SCOPUS 정보 검색 플랫폼

Molecular Endocrinology

Volumn 13, Issue 6, 1999, Pages 812-818

Fertility and infertility: Genetic contributions from the hypothalamic-pituitary-gonadal axis

(2) Achermann, John C a Jameson, J Larry a

a NORTHWESTERN UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVIN; FOLLISTATIN; FOLLITROPIN; GONADORELIN; GONADOTROPIN; GONADOTROPIN RECEPTOR; HORMONE RECEPTOR; INHIBIN; LUTEINIZING HORMONE; SEX HORMONE; STEROIDOGENIC FACTOR 1; TRANSCRIPTION FACTOR;

ADENOHYPOPHYSIS; DEVELOPMENT; FEMALE; FERTILITY; GAMETOGENESIS; GENE MUTATION; GENETIC ANALYSIS; GONAD DEVELOPMENT; HUMAN; HYPOTHALAMUS HYPOPHYSIS GONAD SYSTEM; INFERTILITY; MALE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SHORT SURVEY;

EID: 0033305054 PISSN: 08888809 EISSN: None Source Type: Journal
DOI: 10.1210/mend.13.6.0301 Document Type: Short Survey

Times cited : (53)

References (19)

1
- 0032126769
- The role of DAX-1 in reproduction
- (1998) Trends Endocrinol Metab , vol.9 , pp. 169-175
- Yu, R.N.¹ Achermann, J.C.² Ito, M.³ Jameson, J.L.⁴

2
- 0031796372
- Role of Ahch in gonadal development and gametogenesis
- (1998) Nat Genet , vol.20 , pp. 353-357
- Yu, R.N.¹ Ito, M.² Saunders, T.L.³ Camper, S.A.⁴ Jameson, J.L.⁵

3
- 0031694570
- Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): Pathophysiological and genetic considerations
- (1998) Endocr Rev , vol.19 , pp. 521-539
- Seminara, S.B.¹ Hayes, F.J.² Crowley W.F., Jr.³

4
- 0030698188
- A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor
- (1997) N Engl J Med , vol.337 , pp. 1597-1602
- De Roux, N.¹ Young, J.² Misrahi, M.³ Genet, R.⁴ Chanson, P.⁵ Schaison, G.⁶ Milgrom, E.⁷

5
- 17144439793
- Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism
- (1998) Nat Genet , vol.18 , pp. 14-15
- Layman, L.C.¹ Cohen, D.P.² Jin, M.³ Xie, J.⁴ Li, Z.⁵ Reindollar, R.H.⁶ Bolbolan, S.⁷ Bick, D.P.⁸ Sherins, R.R.⁹ Duck, L.W.¹⁰ Musgrove, L.C.¹¹ Sellers, J.C.¹² Neill, J.D.¹³

6
- 17344362762
- Mutations in the homeobox gene HESX1/ Hesxl associated with septo-optic dysplasia in human and mouse
- (1998) Nat Genet , vol.19 , pp. 125-133
- Dattani, M.T.¹ Martinez-Barbera, J.P.² Thomas, P.Q.³ Brickman, J.M.⁴ Gupta, R.⁵ Martensson, I.L.⁶ Toresson, H.⁷ Fox, M.⁸ Wales, J.K.⁹ Hindmarsh, P.C.¹⁰ Krauss, S.¹¹ Beddington, R.S.P.¹² Robinson, I.C.A.F.¹³

7
- 17344371881
- Mutations in PROP1 cause familial combined pituitary hormone deficiency
- (1998) Nat Genet , vol.18 , pp. 147-149
- Wu, W.¹ Cogan, J.D.² Pfaffle, R.W.³ Dasen, J.S.⁴ Frisch, H.⁵ O'Connell, S.M.⁶ Flynn, S.E.⁷ Brown, M.R.⁸ Mullis, P.E.⁹ Parks, J.S.¹⁰ Phillips, J.A.¹¹ Rosenfeld, M.G.¹²

8
- 0030744037
- Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone β-subunit gene
- (1997) N Engl J Med , vol.337 , pp. 607-611
- Layman, L.C.¹ Lee, E.J.² Peak, D.B.³ Namnoum, A.B.⁴ Vu, K.V.⁵ Van Lingen, B.L.⁶ Gray, M.R.⁷ McDonough, P.G.⁸ Reindollar, R.H.⁹ Jameson, J.L.¹⁰

9
- 0029118115
- Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
- (1995) Cell , vol.82 , pp. 959-968
- Aittomaki, K.¹ Lucena, J.L.² Pakarinen, P.³ Sistonen, P.⁴ Tapanainen, J.⁵ Gromoll, J.⁶ Kaskikari, R.⁷ Sankila, E.M.⁸ Lehvaslaiho, H.⁹ Engel, A.R.¹⁰ Nieschlag, E.¹¹ Huhtaniemi, I.¹² De la Chapelle, A.¹³

10
- 0031054284
- Follicle stimulating hormone is required for ovarian follicle maturation but not male fertility
- (1997) Nat Genet , vol.15 , pp. 201-204
- Kumar, T.R.¹ Wang, Y.² Lu, N.³ Matzuk, M.M.⁴

11
- 0032190476
- A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor
- (1998) J Clin Invest , vol.102 , pp. 1352-1359
- Beau, I.¹ Touraine, P.² Meduri, G.³ Gougeon, A.⁴ Desroches, A.⁵ Matuchansky, C.⁶ Milgrom, E.⁷ Kuttenn, F.⁸ Misrahi, M.⁹

12
- 1842376911
- Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility
- (1997) Nat Genet , vol.15 , pp. 205-206
- Tapanainen, J.S.¹ Aittomaki, K.² Min, J.³ Vaskivuo, T.⁴ Huhtaniemi, I.T.⁵

13
- 0032508059
- Male hypogonadism due to a mutation in the gene for the β-subunit of follicle-stimulating hormone
- (1998) N Engl J Med , vol.338 , pp. 1729-1732
- Phillip, M.¹ Arbelle, J.E.² Segev, Y.³ Parvari, R.⁴

14
- 0031712880
- Follitropin (FSH) deficiency in an infertile male due to FSH β gene mutation. A syndrome of normal puberty and virilization but underdeveloped testicles with azoospermia, low FSH but high lutropin and normal serum testosterone concentrations
- (1998) Clin Chem Lab Med , vol.36 , pp. 663-665
- Lindstedt, G.¹ Nystrom, E.² Matthews, C.³ Ernest, I.⁴ Janson, P.O.⁵ Chatterjee, K.⁶

15
- 0026335545
- Hypogonadism caused by a single amino acid substitution in the β subunit of luteinizing hormone
- (1992) N Engl J Med , vol.326 , pp. 179-183
- Weiss, J.¹ Axelrod, L.² Whitcomb, R.W.³ Harris, P.E.⁴ Crowley, W.F.⁵ Jameson, J.L.⁶

16
- 0032230326
- A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: Correlation between receptor activity and phenotype
- (1998) Mol Endocrinol , vol.12 , pp. 775-784
- Martens, J.W.¹ Verhoef-Post, M.² Abelin, N.³ Ezabella, M.⁴ Toledo, S.P.⁵ Brunner, H.G.⁶ Themmen, A.P.⁷

17
- 0032230361
- A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptor
- (1998) Mol Endocrinol , vol.12 , pp. 442-450
- Latronico, A.C.¹ Chai, Y.² Arnhold, I.J.³ Liu, X.⁴ Mendonca, B.B.⁵ Segaloff, D.L.⁶

18
- 0031941395
- Overexpression of mouse follistatin causes reproductive defects in transgenic mice
- (1998) Mol Endocrinol , vol.12 , pp. 96-106
- Guo, Q.¹ Kumar, T.R.² Woodruff, T.³ Hadsell, L.A.⁴ DeMayo, F.J.⁵ Matzuk, M.M.⁶

19
- 0030238387
- Transgenic mice in the analysis of reproductive development and function
- (1996) Rev Reprod , vol.1 , pp. 203-212
- Nishimori, K.¹ Matzuk, M.M.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.