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Autor: W. W. Weber, J. H. Kurth, M. D. Caldwell

Publikováno v: Current Pharmacogenomics. 1:193-202

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f20db66fdf2882610e438aee0d062d7
https://doi.org/10.2174/1570160033476269

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Gene-Toxin Interaction as a Putative Risk Factor for Parkinson’s Disease with Dementia

Autor: R. E. S. Hassanein, J. P. Hubble, W. C. Koller, S. L. Glatt, Abraham N. Lieberman, M. C. Kurth, Gerard D. Schellenberg, J. H. Kurth

Publikováno v: Neuroepidemiology. 17:96-104

We had previously examined environmental, sociodemographic and clinical variables as predictors for Parkinson’s disease with dementia (PD + D) and found that lower educational attainment, greater motor impairment and advanced age at disease onset w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82e36acab464c8e2616d3dcac0941f43
https://doi.org/10.1159/000026159

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Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig

Autor: E W, Johnson, L M, Iyer, S S, Rich, H T, Orr, A, Gil-Nagel, J H, Kurth, J M, Zabramski, D A, Marchuk, J, Weissenbach, C L, Clericuzio, L E, Davis, B L, Hart, J F, Gusella, B E, Kosofsky, D N, Louis, L A, Morrison, E D, Green, J L, Weber

Publikováno v: Genome research. 5(4)

Cerebral cavernous malformations (CCM) are vascular lesions present in some 20 million people worldwide that are responsible for seizures, migraine, hemorrhage, and other neurologic problems. Familial cases ofCCM can be inherited as an autosomal domi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63bb8ed41f135844a9cf07ee727f798c
https://pubmed.ncbi.nlm.nih.gov/8750196

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Notes on individual sequence variation in humans: immunoglobulin kappa light chain

Autor: J H, Kurth, L L, Cavalli-Sforza

Publikováno v: American journal of human genetics. 54(6)

Little is known concerning the magnitude of variability in the nucleic acid sequence of DNA at the individual level. We have collected a large set of sequence data from the human immunoglobulin kappa light-chain-locus constant region (10,444 bp) and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1bb1e75cf6fdccaa69b0eedc726227e1
https://pubmed.ncbi.nlm.nih.gov/8198126

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HLA-DQa allelic frequencies detected with PCR in a variety of human populations

Autor: J H, Kurth, A M, Bowcock, H A, Erlich, L L, Cavallisforza

Publikováno v: Gene geography : a computerized bulletin on human gene frequencies. 6(3)

Polymerase chain reaction (PCR) amplification and oligonucleotide probe hybridization may be used to detect DNA polymorphisms rapidly in large samples. In this study, 475 individuals from thirteen human populations were allelotyped at the human leuko

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1b96d6d1e3bc03cfdffbe77eed57e3fd
https://pubmed.ncbi.nlm.nih.gov/1339494

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Polymerase chain reaction polymorphisms in HLA-DQ alpha and IL6 from Mongoloid and Caucasoid populations

Autor: N V, Titenko, J H, Kurth, A M, Bowcock, L L, Cavalli-Sforza

Publikováno v: Biomedical science. 2(2)

Polymerase chain reaction polymorphisms have been used to study European, Chinese, Russian and Buryat populations at the HLA-DQ alpha and IL6 loci. DNA from individuals in these populations was specifically amplified at these loci, and analyzed eithe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d647b9c304687f68dcc23d8aa9114d4d
https://pubmed.ncbi.nlm.nih.gov/1772970

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