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Results: 1-7 |
Results: 7
Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation
Authors: Oeffner, F Korn, T Roth, H Ziegler, A Hinney, A Goldschmidt, H Siegfried, W Hebebrand, J Grzeschik, KH
Citation: F. Oeffner et al., Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation, INT J OBES, 25(6), 2001, pp. 767-769
Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents
Authors: Oeffner, F Bornholdt, D Ziegler, A Hinney, A Gorg, T Gerber, G Goldschmidt, HP Siegfried, W Wright, A Hebebrand, J Grzeschik, KH
Citation: F. Oeffner et al., Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents, ACT DIABETO, 37(2), 2000, pp. 93-101
Independent confirmation of a major locus for obesity on chromosome 10
Authors: Hinney, A Ziegler, A Oeffner, F Wedewardt, C Vogel, M Wulftange, H Geller, F Stubing, K Siegfried, W Goldschmidt, HP Remschmidt, H Hebebrand, J
Citation: A. Hinney et al., Independent confirmation of a major locus for obesity on chromosome 10, J CLIN END, 85(8), 2000, pp. 2962-2965
Independent confirmation of a major locus for obesity on chromosome 10 (vol 85, pg 2962, 2000)
Authors: Hinney, A Ziegler, A Oeffner, F Wedewardt, C Vogel, M Wulftange, H Geller, F Stubing, K Siegried, WG Goldschmidt, HP Remschmidt, H Hebegrand, J
Citation: A. Hinney et al., Independent confirmation of a major locus for obesity on chromosome 10 (vol 85, pg 2962, 2000), J CLIN END, 85(11), 2000, pp. 3972-3972
Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.3
Authors: Lisch, W Buttner, A Oeffner, F Boddeker, I Engel, H Lisch, C Ziegler, A Grzeschik, KH
Citation: W. Lisch et al., Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.3, AM J OPHTH, 130(4), 2000, pp. 461-468
Cloning and characterization of gp36, a human mucin-type glycoprotein preferentially expressed in vascular endothelium
Authors: Zimmer, G Oeffner, F von Messling, V Tschernig, T Grone, HJ Klenk, HD Herrler, G
Citation: G. Zimmer et al., Cloning and characterization of gp36, a human mucin-type glycoprotein preferentially expressed in vascular endothelium, BIOCHEM J, 341, 1999, pp. 277-284
The cytoplasmic tail of the influenza C virus glycoprotein HEF negatively affects transport to the cell surface
Authors: Oeffner, F Klenk, HD Herrler, G
Citation: F. Oeffner et al., The cytoplasmic tail of the influenza C virus glycoprotein HEF negatively affects transport to the cell surface, J GEN VIROL, 80, 1999, pp. 363-369
Risultati: 1-7 |