Search | Virtual Health Library

1.

[Study on original investigation, macroscopic and microscopic identification of pharmacopoeia contained species of Epmedii Folium].

Kang, Shuai; Lu, Jing; Zhang, Ji; Lian, Chao-Jie; Wei, Ai-Hua; Ma, Shuang-Cheng.

Zhongguo Zhong Yao Za Zhi ; 43(4): 697-703, 2018 Feb.

Article in Zh | MEDLINE | ID: mdl-29600643

2.

Mutation of SLC35D3 causes metabolic syndrome by impairing dopamine signaling in striatal D1 neurons.

Zhang, Zhe; Hao, Chan-Juan; Li, Chang-Gui; Zang, Dong-Jie; Zhao, Jing; Li, Xiao-Nan; Wei, Ai-Hua; Wei, Zong-Bo; Yang, Lin; He, Xin; Zhen, Xue-Chu; Gao, Xiang; Speakman, John R; Li, Wei.

PLoS Genet ; 10(2): e1004124, 2014 Feb.

Article in English | MEDLINE | ID: mdl-24550737

3.

[Identification of Epmedii Folium and its counterfeit leaf of Quercus variabilis].

Kang, Shuai; Zhou, Chao; He, Yi; Zhang, Ji; Wei, Ai-hua; Lu, Jing; Ma, Shuang-cheng.

Zhongguo Zhong Yao Za Zhi ; 40(9): 1676-80, 2015 May.

Article in Zh | MEDLINE | ID: mdl-26323128

4.

New insights into the pathogenesis of Hermansky-Pudlak syndrome.

Li, Wei; Hao, Chan-Juan; Hao, Zhen-Hua; Ma, Jing; Wang, Qiao-Chu; Yuan, Ye-Feng; Gong, Juan-Juan; Chen, Yuan-Ying; Yu, Jia-Ying; Wei, Ai-Hua.

Pigment Cell Melanoma Res ; 35(3): 290-302, 2022 05.

Article in English | MEDLINE | ID: mdl-35129281

5.

Prenatal genotyping of four common oculocutaneous albinism genes in 51 Chinese families.

Wei, Ai-Hua; Zang, Dong-Jie; Zhang, Zhao; Yang, Xiu-Min; Li, Wei.

J Genet Genomics ; 42(6): 279-86, 2015 Jun 20.

Article in English | MEDLINE | ID: mdl-26165494

6.

A comprehensive study of oculocutaneous albinism type 1 reveals three previously unidentified alleles on the TYR gene.

Lin, Yu-Ying; Wei, Ai-Hua; He, Xin; Zhou, Zhi-Yong; Lian, Shi; Zhu, Wei.

Eur J Dermatol ; 24(2): 168-73, 2014.

Article in English | MEDLINE | ID: mdl-24721949

7.

Application of multiplex ligation-dependent probe amplification in the genetic testing of oculocutaneous albinism.

Zhang, Ying-Zi; Bai, Da-Yong; Qi, Zhan; Zhao, Su-Zhou; Yang, Xiu-Min; Li, Wei; Wei, Ai-Hua.

Chin Med J (Engl) ; 132(16): 2011-2012, 2019 Aug 20.

Article in English | MEDLINE | ID: mdl-31356463

8.

Increasing the complexity: new genes and new types of albinism.

Montoliu, Lluís; Grønskov, Karen; Wei, Ai-Hua; Martínez-García, Mónica; Fernández, Almudena; Arveiler, Benoît; Morice-Picard, Fanny; Riazuddin, Saima; Suzuki, Tamio; Ahmed, Zubair M; Rosenberg, Thomas; Li, Wei.

Pigment Cell Melanoma Res ; 27(1): 11-8, 2014 Jan.

Article in English | MEDLINE | ID: mdl-24066960

9.

Hermansky-Pudlak syndrome: pigmentary and non-pigmentary defects and their pathogenesis.

Wei, Ai-Hua; Li, Wei.

Pigment Cell Melanoma Res ; 26(2): 176-92, 2013 Mar.

Article in English | MEDLINE | ID: mdl-23171219

10.

Hypopigmentation in Hermansky-Pudlak syndrome.

Wei, Ai-Hua; He, Xin; Li, Wei.

J Dermatol ; 40(5): 325-9, 2013 May.

Article in English | MEDLINE | ID: mdl-23668540

11.

Genetic analyses of Chinese patients with digenic oculocutaneous albinism.

Wei, Ai-Hua; Yang, Xiu-Min; Lian, Shi; Li, Wei.

Chin Med J (Engl) ; 126(2): 226-30, 2013 Jan.

Article in English | MEDLINE | ID: mdl-23324268

12.

Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.

Wei, Ai-Hua; Zang, Dong-Jie; Zhang, Zhe; Liu, Xuan-Zhu; He, Xin; Yang, Lin; Wang, Yi; Zhou, Zhi-Yong; Zhang, Ming-Rong; Dai, Lan-Lan; Yang, Xiu-Min; Li, Wei.

J Invest Dermatol ; 133(7): 1834-40, 2013 Jul.

Article in English | MEDLINE | ID: mdl-23364476

13.

A novel missense mutation of the TYR gene in a pedigree with oculocutaneous albinism type 1 from China.

Lin, Yu-Ying; Wei, Ai-Hua; Zhou, Zhi-Yong; Zhu, Wei; He, Xin; Lian, Shi.

Chin Med J (Engl) ; 124(20): 3358-61, 2011 Oct.

Article in English | MEDLINE | ID: mdl-22088535

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