Publikationen von Sigmar Stricker
Alle Typen
Zeitschriftenartikel (57)
41.
Zeitschriftenartikel
6 (8), S. 826 - 834 (2006)
Comparative expression pattern of Odd-skipped related genes Osr1 and Osr2 in chick embryonic development. Gene Expression Patterns 42.
Zeitschriftenartikel
79 (2), S. 303 - 312 (2006)
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit. American Journal of Human Genetics (Chicago, IL) 43.
Zeitschriftenartikel
79 (2), S. 402 - 408 (2006)
Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome. American Journal of Human Genetics (Chicago, IL) 44.
Zeitschriftenartikel
281 (30), S. 21546 - 21557 (2006)
Expression of Type XXIII Collagen mRNA and Protein. Journal of Biological Chemistry 45.
Zeitschriftenartikel
580 (2), S. 455 - 462 (2006)
Mammalian mitochondrial nitric oxide synthase: Characterization of a novel candidate. FEBS Letters 46.
Zeitschriftenartikel
115 (9), S. 2373 - 2381 (2005)
Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2. Journal of Clinical Investigation 47.
Zeitschriftenartikel
9 (12), S. 1227 - 1238 (2004)
Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2. Genes to Cells 48.
Zeitschriftenartikel
13 (20), S. 2351 - 2359 (2004)
A molecular pathogenesis for transcription factor associated poly-alanine tract expansions. Human Molecular Genetics 49.
Zeitschriftenartikel
100 (21), S. 12277 - 12282 (2003)
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2. Proceedings of the National Academy of Sciences of the United States of America 50.
Zeitschriftenartikel
27 (8), S. 673 - 684 (2003)
A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution. Developmental and Comparative Immunology 51.
Zeitschriftenartikel
278 (19), S. 17360 - 17367 (2003)
Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 52.
Zeitschriftenartikel
278 (19), S. 17360 - 17367 (2003)
Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 53.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 54.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 55.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 56.
Zeitschriftenartikel
112 (1-2), S. 53 - 67 (2002)
The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 57.
Zeitschriftenartikel
112 (1-2), S. 53 - 67 (2002)
The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development Hochschulschrift - Habilitation (1)
58.
Hochschulschrift - Habilitation
Molekulargenetik und funktionelle Analyse embryonaler Extremitätenfehlbildungen. Habilitation, Charité- Univeristätsmedizin Berlin, Berlin (2010)