Zobrazeno 1 - 4
of 4
pro vyhledávání: '"521"'
Autor:
Kallel Choumous, Cohen William, Saut Noémie, Blankenberg Stefan, Schnabel Renate, Rupprecht Hans J, Bickel Christoph, Munzel Thomas, Tregouet David-Alexandre, Morange Pierre-Emmanuel
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 103 (2012)
Abstract Background Blood coagulation is an essential determinant of coronary artery disease (CAD). Soluble Endothelial Protein C Receptor (sEPCR) may be a biomarker of a hypercoagulable state. We prospectively investigated the relationship between p
Externí odkaz:
https://doaj.org/article/7322c6d6cea445088fad27dd497e5f88
Autor:
Anantharaman Ramani, Andiappan Anand, Nilkanth Pallavi, Suri Bani, Wang De Yun, Chew Fook Tim
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 170 (2011)
Abstract Background Recent genome-wide association studies (GWAS) for asthma have been successful in identifying novel associations which have been well replicated. The aim of this study is to identify the genetic variants that influence predispositi
Externí odkaz:
https://doaj.org/article/db19594b699e48d19a3e6a07912dbbe7
Autor:
Hočevar Marko, De Grève Jacques, Teugels Erik, Žgajnar Janez, Krajc Mateja, Stegel Vida, Novaković Srdjan
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 9 (2011)
Abstract Background The BRCA1 and BRCA2 mutation spectrum and mutation detection rates according to different family histories were investigated in 521 subjects from 322 unrelated Slovenian cancer families with breast and/or ovarian cancer. Methods T
Externí odkaz:
https://doaj.org/article/31db7c96255c48c18cbc3f1d659c3a79
Autor:
Rief Winfried, Scherag Susann, Vogel Carla IG, Grallert Harald, Scherag André, Greene Brandon H, Nguyen Trang T, Carrie Jophia, Wandolski Melanie, Brönner Günter, Müller Timo D, Wichmann Hans-Erich, Illig Thomas, Schäfer Helmut, Hebebrand Johannes, Hinney Anke
Publikováno v:
BMC Medical Genetics, Vol 11, Iss 1, p 2 (2010)
Abstract Background The orexigenic effects of cannabinoids are limited by activation of the endocannabinoid degrading enzyme fatty acid amide hydrolase (FAAH). The aim of this study was to analyse whether FAAH alleles are associated with early and la
Externí odkaz:
https://doaj.org/article/4f6c5ff5415a4286845afb37052cc712