Výsledky vyhledávání - "Friedel Susann"

Akademický článek

Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry

Autor: Wichmann H-Erich, Illig Thomas, Heid Iris M, Grallert Harald, Friedel Susann, Müller Timo D, Scherag André, Greene Brandon, Vogel Carla IG, Schäfer Helmut, Hebebrand Johannes, Hinney Anke

Publikováno v: BMC Medical Genetics, Vol 10, Iss 1, p 14 (2009)

Abstract Background A recent genome-wide association (GWA) study of U.S. Caucasians suggested that eight single nucleotide polymorphisms (SNPs) in CTNNBL1 are associated with obesity and increased fat mass. We analysed the respective SNPs in data fro

Externí odkaz: https://doaj.org/article/8e24bae71eb44aaaacf9afa8fc903e06

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Akademický článek

Mutation screen and association studies in the Diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13

Autor: Platzer Matthias, Meitinger Thomas, Wabitsch Martin, Koberwitz Kerstin, Fries Hans-Rudolf, Wermter Anne-Kathrin, Brumm Harald, Scherag André, Reichwald Kathrin, Friedel Susann, Biebermann Heike, Hinney Anke, Hebebrand Johannes

Publikováno v: BMC Genetics, Vol 8, Iss 1, p 17 (2007)

Abstract Background DGAT2 is a promising candidate gene for obesity because of its function as a key enzyme in fat metabolism and because of its localization on chromosome 11q13, a linkage region for extreme early onset obesity detected in our sample

Externí odkaz: https://doaj.org/article/f93d77abd4c9418cb22bade5d912d346

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Akademický článek

No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents

Autor: Müller, Timo Dirk, Reichwald, Kathrin, Wermter, Anne-Kathrin, Brönner, Günter, Nguyen, Thuy Trang, Friedel, Susann, Koberwitz, Kerstin, Engeli, Stefan, Lichtner, Peter, Meitinger, Thomas, Schäfer, Helmut, Hebebrand, Johannes, Hinney, Anke ^*

Publikováno v: In Molecular Genetics and Metabolism April 2007 90(4):429-434

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Akademický článek

Mutation screen and association studies in the Diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.

Autor: Friedel, Susann¹ Susann.Friedel@uni-due.de, Reichwald, Kathrin^1,2 KReichwald@fli-leibnitz.de, Scherag, Andre³ Scherag@staff.unimarburg.de, Brumm, Harald⁴ Harald.Brumm@charite.de, Wermter, Anne-Kathrin⁵ Wermtera@med.uni-marburg.de, Fries, Hans-Rudolf⁶ Ruedi.Fries@tierzucht.tum.de, Koberwitz, Kerstin⁷ Koberwitz@gsf.de, Wabitsch, Martin⁸ Martin.Wabitsch@uniklinik-ulm.de, Meitinger, Thomas⁷ Meitinger@gsf.de, Platzer, Matthias² Mplatzer@fli-leibnitz.de, Biebermann, Heike⁴ Heike.Biebermann@charite.de, Hinney, Anke¹ Anke.Hinney@uni-due.de, Hebebrand, Johannes¹ Johannes.Hebebrand@uni-due.de

Publikováno v: BMC Genetics. 2007, Vol. 8, p1-9. 9p. 2 Cartoon or Caricatures.

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Estrogen receptor 1 gene (ESR1) is associated to restrictive anorexia nervosa

Autor: VERSINI, Audrey, RAMOZ, Nicolas, Le Strat, Yann, Friedel, Susann, Ehrlich, Stefan, Boni, Claudette, Hinney, Anke, Hebebrand, Johannes, Romo, Lucia, Guelfi, Julien-Daniel, Gorwood, Philip A.P.M.

Publikováno v: Neuropsychopharmacology
Neuropsychopharmacology, Nature Publishing Group, 2010, 35 (8), pp.1818-25. 〈10.1038/npp.2010.49〉
Neuropsychopharmacology, 2010, 35 (8), pp.1818-25. ⟨10.1038/npp.2010.49⟩
Neuropsychopharmacology, Nature Publishing Group, 2010, 35 (8), pp.1818-25. ⟨10.1038/npp.2010.49⟩

International audience; Anorexia nervosa is a highly heritable young-onset psychiatric illness which aetiology remains unknown. Estrogen alpha- and beta-receptors, encoded by ESR1 and ESR2 genes, are involved in food intake regulation and eating beha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::09c30e143a509e050b570e3b7499f25e
https://hal.archives-ouvertes.fr/hal-00524128

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Molecular genetics of obesity

Autor: Hinney, Anke, Scherag, André, Friedel, Susann, Ganz Vogel, Carla Ivane, Jarick, Ivonne, Schäfer, Helmut, Hebebrand, Johannes

Publikováno v: 54. Jahrestagung der Deutschen Gesellschaft für Medizinische Informatik, Biometrie und Epidemiologie (gmds); 20090907-20090910; Essen; DOC09gmds006 /20090831/

Aims: The molecular genetic analysis of obesity has led to the identification of a limited number of confirmed major genes. While such genes have a clear influence on the development of the phenotype, the underlying mutations are however infrequent a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::324004df6c2d45905d595c4a71724ed8

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