947 results on '"Goedde, H."'
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2. Neuropsychopharmacology of Alcoholism
3. Experimental Section
4. Introduction
5. Biochemical Aspects of Alcoholism
6. Genetic Factors in Alcoholism
7. Alcohol Metabolism: Biochemistry and Genetic Variations
8. Metabolism of Cyclophosphamide by Aldehyde Dehydrogenases
9. Human Liver High Km Aldehyde Dehydrogenase (ALDH4): Properties and Structural Relationship to the Glutamic γ-Semialdehyde Dehydrogenase
10. Tumor-Associated Aldehyde Dehydrogenase (ALDH3): Expression in Diffrent Human Tumor Cell Lines with and without Treatment with 3-Methylcholanthrene
11. Biochemical, Immunological, and Molecular Characterization of a 'High KM' Aldehyde Dehydrogenase
12. Biochemistry and Chemistry of Lipoic Acids
13. Human breast cancer: frequent p53 allele loss and protein overexpression
14. Medicobiological and genetic studies on alcoholism Role of metabolic variation and ethnicity on drinking habits, alcohol abuse and alcohol-related mortality
15. Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?
16. Characterization of long-term cell cultures of human chorion villi and fibroblasts using antibodies to cytoskeletal proteins
17. Genetisch bedingte Variabilität des Alkoholstoffwechsels und ihr Einfluß auf Trinkverhalten und Neigung zum Alkoholismus
18. Drinking Behaviour and Alcoholism
19. Human variability in alcohol and aldehyde metabolism: vulnerability to toxic effects
20. Genetic Markers, Serum Protein and Erythrocyte Enzyme Polymorphisms
21. Topics, Materials and Methods
22. Other Traits
23. Conclusions
24. Ecogenetic and Pharmacogenetic Phenomena
25. Biochemical, Immunological, and Molecular Characterization of a “High KM” Aldehyde Dehydrogenase
26. Alcohol Metabolism, Alcohol Intolerance, and Alcoholism
27. Distribution of ADH2 and ALDH2 genotypes in different populations
28. The ITI system in South Koreans and iranians analysed by an improved classification procedure: Distribution of alleles and description of “new” phenotypes
29. Arbeitsvorschriften : Nachweis, Identifizierung, Anreicherung und Auftrennung von normaler Pseudocholinesterase und Enzymvarianten sowie der Komponenten C1—C5
30. Biochemie und Genetik der Pseudocholinesterasen
31. Zur Variabilität und formalen Genetik der Lippenfurchen
32. Quantitative Parameter der digitalen Hautleisten — ihre Verteilung in Familien
33. Serum protein and erythrocyte enzyme polymorphisms in twelve population groups of Hungary
34. The Acetylator Polymorphism in four Populations of Afghanistan
35. Phenotypes of Gc and Tf in Leprosy Patients of Mali and Ethiopia
36. Pseudocholinesterase Polymorphism among Ålanders (Finno-Swedes), Maris (Cheremisses, USSR) and Greenland Eskimos, and the Segregation of some E₁ and E₂ Locus Types in Finnish Lapp Families
37. Properdin Factor B Polymorphism in Afghanistan
38. Twin Studies and Substrate Differences in Platelet Monoamine Oxidase Activity
39. Distribution of Alpha-1-Antitrypsin and Haptoglobin Phenotypes in Bladder Cancer Patients
40. Polymorphism of Delta-Aminolevulinic Acid Dehydratase in Various Populations
41. Purine Metabolism in Fibroblasts of Patients with Duchenne's Muscular Dystrophy
42. High HPRT Activity in Fibroblasts from Patients with Lesch-Nyhan Syndrome Due to Bacterial 'L-Form' Contamination
43. Genetische Aspekte zur Wirkung von Arzneimitteln
44. Pseudocholinesterase Variation
45. Ultrathin-Layer Isoelectric Focusing of Subtypes of Gc, Tf, Pi, and PGM1
46. Isozymes of Alcohol Dehydrogenase and Aldehyde Dehydrogenase in Japanese and their Role in Alcohol Sensitivity
47. Studies on the Polymorphism of Isoniazid (INH) Acetylation in Rhesus Monkeys (Macaca Mulatta)
48. On Nomenclature of Pseudocholinesterase Polymorphism
49. Taste Thresholds of Thiourea Derivatives and Anetholtrithion in Twins
50. Untersuchungen der Hautfurchen bei Patienten mit endogenem Ekzem mit einem Beitrag zur Technik der Daktyloskopie
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