-
2
-
-
0033581458
-
Pathogenesis of polycystic ovary syndrome - The enigma unravels?
-
Balen A. Pathogenesis of polycystic ovary syndrome - the enigma unravels? Lancet 1999 354 966-967.
-
(1999)
Lancet
, vol.354
, pp. 966-967
-
-
Balen, A.1
-
3
-
-
0001217801
-
Diagnostic criteria for polycystic ovary syndrome: Towards a rational approach
-
Eds A Dunaif, JR Givens, F Haseltine & GR Merriam. Boston, MA: Blackwell
-
Zawadzki JK & Dunaif A. Diagnostic criteria for polycystic ovary syndrome: towards a rational approach. In Polycystic Ovary Syndrome, pp 377-384. Eds A Dunaif, JR Givens, F Haseltine & GR Merriam. Boston, MA: Blackwell, 1992.
-
(1992)
Polycystic Ovary Syndrome
, pp. 377-384
-
-
Zawadzki, J.K.1
Dunaif, A.2
-
4
-
-
0002611248
-
Morphology of the polycystic ovary in polycystic ovary syndrome
-
Eds A Dunai, JR Givens, F Haseltine & GR Merriam. Boston, MA: Blackwell
-
Franks S. Morphology of the polycystic ovary in polycystic ovary syndrome. In Polycystic Ovary Syndrome, pp 19-28. Eds A Dunai, JR Givens, F Haseltine & GR Merriam. Boston, MA: Blackwell, 1992.
-
(1992)
Polycystic Ovary Syndrome
, pp. 19-28
-
-
Franks, S.1
-
5
-
-
0028044645
-
The prevalence of polycystic ovaries on ultrasound scanning in a population of randomly selected women
-
Farquhar CM, Birdsall M, Manning P, Mitchell JM & France JT. The prevalence of polycystic ovaries on ultrasound scanning in a population of randomly selected women. Australian and New Zealand Journal of Obstetrics and Gynaecology 1994 34 67-72.
-
(1994)
Australian and New Zealand Journal of Obstetrics and Gynaecology
, vol.34
, pp. 67-72
-
-
Farquhar, C.M.1
Birdsall, M.2
Manning, P.3
Mitchell, J.M.4
France, J.T.5
-
6
-
-
0033014327
-
The epidemiology of polycystic ovary syndrome. Prevalence and associated disease risk
-
Solomon CG. The epidemiology of polycystic ovary syndrome. Prevalence and associated disease risk. Endocrinology and Metabolism Clinics of North America 1999 28 247-265.
-
(1999)
Endocrinology and Metabolism Clinics of North America
, vol.28
, pp. 247-265
-
-
Solomon, C.G.1
-
7
-
-
0031773509
-
Prevalence of the polycystic ovary syndrome in unselected Black and White women of the Southeastern United States: A prospective study
-
Knochenhauer ES, Key TJ, Kahsar-Miller M, Waggoner W, Boots LR & Azziz R. Prevalence of the polycystic ovary syndrome in unselected Black and White women of the Southeastern United States: a prospective study Journal of Clinical Endocrinology and Metabolism 1998 83 3078-3082.
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, vol.83
, pp. 3078-3082
-
-
Knochenhauer, E.S.1
Key, T.J.2
Kahsar-Miller, M.3
Waggoner, W.4
Boots, L.R.5
Azziz, R.6
-
8
-
-
0033345349
-
A survey of the polycystic ovary syndrome in the Greek island of Lesbos: Hormonal and metabolic profile
-
Diamanti-Kandarakis E, Kouli CR, Bergiele AT, Filandra FA, Tsianateli C, Spina GG et al. A survey of the polycystic ovary syndrome in the Greek island of Lesbos: hormonal and metabolic profile. Journal of Clinical Endocrinology and Metabolism 1999 84 4006-4011.
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, pp. 4006-4011
-
-
Diamanti-Kandarakis, E.1
Kouli, C.R.2
Bergiele, A.T.3
Filandra, F.A.4
Tsianateli, C.5
Spina, G.G.6
-
9
-
-
0034457559
-
A prospective study of the prevalence of the polycystic ovary syndrome in unselected Caucasian women from Spain
-
Asuncion M, Calvo RM, San Millan JL, Sancho J, Avila S & Escobar-Morreale HF. A prospective study of the prevalence of the polycystic ovary syndrome in unselected Caucasian women from Spain. Journal of Clinical Endocrinology and Metabolism 2000 85 2434-2438.
-
(2000)
Journal of Clinical Endocrinology and Metabolism
, vol.85
, pp. 2434-2438
-
-
Asuncion, M.1
Calvo, R.M.2
San Millan, J.L.3
Sancho, J.4
Avila, S.5
Escobar-Morreale, H.F.6
-
10
-
-
0026620885
-
Does ethnicity influence the prevalence of adrenal hyperandrogenism and insulin resistance in polycystic ovary syndrome?
-
Carmina E, Koyama T, Chang L, Stanczyk FZ & Lobo RA. Does ethnicity influence the prevalence of adrenal hyperandrogenism and insulin resistance in polycystic ovary syndrome? American Journal of Obstetrics and Gynecology 1992 167 1807-1812.
-
(1992)
American Journal of Obstetrics and Gynecology
, vol.167
, pp. 1807-1812
-
-
Carmina, E.1
Koyama, T.2
Chang, L.3
Stanczyk, F.Z.4
Lobo, R.A.5
-
11
-
-
0027274710
-
Ethnicity and polycystic ovary syndrome are associated with independent and additive decreases in insulin action in Caribbean-Hispanic women
-
Dunaif A, Sorbara L, Delson R & Green G. Ethnicity and polycystic ovary syndrome are associated with independent and additive decreases in insulin action in Caribbean-Hispanic women. Diabetes 1993 42 1462-1468.
-
(1993)
Diabetes
, vol.42
, pp. 1462-1468
-
-
Dunaif, A.1
Sorbara, L.2
Delson, R.3
Green, G.4
-
13
-
-
0034691269
-
The importance of diagnosing the polycystic ovary syndrome
-
Lobo RA & Carmina E. The importance of diagnosing the polycystic ovary syndrome. Annals of Internal Medicine 2000 132 989-993.
-
(2000)
Annals of Internal Medicine
, vol.132
, pp. 989-993
-
-
Lobo, R.A.1
Carmina, E.2
-
14
-
-
0031434341
-
The genetic basis of polycystic ovary syndrome
-
Franks S, Gharani N, Waterworth D, Batty S, White D, Williamson R et al. The genetic basis of polycystic ovary syndrome. Human Reproduction 1997 12 2641-2648.
-
(1997)
Human Reproduction
, vol.12
, pp. 2641-2648
-
-
Franks, S.1
Gharani, N.2
Waterworth, D.3
Batty, S.4
White, D.5
Williamson, R.6
-
15
-
-
0018606011
-
The inheritance of PCO and possible relationship to premature balding
-
Ferriman D & Purdie A. The inheritance of PCO and possible relationship to premature balding. Clinical Endocrinology 1979 11 291-300.
-
(1979)
Clinical Endocrinology
, vol.11
, pp. 291-300
-
-
Ferriman, D.1
Purdie, A.2
-
16
-
-
0027196489
-
Evidence for a single gene effect causing polycystic ovaries and male pattern baldness
-
Carey AH, Chan KL, Short F, White D, Williamson R & Franks S. Evidence for a single gene effect causing polycystic ovaries and male pattern baldness. Clinical Endocrinology 1993 38 653-658.
-
(1993)
Clinical Endocrinology
, vol.38
, pp. 653-658
-
-
Carey, A.H.1
Chan, K.L.2
Short, F.3
White, D.4
Williamson, R.5
Franks, S.6
-
17
-
-
0024268235
-
Familial polycystic ovaries: A genetic disease
-
Hague WM, Adams J, Reeders ST, Peto TE & Jacobs HS. Familial polycystic ovaries: a genetic disease. Clinical Endocrinology 1988 29 593-605.
-
(1988)
Clinical Endocrinology
, vol.29
, pp. 593-605
-
-
Hague, W.M.1
Adams, J.2
Reeders, S.T.3
Peto, T.E.4
Jacobs, H.S.5
-
19
-
-
0024437305
-
Profound peripheral insulin resistance, independent of obesity in polycystic ovary syndrome
-
Dunaif A, Segal KR, Futterfeit W & Dobrjansky A. Profound peripheral insulin resistance, independent of obesity in polycystic ovary syndrome. Diabetes 1989 38 1165-1174.
-
(1989)
Diabetes
, vol.38
, pp. 1165-1174
-
-
Dunaif, A.1
Segal, K.R.2
Futterfeit, W.3
Dobrjansky, A.4
-
20
-
-
0023392635
-
The insulin receptor: Molecular biology and transmembrane signaling
-
Goldfine ID. The insulin receptor: molecular biology and transmembrane signaling. Endocrine Reviews 1987 8 235-255.
-
(1987)
Endocrine Reviews
, vol.8
, pp. 235-255
-
-
Goldfine, I.D.1
-
21
-
-
0029878178
-
Molecular scanning of the insulin receptor gene in women with polycystic ovarian syndrome
-
Talbot JA, Bicknell EJ, Ranjhowa M, Krook A, O'Rahilly S & Clayton RN. Molecular scanning of the insulin receptor gene in women with polycystic ovarian syndrome. Journal of Clinical Endocrinology and Metabolism 1996 81 1979-1983.
-
(1996)
Journal of Clinical Endocrinology and Metabolism
, vol.81
, pp. 1979-1983
-
-
Talbot, J.A.1
Bicknell, E.J.2
Ranjhowa, M.3
Krook, A.4
O'Rahilly, S.5
Clayton, R.N.6
-
22
-
-
0027984168
-
Absence of insulin receptor gene mutations in three women with polycystic ovary syndrome
-
Sorbara LR, Tang Z, Cama A, Xia J, Schenker E, Kohanski RA et al. Absence of insulin receptor gene mutations in three women with polycystic ovary syndrome. Metabolism 1994 43 1568-1574.
-
(1994)
Metabolism
, vol.43
, pp. 1568-1574
-
-
Sorbara, L.R.1
Tang, Z.2
Cama, A.3
Xia, J.4
Schenker, E.5
Kohanski, R.A.6
-
23
-
-
0029119085
-
Excessive insulin receptor serine phosphorylation in cultured fibroblasts and skeletal muscle: A potential mechanism for insulin resistance in the polycystic ovary syndrome
-
Dunaif A, Xia J & Book C. Excessive insulin receptor serine phosphorylation in cultured fibroblasts and skeletal muscle: a potential mechanism for insulin resistance in the polycystic ovary syndrome. Journal of Clinical Investigation 1995 96 801-810.
-
(1995)
Journal of Clinical Investigation
, vol.96
, pp. 801-810
-
-
Dunaif, A.1
Xia, J.2
Book, C.3
-
24
-
-
0029142760
-
Restored insulin sensitivity but persistent increased early insulin secretion after weight loss in obese women with polycystic ovary syndrome
-
Holte J, Bergh T & Berne C. Restored insulin sensitivity but persistent increased early insulin secretion after weight loss in obese women with polycystic ovary syndrome. Journal of Clinical Endocrinology and Metabolism 1995 80 2586-2593.
-
(1995)
Journal of Clinical Endocrinology and Metabolism
, vol.80
, pp. 2586-2593
-
-
Holte, J.1
Bergh, T.2
Berne, C.3
-
25
-
-
0025691614
-
Report of the committee on the genetic constitution of chromosome 11
-
Junien C & Van Heyningen V. Report of the committee on the genetic constitution of chromosome 11. Cytogenetics and Cell Genetics 1990 55 153-169.
-
(1990)
Cytogenetics and Cell Genetics
, vol.55
, pp. 153-169
-
-
Junien, C.1
Van Heyningen, V.2
-
26
-
-
0020080870
-
The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences
-
Bell GI, Selby MJ & Rutter WJ. The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences. Nature 1982 295 31-35.
-
(1982)
Nature
, vol.295
, pp. 31-35
-
-
Bell, G.I.1
Selby, M.J.2
Rutter, W.J.3
-
27
-
-
0032486384
-
The INS.5′ variable number of tandem repeats is associated with IGF-II expression in humans
-
Paquette J, Giannoukakis N, Polychronakos C, Vafiadis P & Deal C. The INS.5′ variable number of tandem repeats is associated with IGF-II expression in humans. Journal of Biological Chemistry 1998 273 14158-14164.
-
(1998)
Journal of Biological Chemistry
, vol.273
, pp. 14158-14164
-
-
Paquette, J.1
Giannoukakis, N.2
Polychronakos, C.3
Vafiadis, P.4
Deal, C.5
-
28
-
-
0028881617
-
The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription
-
Kennedy G, German MS & Rutter WJ. The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription. Nature Genetics 1995 9 293-298.
-
(1995)
Nature Genetics
, vol.9
, pp. 293-298
-
-
Kennedy, G.1
German, M.S.2
Rutter, W.J.3
-
29
-
-
0026568387
-
Central obesity and hyperinsulinaemia in women are associated with polymorphism in the 5′ flanking region of the human insulin gene
-
Weaver JU, Kopelman PG & Hitman GA. Central obesity and hyperinsulinaemia in women are associated with polymorphism in the 5′ flanking region of the human insulin gene. European Journal of Clinical Investigation 1992 22 265-270.
-
(1992)
European Journal of Clinical Investigation
, vol.22
, pp. 265-270
-
-
Weaver, J.U.1
Kopelman, P.G.2
Hitman, G.A.3
-
31
-
-
0032982032
-
The insulin gene VNTR, type 2 diabetes and birth weight
-
Ong KL, Phillips DI, Fall C, Pouton J, Bennett ST, Golding J et al. The insulin gene VNTR, type 2 diabetes and birth weight. Nature Genetics 1999 21 262-263.
-
(1999)
Nature Genetics
, vol.21
, pp. 262-263
-
-
Ong, K.L.1
Phillips, D.I.2
Fall, C.3
Pouton, J.4
Bennett, S.T.5
Golding, J.6
-
32
-
-
0030444451
-
Human type 1 diabetes and the insulin gene: Principles of mapping polygenes
-
Bennett ST & Todd JA. Human type 1 diabetes and the insulin gene: principles of mapping polygenes. Annual Review of Genetics 1996 30 343-370.
-
(1996)
Annual Review of Genetics
, vol.30
, pp. 343-370
-
-
Bennett, S.T.1
Todd, J.A.2
-
33
-
-
0032982032
-
The insulin gene VNTR, type 2 diabetes and birth weight
-
Ong KK, Phillips DI, Fall C, Poulton J, Bennett ST, Golding J et al. The insulin gene VNTR, type 2 diabetes and birth weight. Nature Genetics 1999 21 262-263.
-
(1999)
Nature Genetics
, vol.21
, pp. 262-263
-
-
Ong, K.K.1
Phillips, D.I.2
Fall, C.3
Poulton, J.4
Bennett, S.T.5
Golding, J.6
-
34
-
-
0030895556
-
Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome
-
Waterworth DM, Bennett ST, Gharani N, McCarthy MI, Hague S, Batty S et al. Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome. Lancet 1997 349 986-990.
-
(1997)
Lancet
, vol.349
, pp. 986-990
-
-
Waterworth, D.M.1
Bennett, S.T.2
Gharani, N.3
McCarthy, M.I.4
Hague, S.5
Batty, S.6
-
35
-
-
0027301374
-
The relationship of insulin sensitivity to menstrual pattern in women with hyperandrogenism and polycystic ovaries
-
Robinson S, Kiddy D & Gelding SV. The relationship of insulin sensitivity to menstrual pattern in women with hyperandrogenism and polycystic ovaries. Clinical Endocrinology 1993 39 351-355.
-
(1993)
Clinical Endocrinology
, vol.39
, pp. 351-355
-
-
Robinson, S.1
Kiddy, D.2
Gelding, S.V.3
-
36
-
-
0009874460
-
Association of insulin gene VNTR polymorphism with polycystic ovary syndrome
-
Bennett ST, Todd JA, Waterworth DM, Franks S & McGarthy MI. Association of insulin gene VNTR polymorphism with polycystic ovary syndrome. Lancet 1997 349 1771-1772.
-
(1997)
Lancet
, vol.349
, pp. 1771-1772
-
-
Bennett, S.T.1
Todd, J.A.2
Waterworth, D.M.3
Franks, S.4
McGarthy, M.I.5
-
37
-
-
0032786945
-
Transmission ratio distortion at the INS-IGF2 VNTR
-
Eaves IA, Bennett ST, Forster P, Ferber KM, Ehrmann D, Wilson AJ et al. Transmission ratio distortion at the INS-IGF2 VNTR. Nature Genetics 1999 22 324-325.
-
(1999)
Nature Genetics
, vol.22
, pp. 324-325
-
-
Eaves, I.A.1
Bennett, S.T.2
Forster, P.3
Ferber, K.M.4
Ehrmann, D.5
Wilson, A.J.6
-
38
-
-
0034797755
-
Clinical features in women with polycystic ovaries: Relationships to insulin sensitivity, insulin gene VNTR and birth weight
-
Michelmore K, Ong K, Mason S, Bennett S, Perry L, Vessey M et al. Clinical features in women with polycystic ovaries: relationships to insulin sensitivity, insulin gene VNTR and birth weight. Clinical Endocrinology 2001 55 439-446.
-
(2001)
Clinical Endocrinology
, vol.55
, pp. 439-446
-
-
Michelmore, K.1
Ong, K.2
Mason, S.3
Bennett, S.4
Perry, L.5
Vessey, M.6
-
40
-
-
0028588696
-
Studies of the nature of 17-hydroxyprogesterone hyperresponsiveness to gonadotropin-releasing-hormone agonist challenge in functional ovarian hyperandrogenism
-
Rosenfield RL, Barnes RB & Ehrmann DA. Studies of the nature of 17-hydroxyprogesterone hyperresponsiveness to gonadotropin-releasing-hormone agonist challenge in functional ovarian hyperandrogenism. Journal of Clinical Endocrinology and Metabolism 1994 79 1686-1692.
-
(1994)
Journal of Clinical Endocrinology and Metabolism
, vol.79
, pp. 1686-1692
-
-
Rosenfield, R.L.1
Barnes, R.B.2
Ehrmann, D.A.3
-
41
-
-
0024064517
-
Molecular biology of steroid hormone synthesis
-
Miller WL. Molecular biology of steroid hormone synthesis. Endocrine Reviews 1988 9 295-318.
-
(1988)
Endocrine Reviews
, vol.9
, pp. 295-318
-
-
Miller, W.L.1
-
42
-
-
0028024363
-
Polycystic ovaries and premature male pattern baldness are associated with one allele of the steroid metabolism gene CYP17
-
Carey AH, Waterworth D, Patel K, White D, Little J, Novelli P et al. Polycystic ovaries and premature male pattern baldness are associated with one allele of the steroid metabolism gene CYP17. Human Molecular Genetics 1994 3 1873-1876.
-
(1994)
Human Molecular Genetics
, vol.3
, pp. 1873-1876
-
-
Carey, A.H.1
Waterworth, D.2
Patel, K.3
White, D.4
Little, J.5
Novelli, P.6
-
44
-
-
0028786656
-
Serine phosphorylation of human P450c17 increases 17,20-lyase activity: Implications for adrenarche and polycystic ovary syndrome
-
Znang LH, Rodriguez H, Ohno S & Miller WL. Serine phosphorylation of human P450c17 increases 17,20-lyase activity: implications for adrenarche and polycystic ovary syndrome. PNAS 1995 92 10619-10623.
-
(1995)
PNAS
, vol.92
, pp. 10619-10623
-
-
Znang, L.H.1
Rodriguez, H.2
Ohno, S.3
Miller, W.L.4
-
46
-
-
0031049755
-
Association of the steroid synthesis gene CYP11α with polycystic ovary syndrome and hyperandrogenism
-
Gharani N, Waterworth DM, Batty S, White D, Gilling-Smith C, Conway GS et al. Association of the steroid synthesis gene CYP11α with polycystic ovary syndrome and hyperandrogenism. Human Molecular Genetics 1997 6 397-402.
-
(1997)
Human Molecular Genetics
, vol.6
, pp. 397-402
-
-
Gharani, N.1
Waterworth, D.M.2
Batty, S.3
White, D.4
Gilling-Smith, C.5
Conway, G.S.6
-
48
-
-
0033587746
-
Thirty-seven candidate genes for polycystic ovary syndrome: Strongest evidence for linkage is with follistatin
-
Urbanek M, Legro RS, Driscoll DA, Azziz R, Ehrmann DA, Norman RJ et al. Thirty-seven candidate genes for polycystic ovary syndrome: strongest evidence for linkage is with follistatin. PNAS 1999 96 8573-8578.
-
(1999)
PNAS
, vol.96
, pp. 8573-8578
-
-
Urbanek, M.1
Legro, R.S.2
Driscoll, D.A.3
Azziz, R.4
Ehrmann, D.A.5
Norman, R.J.6
-
50
-
-
0024550760
-
The P450 gene superfamily: Recommended nomenclature
-
Nebert DW, Nelson DR, Adesnik M, Coon MJ, Estabrook RW, Gonzalez FJ et al. The P450 gene superfamily: recommended nomenclature. DNA 1989 8 1-13.
-
(1989)
DNA
, vol.8
, pp. 1-13
-
-
Nebert, D.W.1
Nelson, D.R.2
Adesnik, M.3
Coon, M.J.4
Estabrook, R.W.5
Gonzalez, F.J.6
-
51
-
-
0026785124
-
Genetic studies to characterize the origin of the mutation in placental aromatase deficiency
-
Harada N, Ogawa H, Shozu M & Yamada K. Genetic studies to characterize the origin of the mutation in placental aromatase deficiency. American Journal of Human Genetics 1992 52 666-672.
-
(1992)
American Journal of Human Genetics
, vol.52
, pp. 666-672
-
-
Harada, N.1
Ogawa, H.2
Shozu, M.3
Yamada, K.4
-
52
-
-
0027133452
-
Molecular basis of aromatase deficiency in an adult female with sexual infantilism and polycystic ovaries
-
Ito Y, Fisher CR, Conte FA, Grumbach MM & Simpson ER. Molecular basis of aromatase deficiency in an adult female with sexual infantilism and polycystic ovaries. PNAS 1993 90 11673-11677.
-
(1993)
PNAS
, vol.90
, pp. 11673-11677
-
-
Ito, Y.1
Fisher, C.R.2
Conte, F.A.3
Grumbach, M.M.4
Simpson, E.R.5
-
53
-
-
0029789197
-
Immunohistochemical study of steroidogenesis and proliferation in polycystic ovarian syndrome
-
Takayama K, Tao T & Hironobu S. Immunohistochemical study of steroidogenesis and proliferation in polycystic ovarian syndrome. Human Reproduction 1996 11 1387-1392.
-
(1996)
Human Reproduction
, vol.11
, pp. 1387-1392
-
-
Takayama, K.1
Tao, T.2
Hironobu, S.3
-
54
-
-
0027949072
-
Estradiol production by granulosa cells of normal and polycystic ovaries: Relationship to menstrual cycle and concentrations of gonadotropins and sex steroids in follicular fluid
-
Mason HD, Willis DS, Beard RW, Winston RML, Margara R & Franks S. Estradiol production by granulosa cells of normal and polycystic ovaries: relationship to menstrual cycle and concentrations of gonadotropins and sex steroids in follicular fluid. Journal of Clinical Endocrinology and Metabolism 1994 79 1355-1360.
-
(1994)
Journal of Clinical Endocrinology and Metabolism
, vol.79
, pp. 1355-1360
-
-
Mason, H.D.1
Willis, D.S.2
Beard, R.W.3
Winston, R.M.L.4
Margara, R.5
Franks, S.6
-
55
-
-
0027131585
-
Hypersecretion of luteinizing hormone: A significant cause of infertility and miscarriage
-
Balen Ah, Tan SL & Jacobs HS. Hypersecretion of luteinizing hormone: a significant cause of infertility and miscarriage. British Journal of Obstetrics and Gynaecology 1995 100 1082-1089.
-
(1995)
British Journal of Obstetrics and Gynaecology
, vol.100
, pp. 1082-1089
-
-
Balen, Ah.1
Tan, S.L.2
Jacobs, H.S.3
-
56
-
-
84995842414
-
Identification of two point mutations in the gene coding luteinizing hormone (LH) β-subunit, associated with immunologically anomalous LH variants
-
Furui K, Suganuma N, Tsukahara S, Asada Y, Kikkawa F, Tanaka M et al. Identification of two point mutations in the gene coding luteinizing hormone (LH) β-subunit, associated with immunologically anomalous LH variants. Journal of Clinical Endocrinology and Metabolism 1994 78 107-113.
-
(1994)
Journal of Clinical Endocrinology and Metabolism
, vol.78
, pp. 107-113
-
-
Furui, K.1
Suganuma, N.2
Tsukahara, S.3
Asada, Y.4
Kikkawa, F.5
Tanaka, M.6
-
57
-
-
0028234997
-
Antigen alteration of an anomalous human luteinizing hormone caused by two gonadotropin-type amino-acid substitutions
-
Okuda K, Yamada T, Imoto H, Komatsubara H & Sugimoto O. Antigen alteration of an anomalous human luteinizing hormone caused by two gonadotropin-type amino-acid substitutions. Biochemical and Biophysical Research Communications 1994 200 584-590.
-
(1994)
Biochemical and Biophysical Research Communications
, vol.200
, pp. 584-590
-
-
Okuda, K.1
Yamada, T.2
Imoto, H.3
Komatsubara, H.4
Sugimoto, O.5
-
58
-
-
0343742651
-
Worldwide frequency of a common genetic variant of luteinizing hormone: An international collaborative research
-
Nilsson C, Pettersson K, Millar R, Coerver K, Matzuk M & Huhtaniemi I. Worldwide frequency of a common genetic variant of luteinizing hormone: an international collaborative research. Fertility and Sterility 1997 67 998-1004.
-
(1997)
Fertility and Sterility
, vol.67
, pp. 998-1004
-
-
Nilsson, C.1
Pettersson, K.2
Millar, R.3
Coerver, K.4
Matzuk, M.5
Huhtaniemi, I.6
-
59
-
-
0028923111
-
Occurrence and biological properties of a common genetic variant of luteinizing hormone
-
Haavisto A, Pettersson K, Bergendahl M, Virkamaki A & Huhtaniemi I. Occurrence and biological properties of a common genetic variant of luteinizing hormone. Journal of Clinical Endocrinology and Metabolism 1995 80 1257-1263.
-
(1995)
Journal of Clinical Endocrinology and Metabolism
, vol.80
, pp. 1257-1263
-
-
Haavisto, A.1
Pettersson, K.2
Bergendahl, M.3
Virkamaki, A.4
Huhtaniemi, I.5
-
60
-
-
0029092526
-
Prevalence of an immunological LH β-subunit variant in a UK population of healthy women and women with polycystic ovary syndrome
-
Rajkhowa M, Talbot JA, Jones PW, Pettersson K, Haavisto AM, Huhtaniemi I et al. Prevalence of an immunological LH β-subunit variant in a UK population of healthy women and women with polycystic ovary syndrome. Clinical Endocrinology 1995 43 297-303.
-
(1995)
Clinical Endocrinology
, vol.43
, pp. 297-303
-
-
Rajkhowa, M.1
Talbot, J.A.2
Jones, P.W.3
Pettersson, K.4
Haavisto, A.M.5
Huhtaniemi, I.6
-
61
-
-
0033331384
-
A new contributing factor to polycystic ovary syndrome: The genetic variant of luteinizing hormone
-
Tapanainen JS, Koivunen R, Fauser BC, Taylor AE, Clayton RN, Rajkowa M et al. A new contributing factor to polycystic ovary syndrome: the genetic variant of luteinizing hormone. Journal of Clinical Endocrinology and Metabolism 1999 84 1711-1715.
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, pp. 1711-1715
-
-
Tapanainen, J.S.1
Koivunen, R.2
Fauser, B.C.3
Taylor, A.E.4
Clayton, R.N.5
Rajkowa, M.6
-
62
-
-
0032775220
-
Association of molecular variants of luteinizing hormone with menstrual disorders
-
Ramanujam LN, Liao WX, Roy AC, Loganath A, Goh HH & Ng SC. Association of molecular variants of luteinizing hormone with menstrual disorders. Clinical Endocrinology 1999 51 243-246.
-
(1999)
Clinical Endocrinology
, vol.51
, pp. 243-246
-
-
Ramanujam, L.N.1
Liao, W.X.2
Roy, A.C.3
Loganath, A.4
Goh, H.H.5
Ng, S.C.6
-
63
-
-
0031929585
-
A new molecular variant of luteinizing hormone associated with female infertility
-
Liao WX, Roy AC, Chan C, Arulkumaran S & Ratnam SS. A new molecular variant of luteinizing hormone associated with female infertility. Fertility and Sterility 1998 69 102-106.
-
(1998)
Fertility and Sterility
, vol.69
, pp. 102-106
-
-
Liao, W.X.1
Roy, A.C.2
Chan, C.3
Arulkumaran, S.4
Ratnam, S.S.5
-
64
-
-
0023910355
-
Cloning of human androgen receptor complementary DNA and localization on the X chromosome
-
Lubahn DB, Joseph DR, Sullivan PM, Willard HF, French FS & Wilson EM. Cloning of human androgen receptor complementary DNA and localization on the X chromosome. Science 1988 240 327-330.
-
(1988)
Science
, vol.240
, pp. 327-330
-
-
Lubahn, D.B.1
Joseph, D.R.2
Sullivan, P.M.3
Willard, H.F.4
French, F.S.5
Wilson, E.M.6
-
65
-
-
0024555077
-
Androgen receptor locus on the human X chromosome: Regional localization to Xq11-12 and description of a DNA polymorphism
-
Brown CJ, Goss SJ, Lubahm DB, Joseph DR, Wilson EM, French FS et al. Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism. American Journal of Human Genetics 1989 44 264-269.
-
(1989)
American Journal of Human Genetics
, vol.44
, pp. 264-269
-
-
Brown, C.J.1
Goss, S.J.2
Lubahm, D.B.3
Joseph, D.R.4
Wilson, E.M.5
French, F.S.6
-
67
-
-
0026551039
-
Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups
-
Edwards A, Hammond HA, Jin L, Caskey T & Chakraborty R. Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics 1992 12 241-253.
-
(1992)
Genomics
, vol.12
, pp. 241-253
-
-
Edwards, A.1
Hammond, H.A.2
Jin, L.3
Caskey, T.4
Chakraborty, R.5
-
68
-
-
0028033594
-
The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function
-
Chamberlain NL, Driver ED & Miesfeld RL. The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function. Nucleic Acids Research 1994 22 3181-3186.
-
(1994)
Nucleic Acids Research
, vol.22
, pp. 3181-3186
-
-
Chamberlain, N.L.1
Driver, E.D.2
Miesfeld, R.L.3
-
69
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
LaSpada AR, Wilson EM, Lubahn DB, Harding AE & Fischbeck KH. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 1991 352 77-79.
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
LaSpada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
70
-
-
0030947287
-
The CAG repeat within the androgen receptor gene and its relationship to prostate cancer
-
Giovannucci E, Stamfer MJ, Krithivas K, Brown M, Brufsky A, Talcott J et al. The CAG repeat within the androgen receptor gene and its relationship to prostate cancer. PNAS 1997 94 3320-3323.
-
(1997)
PNAS
, vol.94
, pp. 3320-3323
-
-
Giovannucci, E.1
Stamfer, M.J.2
Krithivas, K.3
Brown, M.4
Brufsky, A.5
Talcott, J.6
-
71
-
-
0033592186
-
Linkage between male infertility and trinucleotide repeat expansion in the androgen receptor gene
-
Dowsing AT, Yong EL, McLachlan RI, de Kretser D & Trounson A. Linkage between male infertility and trinucleotide repeat expansion in the androgen receptor gene. Lancet 1999 354 640-643.
-
(1999)
Lancet
, vol.354
, pp. 640-643
-
-
Dowsing, A.T.1
Yong, E.L.2
McLachlan, R.I.3
de Kretser, D.4
Trounson, A.5
-
72
-
-
0028238319
-
Size polymorphisms of the androgen receptor among female Hispanics and correlation with androgenic characteristics
-
Legro RS, Shahbahrami B, Lobo RA & Kovacs BW. Size polymorphisms of the androgen receptor among female Hispanics and correlation with androgenic characteristics. Obstetrics and Gynecology 1994 83 701-706.
-
(1994)
Obstetrics and Gynecology
, vol.83
, pp. 701-706
-
-
Legro, R.S.1
Shahbahrami, B.2
Lobo, R.A.3
Kovacs, B.W.4
-
73
-
-
0031829734
-
Androgen receptor polymorphisms (CAG repeat lengths) in androgenetic alopecia, hirsutism and acne
-
Sawaya ME & Shalita AR. Androgen receptor polymorphisms (CAG repeat lengths) in androgenetic alopecia, hirsutism and acne. Journal of Cutaneous Medicine and Surgery 1998 3 9-15.
-
(1998)
Journal of Cutaneous Medicine and Surgery
, vol.3
, pp. 9-15
-
-
Sawaya, M.E.1
Shalita, A.R.2
-
74
-
-
0033027673
-
Androgen receptor-mediated hypersensitivity to androgens in women with nonhyperandrogenic hirsutism: Skewing of X-chromosome inactivation
-
Vottero A, Stratakis CA, Ghizzoni L, Longui CA, Karl M & Chrousos GP. Androgen receptor-mediated hypersensitivity to androgens in women with nonhyperandrogenic hirsutism: skewing of X-chromosome inactivation. Journal of Clinical Endocrinology and Metabolism 1999 84 1091-1095.
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, pp. 1091-1095
-
-
Vottero, A.1
Stratakis, C.A.2
Ghizzoni, L.3
Longui, C.A.4
Karl, M.5
Chrousos, G.P.6
-
75
-
-
0033724587
-
Androgen receptor gene CAG trinucleotide repeats in anovulatory infertility and polycystic ovaries
-
Misfud A, Ramirez S & Yong EL. Androgen receptor gene CAG trinucleotide repeats in anovulatory infertility and polycystic ovaries. Journal of Clinical Endocrinology and Metabolism 2000 85 3484-3488.
-
(2000)
Journal of Clinical Endocrinology and Metabolism
, vol.85
, pp. 3484-3488
-
-
Misfud, A.1
Ramirez, S.2
Yong, E.L.3
-
76
-
-
0025741546
-
Follistatin binds to both activin and inhibin through the common beta-subunit
-
Shimonaka M, Inouye S, Shimasaki S & Ling N. Follistatin binds to both activin and inhibin through the common beta-subunit. Endocrinology 1991 128 3313-3315.
-
(1991)
Endocrinology
, vol.128
, pp. 3313-3315
-
-
Shimonaka, M.1
Inouye, S.2
Shimasaki, S.3
Ling, N.4
-
78
-
-
0029937050
-
Two distinct signaling pathways activated by activin A in glucose responsive pancreatic beta-cells lines
-
Shibata H, Kanzaki M, Takeuchi T, Miyazaki J & Kojima I. Two distinct signaling pathways activated by activin A in glucose responsive pancreatic beta-cells lines. Journal of Molecular Endocrinology 1996 16 249-258.
-
(1996)
Journal of Molecular Endocrinology
, vol.16
, pp. 249-258
-
-
Shibata, H.1
Kanzaki, M.2
Takeuchi, T.3
Miyazaki, J.4
Kojima, I.5
-
79
-
-
0031941395
-
Overexpression of mouse follistatin causes reproductive defects in transgenic mice
-
Guo Q, Kuma TR, Woodruff T, Hadsell LA, DeMayo FJ & Matzuk MM. Overexpression of mouse follistatin causes reproductive defects in transgenic mice. Molecular Endocrinology 1998 12 96-106.
-
(1998)
Molecular Endocrinology
, vol.12
, pp. 96-106
-
-
Guo, Q.1
Kuma, T.R.2
Woodruff, T.3
Hadsell, L.A.4
DeMayo, F.J.5
Matzuk, M.M.6
-
80
-
-
17744382570
-
Allelic variants of the follistatin gene in polycystic ovary syndrome
-
Urbanek M, Wu X, Vickery KR, Kao LC, Christenson LK, Schneyer A et al. Allelic variants of the follistatin gene in polycystic ovary syndrome. Journal of Clinical Endocrinology and Metabolism 2000 85 4455-4461.
-
(2000)
Journal of Clinical Endocrinology and Metabolism
, vol.85
, pp. 4455-4461
-
-
Urbanek, M.1
Wu, X.2
Vickery, K.R.3
Kao, L.C.4
Christenson, L.K.5
Schneyer, A.6
-
81
-
-
0035040378
-
Role of the follistatin gene in women with polycystic ovary syndrome
-
Calvo RM, Villuedas G, Sancho J, San Milian JL, & Escobar-Morreale HF. Role of the follistatin gene in women with polycystic ovary syndrome. Fertility and Sterility 2001 75 1020-1023.
-
(2001)
Fertility and Sterility
, vol.75
, pp. 1020-1023
-
-
Calvo, R.M.1
Villuedas, G.2
Sancho, J.3
San Milian, J.L.4
Escobar-Morreale, H.F.5
-
82
-
-
0035164938
-
Follicle stimulating hormone receptor gene mutations are rare in Japanese women with premature ovarian failure and polycystic ovary syndrome
-
Takakura K, Takebayashi K, Wang HQ, Kimura F, Kassahara K & Noda Y. Follicle stimulating hormone receptor gene mutations are rare in Japanese women with premature ovarian failure and polycystic ovary syndrome. Fertility and Sterility 2001 75 207-209.
-
(2001)
Fertility and Sterility
, vol.75
, pp. 207-209
-
-
Takakura, K.1
Takebayashi, K.2
Wang, H.Q.3
Kimura, F.4
Kassahara, K.5
Noda, Y.6
-
83
-
-
0032800694
-
Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome atid polycystic ovary syndrome
-
Conway GS, Conway E, Walker C, Hoppner W, Gromoll J & Simoni M. Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome atid polycystic ovary syndrome. Clinical Endocrinology 1999 51 97-99.
-
(1999)
Clinical Endocrinology
, vol.51
, pp. 97-99
-
-
Conway, G.S.1
Conway, E.2
Walker, C.3
Hoppner, W.4
Gromoll, J.5
Simoni, M.6
-
84
-
-
0033799366
-
No evidence for mutations of the leptin or leptin receptor genes in women with polycystic ovary syndrome
-
Oksanen L, Tiitinen A, Kaprio, J, Koistinen HA, Karonen S & Kontula K. No evidence for mutations of the leptin or leptin receptor genes in women with polycystic ovary syndrome. Molecular Human Reproduction 2000 6 873-876.
-
(2000)
Molecular Human Reproduction
, vol.6
, pp. 873-876
-
-
Oksanen, L.1
Tiitinen, A.2
Kaprio, J.3
Koistinen, H.A.4
Karonen, S.5
Kontula, K.6
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