Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Junwei Geng"'
Autor:
Zhigang Ren, Wei Guo, Hongquan Ji, Junwei Geng, Jing Cai, Yekun Men, Bo Liu, Yitong Shang, Jin Shuo
Publikováno v:
Frontiers in Energy Research; 2024, p01-10, 10p
Publikováno v:
IET CyberPhysical Systems: Theory & Applications; Mar2024, Vol. 9 Issue 1, p87-98, 12p
Publikováno v:
Energy Reports. 8:1585-1600
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85af8f358aba4fc083ce65193fc92cf2
https://doi.org/10.1016/j.egyr.2022.02.210
https://doi.org/10.1016/j.egyr.2022.02.210
Publikováno v:
Biochemical and Biophysical Research Communications. 495:574-581
Mitochondrial DNA mutations are one of the molecular genetic bases of hypertension. Here, we performed clinical, genetic and mutational evaluation, molecular characterization as well as biochemical analysis of a Chinese Han family with maternally inh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0b8709ed5e02ca8271ceecf2a4afed1
https://doi.org/10.1016/j.bbrc.2017.11.061
https://doi.org/10.1016/j.bbrc.2017.11.061
Autor:
Junwei Geng, Lin Qin
Publikováno v:
BDIOT
With the rapid development of big data and Internet of Things technologies, the amount of population information data has exploded, resulting in a series of research and application of population information data. However, the population information
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b2abf1340cefa71d39021478303b36c
https://doi.org/10.1145/3361758.3361767
https://doi.org/10.1145/3361758.3361767
Publikováno v:
Biochemical and biophysical research communications. 495(1)
Mitochondrial DNA mutations are one of the molecular genetic bases of hypertension. Here, we performed clinical, genetic and mutational evaluation, molecular characterization as well as biochemical analysis of a Chinese Han family with maternally inh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d39cef5962af89f353ce91b22a4c0fa0
https://pubmed.ncbi.nlm.nih.gov/29129694
https://pubmed.ncbi.nlm.nih.gov/29129694
Autor:
Meifen Xu, Yiqun He, Junwei Geng, Zhi Lin, Suxue Shi, Yanzi Meng, Ling Xue, Min-Xin Guan, Han Yu, Zhongqiu Lu
Publikováno v:
Hereditas (Beijing). 36:127-134
Mitochondrial tRNA genes are the hot spots for mutations associated with essential hypertension. We report here the clinical and molecular genetic characterization of two Han Chinese pedigrees with materially inherited essential hypertension. Clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca02921976481e2c8d2777ee2208f79f
https://doi.org/10.3724/sp.j.1005.2014.00127
https://doi.org/10.3724/sp.j.1005.2014.00127
Publikováno v:
Hereditas (Beijing). 35:1237-1243
Dyslipidemia is defined as high levels of serum cholesterol and/or triglycerides. Dyslipidemia often leads to severe cardiovascular diseases including coronary heart disease and stroke as the first clinical manifestation, thus threatening the health
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5216488b8b97f18a8b99447b9b12ddae
https://doi.org/10.3724/sp.j.1005.2013.01237
https://doi.org/10.3724/sp.j.1005.2013.01237
Autor:
Han Yu, Haiying Li, Meng Wang, Min-Xin Guan, Jun Qin Mo, Yanyan Peng, Hong Zhou, Heng Wang, Feng Jiang, Lingling Hou, Junwei Geng, Pingping Jiang, Ling Xue, Zhi Lin
Publikováno v:
Mitochondrion. 30
Mitochondria have the profound impact on vascular function in both health and disease. However, mitochondrial genetic determinants for the development of hypertension remain poorly explored.The Sanger sequence analysis of 22 mitochondrial tRNA genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1f0638a5a900da501ab78dc8ca0729a
https://pubmed.ncbi.nlm.nih.gov/27544295
https://pubmed.ncbi.nlm.nih.gov/27544295
Publikováno v:
Clinical Laboratory. 61
BACKGROUND Establish a method to identify simultaneously mitochondrial DNA 4401A>G and 4435A>G mutations associated with essential hypertension. METHODS The whole genomic DNA of samples carrying mitochondrial DNA 4401A>G and 4435A>G mutations, double
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bffe38411df9a08068df42948b306c3b
https://doi.org/10.7754/clin.lab.2015.150111
https://doi.org/10.7754/clin.lab.2015.150111