Zobrazeno 1 - 10
of 29
pro vyhledávání: '"K H, Buetow"'
Autor:
N Siegelmann-Danieli, K H Buetow
Publikováno v:
British Journal of Cancer
The activity of the aromatase enzyme, which converts androgens into oestrogens and has a major role in regulating oestrogen levels in the breast, is thought to be a contributing factor in the development of breast cancer. We undertook this study to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940e9982b538f1f680f6388d0ef78160
https://doi.org/10.1038/sj.bjc.6690071
https://doi.org/10.1038/sj.bjc.6690071
Autor:
K. H Buetow
Publikováno v:
AACR Education book. 2008:537-539
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::262992b09fbc346e2fbd68237ea3d381
https://doi.org/10.1158/aacr.edb-08-8150
https://doi.org/10.1158/aacr.edb-08-8150
Autor:
B R, Balsara, J, Pei, A, De Rienzo, D, Simon, A, Tosolini, Y Y, Lu, F M, Shen, X, Fan, W Y, Lin, K H, Buetow, W T, London, J R, Testa
Publikováno v:
Genes, chromosomescancer. 30(3)
Comparative genomic hybridization (CGH) analysis was used to identify chromosomal imbalances in 52 human primary hepatocellular carcinomas (HCCs). The most prominent changes were gains of part or all of chromosome arms 8q (83% of cases) and 1q (73%)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0af94c3ecd5fcd5daa58bac4352d2928
https://pubmed.ncbi.nlm.nih.gov/11170281
https://pubmed.ncbi.nlm.nih.gov/11170281
Publikováno v:
International journal of cancer. 77(4)
Metastasis is one of the most important and complex processes in human neoplastic disease. A large number of both positive and negative events must occur to permit a tumor cell to colonize a distant site successfully. To identify mouse strains that h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95954d5c4d93da4d87c92e88681f143d
https://pubmed.ncbi.nlm.nih.gov/9679770
https://pubmed.ncbi.nlm.nih.gov/9679770
Publikováno v:
American journal of human genetics. 60(1)
Two kindreds residing in eastern Missouri and exhibiting X-linked recessive idiopathic hypoparathyroidism have been described. Genealogical records extending back five generations revealed no common ancestor. To investigate the possibility of related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d226c2f21b9ef05369530cd31a7cae5
https://pubmed.ncbi.nlm.nih.gov/8981958
https://pubmed.ncbi.nlm.nih.gov/8981958
Autor:
T R, Rebbeck, A H, Walker, C M, Phelan, A K, Godwin, K H, Buetow, J E, Garber, S A, Narod, B L, Weber
Publikováno v:
Progress in clinical and biological research. 396
Most breast cancer has a complex, multifactorial etiology. One consequence of this multifactorial phenomenon is that etiological heterogeneity may exist. This heterogeneity implies simply that two or more groups of breast cancer cases in the general
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b3e3e81f92db6e3f23bed06ef56fa05a
https://pubmed.ncbi.nlm.nih.gov/9108589
https://pubmed.ncbi.nlm.nih.gov/9108589
Publikováno v:
Molecular carcinogenesis. 17(3)
Genes involved in the metabolic activation or detoxification of environmental carcinogens may contribute to breast cancer susceptibility by influencing rates of somatic mutation. To examine this hypothesis, we studied the association between loss of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c648e3a63bb6bbfdd72afb796cca084d
https://pubmed.ncbi.nlm.nih.gov/8944071
https://pubmed.ncbi.nlm.nih.gov/8944071
Autor:
D C, Schultz, L, Vanderveer, K H, Buetow, M P, Boente, R F, Ozols, T C, Hamilton, A K, Godwin
Publikováno v:
Cancer research. 55(10)
We have examined 41 forms of ovarian cancer for genetic alterations on chromosome 9 using a combination of five RFLP DNA probes and 15 simple tandem repeat polymorphisms. Genetic imbalance (i.e., loss of heterozygosity, microsatellite instability, am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::53f7376e7987aee4f909c7688c07b4bc
https://pubmed.ncbi.nlm.nih.gov/7743516
https://pubmed.ncbi.nlm.nih.gov/7743516
Publikováno v:
Genetic epidemiology. 12(4)
Linkage analysis can be used to test the hypothesis that a marker locus of known location segregates independently from a presumed disease gene. One way to test this hypothesis is to measure the similarity of marker alleles among pairs of relatives a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::462d06bb86a171a44c3e7f491560cdf4
https://pubmed.ncbi.nlm.nih.gov/8536951
https://pubmed.ncbi.nlm.nih.gov/8536951
Autor:
A, Sander, J C, Murray, T, Scherpbier-Heddema, K H, Buetow, J, Weissenbach, M, Zingg, K, Ludwig, R, Schmelzle
Publikováno v:
American journal of human genetics. 56(1)
Van der Woude syndrome (VWS) is an autosomal dominant craniofacial disorder characterized by lip pits, clefting of the primary or secondary palate, and hypodontia. The gene has been localized, by RFLP-based linkage studies, to region 1q32-41 between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7e105d70e6e9532164c82828b498aa5c
https://pubmed.ncbi.nlm.nih.gov/7825592
https://pubmed.ncbi.nlm.nih.gov/7825592