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Entries: 1-9  
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis.
Authors: Klopocki, E.; Lohan, S.; Brancati, F.; Koll, R.; Brehm, A.; Seemann, P.; Dathe, K.; Stricker, S.; Hecht, J.; Bosse, K.; Betz, R. C.; Garaci, F. G.; Dallapiccola, B.; Jain, M.; Muenke, M.; Ng, V. C.; Chan, W.; Chan, D.; Mundlos, S.
Date of Publication (YYYY-MM-DD): 2011-01-07
Title of Journal: American Journal of Human Genetics
Volume: 88
Issue / Number: 1
Start Page: 70
End Page: 75
Document Type: Article
ID: 538366.0
Full text / Content available
Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome
Authors: Brancati, F.; Fortugno, P.; Bottillo, I.; Lopez, M.; Josselin, E.; Boudghene-Stambouli, O.; Agolini, E.; Bernardini, L.; Bellacchio, E.; Iannicelli, M.; Rossi, A.; Dib-Lachachi, A.; Stuppia, L.; Palka, G.; Mundlos, S.; Stricker, S.; Kornak, U.; Zambruno, G.; Dallapiccola, B.
Date of Publication (YYYY-MM-DD): 2010-08-13
Title of Journal: American Journal of Human Genetics
Volume: 87
Issue / Number: 2
Start Page: 265
End Page: 273
Document Type: Article
ID: 539722.0
Full text / Content available
Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region
Authors: Witte, F.; Chan, D.; Economides, A. N.; Mundlos, S.; Stricker, S.
Date of Publication (YYYY-MM-DD): 2010-08-10
Title of Journal: Proceedings of the National Academy of Sciences U S A
Volume: 107
Issue / Number: 32
Start Page: 14211
End Page: 14216
Document Type: Article
ID: 539727.0
Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein.
Authors: Clayton, P.; Fischer, B.; Mann, A.; Mansour, S.; Rossier, E.; Veen, M.; Lang, C.; Baasanjav, S.; Kieslich, M.; Brossuleit, K.; Gravemann, S.; Schnipper, N.; Karbasyian, M.; Demuth, I.; Zwerger, M.; Vaya, A.; Utermann, G.; Mundlos, S.; Stricker, S.; Sperling, K.; Hoffmann, K.
Date of Publication (YYYY-MM-DD): 2010-05-21
Title of Journal: Nucleus
Volume: 1
Issue / Number: 4
Start Page: 354
End Page: 366
Document Type: Article
ID: 540985.0
Full text / Content available
Negative regulation of Wnt signaling mediated by CK1-phosphorylated Dishevelled via Ror2.
Authors: Witte, F.; Bernatik, O.; Kirchner, K.; Masek, J.; Mahl, A.; Krejci, P.; Mundlos, S.; Schambony, A.; Bryja, V.; Stricker, S.
Date of Publication (YYYY-MM-DD): 2010-02-04
Title of Journal: The FASEB Journal
Volume: 24
Issue / Number: 7
Start Page: 2417
End Page: 2426
Document Type: Article
ID: 541114.0
Impairment of Sox9 expression in limb buds of rats homozygous for hypodactyly mutation.
Authors: Liska, F.; Snajdr, P.; Stricker, S.; Gosele, C.; Krenova, D.; Mundlos, S.; Hubner, N.
Date of Publication (YYYY-MM-DD): 2010-01-01
Title of Journal: Folia Biologica
Volume: 56
Issue / Number: 2
Start Page: 58
End Page: 65
Document Type: Article
ID: 541911.0
Full text / Content available
Multiple roles for neurofibromin in skeletal development and growth
Authors: Kolanczyk, M.; Kossler, N.; Kuhnisch, J.; Lavitas, L.; Stricker, S.; Wilkening, U.; Manjubala, I.; Fratzl, P.; Sporle, R.; Herrmann, B. G.; Parada, L. F.; Kornak, U.; Mundlos, S.
Date of Publication (YYYY-MM-DD): 2007-04-15
Title of Journal: Human Molecular Genetics
Volume: 16
Issue / Number: 8
Start Page: 874
End Page: 886
Document Type: Article
ID: 327528.0
Full text / Content available
Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome
Authors: Woods, C. G.; Stricker, S.; Seemann, P.; Stern, R.; Cox, J.; Sherridan, E.; Roberts, E.; Springell, K.; Scott, S.; Karbani, G.; Sharif, S. M.; Toomes, C.; Bond, J.; Kumar, D.; Al-Gazali, L.; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2006-08
Title of Journal: American Journal of Human Genetics (Chicago, IL)
Volume: 79
Issue / Number: 2
Start Page: 402
End Page: 408
Document Type: Article
ID: 313095.0
Full text / Content available
A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution
Authors: Stricker, S.; Poustka, A. J.; Wiecha, U.; Stiege, A.; Hecht, J.; Panopoulou, G.; Vilcinskas, A.; Mundlos, S.; Seitz, V.
Date of Publication (YYYY-MM-DD): 2003-09
Title of Journal: Developmental and Comparative Immunology
Volume: 27
Issue / Number: 8
Start Page: 673
End Page: 684
Document Type: Article
ID: 178596.0
Entries: 1-9  
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