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                             11 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Analyses of Proteins Involved in Vesicular Trafficking in Platelets of Mouse Models of Hermansky Pudlak Syndrome Richards-Smith, Beverly
1999
68 1 p. 14-23
10 p.
artikel
2 A Type 2 Diabetes-Associated Polymorphic ARE Motif Affecting Expression of PPP1R3 Is Involved in RNA–Protein Interactions Xia, James
1999
68 1 p. 48-55
8 p.
artikel
3 Combined Adenine Phosphoribosyltransferase and N-acetylgalactosamine-6-sulfate Sulfatase Deficiency Wang, L.
1999
68 1 p. 78-85
8 p.
artikel
4 Determination of Queuosine Modification System Deficiencies in Cultured Human Cells Morris, Rana C.
1999
68 1 p. 56-67
12 p.
artikel
5 Human Liver-Specific Very-Long-Chain Acyl-Coenzyme A Synthetase: cDNA Cloning and Characterization of a Second Enzymatically Active Protein Steinberg, Steven J.
1999
68 1 p. 32-42
11 p.
artikel
6 Linkage Analysis of the hph-1 Mutation and the GTP Cyclohydrolase I Structural Gene Montañez, Cindy S.
1999
68 1 p. 91-92
2 p.
artikel
7 Metabolic and Secretory Response to d -Fructose in Pancreatic Islets from Adult Rats Injected with Streptozotocin during the Neonatal Period Scruel, Olivier
1999
68 1 p. 86-90
5 p.
artikel
8 Morphine Regulation of a Novel Uridine Diphosphate Glucuronosyl- Transferase in Guinea Pig Pups Following in Utero Exposure Smith, Sue Ann
1999
68 1 p. 68-77
10 p.
artikel
9 Niemann–Pick C1 Is a Late Endosome-Resident Protein That Transiently Associates with Lysosomes and the Trans-Golgi Network Higgins, Maureen E.
1999
68 1 p. 1-13
13 p.
artikel
10 The Mutant Genotype Is the Main Determinant of the Metabolic Phenotype in Phenylalanine Hydroxylase Deficiency Bénit, Paule
1999
68 1 p. 43-47
5 p.
artikel
11 Trimethylaminuria Is Caused by Mutations of the FMO3 Gene in a North American Cohort Akerman, B.R.
1999
68 1 p. 24-31
8 p.
artikel
                             11 gevonden resultaten
 
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