Z. Zhang

发表

Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis

F. Svensson, D. Hellgren, M. Anvret, 2005, Genes and Immunity.

Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I.

M. Blombäck, M. Anvret, N. Egberg, 1992, American journal of human genetics.

Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland Islands.

M. Blombäck, M. Anvret, Z. Zhang, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin.

M. Blombäck, M. Anvret, N. Egberg, 1994, Genomics.

Failure to achieve gene conversion with chimeric circular oligonucleotides: potentially misleading PCR artifacts observed.

M. Blombäck, M. Eriksson, M. Anvret, 1998, Antisense & nucleic acid drug development.

Huntington disease phenocopy is a familial prion disease.

S. Prusiner, L. Edström, M. Anvret, 2001, American journal of human genetics.

Dinucleotide repeat polymorphism in the promoter region of the human von Willebrand factor gene (vWF gene).

M. Blombäck, M. Anvret, Z. Zhang, 1992, Human molecular genetics.

Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III.

M. Blombäck, M. Anvret, N. Egberg, 1992, Human molecular genetics.

Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q.

B. Giometto, L. Edström, M. Anvret, 1999, American journal of human genetics.

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.

A. Clarke, L. Edström, M. Anvret, 1998, Journal of medical genetics.

A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients.

M. Blombäck, M. Anvret, N. Egberg, 1992, Human molecular genetics.

A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.

M. Hayden, L. Edström, M. Anvret, 1998, American journal of human genetics.

APOE genotypes and disease severity in multiple sclerosis

L. Lannfelt, D. Hellgren, M. Anvret, 2002, Multiple sclerosis.

NURR1 mutations in cases of schizophrenia and manic-depressive disorder.

G. Sedvall, E. Jönsson, R. Freedman, 2000, American journal of medical genetics.

Rett syndrome: the bcl-2 gene--a mediator of neurotrophic mechanisms?

M. Anvret, B. Hagberg, Z. Zhang, 1994, Neuropediatrics.

Understanding von Willebrand's disease from gene defects to the patients

M. Blombäck, M. Anvret, Z. Zhang, 1997, Journal of internal medicine. Supplement.