26 results on '"J. Genschel"'
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2. The interleukin-25 gene located in the inflammatory bowel disease (IBD) 4 region: no association with inflammatory bowel disease
3. The C/C_₁₃₉₁₀ and G/G_₂₂₀₁₈ Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel Disease
4. HDL-Stoffwechsel
5. Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease
6. PPARG Agonist führt zu einer Verbesserung der Leberenzyme in einem monogenetischen Modell für NAFLD
7. Einfluss von Polymorphismen des MDR1-Gens auf Ausbruch und Verlauf chronisch entzündlicher Darmerkrankungen
8. Alterationen im PPARG Gen als Ursache einer Familiären Steatosis hepatis
9. Wilson disease: high prevalence in a mountainous area of Crete
10. Genotypen des Multi-Drug-Resistance-Gens MDR1: Prädiktoren für das Steroidansprechen bei chronisch entzündlichen Darmerkrankungen?
11. Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation
12. The interleukin-25 gene located in the inflammatory bowel disease (IBD) 4 region: no association with inflammatory bowel disease
13. Lack of mutations in LMNA, its promoter region, and the cellular retinoic acid binding protein II (CRABP II) in HIV associated lipodystrophy
14. Lipid evaluation in HIV-1-positive patients treated with protease inhibitors
15. Three novel mutations, c314CA, C778insC, and c1285+2TA, in exon 2 of the Wilson disease gene
16. Mutations in the LMNA gene encoding lamin A/C
17. Veränderungen des Lipidstoffwechsels bei HIV-Patienten unter der Therapie mit Proteaseinhibitoren
18. P0184 ATP7B MUTATIONS IN POLISH PEDIATRIC AND ADULT PATIENTS WITH WILSON???S DISEASE
19. R428W mutation within LMNA caused familial partial lipodystrophy
20. Mutation analysis of the HFE gene in hereditary hemochromatosis
21. Mutation analysis of the HFE gene in hereditary hemochromatosis
22. R428W mutation within LMNA caused familial partial lipodystrophy
23. R482W mutation with LMNA causes familial partial lipodystrophy
24. Detection of novel mutations in the wilson disease gene using direct sequence analysis
25. Influence of immunosuppressants on lipoprotein metabolism in a rabbit model
26. Downregulation fof transthyretin-MET30 expression in cell culture with inosine15.1-hammerhead ribozymes
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