Please note that eDoc will be permanently shut down in the first quarter of 2021!      Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Display Documents


Institute:
Collection:
Print in Citation style Print version     Display:
Sort by: Display records with Fulltext only
Entries: 1-8  
 Basket 
Arteries define the position of the thyroid gland during its developmental relocalisation
Authors: Alt, Burkhard; Elsalini, Osama A.; Schrumpf, Pamela; Haufs, Nele; Lawson, Nathan D.; Schwabe, Georg C.; Mundlos, Stefan; Grüters, Annette; Krude, Heiko; Rohr, Klaus B.
Date of Publication (YYYY-MM-DD): 2006-10-01
Title of Journal: Development
Volume: 133
Issue / Number: 19
Start Page: 3797
End Page: 3804
Document Type: Article
ID: 313078.0
 
Full text / Content available
Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2
Authors: Sammar, Marei; Stricker, Sigmar; Schwabe, Georg C.; Sieber, Christina; Hartung, Anke; Hanke, Michael; Oishi, Isao; Pohl, Jens; Minami, Yasuhiro; Sebald, Walter; Mundlos, Stefan; Knaus, Petra
Date of Publication (YYYY-MM-DD): 2004-12
Title of Journal: Genes to Cells
Volume: 9
Issue / Number: 12
Start Page: 1227
End Page: 1238
Document Type: Article
ID: 228826.0
Genetics of congenital hand anomalies
Authors: Schwabe, Georg C.; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2004-04
Title of Journal: Handchirurgie, Mikrochirurgie, Plastische Chirurgie
Volume: 36
Issue / Number: 2-3
Start Page: 85
End Page: 97
Document Type: Article
ID: 228846.0
Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1
Authors: Schwabe, Georg C.; Türkmen, Seval; Leschik, Gundula; Palanduz, Sukru; Stöver, Brigitte; Goecke, Timm O.; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2004-02-01
Title of Journal: American Journal of Medical Genetics
Volume: 124A
Issue / Number: 4
Start Page: 356
End Page: 363
Document Type: Article
ID: 228869.0
Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome
Authors: Schwabe, Georg C.; Trepczik, Britta; Süring, Kathrin; Brieske, Norbert; Tucker, Abigail S.; Sharpe, Paul T.; Minami, Yasuhiro; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2004-02
Title of Journal: Developmental Dynamics
Volume: 229
Issue / Number: 2
Start Page: 400
End Page: 410
Document Type: Article
ID: 228850.0
The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway
Authors: Oishi, Isao; Suzuki, Hiroaki; Onishi, Nobuyuki; Takada, Ritsuko; Kani, Shuichi; Ohkawara, Bisei; Koshida, Ikure; Suzuki, Kentaro; Yamada, General; Schwabe, Georg C.; Mundlos, Stefan; Shibuya, Hiroshi; Takada, Shinji; Minami, Yasuhiro
Date of Publication (YYYY-MM-DD): 2003-07
Title of Journal: Genes to Cells
Volume: 8
Issue / Number: 7
Start Page: 645
End Page: 654
Document Type: Article
ID: 175335.0
The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme
Authors: Albrecht, Andrea N.; Schwabe, Georg C.; Stricker, Sigmar; Böddrich, Annett; Wanker, Erich E.; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2002-01-18
Title of Journal: Mechanisms of Development
Volume: 112
Issue / Number: 1-2
Start Page: 53
End Page: 67
Document Type: Article
ID: 24413.0
The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme
Authors: Albrecht, Andrea N.; Schwabe, Georg C.; Stricker, Sigmar; Böddrich, Annett; Wanker, Erich E.; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2002-01-18
Title of Journal: Mechanisms of Development
Volume: 112
Issue / Number: 1-2
Start Page: 53
End Page: 67
Document Type: Article
ID: 27848.0
Entries: 1-8  
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.