Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Yazhou Huang"'
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background The incidence of spontaneous abortion (SA), which affects approximately 15–20% of pregnancies, is the most common complication of early pregnancy. Pathogenic copy number variations (CNVs) are recognized as potential genetic caus
Externí odkaz:
https://doaj.org/article/eb43b69c8ea349bca659aea0c48fefb1
Autor:
Yazhou Huang, Linya Ma, Zhaoxia Zhang, Shujuan Nie, Yuan Zhou, Jibo Zhang, Chao Wang, Xingxin Fang, Yingting Quan, Ting He, Anhui Liu, Dan Peng
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Background Nance–Horan syndrome (NHS) is a rare and often overlooked X‐linked dominant disorder characterized by dense congenital cataracts, dental abnormalities, and mental retardation. The majority of NHS variations include frameshift
Externí odkaz:
https://doaj.org/article/11788a9a2993478fa010afeef88da7fe
Autor:
Ting Ou, Meng Zhang, Yazhou Huang, Li Wang, Fei Wang, Ruolin Wang, Xiaojiao Liu, Zeyang Zhou, Jie Xie, Zhonghuai Xiang
Publikováno v:
Frontiers in Plant Science, Vol 13 (2022)
Plant growth-promoting rhizobacteria have been shown to play important roles in maintaining host fitness under periods of abiotic stress, and yet their effect on mulberry trees which regularly suffer drought after flooding in the hydro-fluctuation be
Externí odkaz:
https://doaj.org/article/35e14d0d52df4b5ca6da1b68e872b2f4
Autor:
Xi Zhou, Tingbin Ma, Luyao Yang, Shuijiao Peng, Lulu Li, Zhouquan Wang, Zhen Xiao, Qingfeng Zhang, Li Wang, Yazhou Huang, Minzhi Chen, Songping Liang, Xianwei Zhang, Jing Yu Liu, Zhonghua Liu
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
Loss of function of Nav1.7 leads to congenital insensitivity to pain in humans. Here the authors found that activation of Nav1.9 can restore nociception in Nav1.7 knockout mice, revealed by a venom-derived peptide as a probe.
Externí odkaz:
https://doaj.org/article/e93339c156fa489c94f4b1e344ea1aaf
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
BackgroundTyrosinase-positive oculocutaneous albinism (OCA, type II, OCA2) is an autosomal recessive genetic disease in which the biosynthesis of melanin decreases in the skin, hair, and eyes. OCA2 disease is caused by mutations in OCA2 gene. The gen
Externí odkaz:
https://doaj.org/article/cf77786904d04cf7b338b14372a5f9e9
Autor:
Qian Chen, Chaoliang Xiong, Kunyun Jia, Jing Jin, Ziyang Li, Yazhou Huang, Yewen Liu, Lingling Wang, Haitao Luo, Haiyan Li, Qing H. Meng, Wei Li
Publikováno v:
Journal of Lipid Research, Vol 60, Iss 2, Pp 341-352 (2019)
To elucidate the transcriptomic changes of long noncoding RNAs (lncRNAs) in high-fat diet (HFD)-fed mice, we defined their hepatic transcriptome by RNA sequencing. Aberrant expression of 37 representative lncRNAs and 254 protein-coding RNAs was obser
Externí odkaz:
https://doaj.org/article/2d6fad24599a4a46a81f2714528471a7
Publikováno v:
ACS Omega, Vol 3, Iss 3, Pp 3120-3128 (2018)
Externí odkaz:
https://doaj.org/article/8691c332befc45138803d1bde4c1ba3d
Publikováno v:
AIP Advances, Vol 8, Iss 4, Pp 045216-045216-6 (2018)
How to reduce friction for improving efficiency in the usage of energy is a constant challenge. Layered material like MoS2 has long been recognized as an effective surface lubricant. Due to low interfacial shear strengths, MoS2 is endowed with nomina
Externí odkaz:
https://doaj.org/article/77efe82da72c4818b3df80b7ce4d0f3c
Autor:
Yazhou Huang, Linya Ma, Zhaoxia Zhang, Shujuan Nie, Yuan Zhou, Jibo Zhang, Chao Wang, Xingxin Fang, Yingting Quan, Ting He, Anhui Liu, Dan Peng
Publikováno v:
Molecular Genetics & Genomic Medicine. 11
Nance-Horan syndrome (NHS) is a rare and often overlooked X-linked dominant disorder characterized by dense congenital cataracts, dental abnormalities, and mental retardation. The majority of NHS variations include frameshift mutations, nonsense muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64927547cfa6ab585169d9670b2139e9
https://doi.org/10.1002/mgg3.2100
https://doi.org/10.1002/mgg3.2100
Publikováno v:
RSC Advances. 11:26928-26936
Although MoS2 has shown its potential as an electro-catalyst for the oxygen evolution reaction (OER), its research is still insufficient. In this study, as a novel MoS2-based heterostructure electro-catalyst for OER, namely NiSe2@MoS2 nano-heterostru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::171fd76ed7e8b6076e4b4588c15a2b34
https://doi.org/10.1039/d1ra05509g
https://doi.org/10.1039/d1ra05509g