Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Meichao, Men"'
Autor:
Meichao Men, Dan‐Na Chen, Jia‐Da Li, Xinying Wang, Wang Zeng, Fang Jiang, Ruizhi Zheng, Wenting Dai
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background Isolated hypogonadotropic hypogonadism (IHH) is a clinical syndrome described by failure of gonadal function secondary to defects on the synthesis, secretion, or action of the gonadotropin‐releasing hormone (GnRH). The secreted
Externí odkaz:
https://doaj.org/article/7380da4e170b472ea1731bbcf0fa60da
Autor:
Xizi Du, Lin Yuan, Mengping Wu, Meichao Men, Ruoxi He, Leyuan Wang, Shuangyan Wu, Yang Xiang, Xiangping Qu, Huijun Liu, Xiaoqun Qin, Chengping Hu, Ling Qin, Chi Liu
Publikováno v:
Respiratory Research, Vol 20, Iss 1, Pp 1-10 (2019)
Abstract Background Chronic obstructive pulmonary disease (COPD) is a chronic lung inflammatory disease which has a close relationship with aging. Genome-wide analysis reveals that DNA methylation markers vary obviously with age. DNA methylation vari
Externí odkaz:
https://doaj.org/article/3e13b1127e7443d492528ff8ecbce1cc
Autor:
Xinying Wang, Danna Chen, Yaguang Zhao, Meichao Men, Zhiheng Chen, Fang Jiang, Ruizhi Zheng, Maria I Stamou, Lacey Plummer, Ravikumar Balasubramanian, Jia-Da Li
Publikováno v:
Human Molecular Genetics. 32:1722-1729
Isolated hypogonadotropic hypogonadism (IHH) is a rare disease with hypogonadism and infertility caused by the defects in embryonic migration of hypothalamic gonadotropin-releasing hormone (GnRH) neurons, hypothalamic GnRH secretion or GnRH signal tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4dbc1b1bc5ba93483ba327a338c07459
https://doi.org/10.1093/hmg/ddad014
https://doi.org/10.1093/hmg/ddad014
Publikováno v:
Nutrition, Metabolism and Cardiovascular Diseases. 32:2348-2355
Lipid accumulation product (LAP) is a novel, sex-specific, index-describing lipid over accumulation. Previous studies used baseline LAP for predicting hyperuricaemia; however, the relationship between them is unclear. We aimed to investigate the rela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb4c7975e6f0620f936bfb68ca3e9b9a
https://doi.org/10.1016/j.numecd.2022.06.022
https://doi.org/10.1016/j.numecd.2022.06.022
Autor:
Wu Li, Lingyun Mei, Hongsheng Chen, Xinzhang Cai, Yalan Liu, Meichao Men, Xue Zhong Liu, Denise Yan, Jie Ling, Yong Feng
Publikováno v:
Neural Plasticity, Vol 2019 (2019)
Background. Waardenburg syndrome (WS) is one of the most common forms of syndromic deafness with heterogeneity of loci and alleles and variable expressivity of clinical features. Methods. The technology of single-nucleotide variants (SNV) and copy nu
Externí odkaz:
https://doaj.org/article/b8e1cc6bd7974fbf82eef0a2e5546ad1
Autor:
Jiayu Wu, Zhenghuan Fang, Xinying Wang, Wang Zeng, Yaguang Zhao, Fang Jiang, Dan-Na Chen, Ruizhi Zheng, Jinchen Li, Meichao Men, Jia-Da Li
Publikováno v:
Hormone Research in Paediatrics. 95:384-392
Introduction: Idiopathic hypogonadotropic hypogonadism (IHH) is a rare reproductive disorder resulting from gonadotropin-releasing hormone (GnRH) deficiency. However, in only approximately half of patients with IHH is it possible to identify a likely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c784e1e33ee73c950650505b2ad82633
https://doi.org/10.1159/000525769
https://doi.org/10.1159/000525769
Publikováno v:
Journal of Medical Genetics. 58:66-72
BackgroundFGF8-FGFR1 signalling is involved in multiple biological processes, while impairment of this signalling is one of the main reasons for isolated hypogonadotropic hypogonadism (IHH). Recently, several negative modulators of FGF8-FGFR1 signall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6522013c5fdef54da8988847ac2ee138
https://doi.org/10.1136/jmedgenet-2019-106786
https://doi.org/10.1136/jmedgenet-2019-106786
Autor:
Fang Jiang, Meichao Men, Jia-Da Li, Dan-Na Chen, Yaguang Zhao, Jiayu Wu, Wenting Dai, Ruizhi Zheng
Publikováno v:
Clinical Genetics. 97:696-703
Isolated hypogonadotropic hypogonadism (IHH) is a rare disorder characterized by impaired sexual development and infertility, caused by the deficiency of hypothalamic gonadotropin-releasing hormone neurons. IHH is named Kallmann's syndrome (KS) or no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e4264c530bdc5d919b152b4b91738af
https://doi.org/10.1111/cge.13723
https://doi.org/10.1111/cge.13723
Autor:
Jiayu, Wu, Zhenghuan, Fang, Xinying, Wang, Wang, Zeng, Yaguang, Zhao, Fang, Jiang, Dan-Na, Chen, Ruizhi, Zheng, Jinchen, Li, Meichao, Men, Jia-Da, Li
Publikováno v:
Hormone research in paediatrics. 95(4)
Idiopathic hypogonadotropic hypogonadism (IHH) is a rare reproductive disorder resulting from gonadotropin-releasing hormone (GnRH) deficiency. However, in only approximately half of patients with IHH is it possible to identify a likely molecular dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a4b978a7aa94031ea71abad6d6dfe31
https://pubmed.ncbi.nlm.nih.gov/35797970
https://pubmed.ncbi.nlm.nih.gov/35797970
Autor:
Xinying Wang, Dan-Na Chen, Meichao Men, Jia-Da Li, Wang Zeng, Wenting Dai, Ruizhi Zheng, Fang Jiang
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Background Isolated hypogonadotropic hypogonadism (IHH) is a clinical syndrome described by failure of gonadal function secondary to defects on the synthesis, secretion, or action of the gonadotropin‐releasing hormone (GnRH). The secreted glycoprot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2951d7aee5c16aaa7b7ca5dcd19372e5
https://pubmed.ncbi.nlm.nih.gov/34636164
https://pubmed.ncbi.nlm.nih.gov/34636164