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R Spörle

Showing results (1-10 of 10) with videos related to

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Development Genes and Evolution|July 17, 2001
Epaxial-adaxial-hypaxial regionalisation of the vertebrate somite: evidence for a somitic organiser and a mirror-image duplicationR Spörle
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 6, 1997
System to identify individual somites and their derivatives in the developing mouse embryoR Spörle, K Schughart
Current Opinion in Genetics & Development|August 1, 1997
Neural tube morphogenesisR Spörle, K Schughart
Developmental Genetics|July 17, 1998
Paradox segmentation along inter- and intrasomitic borderlines is followed by dysmorphology of the axial skeleton in the open brain (opb) mouse mutantR Spörle, K Schughart
Development (Cambridge, England)|January 1, 1996
Severe defects in the formation of epaxial musculature in open brain (opb) mutant mouse embryosR Spörle, T Günther, M Struwe, et al.
Genomics|April 13, 1999
Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndromeY K Wang, R Spörle, T Paperna, et al.
Developmental Biology|February 15, 1997
The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formationT Nagai, J Aruga, S Takada, et al.
Nature Genetics|June 3, 2000
Computer-based three-dimensional visualization of developmental gene expressionJ Streicher, M A Donat, B Strauss, et al.
Human Molecular Genetics|March 11, 1999
Isolation and embryonic expression of the novel mouse gene Hic1, the homologue of HIC1, a candidate gene for the Miller-Dieker syndromeC Grimm, R Spörle, T E Schmid, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidneyJ Favor, R Sandulache, A Neuhäuser-Klaus, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Development Genes and Evolution|July 17, 2001
Epaxial-adaxial-hypaxial regionalisation of the vertebrate somite: evidence for a somitic organiser and a mirror-image duplicationR Spörle
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 6, 1997
System to identify individual somites and their derivatives in the developing mouse embryoR Spörle, K Schughart
Current Opinion in Genetics & Development|August 1, 1997
Neural tube morphogenesisR Spörle, K Schughart
Developmental Genetics|July 17, 1998
Paradox segmentation along inter- and intrasomitic borderlines is followed by dysmorphology of the axial skeleton in the open brain (opb) mouse mutantR Spörle, K Schughart
Development (Cambridge, England)|January 1, 1996
Severe defects in the formation of epaxial musculature in open brain (opb) mutant mouse embryosR Spörle, T Günther, M Struwe, et al.
Genomics|April 13, 1999
Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndromeY K Wang, R Spörle, T Paperna, et al.
Developmental Biology|February 15, 1997
The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formationT Nagai, J Aruga, S Takada, et al.
Nature Genetics|June 3, 2000
Computer-based three-dimensional visualization of developmental gene expressionJ Streicher, M A Donat, B Strauss, et al.
Human Molecular Genetics|March 11, 1999
Isolation and embryonic expression of the novel mouse gene Hic1, the homologue of HIC1, a candidate gene for the Miller-Dieker syndromeC Grimm, R Spörle, T E Schmid, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidneyJ Favor, R Sandulache, A Neuhäuser-Klaus, et al.
Pageof 1