Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Songya Pang"'
Autor:
Noriyuki Katsumata, Yasuhiro Naiki, Songya Pang, Reiko Horikawa, Maki Fukami, Tsutomu Ogata, Mami Miyado, Masafumi Onodera
Publikováno v:
Endocrine Journal. 63:897-904
Congenital adrenal hyperplasia (CAH) due to steroid 21-hydroxylase (21-OH) deficiency (21-OHD) is an autosomal recessive disorder, in which CYP21A2 mutations or deletions result in underproduction of glucocorticoid and mineralocorticoid, and overprod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f61e4cea178e5927fcfceec6e576d7ce
https://doi.org/10.1507/endocrj.ej16-0112
https://doi.org/10.1507/endocrj.ej16-0112
Autor:
Yasuhiro, Naiki, Mami, Miyado, Reiko, Horikawa, Noriyuki, Katsumata, Masafumi, Onodera, Songya, Pang, Tsutomu, Ogata, Maki, Fukami
Publikováno v:
Endocrine journal. 63(10)
Congenital adrenal hyperplasia (CAH) due to steroid 21-hydroxylase (21-OH) deficiency (21-OHD) is an autosomal recessive disorder, in which CYP21A2 mutations or deletions result in underproduction of glucocorticoid and mineralocorticoid, and overprod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d371d890422839df104a8bb470a4547
https://pubmed.ncbi.nlm.nih.gov/27432820
https://pubmed.ncbi.nlm.nih.gov/27432820
Autor:
Goldy Carbunaru, Songya Pang, Ying Tai Chang, Chantal Lutfallah, Anzar Haider, Kenneth C. Copeland, J. Ian Mason
Publikováno v:
Clinical Endocrinology. 58:323-331
Summary objective We investigated adrenal steroidogenic function relevant to 3β-hydroxysteroid dehydrogenase (HSD3B2) activity in vivo and HSD3B2 genotype in clinically normal family members of patients with HSD3B2 genotype-proven HSD3B2 deficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb6f0e1b67277f19ffadcd4d5bc85819
https://doi.org/10.1046/j.1365-2265.2003.01716.x
https://doi.org/10.1046/j.1365-2265.2003.01716.x
Autor:
Kenneth C. Copeland, Barry H. Rich, Chantal Lutfallah, Weihua Wang, Mariano Castro-Magana, Raphael David, Ying Tai Chang, J. Ian Mason, Anzar Haider, Songya Pang
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 87:2611-2622
To define the hormonal criteria via genotypic proof for 3beta-hydroxysteroid dehydrogenase (3beta-HSD) deficiency in the adrenals and gonads, we investigated the type II 3beta-HSD genotype in 55 patients with clinical and/or hormonal presentation sug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2f087c66d8a59fdd6e3a0179516e13b
https://doi.org/10.1210/jcem.87.6.8615
https://doi.org/10.1210/jcem.87.6.8615
Autor:
John C. Achermann, Songya Pang, A Rosler, M Ito, J L Jameson, Bernard L. Silverman, Reema L. Habiby
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 86:3171-3175
DAX-1 is an orphan nuclear receptor that plays a key role in the development and function of the adrenal gland and hypothalamic-pituitary gonadal axis. Mutations in the gene encoding DAX-1 result in X-linked adrenal hypoplasia congenita (AHC). Affect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25ecd5d7b74a75fe7c2fd34ca68cbe57
https://doi.org/10.1210/jcem.86.7.7660
https://doi.org/10.1210/jcem.86.7.7660
Publikováno v:
Clinical Pediatric Endocrinology. 10:17-28
We investigated ovarian steroidogenic enzyme gene expression in exogenous androgen induced polycystic ovaries (PCO) in rabbits. Twelve 3-month peripubertal, and seven 9-11 month reproductive aged New Zealand White female rabbits were divided into fou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54bff9baff4dc09f48753f07eddf2100
https://doi.org/10.1297/cpe.10.17
https://doi.org/10.1297/cpe.10.17
Autor:
Y. Naiki, T. T. Gordon-Walker, Li Zhang, Kenneth C. Copeland, Mariano Castro-Magana, J. I. Mason, Songya Pang, Ying Tai Chang
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 85:1678-1685
We identified two homozygous missense mutations in the human type II 3beta-hydroxysteroid dehydrogenase (3/betaHSD) gene, the first in codon 6 of exon II [CTT (Leu) to TTT (Phe)] in a male infant with hyperpigmented scrotum and hypospadias, raised as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60b801fbbd65dcb02eaa4b4b4bf557b3
https://doi.org/10.1210/jcem.85.4.6539
https://doi.org/10.1210/jcem.85.4.6539
Publikováno v:
Clinical Pediatric Endocrinology. 8:77-84
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::426d88e2b10eb0871ac8d1a395c86d24
https://doi.org/10.1297/cpe.8.77
https://doi.org/10.1297/cpe.8.77
Autor:
Songya Pang
Publikováno v:
Trends in Endocrinology & Metabolism. 9:82-86
Severe 3beta-hydroxysteroid dehydrogenase (3beta-HSD) deficiency in the adrenals and gonads is a well known cause of salt-wasting and non-salt-wasting forms of congenital adrenal hyperplasia (CAH), male pseudohermaphroditism and mild androgen excess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ba2638457b8179d3795ba0e25eee3d9
https://doi.org/10.1016/s1043-2760(98)00015-0
https://doi.org/10.1016/s1043-2760(98)00015-0
Autor:
Songya Pang, Hala Sakkal-Alkaddour, Fuad Ziai, Linda Riddick, Mary Jean Suriano, Ying T Chang
Publikováno v:
Clinical Pediatric Endocrinology. 7:23-34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9224453327c1c36658eff3ee715c87de
https://doi.org/10.1297/cpe.7.23
https://doi.org/10.1297/cpe.7.23