-
1
-
-
0027960920
-
The first analysis of exon 1 (transactivation domain) of the androgen receptor gene in infertile men with oligospermia or azoospermia
-
Puscheck E.E., Behzadian M.A., McDonough P.G. The first analysis of exon 1 (transactivation domain) of the androgen receptor gene in infertile men with oligospermia or azoospermia. Fertil Steril. 62:1994;1035-1038.
-
(1994)
Fertil Steril
, vol.62
, pp. 1035-1038
-
-
Puscheck, E.E.1
Behzadian, M.A.2
McDonough, P.G.3
-
2
-
-
0023910355
-
Cloning of human androgen receptor complementary DNA and localisation to the X chromosome
-
Lubahn D.B., Joseph D.R., Sullivan P.M.et al. Cloning of human androgen receptor complementary DNA and localisation to the X chromosome. Science. 240:1988;327-330.
-
(1988)
Science
, vol.240
, pp. 327-330
-
-
Lubahn, D.B.1
Joseph, D.R.2
Sullivan, P.M.3
-
3
-
-
0029116783
-
Defects of androgen receptor function: From sex reversal to motor neuron disease
-
MacLean H.E., Warne G.L., Zajac J.D. Defects of androgen receptor function: from sex reversal to motor neuron disease. Mol Cell Endocrinol. 112:1995;133-141.
-
(1995)
Mol Cell Endocrinol
, vol.112
, pp. 133-141
-
-
MacLean, H.E.1
Warne, G.L.2
Zajac, J.D.3
-
4
-
-
0020415365
-
The frequency of androgen receptor deficiency in infertile men
-
Aiman J., Griffin J.E. The frequency of androgen receptor deficiency in infertile men. J Clin Endocrinol Metab. 54:1982;725-732.
-
(1982)
J Clin Endocrinol Metab
, vol.54
, pp. 725-732
-
-
Aiman, J.1
Griffin, J.E.2
-
5
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
LaSpada A.R., Wilson E.M., Lubahn D.B.et al. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature. 352:1991;77-79.
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
Laspada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
-
6
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is unstable on Huntington's disease chromosomes
-
A novel gene containing a trinucleotide repeat that is unstable on Huntington's disease chromosomes. Cell. 72:1993;971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
7
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
Orr H.T., Chung M.Y., Banfi S.et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet. 4:1993;221-226.
-
(1993)
Nat Genet
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.Y.2
Banfi, S.3
-
8
-
-
0028143527
-
CAG expansion in a novel gene for Machado-Joseph disease at chromosome 14q32.1
-
Kawaguchi Y., Okamoto T., Taniwaki M.et al. CAG expansion in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet. 8:1994;221-227.
-
(1994)
Nat Genet
, vol.8
, pp. 221-227
-
-
Kawaguchi, Y.1
Okamoto, T.2
Taniwaki, M.3
-
9
-
-
0028216760
-
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
-
Koide R., Ikeuchi T., Onodera O.et al. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nat Genet. 6:1994;9-13.
-
(1994)
Nat Genet
, vol.6
, pp. 9-13
-
-
Koide, R.1
Ikeuchi, T.2
Onodera, O.3
-
11
-
-
6844254538
-
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)
-
David G., Durr A., Stevanin G.et al. Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7). Hum Mol Genet. 7:1998;165-170.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 165-170
-
-
David, G.1
Durr, A.2
Stevanin, G.3
-
13
-
-
0030947287
-
The CAG repeat within the androgen receptor gene and its relationship to prostate cancer
-
Giovannucci E., Stamper M.J., Krithivas K.et al. The CAG repeat within the androgen receptor gene and its relationship to prostate cancer. Proc Natl Acad Sci USA. 94:1997;3320-3323.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 3320-3323
-
-
Giovannucci, E.1
Stamper, M.J.2
Krithivas, K.3
-
14
-
-
0030694396
-
Long polyglutamine tracts in the androgen receptor are associated with reduced trans-activation, impaired sperm production, and male infertility
-
Tut T.G., Ghadessy F.J., Trifiro M.A.et al. Long polyglutamine tracts in the androgen receptor are associated with reduced trans-activation, impaired sperm production, and male infertility. J Clin Endocrinol Metab. 82:1997;3777-3782.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3777-3782
-
-
Tut, T.G.1
Ghadessy, F.J.2
Trifiro, M.A.3
-
15
-
-
0031266759
-
Preliminary investigations on androgen receptor gene mutations in infertile men
-
Tincello D.G., Saunders P.T.K., Hargreave T.B. Preliminary investigations on androgen receptor gene mutations in infertile men. Mol Hum Genet. 3:1997;941-943.
-
(1997)
Mol Hum Genet
, vol.3
, pp. 941-943
-
-
Tincello, D.G.1
Saunders, P.T.K.2
Hargreave, T.B.3
-
16
-
-
0023273754
-
Towards an objective evaluation of signs and symptoms in male infertility
-
(suppl)
-
Towards an objective evaluation of signs and symptoms in male infertility. Int J Androl. 7:1987;3-9. (suppl).
-
(1987)
Int J Androl
, vol.7
, pp. 3-9
-
-
-
17
-
-
9244243681
-
Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligospermia detected using a sequence-tagged site-based mapping strategy
-
Najmabadi H., Huang V., Yen P.et al. Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligospermia detected using a sequence-tagged site-based mapping strategy. J Clin Endocrinol Metab. 81:1996;1347-1352.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 1347-1352
-
-
Najmabadi, H.1
Huang, V.2
Yen, P.3
-
18
-
-
0028092712
-
Disordered acrosome reaction of spermatozoa bound to the zona pellucida: A newly discovered sperm defect causing infertility with reduced sperm-zona pellucida penetration and reduced fertilisation in vitro
-
Liu D.Y., Baker H.W. Disordered acrosome reaction of spermatozoa bound to the zona pellucida: a newly discovered sperm defect causing infertility with reduced sperm-zona pellucida penetration and reduced fertilisation in vitro. Hum Reprod. 9:1994;1694-1700.
-
(1994)
Hum Reprod
, vol.9
, pp. 1694-1700
-
-
Liu, D.Y.1
Baker, H.W.2
-
20
-
-
0024306555
-
Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity
-
Lubahn D.B., Brown T.R., Simental J.A.et al. Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity. Proc Natl Acad Sci USA. 86:1989;9534-9538.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 9534-9538
-
-
Lubahn, D.B.1
Brown, T.R.2
Simental, J.A.3
-
21
-
-
0028278532
-
Complete androgen insensitivity due to a splice-site mutation in the androgen receptor gene and genetic screening with single stranded conformation polymorphism
-
Yong E.L., Chua K.L., Yang M.et al. Complete androgen insensitivity due to a splice-site mutation in the androgen receptor gene and genetic screening with single stranded conformation polymorphism. Fertil Steril. 61:1994;856-862.
-
(1994)
Fertil Steril
, vol.61
, pp. 856-862
-
-
Yong, E.L.1
Chua, K.L.2
Yang, M.3
-
22
-
-
0029968460
-
Trinucleotide repeats in neurogenetic disorders
-
Paulson H.L., Fischbeck K.H. Trinucleotide repeats in neurogenetic disorders. Annu Rev Neurosci. 19:1996;79-107.
-
(1996)
Annu Rev Neurosci
, vol.19
, pp. 79-107
-
-
Paulson, H.L.1
Fischbeck, K.H.2
-
23
-
-
0030061741
-
The endocrine regulation of spermatogenesis: Independent roles for testosterone and FSH.
-
McLachlan R.I., Wreford N.G., O'Donnett L.et al. The endocrine regulation of spermatogenesis: independent roles for testosterone and FSH. J Endocrinol. 148:1996;1-9.
-
(1996)
J Endocrinol
, vol.148
, pp. 1-9
-
-
McLachlan, R.I.1
Wreford, N.G.2
O'Donnett, L.3
-
24
-
-
0032560349
-
Medical and developmental outcome at 1 year for children conceived by intracytoplasmic sperm injection
-
Bowen J.R., Gibson F.L., Leslie G.I., Saunders D.M. Medical and developmental outcome at 1 year for children conceived by intracytoplasmic sperm injection. Lancet. 351:1998;1529-1534.
-
(1998)
Lancet
, vol.351
, pp. 1529-1534
-
-
Bowen, J.R.1
Gibson, F.L.2
Leslie, G.I.3
Saunders, D.M.4
-
25
-
-
0032560296
-
Mental development of 201 ICSI children at 2 years of age
-
Bonduelle M., Joris H., Hofmans K.et al. Mental development of 201 ICSI children at 2 years of age. Lancet. 351:1998;1553.
-
(1998)
Lancet
, vol.351
, pp. 1553
-
-
Bonduelle, M.1
Joris, H.2
Hofmans, K.3
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