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S Mundlos

Showing results (81-90 of 94) with videos related to

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Gene Expression Patterns : GEP|July 11, 2006
Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2(-/-) mouse modelJ Hecht, V Seitz, M Urban, et al.
American Journal of Human Genetics|October 16, 1999
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasiaI Quack, B Vonderstrass, M Stock, et al.
Zeitschrift Fur Rheumatologie|April 26, 2018
[Osteoimmunology-IMMUNOBONE : Regulation of bone by inflammation]M Rauner, F Buttgereit, J Distler, et al.
American Journal of Human Genetics|August 2, 2007
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGINK Lehmann, P Seemann, F Silan, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 12, 2013
TCR repertoire analysis by next generation sequencing allows complex differential diagnosis of T cell-related pathologyM Dziubianau, J Hecht, L Kuchenbecker, et al.
Neurology|August 22, 2008
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre typeL Van Maldergem, M Yuksel-Apak, H Kayserili, et al.
Cell|May 30, 1997
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone developmentF Otto, A P Thornell, T Crompton, et al.
Leukemia & Lymphoma|October 6, 2007
Immunoglobulin receptor evolution in follicular lymphoma and a review of literatureV Seitz, A Stiege, S Mundlos, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractF R Goodman, S Mundlos, Y Muragaki, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromeC G Woods, S Stricker, P Seemann, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
Gene Expression Patterns : GEP|July 11, 2006
Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2(-/-) mouse modelJ Hecht, V Seitz, M Urban, et al.
American Journal of Human Genetics|October 16, 1999
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasiaI Quack, B Vonderstrass, M Stock, et al.
Zeitschrift Fur Rheumatologie|April 26, 2018
[Osteoimmunology-IMMUNOBONE : Regulation of bone by inflammation]M Rauner, F Buttgereit, J Distler, et al.
American Journal of Human Genetics|August 2, 2007
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGINK Lehmann, P Seemann, F Silan, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 12, 2013
TCR repertoire analysis by next generation sequencing allows complex differential diagnosis of T cell-related pathologyM Dziubianau, J Hecht, L Kuchenbecker, et al.
Neurology|August 22, 2008
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre typeL Van Maldergem, M Yuksel-Apak, H Kayserili, et al.
Cell|May 30, 1997
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone developmentF Otto, A P Thornell, T Crompton, et al.
Leukemia & Lymphoma|October 6, 2007
Immunoglobulin receptor evolution in follicular lymphoma and a review of literatureV Seitz, A Stiege, S Mundlos, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractF R Goodman, S Mundlos, Y Muragaki, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromeC G Woods, S Stricker, P Seemann, et al.
Pageof 10