A screen of candidates from peaks of linkage: evidence for the involvement of myeloperoxidase in multiple sclerosis
暂无分享,去创建一个
P. Goodfellow | S. Sawcer | A. Compston | S. Broadley | H. Jones | J. Chataway | D. Clayton | J. Gray | F. Coraddu | R. Feakes | Alastair Compston
[1] M. J. Walsh,et al. Dual implication of 2',3'-cyclic nucleotide 3' phosphodiesterase as major autoantigen and C3 complement-binding protein in the pathogenesis of multiple sclerosis. , 1998, The Journal of clinical investigation.
[2] M. Daly,et al. Genomewide scan of multiple sclerosis in Finnish multiplex families. , 1997, American journal of human genetics.
[3] M. Carrington,et al. Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients. , 1997 .
[4] D. Douer,et al. An allelic association implicates myeloperoxidase in the etiology of acute promyelocytic leukemia. , 1997, Blood.
[5] B. Becher,et al. Immunohistochemical and genetic evidence of myeloperoxidase involvement in multiple sclerosis , 1997, Journal of Neuroimmunology.
[6] J. Newcombe,et al. The Expression of Tissue‐type Plasminogen Activator, Matrix Metalloproteases and Endogenous Inhibitors in the Central Nervous System in Multiple Sclerosis: Comparison of Stages in Lesion Evolution , 1996, Journal of neuropathology and experimental neurology.
[7] W J Ewens,et al. The TDT and other family-based tests for linkage disequilibrium and association. , 1996, American journal of human genetics.
[8] N Risch,et al. The Future of Genetic Studies of Complex Human Diseases , 1996, Science.
[9] P. Goodfellow,et al. A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 , 1996, Nature Genetics.
[10] D. Hinds,et al. A full genome search in multiple sclerosis , 1996, Nature Genetics.
[11] J. Haines,et al. A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex , 1996, Nature Genetics.
[12] D. Clayton,et al. Age-adjusted recurrence risks for relatives of patients with multiple sclerosis. , 1996, Brain : a journal of neurology.
[13] R. Sobel,et al. Matrix Metalloproteinases in the Normal Human Central Nervous System, Microglial Nodules, and Multiple Sclerosis Lesions , 1996, Journal of neuropathology and experimental neurology.
[14] R. Kucherlapati,et al. Neuronal abnormalities in microtubule-associated protein 1B mutant mice. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[15] E. Goetzl,et al. Matrix metalloproteinases in immunity. , 1996, Journal of immunology.
[16] R. Hughes,et al. Neurofibromatosis 1 and multiple sclerosis. , 1995, Journal of neurology, neurosurgery, and psychiatry.
[17] S. C. Jenkins,et al. Chromosome–specific microsatellite sets for fluorescence–based, semi–automated genome mapping , 1994, Nature Genetics.
[18] W. Ewens,et al. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). , 1993, American journal of human genetics.
[19] A. Sadovnick,et al. Multiple sclerosis: updated risks for relatives. , 1988, American journal of medical genetics.
[20] R. Brady,et al. Myelin‐associated glycoprotein in multiple sclerosis lesions: A quantitative and qualitative analysis , 1987, Annals of neurology.
[21] J. Ott. Analysis of Human Genetic Linkage , 1985 .
[22] D. Silberberg,et al. New diagnostic criteria for multiple sclerosis: Guidelines for research protocols , 1983, Annals of neurology.
[23] Erland Nelson. The Epidemiology of Multiple Sclerosis , 1969 .