Zeitschriftenartikel (1249)
1041.
Zeitschriftenartikel
5 (2), S. 205 - 219 (2013)
Genomics and epigenomics of colorectal cancer. Wiley Interdisciplinary Reviews: Cognitive Science 1042.
Zeitschriftenartikel
72, S. 5 - 5 (2013)
Protein array screening reveals IGA autoantigens predicting therapy response in rheumatoid arthritis patients. Zeitschrift Fur Rheumatologie 1043.
Zeitschriftenartikel
2 (8), S. 771 - 8 (2013)
An integrative computational analysis provides evidence for FBN1-associated network deregulation in trisomy 21. Biol Open 1044.
Zeitschriftenartikel
23 (2), S. 159 - 70 (2013)
Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer. Cancer Cell 1045.
Zeitschriftenartikel
9 (3), S. e1002933 - e1002933 (2013)
Dual Coordination of Post Translational Modifications in Human Protein Networks. PLoS Computational Biology 1046.
Zeitschriftenartikel
7 (12), e52700 (2012)
Functional comparison of chronological and in vitro aging: differential role of the cytoskeleton and mitochondria in mesenchymal stromal cells. PLoS One 1047.
Zeitschriftenartikel
21 (24), S. 5359 - 5372 (2012)
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Human Molecular Genetics 1048.
Zeitschriftenartikel
2012, S. e - e (2012)
A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring. European journal of human genetics: EJHG ; the official journal of the European Society of Human Genetics 1049.
Zeitschriftenartikel
6, S. 317 - 327 (2012)
Methods of Combinatorial Optimization to Reveal Factors Affecting Gene Length. Bioinformatics and Biology Insights 1050.
Zeitschriftenartikel
91 (6), S. 1022 - 1031 (2012)
Deleterious- and Disease-Allele Prevalence in Healthy Individuals: Insights from Current Predictions, Mutation Databases, and Population-Scale Resequencing. The American Journal of Human Genetics 1051.
Zeitschriftenartikel
7 (12), e44591 (2012)
Mutations of the EPHB6 receptor tyrosine kinase induce a pro-metastatic phenotype in non-small cell lung cancer. PLoS One 1052.
Zeitschriftenartikel
2012, S. e - e (2012)
Identification of a Novel Missense Mutation in EDAR Causing Autosomal Recessive Hypohidrotic Ectodermal Dysplasia with Bilateral Amastia and Palmoplantar Hyperkeratosis. British Journal of Dermatology 1053.
Zeitschriftenartikel
48 (3), S. 391 - 398 (2012)
Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS. Neurobiology of Disease 1054.
Zeitschriftenartikel
53 (6), S. 357 - 364 (2012)
Directed evolution of nucleotide-based libraries using lambda exonuclease. Biotechniques 1055.
Zeitschriftenartikel
372 (1), S. 55 - 67 (2012)
In vivo knockdown of Brachyury results in skeletal defects and urorectal malformations resembling caudal regression syndrome. Developmental Biology 1056.
Zeitschriftenartikel
51 (12), S. 1114 - 1124 (2012)
Involvement of the MLL gene in adult T-lymphoblastic leukemia. Genes, Chromosomes and Cancer 1057.
Zeitschriftenartikel
130 (2), S. 427 - 439 (2012)
RNA-Seq provides new insights in the transcriptome responses induced by the carcinogen benzo[a]pyrene. Toxicological Sciences 1058.
Zeitschriftenartikel
7 (11), S. e50393 (2012)
Identification of biomarkers of human skin ageing in both genders. Wnt signalling - a label of skin ageing? PLoS One 1059.
Zeitschriftenartikel
2012, S. e - e (2012)
Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4. European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 1060.
Zeitschriftenartikel
7 (11), S. e50134 - e50134 (2012)
Ataxin-2-like is a regulator of stress granules and processing bodies. PLoS One