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Entries: 1-8  
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The LIM domain protein Wtip interacts with the receptor tyrosine kinase Ror2 and inhibits canonical Wnt signalling
Authors: van Wijk, Nicole Verhey; Witte, Florian; Feike, Ann Carolin; Schambony, Alexandra; Birchmeier, Walter; Mundlos, Stefan; Stricker, Sigmar
Date of Publication (YYYY-MM-DD): 2009-12-11
Title of Journal: Biochemical and Biophysical Research Communications
Volume: 390
Issue / Number: 2
Start Page: 211
End Page: 216
Document Type: Article
ID: 456474.0
A gradient of ROR2 protein stability and membrane
localization confers brachydactyly type B or Robinow syndrome phenotypes
Authors: Schwarzer, Wibke; Witte, Florian; Rajab, Anna; Mundlos, Stefan; Stricker, Sigmar
Date of Publication (YYYY-MM-DD): 2009-11
Title of Journal: Human Molecular Genetics
Volume: 18
Issue / Number: 21
Start Page: 4013
End Page: 4021
Document Type: Article
ID: 456438.0
Analyse der Ror2-Funktion in vivo und in vitro : die Ror2W749X-Maus als Modell für humane Brachydaktylie Typ B
Authors: Witte, Florian
Name of University: Freie Universität
Place of University: Berlin
Date of Approval (YYYY-MM-DD): 2009-05-18
Document Type: PhD-Thesis
ID: 456393.0
 
Full text / Content available
A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range
Authors: Gao, Bo; Hu, Jianxin; Stricker, Sigmar; Cheung, Martin; Ma, Gang; Law, Kit Fong; Witte, Florian; Briscoe, James; Mundlos, Stefan; He, Lin; Cheah, Kathryn S. E.; Chan, Danny
Date of Publication (YYYY-MM-DD): 2009-04-30
Title of Journal: Nature
Volume: 458
Issue / Number: 7242
Start Page: 1196
End Page: 1200
Document Type: Article
ID: 456427.0
Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation
Authors: Witte, Florian; Dokas, Janine; Neuendorf, Franziska; Mundlos, Stefan; Stricker, Sigmar
Date of Publication (YYYY-MM-DD): 2009-04
Title of Journal: Gene Expression Patterns
Volume: 9
Issue / Number: 4
Start Page: 215
End Page: 223
Document Type: Article
ID: 456626.0
Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis
Authors: Kuss, Pia; Villavicencio-Lorini, Pablo; Witte, Florian; Klose, Joachim; Albrecht, Andrea N.; Seemann, Petra; Hecht, Jochen; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2009-01-05
Title of Journal: Journal of Clinical Investigation
Volume: 119
Issue / Number: 1
Start Page: 146
End Page: 156
Document Type: Article
ID: 448428.0
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
Authors: Raz, Regina; Stricker, Sigmar; Elizabetta Gazzerro, Elizabetta; Clor, Julie L.; Witte, Florian; Nistala, Harakiran; Zabski, Stefanie; Pereira, Renata C.; Stadmeyer, Lisa; Wang, Xiangmin; Gowen, Lori; Sleeman, Mark W.; Yancopoulos, George D.; Canalis, Ernesto; Mundlos, Stefan; Valenzuela, David M. V; Economides, Aris N.
Date of Publication (YYYY-MM-DD): 2008-03-19
Title of Journal: Development
Volume: 135
Issue / Number: 9
Start Page: 1713
End Page: 1723
Document Type: Article
ID: 411679.0
 
Full text / Content available
Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome
Authors: Stricker, Sigmar; Van Wijk, Nicole Verhey; Witte, Florian; Brieske, Norbert; Seidel, Kathrin; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2006-12
Title of Journal: Developmental Dynamics
Volume: 235
Issue / Number: 12
Start Page: 3456
End Page: 3465
Document Type: Article
ID: 313092.0
 
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Entries: 1-8  
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