Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Jian-Hang Leng"'
Autor:
Ou Wu, Jian-hang Leng, Fen-fang Yang, Hai-ming Yang, Hu Zhang, Zeng-fang Li, Xing-yu Zhang, Cheng-Da Yuan, Jia-jia Li, Qi Pan, Wei Liu, Yan-jun Ren, Bing Liu, Qing-min Liu, Cheng-jian Cao
Publikováno v:
Clinical and Experimental Hypertension, Vol 40, Iss 1, Pp 16-21 (2018)
Background: The obesity-hypertension pathogenesis is complex. From the phenotype to molecular mechanism, there is a long way to clarify the mechanism. To explore the association between obesity and hypertension, we correlate the phenotypes such as th
Externí odkaz:
https://doaj.org/article/c7f48c49a4cf42109447c76bbd48232e
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 4, Iss 1, Pp 1347-1349 (2019)
Mutations in mitochondrial DNA (mtDNA) were the important causes for non-syndromic hearing loss (NSHL). However, the molecular mechanism underlying mt-tRNA mutations and NSHL remained poorly understood. In this study, we reported here the clinical, g
Externí odkaz:
https://doaj.org/article/b1ce2bf334b449a099759af42cb10d4a
Autor:
Wen-Xin Hang, Yan-Chang Yang, Yu-Han Hu, Fu-Quan Fang, Lang Wang, Xing-Hua Qian, McQuillan, Patrick M., Hui Xiong, Jian-Hang Leng, Zhi-Yong Hu
Publikováno v:
Zoological Research; 2024, Vol. 45 Issue 3, p691-703, 13p
Autor:
Jian Hang Leng, Xi Lu, Xingyu Zhang, Hu Zhang, Wei Liu, Guo Zhong Zhang, Fen Fang Yang, Ou Wu, Jia Jia Li
Publikováno v:
Clinical and Experimental Hypertension. 44:40-45
To explore the role of adiponectin-resistin (AR) index as a better indicator of obesity-related hypertension.This study continued a case control study that had finished recruiting 153 subjects divided as four characteristic groups. Fasting serum resi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::affe32deea9b218f6202b86f8de86081
https://doi.org/10.1080/10641963.2021.1984500
https://doi.org/10.1080/10641963.2021.1984500
Publikováno v:
Clinical and Experimental Hypertension. :1-7
Objective: To explore the role of resistin in the onset and development of obesity-related hypertension.Methods: Resistin serum levels were tested by ELISA in 153 adult subjects among four characteristic Chinese adult physical examination groups. Wai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::373e588ff1e07fe031907f23c7299718
https://doi.org/10.1080/10641963.2021.1883049
https://doi.org/10.1080/10641963.2021.1883049
Autor:
Ou Wu, Jian Hang Leng, Xingyu Zhang, Wei Liu, Fen Fang Yang, Hu Zhang, Jia Jia Li, Guo Zhong Zhang, Xi Lu
Publikováno v:
Clinical and experimental hypertension (New York, N.Y. : 1993). 44(6)
To explore the role of leptin in the onset and development of obesity-associated hypertension.A case-control study that had finished recruiting 153 subjects divided as four characteristic groups. Leptin serum levels were tested by ELISA in these subj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4076996e051e39ece09b152d34e511d6
https://pubmed.ncbi.nlm.nih.gov/35531968
https://pubmed.ncbi.nlm.nih.gov/35531968
Publikováno v:
Molecular Medicine Reports
Certain mutations in mitochondrial DNA (mtDNA) are associated with Leber's hereditary optic neuropathy (LHON). In particular, the well‑known NADH dehydrogenase 4 (ND4) m.11778G>A mutation is one of the most common LHON‑associated primary mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6d41f72012f63ed62edb3bac14e4085
http://europepmc.org/articles/PMC6896293
http://europepmc.org/articles/PMC6896293
Publikováno v:
Endocrine Journal. 66:81-88
Premature ovarian insufficiency (POI) is a common endocrine disorder featured by the triad constituting of amenorrhea for at least four months, to date, the molecular pathogenesis of POI is largely undetermined. Despite several investigations have re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::941c1e0066588cca51b07e1730003592
https://doi.org/10.1507/endocrj.ej18-0308
https://doi.org/10.1507/endocrj.ej18-0308
Publikováno v:
International Journal of Molecular Medicine
Polycystic ovary syndrome (PCOS) is a common endocrine disorder with unknown etiology and unsatisfactory clinical treatment. Considering the ethical limitations of studies involving humans, animal models that reflect features of PCOS and insulin resi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aea70b5ad3422740fde00f8dc54dc51
http://europepmc.org/articles/PMC6257859
http://europepmc.org/articles/PMC6257859
Publikováno v:
Current molecular medicine. 19(2)
Background:Mutations in mitochondrial tRNA (mt-tRNA) genes have been found to be associated with both syndromic and non-syndromic hearing impairment. However, the pathophysiology underlying mt-tRNA mutations in clinical expression of hearing loss rem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f9518a68c5db821e71a381826f467d
https://pubmed.ncbi.nlm.nih.gov/30854964
https://pubmed.ncbi.nlm.nih.gov/30854964