Zeitschriftenartikel (195)
121.
Zeitschriftenartikel
82 (5), S. 1165 - 1170 (2008)
Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly. The American Journal of Human Genetics 122.
Zeitschriftenartikel
14 (8), S. 2270 - 2275 (2008)
Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research 123.
Zeitschriftenartikel
16 (9), S. 1029 - 1037 (2008)
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression. European Journal of Human Genetics 124.
Zeitschriftenartikel
38 (12), S. 1411 - 1423 (2008)
Identification of a Leishmania infantum gene mediating resistance to miltefosine and SbIII. International Journal for Parasitology 125.
Zeitschriftenartikel
4 (6), S. 589 - 598 (2008)
Prediction of cardiac transcription networks based on molecular data and complex clinical phenotypes. Molecular BioSystems: A New High Quality Chemical Biology Journal with A Particular Focus on the Interface between Chemistry and the -Omic Sciences and Systems Biology 126.
Zeitschriftenartikel
32 (4), S. 579 - 585 (2008)
A multiplex PCR for improved detection of typical and atypical BCR-ABL fusion transcripts. Leukemea Research 127.
Zeitschriftenartikel
26 (4), S. 407 - 415 (2008)
Discovering microRNAs from deep sequencing data using miRDeep. Nature Biotechnology 128.
Zeitschriftenartikel
40 (4), S. 638 - 650 (2008)
A short ultraconserved sequence drives transcription from an alternate FBN1 promoter. The International Journal of Biochemistry & Cell Biology 129.
Zeitschriftenartikel
111 (7), S. 3830 - 3837 (2008)
Human antibody RNase fusion protein targeting CD30+ lymphomas. Blood 130.
Zeitschriftenartikel
76 (4), S. 404 - 416 (2008)
Follistatin antagonizes transforming growth factor-β3-induced epithelial–mesenchymal transition in vitro: implications for murine palatal development supported by microarray analysis. Differentiation 131.
Zeitschriftenartikel
16, S. 1070 - 1074 (2008)
Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor gene. European Journal of Human Genetics 132.
Zeitschriftenartikel
4 (3), S. e1000025 - e1000025 (2008)
Evolution of a core gene network for skeletogenesis in chordates. PLoS Genetics 133.
Zeitschriftenartikel
4 (3), S. e1000039 - e1000039 (2008)
Statistical Modeling of Transcription Factor Binding Affinities Predicts Regulatory Interactions. PLoS Computational Biology 134.
Zeitschriftenartikel
135 (9), S. 1713 - 1723 (2008)
The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome. Development 135.
Zeitschriftenartikel
36 (7), S. e39 - e39 (2008)
High-resolution array comparative genomic hybridization of single micrometastatic tumor cells. Nucleic Acids Research 136.
Zeitschriftenartikel
92 (2), S. 189 - 205 (2008)
Petri net modelling of gene regulation of the Duchenne muscular dystrophy. Biosystems 137.
Zeitschriftenartikel
18 (7), S. 1143 - 1149 (2008)
Mapping translocation breakpoints by next-generation sequencing. Genome Research 138.
Zeitschriftenartikel
26, S. 305 - 312 (2008)
Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE). Nature Biotechnology 139.
Zeitschriftenartikel
58 (Pt 3), S. 585 - 590 (2008)
Spongiibacter marinus gen. nov., sp. nov., a halophilic marine bacterium isolated from the boreal sponge Haliclona sp. 1. International Journal of Sytematic and Evolutionary Micro 140.
Zeitschriftenartikel
17 (3), S. 458 - 465 (2008)
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics