Zeitschriftenartikel (223)
81.
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328 (5984), S. 1401 - 1403 (2010)
Lysosomal pathology and osteopetrosis upon loss of H+-driven lysosomal Cl- accumulation. Science 82.
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11, S. 11:354 - 11:354 (2010)
Development of an oligo DNA microarray for the European sea bass and its application to expression profiling of jaw deformity. BMC Genomics 83.
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31 (8), S. E1587 - 93 (2010)
Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Human Mutation 84.
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20 (7), S. 989 - 999 (2010)
Strand-specific deep sequencing of the transcriptome. Genome Research 85.
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29 (11), S. 1877 - 1888 (2010)
Dynamic link of DNA demethylation, DNA strand breaks and repair in mouse zygotes. EMBO Journal 86.
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38 (11), S. 3523 - 3532 (2010)
GOing Bayesian: model-based gene set analysis of genome-scale data. Nucleic Acids Research 87.
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184 (11), S. 6407 - 6417 (2010)
CD93/AA4.1: a novel regulator of inflammation in murine focal cerebral ischemia. Journal of Immunology 88.
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38 (10), S. e112 - e112 (2010)
Prediction of alternative isoforms from exon expression levels in RNA-Seq experiments. Nucleic Acids Research 89.
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120 (6), S. 1994 - 2004 (2010)
Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation. Journal of Clinical Investigation 90.
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5 (2), S. 171 - 177 (2010)
Multi-transcript expression patterns in the gastrolith disk and the hypodermis of the crayfish Cherax quadricarinatus at premolt. Comparative Biochemistry and Physiology, Part D: Genomics and Proteomics 91.
Zeitschriftenartikel
27 (2), S. 108 - 111 (2010)
V-gene amplification revisited - An optimised procedure for amplification of rearranged human antibody genes of different isotypes. Nature biotechnology 92.
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139 (Suppl 1), S. S64 - 78 (2010)
Ecophysiology of food-borne pathogens: Essential knowledge to improve food safety. International Journal of Food Microbiology 93.
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152A (7), S. 1724 - 1729 (2010)
Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome. American Journal of Medical Genetics Part A 94.
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88 (9), S. 931 - 939 (2010)
The difference between rare and exceptionally rare: molecular characterization of ribose 5-phosphate isomerase deficiency. Journal of Molecular Medicine 95.
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22, S. 235 - 241 (2010)
Online-Datenbanken und systematische Metaanalysen komplex-genetischer Erkrankungen. Medizinische Genetik 96.
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1 (4), S. 354 - 366 (2010)
Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein. Nucleus 97.
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5 (5), S. e10709 - e10709 (2010)
A data integration approach to mapping OCT4 gene regulatory networks operative in embryonic stem cells and embryonal carcinoma cells. PLoS ONE 98.
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123 (12), S. 2045 - 2057 (2010)
TRPV1 acts as a synaptic protein and regulates vesicle recycling. Journal of Cell Science 99.
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285 (20), S. 14848 - 14851 (2010)
Mechanism of eIF6-mediated inhibition of ribosomal subunit joining. The Journal of Biological Chemistry 100.
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8 (1), S. 6 - 6 (2010)
Cancer stem cells in solid tumors: elusive or illusive? Cell Communication and Signaling