scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF00866919 |
P698 | PubMed publication ID | 8568530 |
P50 | author | Peter Holmans | Q37649643 |
Nicholas W. Wood | Q42592839 | ||
P2093 | author name string | D Clayton | |
N Robertson | |||
D A Compston | |||
H F Kellar-Wood | |||
S J Sawcer | |||
P2860 | cites work | Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 |
Somatic generation of antibody diversity | Q29616439 | ||
Cytokine cytotoxicity against oligodendrocytes. Apoptosis induced by lymphotoxin | Q33393620 | ||
Multiple sclerosis in the Cambridge health district of east Anglia. | Q33591691 | ||
Myelin autoreactivity in multiple sclerosis: recognition of myelin basic protein in the context of HLA-DR2 products by T lymphocytes of multiple-sclerosis patients and healthy donors. | Q33842739 | ||
Susceptibility to multiple sclerosis is associated with the proximal immunoglobulin heavy chain variable region | Q34183158 | ||
New diagnostic criteria for multiple sclerosis: guidelines for research protocols | Q34271601 | ||
Combined influences of Gm and HLA phenotypes upon multiple sclerosis susceptibility and severity | Q34534456 | ||
Susceptibility to multiple sclerosis associated with an immunoglobulin gamma 3 restriction fragment length polymorphism | Q34556850 | ||
The British Isles survey of multiple sclerosis in twins | Q34729146 | ||
Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs | Q35201281 | ||
Linkage strategies for genetically complex traits. II. The power of affected relative pairs | Q35201348 | ||
Immunoglobulin G heavy chain (Gm) allotypes in multiple sclerosis | Q37000386 | ||
Linkage analysis of "necessary" disease loci versus "susceptibility" loci. | Q40531758 | ||
Asymptotic properties of affected-sib-pair linkage analysis. | Q40535037 | ||
Linkage analysis versus association analysis: distinguishing between two models that explain disease-marker associations | Q40540349 | ||
A simple method to detect linkage for rare recessive diseases: An application to juvenile diabetes | Q40990574 | ||
Patterns of blood-brain barrier breakdown in inflammatory demyelination | Q41186929 | ||
The affected sib method. IV. Sib trios | Q41483807 | ||
Immunoglobulin heavy chain variable region polymorphisms and multiple sclerosis susceptibility. | Q42622566 | ||
Antimyelin basic protein and antimyelin antibody-producing cells in multiple sclerosis | Q45007793 | ||
Interactions between oligodendrocytes and microglia. A major role for complement and tumour necrosis factor in oligodendrocyte adherence and killing | Q48397929 | ||
Histopathology of multiple sclerosis lesions detected by magnetic resonance imaging in unfixed postmortem central nervous system tissue | Q48744978 | ||
Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q | Q59064472 | ||
Autoreactive T and B cells responding to myelin proteolipid protein in multiple sclerosis and controls | Q67691159 | ||
T and B cell responses to myelin-oligodendrocyte glycoprotein in multiple sclerosis | Q67983602 | ||
Oligodendrocyte-macrophage interactions in vitro triggered by specific antibodies | Q68202255 | ||
A comparison of sporadic and familial multiple sclerosis | Q68899429 | ||
Organization and evolution of variable region genes of the human immunoglobulin heavy chain | Q70313336 | ||
Gm allotypes and multiple sclerosis | Q70604639 | ||
Immunoglobulin gamma constant gene region polymorphisms in multiple sclerosis | Q72214192 | ||
P433 | issue | 10 | |
P921 | main subject | multiple sclerosis | Q8277 |
P304 | page(s) | 677-682 | |
P577 | publication date | 1995-10-01 | |
P1433 | published in | Journal of Neurology | Q6295649 |
P1476 | title | Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region | |
P478 | volume | 242 |
Q71230101 | A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group |
Q57264092 | A full genome search in multiple sclerosis |
Q28283861 | A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 |
Q77910744 | Changes in Bruch's membrane and related structures with age |
Q52911420 | Comparison of clinical and demographic features between affected pairs of Italian multiple sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms. |
Q38959483 | Differential reactivity of germ line allelic variants of a broadly neutralizing HIV-1 antibody to a gp41 fusion intermediate conformation |
Q40470037 | Genes and susceptibility to multiple sclerosis |
Q35030955 | Genetic diversity of the human immunoglobulin heavy chain VH region |
Q33735806 | Genetic epidemiology of multiple sclerosis |
Q47817624 | HLA associations with multiple sclerosis in the Canary Islands |
Q73835063 | IgG allotypes and subclasses in Norwegian patients with multiple sclerosis |
Q73846707 | Immune system genes in multiple sclerosis: genetic association and linkage analyses on TCR beta, IGH, IFN-gamma and IL-1ra/IL-1 beta loci |
Q35120453 | Influence of histocompatibility genes on disease susceptibility and treatment response in patients with relapsing-remitting multiple sclerosis treated with interferon β-1a |
Q73270575 | Polygenic control of experimental allergic encephalomyelitis in Biozzi ABH and BALB/c mice |
Q37834024 | Regulatory T-cell as orchestra leader in immunosuppression process of multiple sclerosis |
Q37845414 | Th17 cell, the new player of neuroinflammatory process in multiple sclerosis. |
Q41509957 | The genetic analysis of multiple sclerosis |
Q33770454 | The genetics of multiple sclerosis. A review |
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