Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ai Hua Wei"'
Autor:
Wei, Li, Chan-Juan, Hao, Zhen-Hua, Hao, Jing, Ma, Qiao-Chu, Wang, Ye-Feng, Yuan, Juan-Juan, Gong, Yuan-Ying, Chen, Jia-Ying, Yu, Ai-Hua, Wei
Publikováno v:
Pigment Cell & Melanoma Research. 35:290-302
Hermansky-Pudlak syndrome (HPS) is characterized by defects of multiple tissue-specific lysosome-related organelles (LROs), typically manifesting with oculocutaneous albinism or ocular albinism, bleeding tendency, and in some cases with pulmonary fib
Autor:
Ying-Zi Zhang, Da-Yong Bai, Zhan Qi, Su-Zhou Zhao, Xiu-Min Yang, Wei Li, Ai-Hua Wei, Qiang Shi
Publikováno v:
Chinese Medical Journal, Vol 132, Iss 16, Pp 2011-2012 (2019)
Externí odkaz:
https://doaj.org/article/98dfac9e7d524cc4888449780f6257a3
Autor:
Zhe Zhang, Chan-Juan Hao, Chang-Gui Li, Dong-Jie Zang, Jing Zhao, Xiao-Nan Li, Ai-Hua Wei, Zong-Bo Wei, Lin Yang, Xin He, Xue-Chu Zhen, Xiang Gao, John R Speakman, Wei Li
Publikováno v:
PLoS Genetics, Vol 10, Iss 2, p e1004124 (2014)
Obesity is one of the largest health problems facing the world today. Although twin and family studies suggest about two-thirds of obesity is caused by genetic factors, only a small fraction of this variance has been unraveled. There are still large
Externí odkaz:
https://doaj.org/article/f408cd8a51894ff09a38d4eeee155f40
Publikováno v:
Journal of Genetics and Genomics. 42:279-286
Oculocutaneous albinism (OCA) is an autosomal recessive disorder characterized by hypopigmentation in eyes, hair and skin, accompanied with vision loss. Currently, six genes have been identified as causative genes for non-syndromic OCA (OCA-1∼4, 6,
Publikováno v:
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 43(4)
Epimedii Folium is a commonly used traditional Chinese drug, and now still depends on the wild resource. In recent years, with the surge in consumption, the resources are declining, the use of market varieties are constantly changing. In this paper,
Autor:
Zubair M. Ahmed, Tamio Suzuki, Benoit Arveiler, Ai-Hua Wei, Almudena Fernández, Fanny Morice-Picard, Thomas Rosenberg, Wei Li, Lluis Montoliu, Saima Riazuddin, Karen Grønskov, Mónica Martínez-García
Publikováno v:
Pigment Cell & Melanoma Research. 27:11-18
Albinism is a rare genetic condition globally characterized by a number of specific deficits in the visual system, resulting in poor vision, in association with a variable hypopigmentation phenotype. This lack or reduction in pigment might affect the
Autor:
Lan-Lan Dai, Xiumin Yang, Ming-Rong Zhang, Yi Wang, Xin He, Lin Yang, Dong-Jie Zang, Zhe Zhang, Ai-Hua Wei, Zhiyong Zhou, Xuan-Zhu Liu, Wei Li
Publikováno v:
Journal of Investigative Dermatology. 133(7):1834-1840
Oculocutaneous albinism (OCA) is a heterogeneous and autosomal recessive disorder with hypopigmentation in the eye, hair, and skin color. Four genes, TYR, OCA2, TYRP1, and SLC45A2, have been identified as causative genes for nonsyndromic OCA1–4, re
Publikováno v:
Advanced Materials Research. :2520-2524
To indentify the influence of human activities on groundwater chemistry, fifteen groundwater samples, from the mostly exploited aquifers, were collected at Tanghai County. Considering the multivariable statistical method is reliable to study the anth
Publikováno v:
Advanced Materials Research. :1503-1509
Ground subsidence is aggravated and becomes a prominent phenomenon recently in Tanggu, China. The subsidence reached its most critic state because of intensive water over-extraction in 1980s. Thereafter, over-draft withdraw of groundwater has been st
Publikováno v:
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 40(9)
Epmedii Folium is a commonly used traditional Chinese drug, and is beneficial for the "liver" and "kidney" s function in Chinese medicine. Recently, the origin of this drug is more complex. Most of the identification studies are emphasized on the spe