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                             41 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Analysis of the glutathione S-transferase (GST) gene family Nebert, Daniel W
2004
6 p. 460-464
artikel
2 An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) gene Millar, David S
2010
6 p. 384-393
artikel
3 A non-parametric approach to population structure inference using multilocus genotypes Liu, Nianjun
2006
6 p. 353-367
artikel
4 Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels Hinds, David A
2004
6 p. 421-434
artikel
5 A review of the 'Statistical Analysis for Genetic Epidemiology' (SAGE) software package Elston, Robert C
2004
6 p. 456-459
artikel
6 ArrayTrack: a free FDA bioinformatics tool to support emerging biomedical research -- an update Xu, Joshua
2010
6 p. 428-434
artikel
7 A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation Karimpour-Fard, Anis
2010
6 p. 421-427
artikel
8 Bioinformatics methods for identifying candidate disease genes van Driel, Marc A
2006
6 p. 429-432
artikel
9 Color Atlas of Pharmacology Konstandi, Maria
2010
6 artikel
10 Comparison of regional gene expression differences in the brains of the domestic dog and human Kennerly, Erin
2004
6 p. 435-443
artikel
11 Design and Analysis of DNA Microarray Investigations Wit, Ernst
2004
6 artikel
12 Editorial Jin, Li
2004
6 artikel
13 Emerging strategies and applications of pharmacogenomics Milos, Patrice M
2004
6 p. 444-455
artikel
14 Endothelial nitric oxide synthase gene polymorphisms -786T >C and 894G >T in coronary artery bypass graft surgery patients Ragia, Georgia
2010
6 p. 375-383
artikel
15 Evolutionary divergence and functions of the human acyl-CoA thioesterase gene (ACOT) family Brocker, Chad
2010
6 p. 411-420
artikel
16 From DNA to RNA to disease and back: The 'central dogma' of regulatory disease variation Stranger, Barbara E
2006
6 p. 383-390
artikel
17 Functional single nucleotide polymorphism-based association studies Carlton, Victoria EH
2006
6 p. 391-402
artikel
18 General considerations for integrating pharmacogenomics into mainstream medical practice Patrinos, George P
2010
6 p. 371-374
artikel
19 Genetic association studies in cancer: Good, bad or no longer ugly? Savage, Sharon A
2006
6 p. 415-421
artikel
20 Genetic factors leading to chronic Epstein-Barr virus infection and nasopharyngeal carcinoma in South East China: Study design, methods and feasibility Guo, Xiu Chan
2006
6 p. 365-375
artikel
21 Genome-wide approaches to understanding human ageing Kaeberlein, Matt
2006
6 p. 422-428
artikel
22 Genome-wide association studies getting more complicated but help is on the way Kwok, Pui-Yan
2006
6 p. 341-342
artikel
23 Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22 González-Neira, Anna
2004
6 p. 399-409
artikel
24 Human genetics and genomics a decade after the release of the draft sequence of the human genome Naidoo, Nasheen
2011
6 p. 577-622
artikel
25 In-silico human genomics with GeneCards Stelzer, Gil
2011
6 p. 709-717
artikel
26 Intronic polymorphisms of cytochromes P450 Ingelman-Sundberg, Magnus
2010
6 p. 402-405
artikel
27 KinSNP software for homozygosity mapping of disease genes using SNP microarrays Amir, El-Ad David
2010
6 p. 394-401
artikel
28 Letter to the Editor Levan, Göran
2006
6 p. 343-344
artikel
29 Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides, as well as in CpG dinucleotides Cooper, David N
2010
6 p. 406-410
artikel
30 Neurofibromatosis type 1-associated tumours: Their somatic mutational spectrum and pathogenesis Spyk, Sebastian Laycock-van
2011
6 p. 623-690
artikel
31 Overview of biological database mapping services for interoperation between different 'omics' datasets Chavan, Shweta S
2011
6 p. 703-708
artikel
32 Research Highlights Scheinman, Robert I
2011
6 p. 522-529
artikel
33 Role of CYP2E1 genotypes in susceptibility to colorectal cancer in the Kashmiri population Sameer, A Syed
2011
6 p. 530-537
artikel
34 Stepwise haplotype analysis: Are LD patterns repeatable? Mander, A P
2006
6 p. 376-382
artikel
35 Strategies for the detection of copy number and other structural variants in the human genome Carson, Andrew R
2006
6 p. 403-414
artikel
36 Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration Morrison, Margaux A
2011
6 p. 538-568
artikel
37 Testing groups of genomic locations for enrichment in disease loci using linkage scan data: A method for hypothesis testing Avramopoulos, Dimitrios
2006
6 p. 345-352
artikel
38 The extent and importance of intragenic recombination de Silva, Eric
2004
6 p. 410-420
artikel
39 The role of ALDH2 and ADH1B polymorphism in alcohol consumption and stroke in Han Chinese Yao, Chung-Tay
2011
6 p. 569-576
artikel
40 Update of the human secretoglobin (SCGB) gene superfamily and an example of 'evolutionary bloom' of androgen-binding protein genes within the mouse Scgb gene superfamily Jackson, Brian C
2011
6 p. 691-702
artikel
41 Visionary genomics Petrash, J Mark
2011
6 p. 519-521
artikel
                             41 gevonden resultaten
 
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