Suchergebnisse
Alle Typen
Zeitschriftenartikel (3246)
2881.
Zeitschriftenartikel
130 (24), S. 5903 - 5914 (2003)
The amphioxus Hairy family: differential fate after duplication. Development 2882.
Zeitschriftenartikel
4 (4), S. 217 - 225 (2003)
Rapid purification and crystal structure analysis of a small protein carrying two terminal affinity tags. Journal of Structural and Functional Genomics 2883.
Zeitschriftenartikel
13 (12), S. 2736 - 2746 (2003)
Generation, annotation, evolutionary analysis, and database integration of 20,000 unique sea urchin EST clusters. Genome Research 2884.
Zeitschriftenartikel
55 (9), S. 605 - 614 (2003)
The properties of the single chicken MHC classical class II alpha chain (B-LA) gene indicate an ancient origin for the DR/E-like isotype of class II molecules. Immunogenetics 2885.
Zeitschriftenartikel
Protein and antibody microarray technology. Interactions in Biological Systems, S. 229 - 240 (2003)
2886.
Zeitschriftenartikel
311 (3), S. 641 - 648 (2003)
Demethylation of host-cell DNA at the site of avian retrovirus integration. Biochemical and Biophysical Research Communications 2887.
Zeitschriftenartikel
554 (1-2), S. 55 - 58 (2003)
Physical and functional interaction of the Werner syndrome protein with poly-ADP ribosyl transferase. FEBS Letters 2888.
Zeitschriftenartikel
20 (11), S. 1887 - 1896 (2003)
Distinct changes of genomic biases in nucleotide substitution at the time of mammalian radiation. Molecular Biology and Evolution 2889.
Zeitschriftenartikel
14 (Suppl. S), S. 359A - 359A (2003)
Mutational analysis in nephronophthisis type 4. Journal of the American Society of Nephrology 2890.
Zeitschriftenartikel
4 (6), S. 351 - 378 (2003)
Human inter-individual DNA sequence variation in candidate genes, drug targets, the importance of haplotypes and pharmacogenomics. Current Pharmaceutical Biotechnology 2891.
Zeitschriftenartikel
100 (11), S. 979 - 983 (2003)
Schnyder's crystalline corneal dystrophy. Further narrowing of the linkage interval at chromosome 1p34.1-p36? Ophthalmologe 2892.
Zeitschriftenartikel
73 (6), S. 1341 - 1354 (2003)
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation. American Journal of Human Genetics 2893.
Zeitschriftenartikel
11 (11), S. 858 - 865 (2003)
Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes. European Journal of Human Genetics 2894.
Zeitschriftenartikel
66 (9), S. 1673 - 1680 (2003)
A unique central tryptophan hydroxylase isoform. Biochemical Pharmacology 2895.
Zeitschriftenartikel
278 (42), S. 41452 - 41461 (2003)
Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin - A potential mechanism for loss of huntingtin function in Huntington's disease. Journal of Biological Chemistry 2896.
Zeitschriftenartikel
278 (42), S. 41452 - 41461 (2003)
Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin - A potential mechanism for loss of huntingtin function in Huntington's disease. Journal of Biological Chemistry 2897.
Zeitschriftenartikel
31 (20), S. 5917 - 5929 (2003)
Hexameric RSF1010 helicase RepA: the structural and functional importance of single amino acid residues. Nucleic Acids Research 2898.
Zeitschriftenartikel
100 (21), S. 12277 - 12282 (2003)
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2. Proceedings of the National Academy of Sciences of the United States of America 2899.
Zeitschriftenartikel
163 (1), S. 15 - 20 (2003)
H2AX regulates meiotic telomere clustering. Journal of Cell Biology 2900.
Zeitschriftenartikel
333 (1), S. 75 - 85 (2003)
Correlating protein-DNA and protein-protein interaction networks. Journal of Molecular Biology