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                             42 results found
no title author magazine year volume issue page(s) type
1 Aldo-keto reductase (AKR) superfamily: Genomics and annotation Mindnich, Rebekka D
2009
4 p. 362-370
article
2 A meta-analysis of single base-pair substitutions in translational termination codons ('nonstop' mutations) that cause human inherited disease Hamby, Stephen E
2011
4 p. 241-264
article
3 Analysis of pharmacogenetic traits in two distinct South African populations Ikediobi, Ogechi
2011
4 p. 265-282
article
4 Animal Models in Eye Research Robinson, Michael L
2009
4 p. 381-382
article
5 A review of software for microarray genotyping Lamy, Philippe
2011
4 p. 304-309
article
6 Collection of variation causing disease - The Human Variome Project Cotton, Richard GH
2009
4 p. 301-303
article
7 Comparative transcriptome analyses of Pseudomonas aeruginosa Balasubramanian, Deepak
2009
4 p. 349-361
article
8 Comparison of human (and other) genome browsers Furey, Terrence S
2006
4 p. 266-270
article
9 Current software for genotype imputation Ellinghaus, David
2009
4 p. 371-380
article
10 Cytochrome P450 humanised mice Gonzalez, Frank J
2004
4 p. 300-306
article
11 Designer Genes: A new Era in the Evolution of Man Nebert, Daniel W
2011
4 article
12 Editorial Jin, Li
2006
4 article
13 Editorial Jin, Li
2004
4 article
14 Editorial Vasiliou, Vasilis
2011
4 article
15 FDA perspectives on potential microarray-based clinical diagnostics Težak, Živana
2006
4 p. 236-243
article
16 'Frankenstein genes', or the Mad Magazine version of the human pseudogenome Nelson, David R
2004
4 p. 310-316
article
17 From DNA to proteins via the ribosome: Structural insights into the workings of the translation machinery Agirrezabala, Xabier
2010
4 p. 226-237
article
18 Further statistical analysis for genome-wide expression evolution in primate brain/liver/fibroblast tissue Gu, Jianying
2004
4 p. 247-254
article
19 Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population Walsh, Tom
2006
4 p. 203-211
article
20 Given the complexity of the human genome, can 'personalised medicine' or 'individualised drug therapy' ever be achieved? Nebert, Daniel W
2009
4 p. 299-300
article
21 Haplotype structure and linkage disequilibrium in chemokine and chemokine receptor genes Clark, Vanessa J
2004
4 p. 255-273
article
22 Human genomic diversity, viral genomics and proteomics, as exemplified by human papillomaviruses and H5N1 influenza viruses Sakharkar, Meena K
2009
4 p. 320-331
article
23 Hyperferritinaemia-cataract syndrome: Worldwide mutations and phenotype of an increasingly diagnosed genetic disorder Millonig, Gunda
2010
4 p. 250-262
article
24 Identification of a novel cytosolic aldehyde dehydrogenase allele, ALDHIAI*4 Moore, Shelley M
2009
4 p. 304-307
article
25 Immunogenomics: Molecular hide and seek Miretti, Marcos M
2006
4 p. 244-251
article
26 Inference of ancestry: constructing hierarchical reference populations and assigning unknown individuals Ekins, Jayne E
2006
4 p. 212-235
article
27 Integrated analysis of genetic data with R Zhao, Jing Hua
2006
4 p. 258-265
article
28 Inter-chromosomal variation in the pattern of human population genetic structure Baye, Tesfaye M
2011
4 p. 220-240
article
29 Krüppel-like factors: Three fingers in control Swamynathan, Shivalingappa K
2010
4 p. 263-270
article
30 Metagenomics: Theory, methods, and applications Chroneos, Zissis C
2010
4 p. 282-283
article
31 Mitochondrial DNA as a potential tool for early cancer detection Parr, Ryan L
2005
4 p. 252-257
article
32 Pathway annotation and analysis with Reactome: The solute carrier class of membrane transporters Jassal, Bijay
2011
4 p. 310-315
article
33 Recommendations for using standardised phenotypes in genetic association studies Naylor, Melissa G
2009
4 p. 308-319
article
34 Research Highlights Scheinman, Robert I
2011
4 p. 216-219
article
35 State of the art de novo assembly of human genomes from massively parallel sequencing data Li, Yingrui
2010
4 p. 271-277
article
36 The clinical application of UGT1A1 pharmacogenetic testing: Gene-environment interactions Marques, Sara Correia
2010
4 p. 238-249
article
37 The clinical pharmacogeneticist: An emerging regulatory scientist at the US Food and Drug Administration Zineh, Issam
2010
4 p. 221-225
article
38 The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs Shriver, Mark D
2004
4 p. 274-286
article
39 The Human Cytochrome P450 (CYP) Allele Nomenclature website: a peer-reviewed database of CYP variants and their associated effects Sim, Sarah C
2010
4 p. 278-281
article
40 The tiny world of microRNAs in the cross hairs of the mammalian eye Lavker, Robert M
2009
4 p. 332-348
article
41 Update on the aldehyde dehydrogenase gene (ALDH) superfamily Jackson, Brian
2011
4 p. 283-303
article
42 Whole genome DNA copy number changes identified by high density oligonucleotide arrays Huang, Jing
2004
4 p. 287-299
article
                             42 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands