Zeitschriftenartikel (1119)
1081.
Zeitschriftenartikel
7 (10), S. 4566 - 4576 (2008)
Quantitative analysis of global ubiquitination in HeLa cells by mass spectrometry. Journal of Proteome Research 1082.
Zeitschriftenartikel
14 (8), S. 2270 - 2275 (2008)
Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research 1083.
Zeitschriftenartikel
26, S. 305 - 312 (2008)
Minimum Information Specification For In Situ Hybridization and Immunohistochemistry Experiments (MISFISHIE). Nature biotechnology 1084.
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 1085.
Zeitschriftenartikel
6 (5), S. 268 - 269 (2006)
Biochemical consequences of a pathogenic A3243G mtDNA mutation. Mitochondrion 1086.
Zeitschriftenartikel
27 (19), S. 3864 - 2868 (2006)
Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis 1087.
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 1088.
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. 1089.
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 1090.
Zeitschriftenartikel
49 (3), S. 225 - 34 (2006)
First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization. Eur J Med Genet 1091.
Zeitschriftenartikel
14 (12), S. 1317 - 20 (2006)
Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3. Eur J Hum Genet 1092.
Zeitschriftenartikel
5 (4), S. 282 - 296 (2005)
Rapid screening of the entire mitochondrial DNA for low-level heteroplasmic mutations. Mitochondrion 1093.
Zeitschriftenartikel
579 (5), S. 1101 - 1108 (2005)
In silico identification of the key components and steps in IFN-γ induced JAK-STAT signaling pathway. FEBS Letters 1094.
Zeitschriftenartikel
132A (3), S. 324 - 8 (2005)
Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome. Am J Med Genet A 1095.
Zeitschriftenartikel
135 (3), S. 339 - 41 (2005)
Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome. Am J Med Genet A 1096.
Zeitschriftenartikel
25 (6), S. 1005 - 1010 (2004)
Decrease of mitochondrial DNA content and energy metabolism in renal cell carcinoma. Carcinogenesis 1097.
Zeitschriftenartikel
105 (3), S. 245 - 251 (2003)
Severe depletion of mitochondrial DNA in spinal muscular atrophy. Acta Neuropathologica 1098.
Zeitschriftenartikel
77 (1-2), S. 8 - 17 (2001)
Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1. Genomics 1099.
Zeitschriftenartikel
9 (12), S. 910 - 6 (2001)
Low incidence of UPD in spontaneous abortions beyond the 5th gestational week. Eur J Hum Genet 1100.
Zeitschriftenartikel
68 (2), S. 543 - 5 (2001)
Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression? Am J Hum Genet