-
1
-
-
84883954825
-
Physiology of the GnRH neuronal network
-
3rd edition. J.D. Neill, editor. Academic Press. San Diego, California, USA
-
Herbison, A.E. 2006. Physiology of the GnRH neuronal network. In Knobil and Neill's physiology of reproduction. 3rd edition. J.D. Neill, editor. Academic Press. San Diego, California, USA. 1415-1482.
-
(2006)
Knobil and Neill's physiology of reproduction
, pp. 1415-1482
-
-
Herbison, A.E.1
-
2
-
-
0014245370
-
Influence of hypophysectomy, sham hypophysectomy and other surgical procedures on luteal function in the rhesus monkey
-
Knobil, E., Neill, J.D., and Johansson, E.D. 1968. Influence of hypophysectomy, sham hypophysectomy and other surgical procedures on luteal function in the rhesus monkey. Endocrinology. 82:410-415.
-
(1968)
Endocrinology
, vol.82
, pp. 410-415
-
-
Knobil, E.1
Neill, J.D.2
Johansson, E.D.3
-
3
-
-
11144235562
-
Live view of gonadotropin-releasing hormone containing neuron migration
-
Bless, E.P., et al. 2005. Live view of gonadotropin-releasing hormone containing neuron migration. Endocrinology. 146:463-468.
-
(2005)
Endocrinology
, vol.146
, pp. 463-468
-
-
Bless, E.P.1
-
4
-
-
9644281869
-
Ontogeny of GnRH and olfactory neuronal systems in man: Novel insights from the investigation of inherited forms of Kallmann's syndrome
-
Gonzalez-Martinez, D., Hu, Y., and Bouloux, P.M. 2004. Ontogeny of GnRH and olfactory neuronal systems in man: novel insights from the investigation of inherited forms of Kallmann's syndrome. Front. Neuroendocrinol. 25:108-130.
-
(2004)
Front. Neuroendocrinol
, vol.25
, pp. 108-130
-
-
Gonzalez-Martinez, D.1
Hu, Y.2
Bouloux, P.M.3
-
5
-
-
0031694570
-
Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): Pathophysiological and genetic considerations
-
Seminara, S.B., Hayes, F.J., and Crowley, W.F., Jr. 1998. Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations. Endocr. Rev. 19:521-539.
-
(1998)
Endocr. Rev
, vol.19
, pp. 521-539
-
-
Seminara, S.B.1
Hayes, F.J.2
Crowley Jr., W.F.3
-
6
-
-
0031059199
-
Adult-onset idiopathic hypogonadotropic hypogonadism-a treatable form of male infertility
-
Nachtigall, L.B., Boepple, P.A., Pralong, F.P., and Crowley, W.F., Jr. 1997. Adult-onset idiopathic hypogonadotropic hypogonadism-a treatable form of male infertility. N. Engl. J. Med. 336:410-415.
-
(1997)
N. Engl. J. Med
, vol.336
, pp. 410-415
-
-
Nachtigall, L.B.1
Boepple, P.A.2
Pralong, F.P.3
Crowley Jr., W.F.4
-
7
-
-
34548331152
-
Reversal of idiopathic hypogonadotropic hypogonadism
-
Raivio, T., et al. 2007. Reversal of idiopathic hypogonadotropic hypogonadism. N. Engl. J. Med. 357:863-873.
-
(2007)
N. Engl. J. Med
, vol.357
, pp. 863-873
-
-
Raivio, T.1
-
8
-
-
33846841151
-
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism
-
Pitteloud, N., et al. 2007. Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism. J. Clin. Invest. 117:457-463.
-
(2007)
J. Clin. Invest
, vol.117
, pp. 457-463
-
-
Pitteloud, N.1
-
9
-
-
33750471153
-
Kallmann syndrome: Mutations in the genes encoding prokineticin-2 and prokineticin receptor-2
-
Dodé, C., et al. 2006. Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2. PLoS Genet. 2:e175.
-
(2006)
PLoS Genet
, vol.2
-
-
Dodé, C.1
-
10
-
-
20244366799
-
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
-
Dode, C., et al. 2003. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat. Genet. 33:463-465.
-
(2003)
Nat. Genet
, vol.33
, pp. 463-465
-
-
Dode, C.1
-
11
-
-
33646567190
-
Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism
-
Pitteloud, N., et al. 2006. Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism. Proc. Natl. Acad. Sci. U. S. A. 103:6281-6286.
-
(2006)
Proc. Natl. Acad. Sci. U. S. A
, vol.103
, pp. 6281-6286
-
-
Pitteloud, N.1
-
12
-
-
18144423534
-
Structural basis for fibroblast growth factor receptor activation
-
Mohammadi, M., Olsen, S.K., and Ibrahimi, O.A. 2005. Structural basis for fibroblast growth factor receptor activation. Cytokine Growth Factor Rev. 16:107-137.
-
(2005)
Cytokine Growth Factor Rev
, vol.16
, pp. 107-137
-
-
Mohammadi, M.1
Olsen, S.K.2
Ibrahimi, O.A.3
-
13
-
-
33744937606
-
Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family
-
Zhang, X., et al. 2006. Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family. J. Biol. Chem. 281:15694-15700.
-
(2006)
J. Biol. Chem
, vol.281
, pp. 15694-15700
-
-
Zhang, X.1
-
14
-
-
0031916557
-
An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination
-
Meyers, E.N., Lewandoski, M., and Martin, G.R. 1998. An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination. Nat. Genet. 18:136-141.
-
(1998)
Nat. Genet
, vol.18
, pp. 136-141
-
-
Meyers, E.N.1
Lewandoski, M.2
Martin, G.R.3
-
15
-
-
0026738943
-
Cloning and characterization of an androgen-induced growth factor essential for the androgen-dependent growth of mouse mammary carcinoma cells
-
Tanaka, A., et al. 1992. Cloning and characterization of an androgen-induced growth factor essential for the androgen-dependent growth of mouse mammary carcinoma cells. Proc. Natl. Acad. Sci. U. S. A. 89:8928-8932.
-
(1992)
Proc. Natl. Acad. Sci. U. S. A
, vol.89
, pp. 8928-8932
-
-
Tanaka, A.1
-
16
-
-
0035798089
-
Neocortex patterning by the secreted signaling molecule FGF8
-
Fukuchi-Shimogori, T., and Grove, E.A. 2001. Neocortex patterning by the secreted signaling molecule FGF8. Science. 294:1071-1074.
-
(2001)
Science
, vol.294
, pp. 1071-1074
-
-
Fukuchi-Shimogori, T.1
Grove, E.A.2
-
17
-
-
0038635952
-
Molecular regionalization of the neocortex is disrupted in Fgf8 hypomorphic mutants
-
Garel, S., Huffman, K.J., and Rubenstein, J.L. 2003. Molecular regionalization of the neocortex is disrupted in Fgf8 hypomorphic mutants. Development. 130:1903-1914.
-
(2003)
Development
, vol.130
, pp. 1903-1914
-
-
Garel, S.1
Huffman, K.J.2
Rubenstein, J.L.3
-
18
-
-
0033959238
-
Signalling by FGF8 from the isthmus patterns anterior hindbrain and establishes the anterior limit of Hox gene expression
-
Irving, C., and Mason, I. 2000. Signalling by FGF8 from the isthmus patterns anterior hindbrain and establishes the anterior limit of Hox gene expression. Development. 127:177-186.
-
(2000)
Development
, vol.127
, pp. 177-186
-
-
Irving, C.1
Mason, I.2
-
19
-
-
0037083449
-
Role of the isthmus and FGFs in resolving the paradox of neural crest plasticity and prepatterning
-
Trainor, P.A., Ariza-McNaughton, L., and Krumlauf, R. 2002. Role of the isthmus and FGFs in resolving the paradox of neural crest plasticity and prepatterning. Science. 295:1288-1291.
-
(2002)
Science
, vol.295
, pp. 1288-1291
-
-
Trainor, P.A.1
Ariza-McNaughton, L.2
Krumlauf, R.3
-
20
-
-
0041409985
-
The isthmic organizer signal FGF8 is required for cell survival in the prospective midbrain and cerebellum
-
Chi, C.L., Martinez, S., Wurst, W., and Martin, G.R. 2003. The isthmic organizer signal FGF8 is required for cell survival in the prospective midbrain and cerebellum. Development. 130:2633-2644.
-
(2003)
Development
, vol.130
, pp. 2633-2644
-
-
Chi, C.L.1
Martinez, S.2
Wurst, W.3
Martin, G.R.4
-
21
-
-
0037452624
-
Dosage of Fgf8 determines whether cell survival is positively or negatively regulated in the developing forebrain
-
Storm, E.E., Rubenstein, J.L., and Martin, G.R. 2003. Dosage of Fgf8 determines whether cell survival is positively or negatively regulated in the developing forebrain. Proc. Natl. Acad. Sci. U. S. A. 100:1757-1762.
-
(2003)
Proc. Natl. Acad. Sci. U. S. A
, vol.100
, pp. 1757-1762
-
-
Storm, E.E.1
Rubenstein, J.L.2
Martin, G.R.3
-
22
-
-
0030200887
-
Structure and sequence of human FGF8
-
Gemel, J., Gorry, M., Ehrlich, G.D., and MacArthur, C.A. 1996. Structure and sequence of human FGF8. Genomics. 35:253-257.
-
(1996)
Genomics
, vol.35
, pp. 253-257
-
-
Gemel, J.1
Gorry, M.2
Ehrlich, G.D.3
MacArthur, C.A.4
-
23
-
-
30944448671
-
Structural basis by which alternative splicing modulates the organizer activity of FGF8 in the brain
-
Olsen, S.K., et al. 2006. Structural basis by which alternative splicing modulates the organizer activity of FGF8 in the brain. Genes Dev. 20:185-198.
-
(2006)
Genes Dev
, vol.20
, pp. 185-198
-
-
Olsen, S.K.1
-
24
-
-
0033635299
-
Crystal structure of a ternary FGF-FGFR-heparin complex reveals a dual role for heparin in FGFR binding and dimerization
-
Schlessinger, J., et al. 2000. Crystal structure of a ternary FGF-FGFR-heparin complex reveals a dual role for heparin in FGFR binding and dimerization. Mol. Cell. 6:743-750.
-
(2000)
Mol. Cell
, vol.6
, pp. 743-750
-
-
Schlessinger, J.1
-
25
-
-
0031023520
-
Overlapping expression and redundant activation of mesenchymal fibroblast growth factor (FGF) receptors by alternatively spliced FGF-8 ligands
-
Blunt, A.G., et al. 1997. Overlapping expression and redundant activation of mesenchymal fibroblast growth factor (FGF) receptors by alternatively spliced FGF-8 ligands. J. Biol. Chem. 272:3733-3738.
-
(1997)
J. Biol. Chem
, vol.272
, pp. 3733-3738
-
-
Blunt, A.G.1
-
26
-
-
29644446379
-
Fgf8 expression defines a morphogenetic center required for olfactory neurogenesis and nasal cavity development in the mouse
-
Kawauchi, S., et al. 2005. Fgf8 expression defines a morphogenetic center required for olfactory neurogenesis and nasal cavity development in the mouse. Development. 132:5211-5223.
-
(2005)
Development
, vol.132
, pp. 5211-5223
-
-
Kawauchi, S.1
-
27
-
-
0024598702
-
Spatio-temporal cell expression of luteinizing hormone-releasing hormone in the prenatal mouse: Evidence for an embryonic origin in the olfactory placode
-
Wray, S., Nieburgs, A., and Elkabes, S. 1989. Spatio-temporal cell expression of luteinizing hormone-releasing hormone in the prenatal mouse: evidence for an embryonic origin in the olfactory placode. Brain Res. Dev. Brain Res. 46:309-318.
-
(1989)
Brain Res. Dev. Brain Res
, vol.46
, pp. 309-318
-
-
Wray, S.1
Nieburgs, A.2
Elkabes, S.3
-
28
-
-
3843073092
-
Developmental regulation of gonadotropin-releasing hormone neurons by Fgf signaling
-
Gill, J.C., Moenter, S.M., and Tsai, P.S. 2004. Developmental regulation of gonadotropin-releasing hormone neurons by Fgf signaling. Endocrinology. 145:3830-3839.
-
(2004)
Endocrinology
, vol.145
, pp. 3830-3839
-
-
Gill, J.C.1
Moenter, S.M.2
Tsai, P.S.3
-
29
-
-
0034457870
-
Soluble factors guide gonadotropin-releasing hormone axonal targeting to the median eminence
-
Gibson, M.J., Ingraham, L., and Dobrjansky, A. 2000. Soluble factors guide gonadotropin-releasing hormone axonal targeting to the median eminence. Endocrinology. 141:3065-3071.
-
(2000)
Endocrinology
, vol.141
, pp. 3065-3071
-
-
Gibson, M.J.1
Ingraham, L.2
Dobrjansky, A.3
-
30
-
-
0028959288
-
The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo
-
Crossley, P.H., and Martin, G.R. 1995. The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo. Development. 121:439-451.
-
(1995)
Development
, vol.121
, pp. 439-451
-
-
Crossley, P.H.1
Martin, G.R.2
-
31
-
-
0033565746
-
Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo
-
Sun, X., Meyers, E.N., Lewandoski, M., and Martin, G.R. 1999. Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo. Genes Dev. 13:1834-1846.
-
(1999)
Genes Dev
, vol.13
, pp. 1834-1846
-
-
Sun, X.1
Meyers, E.N.2
Lewandoski, M.3
Martin, G.R.4
-
32
-
-
33745948557
-
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes
-
Pitteloud, N., et al. 2006. Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes. Mol. Cell. Endocrinol. 254-255:60-69.
-
(2006)
Mol. Cell. Endocrinol
, vol.254-255
, pp. 60-69
-
-
Pitteloud, N.1
-
33
-
-
34248347081
-
Impaired FGF signaling contributes to cleft lip and palate
-
Riley, B.M., et al. 2007. Impaired FGF signaling contributes to cleft lip and palate. Proc. Natl. Acad. Sci. U. S. A. 104:4512-4517.
-
(2007)
Proc. Natl. Acad. Sci. U. S. A
, vol.104
, pp. 4512-4517
-
-
Riley, B.M.1
-
34
-
-
84920355419
-
Osteoporosis in men with idiopathic hypogonadotropic hypogonadism
-
Finkelstein, J.S., et al. 1987. Osteoporosis in men with idiopathic hypogonadotropic hypogonadism. Ann. Intern. Med. 104:777-782.
-
(1987)
Ann. Intern. Med
, vol.104
, pp. 777-782
-
-
Finkelstein, J.S.1
-
35
-
-
43749110077
-
Genetic evidence that FGFs have an instructive role in limb proximal-distal patterning
-
Mariani, F.V., Ahn, C.P., and Martin, G.R. 2008. Genetic evidence that FGFs have an instructive role in limb proximal-distal patterning. Nature. 453:401-405.
-
(2008)
Nature
, vol.453
, pp. 401-405
-
-
Mariani, F.V.1
Ahn, C.P.2
Martin, G.R.3
-
36
-
-
33645890305
-
Regulation of osteoblast differentiation: A novel function for fibroblast growth factor 8
-
Valta, M.P., et al. 2006. Regulation of osteoblast differentiation: a novel function for fibroblast growth factor 8. Endocrinology. 147:2171-2182.
-
(2006)
Endocrinology
, vol.147
, pp. 2171-2182
-
-
Valta, M.P.1
-
37
-
-
11244325104
-
Targeted expression of a dominant-negative fibroblast growth factor (FGF) receptor in gonadotropin-releasing hormone (GnRH) neurons reduces FGF responsiveness and the size of GnRH neuronal population
-
Tsai, P.S., et al. 2005. Targeted expression of a dominant-negative fibroblast growth factor (FGF) receptor in gonadotropin-releasing hormone (GnRH) neurons reduces FGF responsiveness and the size of GnRH neuronal population. Mol. Endocrinol. 19:225-236.
-
(2005)
Mol. Endocrinol
, vol.19
, pp. 225-236
-
-
Tsai, P.S.1
-
38
-
-
0033739538
-
Genetics of Hirschsprung disease
-
Parisi, M.A., and Kapur, R.P. 2000. Genetics of Hirschsprung disease. Curr. Opin. Pediatr. 12:610-617.
-
(2000)
Curr. Opin. Pediatr
, vol.12
, pp. 610-617
-
-
Parisi, M.A.1
Kapur, R.P.2
-
39
-
-
0028245437
-
Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
-
Kajiwara, K., Berson, E.L., and Dryja, T.P. 1994. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci. Science. 264:1604-1608.
-
(1994)
Science
, vol.264
, pp. 1604-1608
-
-
Kajiwara, K.1
Berson, E.L.2
Dryja, T.P.3
-
40
-
-
0037351187
-
FGF signaling through FGFR1 is required for olfactory bulb morphogenesis
-
Hebert, J.M., Lin, M., Partanen, J., Rossant, J., and McConnell, S.K. 2003. FGF signaling through FGFR1 is required for olfactory bulb morphogenesis. Development. 130:1101-1111.
-
(2003)
Development
, vol.130
, pp. 1101-1111
-
-
Hebert, J.M.1
Lin, M.2
Partanen, J.3
Rossant, J.4
McConnell, S.K.5
-
41
-
-
18844367672
-
A window of opportunity: The diagnosis of gonadotropin deficiency in the male infant
-
Grumbach, M.M. 2005. A window of opportunity: the diagnosis of gonadotropin deficiency in the male infant. J. Clin. Endocrinol. Metab. 90:3122-3127.
-
(2005)
J. Clin. Endocrinol. Metab
, vol.90
, pp. 3122-3127
-
-
Grumbach, M.M.1
-
42
-
-
0030846217
-
Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes
-
Yoshiura, K., et al. 1997. Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes. Am. J. Med. Genet. 72:354-362.
-
(1997)
Am. J. Med. Genet
, vol.72
, pp. 354-362
-
-
Yoshiura, K.1
-
43
-
-
0031612929
-
Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group
-
Antonarakis, S.E. 1998. Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group. Hum. Mutat. 11:1-3.
-
(1998)
Hum. Mutat
, vol.11
, pp. 1-3
-
-
Antonarakis, S.E.1
-
44
-
-
17744373868
-
The importance of autosomal genes in Kallmann syndrome: Genotype-phenotype correlations and neuroendocrine characteristics
-
Oliveira, L.M., et al. 2001. The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. J. Clin. Endocrinol. Metab. 86:1532-1538.
-
(2001)
J. Clin. Endocrinol. Metab
, vol.86
, pp. 1532-1538
-
-
Oliveira, L.M.1
-
45
-
-
0030698188
-
A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor
-
de Roux, N., et al. 1997. A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor. N. Engl. J. Med. 337:1597-1602.
-
(1997)
N. Engl. J. Med
, vol.337
, pp. 1597-1602
-
-
de Roux, N.1
-
46
-
-
15944364441
-
Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene
-
Pitteloud, N., et al. 2005. Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene. J. Clin. Endocrinol. Metab. 90:1317-1322.
-
(2005)
J. Clin. Endocrinol. Metab
, vol.90
, pp. 1317-1322
-
-
Pitteloud, N.1
-
47
-
-
0142091653
-
The GPR54 gene as a regulator of puberty
-
Seminara, S.B., et al. 2003. The GPR54 gene as a regulator of puberty. N. Engl. J. Med. 349:1614-1627.
-
(2003)
N. Engl. J. Med
, vol.349
, pp. 1614-1627
-
-
Seminara, S.B.1
-
48
-
-
36849044530
-
From the Cover: Lossof-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism
-
Pitteloud, N., et al. 2007. From the Cover: Lossof-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism. Proc. Natl. Acad. Sci. U. S. A. 104:17447-17452.
-
(2007)
Proc. Natl. Acad. Sci. U. S. A
, vol.104
, pp. 17447-17452
-
-
Pitteloud, N.1
-
49
-
-
0036149989
-
The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism
-
Pitteloud, N., et al. 2002. The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism. J. Clin. Endocrinol. Metab. 87:152-160.
-
(2002)
J. Clin. Endocrinol. Metab
, vol.87
, pp. 152-160
-
-
Pitteloud, N.1
-
50
-
-
0021796858
-
Sex differences in odor identification ability: A cross-cultural analysis
-
Doty, R.L., Applebaum, S., Zusho, H., and Settle, R.G. 1985. Sex differences in odor identification ability: a cross-cultural analysis. Neuropsychologia. 23:667-672.
-
(1985)
Neuropsychologia
, vol.23
, pp. 667-672
-
-
Doty, R.L.1
Applebaum, S.2
Zusho, H.3
Settle, R.G.4
-
51
-
-
0033059856
-
Free alpha-subunit is superior to luteinizing hormone as a marker of gonadotropin-releasing hormone despite desensitization at fast pulse frequencies
-
Hayes, F.J., McNicholl, D.J., Schoenfeld, D., Marsh, E.E., and Hall, J.E. 1999. Free alpha-subunit is superior to luteinizing hormone as a marker of gonadotropin-releasing hormone despite desensitization at fast pulse frequencies. J. Clin. Endocrinol. Metab. 84:1028-1036.
-
(1999)
J. Clin. Endocrinol. Metab
, vol.84
, pp. 1028-1036
-
-
Hayes, F.J.1
McNicholl, D.J.2
Schoenfeld, D.3
Marsh, E.E.4
Hall, J.E.5
-
52
-
-
0019914160
-
Induction of puberty in men by long-term pulsatile administration of low-dose gonadotropin-releasing hormone
-
Hoffman, A.R., and Crowley, W.F., Jr. 1982. Induction of puberty in men by long-term pulsatile administration of low-dose gonadotropin-releasing hormone. N. Engl. J. Med. 307:1237-1241.
-
(1982)
N. Engl. J. Med
, vol.307
, pp. 1237-1241
-
-
Hoffman, A.R.1
Crowley Jr., W.F.2
-
53
-
-
0022669377
-
Hypogonadotropic disorders in men and women: Diagnosis and therapy with pulsatile gonadotropin-releasing hormone
-
Santoro, N., Filicori, M., and Crowley, W.F., Jr. 1986. Hypogonadotropic disorders in men and women: diagnosis and therapy with pulsatile gonadotropin-releasing hormone. Endocr. Rev. 7:11-23.
-
(1986)
Endocr. Rev
, vol.7
, pp. 11-23
-
-
Santoro, N.1
Filicori, M.2
Crowley Jr., W.F.3
-
54
-
-
0034912866
-
Testosterone and estrogen act via different pathways to inhibit puberty in the male Siberian hamster (Phodopus sungorus)
-
Pak, T.R., Lynch, G.R., and Tsai, P.S. 2001. Testosterone and estrogen act via different pathways to inhibit puberty in the male Siberian hamster (Phodopus sungorus). Endocrinology. 142:3309-3316.
-
(2001)
Endocrinology
, vol.142
, pp. 3309-3316
-
-
Pak, T.R.1
Lynch, G.R.2
Tsai, P.S.3
|