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@ARTICLE{Wu:1500,
author = {Wu, Y. and Lücke, A. and Sumin, W.},
title = {{A}ssessment of nutrient sources and paleoproductivity
during the past century in {L}onggan {L}ake, middle reaches
of the {Y}angtze {R}iver, {C}hina},
journal = {Journal of paleolimnology},
volume = {39},
issn = {0921-2728},
address = {Dordrecht [u.a.]},
publisher = {Springer Science + Business Media B.V},
reportid = {PreJuSER-1500},
pages = {451 - 462},
year = {2008},
note = {Record converted from VDB: 12.11.2012},
abstract = {Previous genome-wide association studies have identified
two independent variants in HNF1B as susceptibility loci for
prostate cancer risk. To fine-map common genetic variation
in this region, we genotyped 79 single nucleotide
polymorphisms (SNPs) in the 17q12 region harboring HNF1B in
10 272 prostate cancer cases and 9123 controls of European
ancestry from 10 case-control studies as part of the Cancer
Genetic Markers of Susceptibility (CGEMS) initiative. Ten
SNPs were significantly related to prostate cancer risk at a
genome-wide significance level of P < 5 × 10(-8) with the
most significant association with rs4430796 (P = 1.62 ×
10(-24)). However, risk within this first locus was not
entirely explained by rs4430796. Although modestly
correlated (r(2)= 0.64), rs7405696 was also associated with
risk (P = 9.35 × 10(-23)) even after adjustment for
rs4430769 (P = 0.007). As expected, rs11649743 was related
to prostate cancer risk (P = 3.54 × 10(-8)); however, the
association within this second locus was stronger for
rs4794758 (P = 4.95 × 10(-10)), which explained all of the
risk observed with rs11649743 when both SNPs were included
in the same model (P = 0.32 for rs11649743; P = 0.002 for
rs4794758). Sequential conditional analyses indicated that
five SNPs (rs4430796, rs7405696, rs4794758, rs1016990 and
rs3094509) together comprise the best model for risk in this
region. This study demonstrates a complex relationship
between variants in the HNF1B region and prostate cancer
risk. Further studies are needed to investigate the
biological basis of the association of variants in 17q12
with prostate cancer.},
keywords = {Alleles / Genetic Loci: genetics / Genetic Predisposition
to Disease / Genome, Human: genetics / Hepatocyte Nuclear
Factor 1-beta: genetics / Humans / Male / Models, Genetic /
Physical Chromosome Mapping: methods / Polymorphism, Single
Nucleotide: genetics / Prostatic Neoplasms: genetics /
Regression Analysis / Risk Factors / HNF1B protein, human
(NLM Chemicals) / Hepatocyte Nuclear Factor 1-beta (NLM
Chemicals) / J (WoSType)},
cin = {ICG-5},
ddc = {930},
cid = {I:(DE-Juel1)VDB143},
pnm = {Geosysteme - Erde im Wandel},
pid = {G:(DE-Juel1)FUEK405},
shelfmark = {Environmental Sciences / Geosciences, Multidisciplinary /
Limnology},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:21576123},
pmc = {pmc:PMC3140817},
UT = {WOS:000254905100002},
doi = {10.1007/s10933-007-9123-0},
url = {https://juser.fz-juelich.de/record/1500},
}