Zobrazeno 1 - 10
of 1 718
pro vyhledávání: '"Illig Thomas"'
Autor:
Tang, Ming, Antić, Željko, Fardzadeh, Pedram, Pietzsch, Stefan, Schröder, Charlotte, Eberhardt, Adrian, van Bömmel, Alena, Escherich, Gabriele, Hofmann, Winfried, Horstmann, Martin A., Illig, Thomas, McCrary, J. Matt, Lentes, Jana, Metzler, Markus, Nejdl, Wolfgang, Schlegelberger, Brigitte, Schrappe, Martin, Zimmermann, Martin, Miarka-Walczyk, Karolina, Pastorczak, Agata, Cario, Gunnar, Renard, Bernhard Y., Stanulla, Martin, Bergmann, Anke Katharina
Publikováno v:
In eBioMedicine June 2024 104
Autor:
Volckmar Anna-Lena, Bolze Florian, Jarick Ivonne, Knoll Nadja, Scherag André, Reinehr Thomas, Illig Thomas, Grallert Harald, Wichmann Heinz-Erich, Wiegand Susanna, Biebermann Heike, Krude Heiko, Fischer-Posovszky Pamela, Rief Winfried, Wabitsch Martin, Klingenspor Martin, Hebebrand Johannes, Hinney Anke
Publikováno v:
BMC Medical Genomics, Vol 5, Iss 1, p 65 (2012)
Abstract Background The SH2B1 gene (Src-homology 2B adaptor protein 1 gene) is a solid candidate gene for obesity. Large scale GWAS studies depicted markers in the vicinity of the gene; animal models suggest a potential relevance for human body weigh
Externí odkaz:
https://doaj.org/article/7f79fb8d6c934df2ab10ebc95f475b8c
Autor:
Arnold Matthias, Hartsperger Mara L, Baurecht Hansjörg, Rodríguez Elke, Wachinger Benedikt, Franke Andre, Kabesch Michael, Winkelmann Juliane, Pfeufer Arne, Romanos Marcel, Illig Thomas, Mewes Hans-Werner, Stümpflen Volker, Weidinger Stephan
Publikováno v:
BMC Genomics, Vol 13, Iss 1, p 490 (2012)
Abstract Background Genome-wide association studies (GWAS) have provided a large set of genetic loci influencing the risk for many common diseases. Association studies typically analyze one specific trait in single populations in an isolated fashion
Externí odkaz:
https://doaj.org/article/6cadd4efe8ed4d738e9da9b2e6ab2709
Autor:
Raum Elke, Illig Thomas, Klopp Norman, Weck Melanie, Müller Heiko, Frank Bernd, Brenner Hermann
Publikováno v:
BMC Cancer, Vol 11, Iss 1, p 440 (2011)
Abstract Background Recent studies have reported associations of DNA repair pathway gene variants and risk of various cancers and precancerous lesions, such as chronic atrophic gastritis (CAG). Methods A nested case-control study within the German po
Externí odkaz:
https://doaj.org/article/54bc0c66cd4d4464bfa198262e79ad96
Autor:
Vogelberg Christian, Illig Thomas, Klopp Norman, Depner Martin, Pinto Leonardo A, von Mutius Erika, Kabesch Michael
Publikováno v:
Respiratory Research, Vol 11, Iss 1, p 23 (2010)
Abstract Background Atopic and non-atopic wheezing may be caused by different etiologies: while eosinophils are more important in atopic asthmatic wheezers, neutrophils are predominantly found in BAL samples of young children with wheezing. Both neut
Externí odkaz:
https://doaj.org/article/df0369d6bf464f579d1fb8ca9f506ac6
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
Autor:
Kimmig Rainer, Vogel Carla, Grallert Harald, Scherag Susann, Dietz Tiina, Lahner Harald, Hahn Susanne, Janssen Onno, Scherag André, Tan Susanne, Illig Thomas, Mann Klaus, Hebebrand Johannes, Hinney Anke
Publikováno v:
BMC Medical Genetics, Vol 11, Iss 1, p 12 (2010)
Abstract Background The polycystic ovary syndrome (PCOS), a common endocrine disorder in women of child-bearing age, mainly characterised by chronic anovulation and hyperandrogenism, is often associated with insulin resistance (IR) and obesity. Its e
Externí odkaz:
https://doaj.org/article/de1f6e0dd4f04d878762be7282a87f34
Autor:
McArdle Wendy, Lewis David H, Laiho Päivi, Lagerberg Camilla, Krinka Dagni, Ke Xiayi, Illig Thomas, Hardy Matthew, Gwilliam Rhian, Foedinger Manuela, Dixon Katherine P, Bracegirdle Pippa, Aslanidis Charalampos, Donev Alexander N, Brown Jay, Patton Simon, Ring Susan M, Schmitz Gerd, Stevens Helen, Tybring Gunnel, Wichmann H Erich, Ollier William ER, Yuille Martin A
Publikováno v:
BMC Research Notes, Vol 2, Iss 1, p 208 (2009)
Abstract Background There is little confidence in the consistency of estimation of DNA concentrations when samples move between laboratories. Evidence on this consistency is largely anecdotal. Therefore there is a need first to measure this consisten
Externí odkaz:
https://doaj.org/article/504f2ce5bb6c420f8ba97ce3aabd5970
Autor:
Khuseyinova Natalie, Winkelmann Bernhard, Meisinger Christa, Rothenbacher Dietrich, Vollmert Caren, Hoffmann Michael M, Karakas Mahir, Böhm Bernhard O, Illig Thomas, März Winfried, Koenig Wolfgang
Publikováno v:
BMC Medical Genetics, Vol 10, Iss 1, p 46 (2009)
Abstract Background The role of the Fcγ receptor IIa (FcγRIIa), a receptor for C-reactive protein (CRP), the classical acute phase protein, in atherosclerosis is not yet clear. We sought to investigate the association of FcγRIIa genotype with risk
Externí odkaz:
https://doaj.org/article/568aef6b01404aa0879cebb246d9bd6f
Autor:
Rief Winfried, Reinehr Thomas, Völzke Henry, Rosskopf Dieter, Bornhorst Alexa, Grallert Harald, Wang Hai-Jun, Nguyen Thuy T, Brönner Günter, Scherag André, Vogel Carla IG, Illig Thomas, Wichmann H-Erich, Schäfer Helmut, Hebebrand Johannes, Hinney Anke
Publikováno v:
BMC Medical Genetics, Vol 10, Iss 1, p 19 (2009)
Abstract Background Gastric inhibitory polypeptide (GIP) is postulated to be involved in type 2 diabetes mellitus and obesity. It exerts its function through its receptor, GIPR. We genotyped three GIPR SNPs (rs8111428, rs2302382 and rs1800437) in Ger
Externí odkaz:
https://doaj.org/article/9fa39def1e7749a7975678e37bd6c86f