Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Chizuko Kimura"'
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Identification of a novel mutation in the exon 2 splice donor site of the POU1F1/PIT-1 gene in Japanese identical twins with mild combined pituitary hormone deficiency
Autor: Tsutomu Ogata, Tokuo Mukai, Yoshiya Ito, Kenji Fujieda, Mitsuo Itakura, Hiroshi Inoue, Yukiko Sakamoto, Chizuko Kimura, Natsumi Kangawa
Publikováno v: Clinical Endocrinology. 76:78-87
Summary Context To date, approximately 35 different POU1F1 mutations have been described in patients with familial and sporadic combined pituitary hormone deficiency (CPHD) from different ethnic backgrounds. The majority are missense mutations cluste
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d156580f865e3724972f491dc2b57401
https://doi.org/10.1111/j.1365-2265.2011.04165.x
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3
Analysis of expression and structure of the rat GH-secretagogue/ghrelin receptor (Ghsr) gene: Roles of epigenetic modifications in transcriptional regulation
Autor: Hiroshi Inoue, Toshiaki Sano, Natsumi Kangawa, Yukiko Sakamoto, Tsutomu Ogata, Chizuko Kimura, Zhi Rong Qian, Kenji Fujieda, Mitsuo Itakura
Publikováno v: Molecular and Cellular Endocrinology. 345:1-15
In the current study, to elucidate the molecular basis of cell type-specific expression of the GH-secretagogue/ghrelin receptor type 1A (GHSR1A), we characterized the structure and putative promoter region of the rat Ghsr gene. We identified an alter
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81feb3d4471fe321d11c968fecc47eab
https://doi.org/10.1016/j.mce.2011.06.034
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4
Identification and functional analysis of novel human growth hormone-releasing hormone receptor (GHRHR) gene mutations in Japanese subjects with short stature
Autor: Tsutomu Ogata, Yukiko Sakamoto, Kenji Fujieda, Atsuko Kinouchi, Chizuko Kimura, Mitsuo Itakura, Yosuke Shigematsu, Reiko Horikawa, Natsumi Kangawa, Hiroshi Inoue
Publikováno v: Clinical Endocrinology. 74:223-233
Summary Context Growth hormone–releasing hormone receptor (GHRHR) gene mutations have been identified in patients of different ethnic origins with isolated GH deficiency (IGHD) type IB. However, the prevalence of these mutations in the Japanese pop
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f3a378ea91fb93cf7a38d468793e31c8
https://doi.org/10.1111/j.1365-2265.2010.03911.x
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6
Identification of a novel mutation in the exon 2 splice donor site of the POU1F1/PIT-1 gene in Japanese identical twins with mild combined pituitary hormone deficiency
Autor: Hiroshi, Inoue, Tokuo, Mukai, Yukiko, Sakamoto, Chizuko, Kimura, Natsumi, Kangawa, Mitsuo, Itakura, Tsutomu, Ogata, Yoshiya, Ito, Kenji, Fujieda
Publikováno v: Clinical endocrinology. 76(1)
To date, approximately 35 different POU1F1 mutations have been described in patients with familial and sporadic combined pituitary hormone deficiency (CPHD) from different ethnic backgrounds. The majority are missense mutations clustered within the c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::767b65289a41377fb9f47a895c378a8a
https://pubmed.ncbi.nlm.nih.gov/21722153
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7
Identification and functional analysis of novel human growth hormone secretagogue receptor (GHSR) gene mutations in Japanese subjects with short stature
Autor: Chizuko Kimura, Hiroshi Inoue, Yukiko Sakamoto, Tsutomu Ogata, Atsuko Kinouchi, Mitsuo Itakura, Kenji Fujieda, Yosuke Shigematsu, Reiko Horikawa, Natsumi Kangawa
Publikováno v: The Journal of clinical endocrinology and metabolism. 96(2)
Context: Short stature (SS) is a multifactorial developmental condition with a significant genetic component. Recent studies have revealed that rare deleterious mutations in the GH-secretagogue receptor type 1A (GHSR1A) gene could be a cause of famil
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6879050193c4c0213ee86ebd6fe8f44a
https://pubmed.ncbi.nlm.nih.gov/21084395
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8
Identification and functional analysis of novel human growth hormone-releasing hormone receptor (GHRHR) gene mutations in Japanese subjects with short stature
Autor: Hiroshi, Inoue, Natsumi, Kangawa, Atsuko, Kinouchi, Yukiko, Sakamoto, Chizuko, Kimura, Reiko, Horikawa, Yosuke, Shigematsu, Mitsuo, Itakura, Tsutomu, Ogata, Kenji, Fujieda
Publikováno v: Clinical endocrinology. 74(2)
Growth hormone-releasing hormone receptor (GHRHR) gene mutations have been identified in patients of different ethnic origins with isolated GH deficiency (IGHD) type IB. However, the prevalence of these mutations in the Japanese population has yet to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bfbbec40154c6c337f6d20d3e7803d2e
https://pubmed.ncbi.nlm.nih.gov/21044116
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9
Rousselianone A, novel antibiotic related to phenalenone produced by Phaeosphaeria rousseliana
Autor: Chizuko Kimura, Nobuji Yoshikawa, Takashi Mikawa, Hirofumi Tomita, Shigenori Kumazawa, Jin-Zhong Xiao
Publikováno v: The Journal of antibiotics. 46(10)
Novel antibiotic, rousselianone A, was produced by fermentation of Phaeosphaeria rousseliana L2144. Rousselianone A was characterized as a new derivative of phenalenone. The antibiotic showed no antimicrobial activity in vitro, but exhibited in vivo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51d42fe7d596d5bd349f320fb25af7d8
https://pubmed.ncbi.nlm.nih.gov/8244885
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