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Zeitschriftenartikel (120)
101.
Zeitschriftenartikel
335 (6070), S. 823 - 828 (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 102.
Zeitschriftenartikel
7 (12), e1002304 (2011)
Combinatorial binding in human and mouse embryonic stem cells identifies conserved enhancers active in early embryonic development. PLoS Comput Biol 103.
Zeitschriftenartikel
4, S. 68 (2011)
Targeted high throughput sequencing in clinical cancer settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity. BMC Med Genomics 104.
Zeitschriftenartikel
25 (12), S. 1840 - 8 (2011)
The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories. Leukemia: Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K 105.
Zeitschriftenartikel
29 (9), S. 1338 - 48 (2011)
Human induced pluripotent stem cells harbor homoplasmic and heteroplasmic mitochondrial DNA mutations while maintaining human embryonic stem cell-like metabolic reprogramming. Stem Cells 106.
Zeitschriftenartikel
30 (2), S. 199 - 210 (2011)
The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations. Cancer Metastasis Reviews 107.
Zeitschriftenartikel
5 (12), S. e15661 - e15661 (2010)
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis. PLoS ONE 108.
Zeitschriftenartikel
31 (suppl 2), S. 255 - 257 (2010)
High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue. Pathologe 109.
Zeitschriftenartikel
20, S. 1441 - 1450 (2010)
Computational analysis of genome-wide DNA methylation during the differentiation of human embryonic stem cells along the endodermal lineage. Genome Research 110.
Zeitschriftenartikel
2 (8), S. 475 - 486 (2010)
A new dominant peroxiredoxin allele identified by whole-genome re-sequencing of random mutagenized yeast causes oxidant-resistance and premature aging. Aging (Albany NY) 111.
Zeitschriftenartikel
2, S. 2:59 - 2:59 (2010)
The application of massively parallel sequencing technologies in diagnostics. F1000 Biology Reports 112.
Zeitschriftenartikel
High-throughput sequencing of microdissected chromosomal regions. European Journal of Human Genetics, ejhg.2009.196, S. 1 - 6 (2009)
113.
Zeitschriftenartikel
4 (5), S. e5548 - e5548 (2009)
Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis. PLoS ONE 114.
Zeitschriftenartikel
9, S. 9:38 - 9:38 (2008)
Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans. BMC Genetics 115.
Zeitschriftenartikel
9, S. 9:38 - 9:38 (2008)
Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans. BMC Genetics 116.
Zeitschriftenartikel
5 (5), S. 31 - 32 (2004)
Genetische Variabilität des Menschen: Hochdurchsatz- Technologien und Datenanalyse. Laborwelt 117.
Zeitschriftenartikel
2004 (1), S. 17 - 19 (2004)
Vergleichende Sequenzierung von Kandidatengenen: die Resequencing-Plattform am MPI-MG. GenomXPress: Informationen aus der Deutschen Genomforschung 118.
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 119.
Zeitschriftenartikel
61 (1 - 2), S. 97 - 109 (2002)
Beta-2 Adrenergic receptor gene variations and coping styles in twins. Biological Psychology 120.
Zeitschriftenartikel
Haplotypen und die systematische Analyse genetischer Variation: Krankheitsgene, „Drug Targets“ und Pharmakogenomik. Proteomics & Drug Development, S. 478 - 485 (2002)