Zeitschriftenartikel (1110)
1061.
Zeitschriftenartikel
10 (1) (2011)
Modeling read counts for CNV detection in exome sequencing data. Statistical Applications in Genetics and Molecular Biology 1062.
Zeitschriftenartikel
177 (2), S. 840 - 853 (2010)
Long-Term Expression of Tissue-Inhibitor of Matrix Metalloproteinase-1 in the Murine Central Nervous System Does Not Alter the Morphological and Behavioral Phenotype but Alleviates the Course of Experimental Allergic Encephalomyelitis. The American Journal of Pathology 1063.
Zeitschriftenartikel
137, S. 2723 - 2731 (2010)
Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling. Development 1064.
Zeitschriftenartikel
7, S. 242 - 243 (2010)
Embryology meets cancer research. Public Service Review: Science and Technology 1065.
Zeitschriftenartikel
5 (3), e9522 (2010)
A quantitative study of the Hog1 MAPK response to fluctuating osmotic stress in Saccharomyces cerevisiae. A Quantitative Study of the Hog1 MAPK Response to Fluctuating Osmotic Stress in Saccharomyces cerevisiae 1066.
Zeitschriftenartikel
42 (11), S. 1021 - 6 (2010)
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet 1067.
Zeitschriftenartikel
88 (8), S. 626 - 632 (2010)
Mosaic Expression of Med12 in Female Mice Leads to Exencephaly, Spina Bifida, and Craniorachischisis. Birth Defects Research Part A: Clinical and Molecular Teratology 1068.
Zeitschriftenartikel
19 (3), S. 157 - 60 (2010)
Noonan-like/multiple giant cell lesion syndrome in two adult patients with SOS1 gene mutations. Clin Dysmorphol 1069.
Zeitschriftenartikel
18 (3), S. 291 - 5 (2010)
Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11. Eur J Hum Genet 1070.
Zeitschriftenartikel
30 (5), S. 673 - 683 (2009)
Sequential polarization and imprinting of type 1 T-helper lymphocytes by interferon-γ and interleukin-12. Immunity 1071.
Zeitschriftenartikel
3 (1-4), S. 41 - 9 (2009)
Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing. Hugo J 1072.
Zeitschriftenartikel
7 (10), S. 4566 - 4576 (2008)
Quantitative analysis of global ubiquitination in HeLa cells by mass spectrometry. Journal of Proteome Research 1073.
Zeitschriftenartikel
14 (8), S. 2270 - 2275 (2008)
Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research 1074.
Zeitschriftenartikel
26, S. 305 - 312 (2008)
Minimum Information Specification For In Situ Hybridization and Immunohistochemistry Experiments (MISFISHIE). Nature biotechnology 1075.
Zeitschriftenartikel
146A (19), S. 2501 - 11 (2008)
Agenesis and dysgenesis of the corpus callosum: clinical, genetic and neuroimaging findings in a series of 41 patients. Am J Med Genet A 1076.
Zeitschriftenartikel
6 (5), S. 268 - 269 (2006)
Biochemical consequences of a pathogenic A3243G mtDNA mutation. Mitochondrion 1077.
Zeitschriftenartikel
27 (19), S. 3864 - 2868 (2006)
Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis 1078.
Zeitschriftenartikel
10 (3), S. 355 - 366 (2006)
Oscillations of the Snail Genes in the Presomitic Mesoderm Coordinate Segmental Patterning and Morphogenesis in Vertebrate Somitogenesis. Developmental Cell 1079.
Zeitschriftenartikel
20 (2), S. 362 - 363 (2006)
Platelet transfusion can mimic somatic mtDNA mutations. Leukemia: the Journal of Normal and Malignant Hemopoiese ; Official Journal of the Leukemia Research Fund U.K. 1080.
Zeitschriftenartikel
94 (2), S. 268 - 274 (2006)
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism. British Journal of Cancer