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Showing results (71-80 of 120) with videos related to

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Archives of Dermatological Research|January 1, 1994
Ehlers-Danlos syndrome type VII: phenotype and genotypeH W Lehmann, S Mundlos, A Winterpacht, et al.
Journal of Medical Genetics|August 1, 1996
The deletion of six amino acids at the C-terminus of the alpha 1 (II) chain causes overmodification of type II and type XI collagen: further evidence for the association between small deletions in COL2A1 and Kniest dysplasiaA Winterpacht, A Superti-Furga, U Schwarze, et al.
Development (Cambridge, England)|November 1, 1992
PAX8, a human paired box gene: isolation and expression in developing thyroid, kidney and Wilms' tumorsA Poleev, H Fickenscher, S Mundlos, et al.
Physiological Genomics|October 4, 2000
A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasiaA Winterpacht, K Hilbert, C Stelzer, et al.
Cytogenetic and Genome Research|July 9, 2004
RNAi knock-down mice: an emerging technology for post-genomic functional geneticsD Prawitt, L Brixel, C Spangenberg, et al.
Genomics|July 25, 2000
Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene familyT Enklaar, M Esswein, M Oswald, et al.
Molecular and Cellular Biology|February 18, 1999
The Wilms' tumor suppressor gene (wt1) product regulates Dax-1 gene expression during gonadal differentiationJ Kim, D Prawitt, N Bardeesy, et al.
Human Genetics|August 14, 2001
Improved definition of chromosomal breakpoints using high-resolution multicolour bandingJ Lemke, I Chudoba, G Senger, et al.
Genes & Development|November 1, 1994
A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament proteinY Chan, I Anton-Lamprecht, Q C Yu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 28, 1998
Cloning, characterization, and chromosomal assignment of the human ortholog of murine Zfp-37, a candidate gene for Nager syndromeS D Dreyer, L Zhou, M A Machado, et al.
Pageof 12

Showing results (71-80 of 120) with videos related to

Sort By:
Pageof 12
Archives of Dermatological Research|January 1, 1994
Ehlers-Danlos syndrome type VII: phenotype and genotypeH W Lehmann, S Mundlos, A Winterpacht, et al.
Journal of Medical Genetics|August 1, 1996
The deletion of six amino acids at the C-terminus of the alpha 1 (II) chain causes overmodification of type II and type XI collagen: further evidence for the association between small deletions in COL2A1 and Kniest dysplasiaA Winterpacht, A Superti-Furga, U Schwarze, et al.
Development (Cambridge, England)|November 1, 1992
PAX8, a human paired box gene: isolation and expression in developing thyroid, kidney and Wilms' tumorsA Poleev, H Fickenscher, S Mundlos, et al.
Physiological Genomics|October 4, 2000
A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasiaA Winterpacht, K Hilbert, C Stelzer, et al.
Cytogenetic and Genome Research|July 9, 2004
RNAi knock-down mice: an emerging technology for post-genomic functional geneticsD Prawitt, L Brixel, C Spangenberg, et al.
Genomics|July 25, 2000
Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene familyT Enklaar, M Esswein, M Oswald, et al.
Molecular and Cellular Biology|February 18, 1999
The Wilms' tumor suppressor gene (wt1) product regulates Dax-1 gene expression during gonadal differentiationJ Kim, D Prawitt, N Bardeesy, et al.
Human Genetics|August 14, 2001
Improved definition of chromosomal breakpoints using high-resolution multicolour bandingJ Lemke, I Chudoba, G Senger, et al.
Genes & Development|November 1, 1994
A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament proteinY Chan, I Anton-Lamprecht, Q C Yu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 28, 1998
Cloning, characterization, and chromosomal assignment of the human ortholog of murine Zfp-37, a candidate gene for Nager syndromeS D Dreyer, L Zhou, M A Machado, et al.
Pageof 12