Zobrazeno 1 - 10
of 13
pro vyhledávání: '"D J Nancarrow"'
Publikováno v:
Melanoma Research. 4:29-34
A gene for familial melanoma (MLM) has been mapped to 9p22-p13 by linkage analysis using simple tandem repeat polymorphisms (STRPs) at the IFNA and D9S126 loci. This localization is consistent with the finding of homozygous deletions of these markers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d58f2121d89d322e15d9b58de6a4df0
https://doi.org/10.1097/00008390-199402000-00005
https://doi.org/10.1097/00008390-199402000-00005
Autor:
M M White, D J Nancarrow
Publikováno v:
Journal of radiological protection : official journal of the Society for Radiological Protection. 24(1)
A short study has been carried out of the potential radioactive waste disposal issues associated with the proposed extension of Part IIA of the Environmental Protection Act 1990 to include radioactively contaminated land, where there is no other suit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc8e781b1e427e838b0186ceba9a8ba
https://pubmed.ncbi.nlm.nih.gov/15080549
https://pubmed.ncbi.nlm.nih.gov/15080549
Autor:
B J, Mowry, D J, Nancarrow
Publikováno v:
Clinical and experimental pharmacologyphysiology. 28(1-2)
1. Schizophrenia is a chronic, disabling brain disease that affects approximately 1% of the world's population. It is characterized by delusions, hallucinations and formal thought disorder, together with a decline in socio-occupational functioning. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7e4a9855b4bb0ab75a6c32308987d5aa
https://pubmed.ncbi.nlm.nih.gov/11153540
https://pubmed.ncbi.nlm.nih.gov/11153540
Second stage of a genome scan of schizophrenia: study of five positive regions in an expanded sample
Autor:
B J, Mowry, K R, Ewen, D J, Nancarrow, D P, Lennon, D A, Nertney, H L, Jones, M S, O'Brien, C E, Thornley, M K, Walters, R R, Crowe, J M, Silverman, J, Endicott, L, Sharpe, N K, Hayward, M M, Gladis, S J, Foote, D F, Levinson
Publikováno v:
American journal of medical genetics. 96(6)
In a previous genome scan of 43 schizophrenia pedigrees, nonparametric linkage (NPL) scores with empirically derived pointwise P-values less than 0.01 were observed in two regions (chromosomes 2q12-13 and 10q23) and less than 0.05 in three regions (4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31df1597e929b69dc9637b3d5e1fa106
https://pubmed.ncbi.nlm.nih.gov/11121199
https://pubmed.ncbi.nlm.nih.gov/11121199
Autor:
M, Martinez, L R, Goldin, Q, Cao, J, Zhang, A R, Sanders, D J, Nancarrow, J M, Taylor, D F, Levinson, A, Kirby, R R, Crowe, N C, Andreasen, D W, Black, J M, Silverman, D P, Lennon, D A, Nertney, D M, Brown, B J, Mowry, E S, Gershon, P V, Gejman
Publikováno v:
American journal of medical genetics. 88(4)
Evidence for suggestive linkage to schizophrenia with chromosome 6q markers was previously reported from a two-stage approach. Using nonparametric affected sib pairs (ASP) methods, nominal p-values of 0.00018 and 0.00095 were obtained in the screenin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::13a80dfd98fa94cf91c9fdbb3f180a44
https://pubmed.ncbi.nlm.nih.gov/10402499
https://pubmed.ncbi.nlm.nih.gov/10402499
Autor:
D J, Nancarrow, B J, Mowry
Publikováno v:
Genetic epidemiology. 14(6)
From a single extended pedigree simulation replicate, high density, affected only subpedigrees were isolated, based on the T40 affected status for the disease trait, Q1. On this sample of 14 pedigrees, with a range of two to six affected members (48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::27c10389a770f6c6a18627f0e71f13f9
https://pubmed.ncbi.nlm.nih.gov/9433619
https://pubmed.ncbi.nlm.nih.gov/9433619
Publikováno v:
Genes, chromosomescancer. 15(2)
Little is known about the biology of Merkel cell carcinoma (MCC), also called small cell carcinoma of the skin. MCC has similarities with small cell lung cancer (SCLC): both are neuroendocrine malignancies with early metastasis to distant sites and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e44930a2a3b3f8f8e249664a94aea13
https://pubmed.ncbi.nlm.nih.gov/8834173
https://pubmed.ncbi.nlm.nih.gov/8834173
Autor:
M A, Maw, D R, Allen-Powell, R J, Goodey, I A, Stewart, D J, Nancarrow, N K, Hayward, R J, Gardner
Publikováno v:
American journal of human genetics. 57(3)
Classical studies have demonstrated genetic heterogeneity for nonsyndromic autosomal recessive congenital neurosensory deafness, with at least six loci postulated. Linkage analysis in two consanguineous Tunisian kindreds has demonstrated that one suc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d5fec3104601434e7893a6878d6f7d9
https://pubmed.ncbi.nlm.nih.gov/7668291
https://pubmed.ncbi.nlm.nih.gov/7668291
Publikováno v:
Melanoma Research. 4:267-268
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b92369b5b38ee347bfe9fed1e29e7d7e
https://doi.org/10.1097/00008390-199408000-00009
https://doi.org/10.1097/00008390-199408000-00009
Autor:
D J Nancarrow and M M White
Publikováno v:
Journal of Radiological Protection; Mar2004, Vol. 24 Issue 1, p61-73, 13p