Publications of Sigmar Stricker
All genres
Journal Article (57)
21.
Journal Article
3, p. 2 - 2 (2010)
A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. Pathogenetics 22.
Journal Article
2 (3), p. 2 - 2 (2010)
A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylose KDM5C. Pathogenetics 23.
Journal Article
56 (2), pp. 58 - 65 (2010)
Impairment of Sox9 expression in limb buds of rats homozygous for hypodactyly mutation. Folia Biologica 24.
Journal Article
390 (2), pp. 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.
Journal Article
5 (11), p. e1000747 - e1000747 (2009)
Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN. PLoS Genetics 26.
Journal Article
18 (21), pp. 4013 - 4021 (2009)
A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes. Human Molecular Genetics 27.
Journal Article
41 (8), pp. 862 - 863 (2009)
Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia. Nature Genetics 28.
Journal Article
458 (7242), pp. 1196 - 1200 (2009)
A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range. Nature 29.
Journal Article
9 (4), pp. 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.
Journal Article
20 (11), pp. 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.
Journal Article
74 (6), pp. 560 - 565 (2008)
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4. Clinical Genetics 32.
Journal Article
74 (6), pp. 560 - 565 (2008)
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4. Clinical Genetics 33.
Journal Article
4 (3), p. e1000025 - e1000025 (2008)
Evolution of a core gene network for skeletogenesis in chordates. PLoS Genetics 34.
Journal Article
135 (9), pp. 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.
Journal Article
82 (2), pp. 464 - 476 (2008)
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. The American Journal of Human Genetics, 36.
Journal Article
51 (8), pp. 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.
Journal Article
16 (8), pp. 232 - 240 (2007)
Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics 38.
Journal Article
7 (1 - 2), pp. 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.
Journal Article
235 (12), pp. 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.
Journal Article
17, pp. 1855 - 1862 (2006)
Induction of Macrophage Chemotaxis by Aortic Extracts of the mgR Marfan Mouse Model and a GxxPG-Containing Fibrillin-1 Fragment. Circulation