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                             17 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A 3-Mb Map of a Large Segmental Duplication Overlapping the α7-Nicotinic Acetylcholine Receptor Gene (CHRNA7) at Human 15q13–q14 Riley, Brien
2002
79 2 p. 197-209
13 p.
artikel
2 Candidate Genes Required for Embryonic Development: A Comparative Analysis of Distal Mouse Chromosome 14 and Human Chromosome 13q22 Kurihara, Laurie Jo
2002
79 2 p. 154-161
8 p.
artikel
3 Conservation of the T-Cell Receptor α/δ Linkage in the Teleost Fish Tetraodon nigroviridis Fischer, Cécile
2002
79 2 p. 241-248
8 p.
artikel
4 Evolution of the Regulators of G-Protein Signaling Multigene Family in Mouse and Human Sierra, David A.
2002
79 2 p. 177-185
9 p.
artikel
5 Genetic “Differences” Steele, Fintan R.
2002
79 2 p. 145-
1 p.
artikel
6 Genomic Analysis of Human Chromosome 10q and 4q Telomeres Suggests a Common Origin van Geel, Michel
2002
79 2 p. 210-217
8 p.
artikel
7 Identification and Characterization of a Dense Cluster of Placenta-Specific Cysteine Peptidase Genes and Related Genes on Mouse Chromosome 13 Deussing, Jan
2002
79 2 p. 225-240
16 p.
artikel
8 Identification of a Mutation Causing Mucopolysaccharidosis Type IIIA in New Zealand Huntaway Dogs Yogalingam, Gouri
2002
79 2 p. 150-153
4 p.
artikel
9 Insertional Mutagenesis of the Mouse Acid Ceramidase Gene Leads to Early Embryonic Lethality in Homozygotes and Progressive Lipid Storage Disease in Heterozygotes Li, Chi-Ming
2002
79 2 p. 218-224
7 p.
artikel
10 In Silico Comparison of the Transcriptome Derived from Purified Normal Breast Cells and Breast Tumor Cell Lines Reveals Candidate Upregulated Genes in Breast Tumor Cells Leerkes, Maarten R.
2002
79 2 p. 257-265
9 p.
artikel
11 Molecular Cloning of SLC26A7, a Novel Member of the SLC26 Sulfate/Anion Transporter Family, from High Endothelial Venules and Kidney Vincourt, Jean-Baptiste
2002
79 2 p. 249-256
8 p.
artikel
12 Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome Nakabayashi, Kazuhiko
2002
79 2 p. 186-196
11 p.
artikel
13 Pex13, the Mouse Ortholog of the Human Peroxisome Biogenesis Disorder PEX13 Gene: Gene Structure, Tissue Expression, and Localization of the Protein to Peroxisomes Björkman, Jonas
2002
79 2 p. 162-168
7 p.
artikel
14 Profiling Gene Expression Using Onto-Express Khatri, Purvesh
2002
79 2 p. 266-270
5 p.
artikel
15 SAGE Identification of Gene Transcripts with Profiles Unique to Pluripotent Mouse R1 Embryonic Stem Cells Anisimov, Sergey V.
2002
79 2 p. 169-176
8 p.
artikel
16 Single-Nucleotide Polymorphism Alleles in the Insulin Receptor Gene Are Associated with Typical Migraine McCarthy, Linda C.
2002
79 2 p. 271-
1 p.
artikel
17 The Muscular Dystrophy with Myositis (mdm) Mouse Mutation Disrupts a Skeletal Muscle-Specific Domain of Titin Garvey, Sean M.
2002
79 2 p. 146-149
4 p.
artikel
                             17 gevonden resultaten
 
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