Wei-min Zhang

发表

New Insights into the Pharmacological Chaperone Activity of C2‐Substituted Glucoimidazoles for the Treatment of Gaucher Disease

Wei Zhao, Tiehai Li, P. Wang, 2013, Chembiochem : a European journal of chemical biology.

A novel mutation of α-galactosidase A gene causes Fabry disease mimicking primary erythromelalgia in a Chinese family

B. Wei, Cuihua Leng, Xingshun Xu, 2017, The International journal of neuroscience.

Lack of support for an association between CLEC4M homozygosity and protection against SARS coronavirus infection

F. Chan, J. Sung, K. To, 2007, Nature Genetics.

Novel mutations in type 2 Gaucher disease in Chinese and their functional characterization by heterologous expression

K. To, N. Tang, G. Grabowski, 2005, Human mutation.

Three novel homozygous mutations in the GNPTG gene that cause mucolipidosis type III gamma.

Y. Meng, Wei-min Zhang, Shuang Liu, 2014, Gene.

SNORA42 Promote Oesophageal Squamous Cell Carcinoma Development Through Interacting With Dhx9

Lianmei Zhao, B. Shan, Cong Zhang, 2020 .

CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency

Shangzhi Huang, Q. Tian, Wei-min Zhang, 2013, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Gaucher disease among Chinese patients: review on genotype/phenotype correlation from 29 patients and identification of novel and rare alleles.

N. Tang, F. Choy, Wei-min Zhang, 2007, Blood cells, molecules & diseases.

Mutational analysis of ATP7B in north Chinese patients with Wilson disease

Sheng Lin, Marie C. M. Lin, D. Xie, 2012, Journal of Human Genetics.

Surgical Treatment of Complex Malignant Anterior Mediastinal Tumors Invading the Superior Vena Cava

Ji‐you Li, Ke-Neng Chen, Zhen-dong Gu, 2006, World Journal of Surgery.

[An analysis of mutations causing Gaucher disease in Chinese population].

Y. Meng, N. Tang, Wei-min Zhang, 2009, Zhonghua yi xue za zhi.

Mutation Analysis of 16 Mucolipidosis II and III Alpha/Beta Chinese Children Revealed Genotype-Phenotype Correlations

Wei-min Zhang, Shuang Liu, M. Wei, 2016, PloS one.

Mucopolysaccharidosis IVA mutations in Chinese patients: 16 novel mutations

Y. Meng, Z. Wang, Shangzhi Huang, 2010, Journal of Human Genetics.

Phenotypic and genetic characteristics of 130 patients with mucopolysaccharidosis type II: A single-center retrospective study in China

Lisi Zhu, Wei-min Zhang, M. Ma, 2023, Frontiers in Genetics.

Two novel mutations of the arylsulfatase B gene in a Chinese MPS VI child undergoing bone marrow transplantation therapy.

J. Chen, Xuefan Gu, Shangzhi Huang, 2006, Clinica chimica acta; international journal of clinical chemistry.

[Postnatal and prenatal diagnosis of mucopolysaccharidosis type III (Sanfilippo syndrome)].

Y. Meng, Wei-min Zhang, Hui-ping Shi, 2008, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Prenatal diagnosis of Duchenne muscular dystrophy and cytogenetic analysis in 303 Chinese families

Wei-min Zhang, Juntao Liu, N. Hao, 2020 .

Clinical and genetic characteristics of 17 Chinese patients with glycogen storage disease type IXa.

Wei-min Zhang, M. Ma, Jiangwei Zhang, 2017, Gene.

[Clinical and molecular genetic study on two patients of the juvenile form of Pompe disease in China].

Wei-min Zhang, M. Wei, Hui-ping Shi, 2007, Zhonghua er ke za zhi = Chinese journal of pediatrics.

ARSA gene mutations in five Chinese metachromatic leukodystrophy patients.

X. Bao, Yuwu Jiang, H. Pan, 2007, Pediatric neurology.

[Postnatal and prenatal diagnosis of mucopolysaccharidosis type II (Hunter syndrome)].

Wei-min Zhang, Q. Qi, Hui-ping Shi, 2006, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[Clinical manifestations and mutation study in 16 Chinese patients with Fabry disease].

Y. Meng, Wei-min Zhang, M. Wei, 2010, Zhonghua yi xue za zhi.

Gene symbol: SGSH. Disease: Sanfilippo syndrome type A.

Wei-min Zhang, S. Huiping, 2008, Human genetics.

Mucopolysaccharidosis I mutations in Chinese patients: identification of 27 novel mutations and 6 cases involving prenatal diagnosis

Y. Meng, W. Zhang, Wei-min Zhang, 2012, Clinical genetics.

New Insights into the Pharmacological Chaperone Activity of C2‐Substituted Glucoimidazoles for the Treatment of Gaucher Disease

Wei Zhao, Tiehai Li, P. Wang, 2013, Chembiochem : a European journal of chemical biology.

Lack of support for an association between CLEC4M homozygosity and protection against SARS coronavirus infection

Wuchun Cao, F. Chan, J. Sung, 2007, Nature Genetics.

[A retrospective study on enzyme replacement therapy in patients with Gaucher disease].

Yong-hong Zhang, Wei-min Zhang, Y. Zang, 2006, Zhonghua er ke za zhi = Chinese journal of pediatrics.