Follow-up investigation of 12 proposed linkage regions in multiple sclerosis.

Follow-up investigation of 12 proposed linkage regions in multiple sclerosis.

Multiple sclerosis (MS) is an autoimmune disease with overwhelming evidence for genetic determination, and for which a maternal parent-of-origin effect has been reported. As with many complex diseases, multiple suggestive linkage signals have been observed. However, the only unambiguous association...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Herrera, B, Cader, M, Dyment, D, Bell, J, Ramagopalan, S, Lincoln, MR, Orton, S, Chao, M, Sadovnick, A, Ebers, G
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	2006

Παρόμοια τεκμήρια

Multiple sclerosis susceptibility and the X chromosome.
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Parental transmission of HLA-DRB1*15 in multiple sclerosis.
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Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility.
ανά: Lincoln, MR, κ.ά.
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Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex.
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Epistasis among HLA-DRB1, HLA-DQA1 and HLA-DQB1 Loci Determines Multiple Sclerosis Susceptibility
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Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex
ανά: Chao, M, κ.ά.
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Methylation of class II transactivator gene promoter IV is not associated with susceptibility to Multiple Sclerosis
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Parental non-inherited HLA resistance alleles do not confer protection against multiple sclerosis.
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Gestational diabetes and multiple sclerosis.
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Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium
ανά: Chao, M, κ.ά.
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Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis.
ανά: Chao, M, κ.ά.
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Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis.
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Congenital abnormalities and multiple sclerosis.
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Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis.
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Parent-of-origin effect in multiple sclerosis: observations from interracial matings.
ανά: Ramagopalan, S, κ.ά.
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Effect of immigration on multiple sclerosis sex ratio in Canada: the Canadian Collaborative Study.
ανά: Orton, S, κ.ά.
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MHC transmission: insights into gender bias in MS susceptibility.
ανά: Chao, M, κ.ά.
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The role of hereditary spastic paraplegia related genes in multiple sclerosis. A study of disease susceptibility and clinical outcome.
ανά: DeLuca, G, κ.ά.
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Congenital abnormalities and multiple sclerosis
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Childhood cow's milk allergy and the risk of multiple sclerosis: a population based study
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Childhood cow's milk allergy and the risk of multiple sclerosis: a population based study.
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Expression of the multiple sclerosis-associated MHC class II Allele HLA-DRB1*1501 is regulated by vitamin D.
ανά: Ramagopalan, S, κ.ά.
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Sex ratio of multiple sclerosis and clinical phenotype.
ανά: Ramagopalan, S, κ.ά.
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Fine Mapping of Epigenetic Modifications in Multiple Sclerosis Susceptibility
ανά: Chao, M, κ.ά.
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Parent-of-origin effects in MS: observations from avuncular pairs.
ανά: Herrera, B, κ.ά.
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A first stage genome-wide screen for regions shared identical-by-descent in Hutterite families with multiple sclerosis.
ανά: Dyment, D, κ.ά.
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HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility.
ανά: Chao, M, κ.ά.
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Vitamin-D Receptor and 1-alpha-hydroxylase Genes in Risk and Outcome of Multiple Sclerosis in Canadians
ανά: Orton, S, κ.ά.
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No effect of birth weight on the risk of multiple sclerosis. A population-based study.
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Clustering of autoimmune disease in families at high risk for multiple sclerosis?
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Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene.
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No effect of preterm birth on the risk of multiple sclerosis: a population based study
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A multigenerational family with multiple sclerosis.
ανά: Dyment, D, κ.ά.
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Vitamin D metabolic pathway genes and risk of multiple sclerosis in Canadians.
ανά: Orton, S, κ.ά.
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