Publikationen von Sigmar Stricker
Alle Typen
Zeitschriftenartikel (57)
21.
Zeitschriftenartikel
3, S. 2 - 2 (2010)
A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. Pathogenetics 22.
Zeitschriftenartikel
2 (3), S. 2 - 2 (2010)
A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylose KDM5C. Pathogenetics 23.
Zeitschriftenartikel
56 (2), S. 58 - 65 (2010)
Impairment of Sox9 expression in limb buds of rats homozygous for hypodactyly mutation. Folia Biologica 24.
Zeitschriftenartikel
390 (2), S. 211 - 216 (2009)
The LIM domain protein Wtip interacts with the receptor tyrosine kinase Ror2 and inhibits canonical Wnt signalling. Biochemical and Biophysical Research Communications 25.
Zeitschriftenartikel
5 (11), S. e1000747 - e1000747 (2009)
Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN. PLoS Genetics 26.
Zeitschriftenartikel
18 (21), S. 4013 - 4021 (2009)
A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes. Human Molecular Genetics 27.
Zeitschriftenartikel
41 (8), S. 862 - 863 (2009)
Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia. Nature Genetics 28.
Zeitschriftenartikel
458 (7242), S. 1196 - 1200 (2009)
A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range. Nature 29.
Zeitschriftenartikel
9 (4), S. 215 - 223 (2009)
Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation. Gene Expression Patterns 30.
Zeitschriftenartikel
20 (11), S. 2134 - 2144 (2008)
Wnt-ligand-dependent interaction of TAK1 (TGF-beta-activated kinase-1) with the receptor tyrosine kinase Ror2 modulates canonical Wnt-signalling. Cellular Signalling 31.
Zeitschriftenartikel
74 (6), S. 560 - 565 (2008)
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4. Clinical Genetics 32.
Zeitschriftenartikel
74 (6), S. 560 - 565 (2008)
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4. Clinical Genetics 33.
Zeitschriftenartikel
4 (3), S. e1000025 - e1000025 (2008)
Evolution of a core gene network for skeletogenesis in chordates. PLoS Genetics 34.
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 35.
Zeitschriftenartikel
82 (2), S. 464 - 476 (2008)
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. The American Journal of Human Genetics, 36.
Zeitschriftenartikel
51 (8), S. 753 - 759 (2007)
A comparative analysis of Meox1 and Meox2 in the developing somites and limbs of the chick embryo. International Journal of Developmental Biology (Ijdb) 37.
Zeitschriftenartikel
16 (8), S. 232 - 240 (2007)
Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics 38.
Zeitschriftenartikel
7 (1 - 2), S. 102 - 112 (2007)
Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2−/− mouse model. Gene Expression Patterns: A Section of Brain Research Devoted to Patterns of Expression of Genes during the Development, Maturity and Aging of the Central Nervous System 39.
Zeitschriftenartikel
235 (12), S. 3456 - 3465 (2006)
Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome. Developmental Dynamics 40.
Zeitschriftenartikel
17, S. 1855 - 1862 (2006)
Induction of Macrophage Chemotaxis by Aortic Extracts of the mgR Marfan Mouse Model and a GxxPG-Containing Fibrillin-1 Fragment. Circulation