-
1
-
-
78049379286
-
Progress of precocious puberty in children
-
Cai D.P. Progress of precocious puberty in children. J. Appl. Clin. Pediatr. 2005, 6:1.
-
(2005)
J. Appl. Clin. Pediatr.
, vol.6
, pp. 1
-
-
Cai, D.P.1
-
2
-
-
16544370834
-
The neural basis of puberty and adolescence
-
Cheryl L.S., Douglas L.F. The neural basis of puberty and adolescence. Nat. Neurosci. 2004, 7:1040-1047.
-
(2004)
Nat. Neurosci.
, vol.7
, pp. 1040-1047
-
-
Cheryl, L.S.1
Douglas, L.F.2
-
4
-
-
21044448847
-
The neuroendocrine timing of puberty
-
Ebling F.J. The neuroendocrine timing of puberty. Reproduction 2005, 129:675-683.
-
(2005)
Reproduction
, vol.129
, pp. 675-683
-
-
Ebling, F.J.1
-
5
-
-
84995842414
-
Identification of two point mutations in the gene coding luteinizing hormone (LH) beta-subunit, associated with immunologically anomalous LH variants
-
Furui K., Suganuma N., Tsukahara S., Asada Y., Kikkawa F., Tanaka M., Ozawa T., Tomoda S Y. Identification of two point mutations in the gene coding luteinizing hormone (LH) beta-subunit, associated with immunologically anomalous LH variants. J. Clin. Endocrinol. Metab. 1994, 78:107-113.
-
(1994)
J. Clin. Endocrinol. Metab.
, vol.78
, pp. 107-113
-
-
Furui, K.1
Suganuma, N.2
Tsukahara, S.3
Asada, Y.4
Kikkawa, F.5
Tanaka, M.6
Ozawa, T.7
Tomoda S, Y.8
-
6
-
-
0002964154
-
Puberty: ontogeny, neuroendocrinology, physiology, and disorders
-
WB Saunders Co., Philadelphia, J.D. Wilson, D.W. Foster, H.M. Kronenberg, P.R. Larsen (Eds.)
-
Grumbach M.M, Styne D.M. Puberty: ontogeny, neuroendocrinology, physiology, and disorders. Williams Textbook of Endocrinology 1998, 1509-1625. WB Saunders Co., Philadelphia. 9th ed. J.D. Wilson, D.W. Foster, H.M. Kronenberg, P.R. Larsen (Eds.).
-
(1998)
Williams Textbook of Endocrinology
, pp. 1509-1625
-
-
Grumbach, M.M.1
Styne, D.M.2
-
7
-
-
0028923111
-
Occurrence and biological properties of a common genetic variant of luteinizing hormone
-
Haavisto A.M., Pettersson K., Bergendahl M., Virkamaki A., Huhtaniemi I. Occurrence and biological properties of a common genetic variant of luteinizing hormone. J. Clin. Endocrinol. Metab. 1995, 80:1257-1263.
-
(1995)
J. Clin. Endocrinol. Metab.
, vol.80
, pp. 1257-1263
-
-
Haavisto, A.M.1
Pettersson, K.2
Bergendahl, M.3
Virkamaki, A.4
Huhtaniemi, I.5
-
8
-
-
0026032263
-
A pulsatile gonadotropin-releasing hormone stimulus is required to increase transcription of the gonadotropin subunit genes: evidence for differential regulation of transcription by pulse frequency in vivo
-
Haisenleder D.J., Dalkin A.C., Ortolano G.A., Marshall J.C., Shupnik M.A. A pulsatile gonadotropin-releasing hormone stimulus is required to increase transcription of the gonadotropin subunit genes: evidence for differential regulation of transcription by pulse frequency in vivo. Endocrinology 1991, 128:509-517.
-
(1991)
Endocrinology
, vol.128
, pp. 509-517
-
-
Haisenleder, D.J.1
Dalkin, A.C.2
Ortolano, G.A.3
Marshall, J.C.4
Shupnik, M.A.5
-
9
-
-
0032883294
-
A common polymorphic allele of the human luteinizing hormone beta-subunit gene: additional mutations and differential function of the promoter sequence
-
Jiang M., Pakarinen P., Zhang F.P., El-Hefnawy T., Koskimies P., Pettersson K., Huhtaniemi I. A common polymorphic allele of the human luteinizing hormone beta-subunit gene: additional mutations and differential function of the promoter sequence. Hum. Mol. Genet. 1999, 8:2037-2046.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 2037-2046
-
-
Jiang, M.1
Pakarinen, P.2
Zhang, F.P.3
El-Hefnawy, T.4
Koskimies, P.5
Pettersson, K.6
Huhtaniemi, I.7
-
10
-
-
27144477692
-
Human FSHβ subunit gene is highly conserved
-
Lamminen T., Jokinen P., Jiang M., Pakarinen P., Simonsen H., Huhtaniemi I. Human FSHβ subunit gene is highly conserved. Mol. Hum. Reprod. 2005, 11:601-605.
-
(2005)
Mol. Hum. Reprod.
, vol.11
, pp. 601-605
-
-
Lamminen, T.1
Jokinen, P.2
Jiang, M.3
Pakarinen, P.4
Simonsen, H.5
Huhtaniemi, I.6
-
11
-
-
0030744037
-
Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone b-subunit gene
-
Layman L.C., Lee E.J., Peak D.B., Namnoum A.B., Vu K.V., van Lingen B.L., Gray M.R., McDonough P.G., Reindollar R.H., Jameson J.L. Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone b-subunit gene. N. Engl. J. Med. 1997, 337:607-611.
-
(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
-
12
-
-
0034732237
-
Mutations of follicle stimulating hormone-β and its receptor in human and mouse: gentype/phenotype
-
Layman L.C., McDonough P.G. Mutations of follicle stimulating hormone-β and its receptor in human and mouse: gentype/phenotype. Mol. Cell. Endocrinol. 2000, 161:9-17.
-
(2000)
Mol. Cell. Endocrinol.
, vol.161
, pp. 9-17
-
-
Layman, L.C.1
McDonough, P.G.2
-
13
-
-
0031712880
-
Follitropin (FSH) deficiency in an infertile male due to FSHβ gene mutation. A syndrome of normal puberty and virilization but underdeveloped testicles with azoospermia, low FSH but high lutropin and normal serum testosterone concentrations
-
Lindstedt G., Nyström E., Matthews C., Ernest I., Janson P.O., Chatterjee K. Follitropin (FSH) deficiency in an infertile male due to FSHβ gene mutation. A syndrome of normal puberty and virilization but underdeveloped testicles with azoospermia, low FSH but high lutropin and normal serum testosterone concentrations. Clin. Chem. Lab. Med. 1998, 36:663-665.
-
(1998)
Clin. Chem. Lab. Med.
, vol.36
, pp. 663-665
-
-
Lindstedt, G.1
Nyström, E.2
Matthews, C.3
Ernest, I.4
Janson, P.O.5
Chatterjee, K.6
-
14
-
-
34848919226
-
GPR54 polymorphisms in Chinese girls with central precocious puberty
-
Luan X., Yu H., Wei X., Zhou Y., Wang W., Li P., Gan X., Wei D., Xiao J. GPR54 polymorphisms in Chinese girls with central precocious puberty. Neuroendocrinology 2007, 86:77-83.
-
(2007)
Neuroendocrinology
, vol.86
, pp. 77-83
-
-
Luan, X.1
Yu, H.2
Wei, X.3
Zhou, Y.4
Wang, W.5
Li, P.6
Gan, X.7
Wei, D.8
Xiao, J.9
-
15
-
-
85047684917
-
Variation in the timing of puberty: clinical spectrum and genetic investigation
-
Mark R.P., Paul A.B. Variation in the timing of puberty: clinical spectrum and genetic investigation. J. Clin. Endocrinol. Metab. 2001, 86:2364-2368.
-
(2001)
J. Clin. Endocrinol. Metab.
, vol.86
, pp. 2364-2368
-
-
Mark, R.P.1
Paul, A.B.2
-
16
-
-
0027324274
-
Primary amenorrhoea and infertility due to a mutation in the β-subunit of follicle-stimulating hormone
-
Matthews C.H., Borgato S., Beck-Peccoz P., Adams M., Tone Y., Gambino G., Casagrande S., Tedeschini G., Benedetti A., Chatterjee V.K. Primary amenorrhoea and infertility due to a mutation in the β-subunit of follicle-stimulating hormone. Nat. Genet. 1993, 5:83-86.
-
(1993)
Nat. Genet.
, vol.5
, pp. 83-86
-
-
Matthews, C.H.1
Borgato, S.2
Beck-Peccoz, P.3
Adams, M.4
Tone, Y.5
Gambino, G.6
Casagrande, S.7
Tedeschini, G.8
Benedetti, A.9
Chatterjee, V.K.10
-
17
-
-
0025001255
-
Gonadotropin secretory dynamics during puberty in normal girls and boys
-
Oerter K.E., Uriarte M.M., Rose S.R., Barnes K.M., Cutler G.B.Jr. Gonadotropin secretory dynamics during puberty in normal girls and boys. J. Clin. Endocrinol. Metab. 1990, 71:1251-1258.
-
(1990)
J. Clin. Endocrinol. Metab.
, vol.71
, pp. 1251-1258
-
-
Oerter, K.E.1
Uriarte, M.M.2
Rose, S.R.3
Barnes, K.M.4
Cutler, G.5
-
18
-
-
0032508059
-
Male hypogonadism due to a mutation in the gene for the beta-subunit of follicle-stimulating hormone
-
Phillip M., Arbelle J.E., Segev Y., Parvari R. Male hypogonadism due to a mutation in the gene for the beta-subunit of follicle-stimulating hormone. N. Engl. J. Med. 1998, 338:1729-1732.
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 1729-1732
-
-
Phillip, M.1
Arbelle, J.E.2
Segev, Y.3
Parvari, R.4
-
19
-
-
0029843892
-
The role of luteinizing hormone-beta gene polymorphism in the onset and progression of puberty in healthy boys
-
Raivio T., Huhtaniemi I., Anttila R., Siimes M.A., Hagenäs L., Nilsson C., Pettersson K., Dunkel L. The role of luteinizing hormone-beta gene polymorphism in the onset and progression of puberty in healthy boys. J. Clin. Endocrinol. Metab. 1996, 81:3278-3282.
-
(1996)
J. Clin. Endocrinol. Metab.
, vol.81
, pp. 3278-3282
-
-
Raivio, T.1
Huhtaniemi, I.2
Anttila, R.3
Siimes, M.A.4
Hagenäs, L.5
Nilsson, C.6
Pettersson, K.7
Dunkel, L.8
-
20
-
-
20044396569
-
Determination of sequence variation and haplotype structure for the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes: investigation of role in pubertal timing
-
Sedlmeyer I.L., Pearce C.L., Trueman J.A., Butler J.L., Bersaglieri T., Read A.P., Clayton P.E., Kolonel L.N., Henderson B.E., Hirschhorn J.N., Palmert M.R. Determination of sequence variation and haplotype structure for the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes: investigation of role in pubertal timing. J. Clin. Endocrinol. Metab. 2005, 90:1091-1099.
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 1091-1099
-
-
Sedlmeyer, I.L.1
Pearce, C.L.2
Trueman, J.A.3
Butler, J.L.4
Bersaglieri, T.5
Read, A.P.6
Clayton, P.E.7
Kolonel, L.N.8
Henderson, B.E.9
Hirschhorn, J.N.10
Palmert, M.R.11
-
21
-
-
18944381751
-
SHEsis a powerful software platform for analyzes of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci
-
Shi Y.Y., He L. SHEsis a powerful software platform for analyzes of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci. Cell Res. 2005, 15:97-98.
-
(2005)
Cell Res.
, vol.15
, pp. 97-98
-
-
Shi, Y.Y.1
He, L.2
-
22
-
-
0028578737
-
Pulsatile GnRH regulation of gonadotropin subunit gene transcription
-
Shupnik M.A, Fallest P.C. Pulsatile GnRH regulation of gonadotropin subunit gene transcription. Neurosci. Biobehav. Rev. 1994, 18:597-599.
-
(1994)
Neurosci. Biobehav. Rev.
, vol.18
, pp. 597-599
-
-
Shupnik, M.A.1
Fallest, P.C.2
-
23
-
-
0035919656
-
Haplotype variation and linkage disequilibrium in 313 human genes
-
Stephens J.C., Schneider J.A., Tanguay D.A., Choi J., Acharya T., Stanley S.E., Jiang R., Messer C.J., Chew A., Han J.H., Duan J., Carr J.L., Lee M.S., Koshy B., Kumar A.M., Zhang G., Newell W.R., Windemuth A., Xu C., Kalbfleisch T.S., Shaner S.L., Arnold K., Schulz V., Drysdale C.M., Nandabalan K., Judson R.S., Ruano G., Vovis G.F. Haplotype variation and linkage disequilibrium in 313 human genes. Science 2001, 293:489-493.
-
(2001)
Science
, vol.293
, pp. 489-493
-
-
Stephens, J.C.1
Schneider, J.A.2
Tanguay, D.A.3
Choi, J.4
Acharya, T.5
Stanley, S.E.6
Jiang, R.7
Messer, C.J.8
Chew, A.9
Han, J.H.10
Duan, J.11
Carr, J.L.12
Lee, M.S.13
Koshy, B.14
Kumar, A.M.15
Zhang, G.16
Newell, W.R.17
Windemuth, A.18
Xu, C.19
Kalbfleisch, T.S.20
Shaner, S.L.21
Arnold, K.22
Schulz, V.23
Drysdale, C.M.24
Nandabalan, K.25
Judson, R.S.26
Ruano, G.27
Vovis, G.F.28
more..
-
24
-
-
0030907986
-
New aspects in the diagnosis and treatment of pubertal disorders
-
Styne D.M. New aspects in the diagnosis and treatment of pubertal disorders. Pediatr. Clin. North Am. 1997, 44:505-529.
-
(1997)
Pediatr. Clin. North Am.
, vol.44
, pp. 505-529
-
-
Styne, D.M.1
-
25
-
-
0033711033
-
Mutations of gonadotropins and gonadotropin receptors: elucidating the physiology and pathophysiology of pituitary-gonadal function
-
Themmen A.P., Huhtaniemi I. Mutations of gonadotropins and gonadotropin receptors: elucidating the physiology and pathophysiology of pituitary-gonadal function. Endocr. Rev. 2000, 21:551-583.
-
(2000)
Endocr. Rev.
, vol.21
, pp. 551-583
-
-
Themmen, A.P.1
Huhtaniemi, I.2
-
26
-
-
0036716853
-
Episodic activation of the rat GnRH promoter: role of the homeoprotein Oct-1
-
Vazquez-Mzrtinez R., Leclerc G.M., Wierman M.E., Boockfor F.R. Episodic activation of the rat GnRH promoter: role of the homeoprotein Oct-1. Mol. Endocrinol. 2002, 16:2093-2100.
-
(2002)
Mol. Endocrinol.
, vol.16
, pp. 2093-2100
-
-
Vazquez-Mzrtinez, R.1
Leclerc, G.M.2
Wierman, M.E.3
Boockfor, F.R.4
-
27
-
-
0026335545
-
Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone
-
Weiss J., Axelrod L., Whitcomb R.W., Harris P.E., Crowley W.F., Jameson J.L. Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. N. Engl. J. Med. 1992, 326:179-183.
-
(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
-
28
-
-
33644621288
-
A novel method based on ligase detection reaction for low abundant YIDD mutants detection in hepatitis B virus
-
Xiao Z., Xiao J., Jiang Y., Zhang S., Yu M., Zhao J., Wei D., Cao H. A novel method based on ligase detection reaction for low abundant YIDD mutants detection in hepatitis B virus. Hepatol. Res. 2006, 34:150-155.
-
(2006)
Hepatol. Res.
, vol.34
, pp. 150-155
-
-
Xiao, Z.1
Xiao, J.2
Jiang, Y.3
Zhang, S.4
Yu, M.5
Zhao, J.6
Wei, D.7
Cao, H.8
-
29
-
-
19444385261
-
Association study of four activity SNPs of CYP3A4 with the precocious puberty in Chinese girls
-
Xin X., Luan X., Xiao J., Wei D., Wang J., Lu D., Yang S. Association study of four activity SNPs of CYP3A4 with the precocious puberty in Chinese girls. Neurosci. Lett. 2005, 381:284-288.
-
(2005)
Neurosci. Lett.
, vol.381
, pp. 284-288
-
-
Xin, X.1
Luan, X.2
Xiao, J.3
Wei, D.4
Wang, J.5
Lu, D.6
Yang, S.7
-
30
-
-
33745673377
-
Association study of six activity SNPS in adrenal steroid hormone metabolism and IBM related genes with precocious puberty in Chinese girls
-
Xin X., Xiao J., Luan X., Zhou Y., Lu D., Wei D., Yang S. Association study of six activity SNPS in adrenal steroid hormone metabolism and IBM related genes with precocious puberty in Chinese girls. Neuro. Endocrinol. Lett. 2006, 27:101-106.
-
(2006)
Neuro. Endocrinol. Lett.
, vol.27
, pp. 101-106
-
-
Xin, X.1
Xiao, J.2
Luan, X.3
Zhou, Y.4
Lu, D.5
Wei, D.6
Yang, S.7
-
31
-
-
34547466053
-
Diagnosis and treatment of precocious puberty
-
Zhang L.J. Diagnosis and treatment of precocious puberty. J. Pract. Train Med. 2005, 33:5-6.
-
(2005)
J. Pract. Train Med.
, vol.33
, pp. 5-6
-
-
Zhang, L.J.1
|