M Anvret
Overview
Explore the profile of M Anvret including associated specialties, affiliations and a list of published articles.
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Articles
138
Citations
1463
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Recent Articles
1.
Zhang Z, Duvefelt K, Svensson F, Masterman T, Jonasdottir G, Salter H, et al.
Genes Immun
. 2005 Jan;
6(2):145-52.
PMID: 15674389
Multiple sclerosis (MS) is a T-cell-mediated disease of the central nervous system, characterized by damage to myelin and axons, resulting in progressive neurological disability. Genes may influence susceptibility to MS,...
2.
Xiang F, Stenbom Y, Anvret M
Clin Genet
. 2002 Jun;
61(5):384-5.
PMID: 12081725
No abstract available.
3.
Masterman T, Zhang Z, Hellgren D, Salter H, Anvret M, Lilius L, et al.
Mult Scler
. 2002 May;
8(2):98-103.
PMID: 11990879
Apolipoprotein E (opoE) is involved in the transport of lipids necessary for membrane repair and is encoded by a gene on chromosome 19q13, a region positive for linkage in two...
4.
Moore R, Xiang F, Monaghan J, Han D, Zhang Z, Edstrom L, et al.
Am J Hum Genet
. 2001 Oct;
69(6):1385-8.
PMID: 11593450
Huntington disease (HD) is a common autosomal dominant neurodegenerative disease with early adult-onset motor abnormalities and dementia. Many studies of HD show that huntingtin (CAG)n repeat-expansion length is a sensitive...
5.
Xiang F, Stenbom Y, Anvret M, Hagberg B
Neuropediatrics
. 2001 Sep;
32(4):217-8.
PMID: 11571704
Mutations in the MECP2 gene are known to be associated with Rett Syndrome (RTT) in the large majority of sporadic cases. Four Swedish families with a total of eight RTT...
6.
Vorechovsky I, Kralovicova J, Tchilian E, Masterman T, Zhang Z, Ferry B, et al.
Nat Genet
. 2001 Sep;
29(1):22-3.
PMID: 11548742
A 77G allele of the gene encoding CD45, also known as the protein tyrosine phosphatase receptor-type C gene (PTPRC), has been associated with multiple sclerosis (MS). Here we determine allele...
7.
Villard L, Levy N, Xiang F, Kpebe A, Labelle V, Chevillard C, et al.
J Med Genet
. 2001 Jul;
38(7):435-42.
PMID: 11432961
Background: Rett syndrome is a neurodevelopmental disorder affecting only girls; 99.5% of Rett syndrome cases are sporadic, although several familial cases have been reported. Mutations in the MECP2 gene were...
8.
Kerr A, Nomura Y, Armstrong D, Anvret M, Belichenko P, Budden S, et al.
Brain Dev
. 2001 May;
23(4):208-11.
PMID: 11376997
An international group recommends that papers relating phenotypes to genotypes involving mutations in the X chromosome gene MECP2 should provide a minimum data set reporting the range of disturbances frequently...
9.
Buervenich S, Xiang F, Sydow O, Jonsson E, Sedvall G, Anvret M, et al.
Hum Mutat
. 2001 Apr;
17(5):435-6.
PMID: 11317366
We identified novel polymorphisms in the calcitonin/CGRPalpha (CALCA) gene by direct sequencing of genomic DNA and subsequent genotyping by RFLP (restriction fragment length polymorphism) detection and investigated association with neurological...
10.
Eriksson M, Ansved T, Anvret M, Carey N
Biochem Biophys Res Commun
. 2001 Mar;
281(4):835-41.
PMID: 11237735
Ciliary function is essential for normal cellular activity in all species from simple protozoa upwards. In humans, ciliary dysmotility or complete immobility have been identified in autosomal recessive multisystemic diseases...