Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nature Genet., 16, 54-63.
-
(1997)
Nature Genet.
, vol.16
, pp. 54-63
-
-
Rao, E.1
Weiss, B.2
Fukami, M.3
Rump, A.4
Niesler, B.5
Mertz, A.6
-
34
-
-
0029001726
-
Viability, development and incidence of chromosome anomalies of preimplantation embryos from XO mice
-
Banzai, M., Omoe, K., Ishikawa, H. and Endo, A. (1995) Viability, development and incidence of chromosome anomalies of preimplantation embryos from XO mice. Cytogenet. Cell Genet., 70, 273-277.
-
(1995)
Cytogenet. Cell Genet.
, vol.70
, pp. 273-277
-
-
Banzai, M.1
Omoe, K.2
Ishikawa, H.3
Endo, A.4
-
35
-
-
0027183088
-
The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acctylation, a cytogenetic marker for gene expression
-
Jeppesen, P. and Turner, B.M. (1993) The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acctylation, a cytogenetic marker for gene expression. Cell, 74, 281-289.
-
(1993)
Cell
, vol.74
, pp. 281-289
-
-
Jeppesen, P.1
Turner, B.M.2
-
37
-
-
0029161999
-
Expression of a linear Sry transcript in the mouse genital ridge
-
Jeske, Y.W.A., Bowles, J., Greenfield, A. and Koopman, P. (1995) Expression of a linear Sry transcript in the mouse genital ridge. Nature Genet., 10, 480-482.
-
(1995)
Nature Genet.
, vol.10
, pp. 480-482
-
-
Jeske, Y.W.A.1
Bowles, J.2
Greenfield, A.3
Koopman, P.4
|