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B Knebelmann

Showing results (11-20 of 25) with videos related to

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Human Molecular Genetics|April 1, 1995
Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndromeB Knebelmann, L Forestier, L Drouot, et al.
Physiological Genomics|April 4, 2001
VHL tumor suppressor regulates Cl-/HCO3- exchange and Na+/H+ exchange activities in renal carcinoma cellsS A Karumanchi, L Jiang, B Knebelmann, et al.
Biochemical and Biophysical Research Communications|May 18, 1999
Kringle 5 causes cell cycle arrest and apoptosis of endothelial cellsH Lu, M Dhanabal, R Volk, et al.
Biochemical and Biophysical Research Communications|March 2, 1999
Antiangiogenic activity of restin, NC10 domain of human collagen XV: comparison to endostatinR Ramchandran, M Dhanabal, R Volk, et al.
Kidney International|April 1, 1995
Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distributionM C Gubler, B Knebelmann, A Beziau, et al.
The Journal of Clinical Investigation|September 1, 1993
Deletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the youngF Sun, B Knebelmann, M E Pueyo, et al.
American Journal of Human Genetics|July 1, 1992
Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragmentsB Knebelmann, G Deschenes, F Gros, et al.
Kidney International|November 1, 1992
Alport syndrome and diffuse leiomyomatosis: deletions in the 5' end of the COL4A5 collagen geneC Antignac, J Zhou, M Sanak, et al.
The Journal of Clinical Investigation|March 1, 1994
Deletions in the COL4A5 collagen gene in X-linked Alport syndrome. Characterization of the pathological transcripts in nonrenal cells and correlation with disease expressionC Antignac, B Knebelmann, L Drouot, et al.
Biochemical and Biophysical Research Communications|December 3, 1999
An important von Hippel-Lindau tumor suppressor domain mediates Sp1-binding and self-associationH T Cohen, M Zhou, A M Welsh, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|April 1, 1995
Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndromeB Knebelmann, L Forestier, L Drouot, et al.
Physiological Genomics|April 4, 2001
VHL tumor suppressor regulates Cl-/HCO3- exchange and Na+/H+ exchange activities in renal carcinoma cellsS A Karumanchi, L Jiang, B Knebelmann, et al.
Biochemical and Biophysical Research Communications|May 18, 1999
Kringle 5 causes cell cycle arrest and apoptosis of endothelial cellsH Lu, M Dhanabal, R Volk, et al.
Biochemical and Biophysical Research Communications|March 2, 1999
Antiangiogenic activity of restin, NC10 domain of human collagen XV: comparison to endostatinR Ramchandran, M Dhanabal, R Volk, et al.
Kidney International|April 1, 1995
Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distributionM C Gubler, B Knebelmann, A Beziau, et al.
The Journal of Clinical Investigation|September 1, 1993
Deletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the youngF Sun, B Knebelmann, M E Pueyo, et al.
American Journal of Human Genetics|July 1, 1992
Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragmentsB Knebelmann, G Deschenes, F Gros, et al.
Kidney International|November 1, 1992
Alport syndrome and diffuse leiomyomatosis: deletions in the 5' end of the COL4A5 collagen geneC Antignac, J Zhou, M Sanak, et al.
The Journal of Clinical Investigation|March 1, 1994
Deletions in the COL4A5 collagen gene in X-linked Alport syndrome. Characterization of the pathological transcripts in nonrenal cells and correlation with disease expressionC Antignac, B Knebelmann, L Drouot, et al.
Biochemical and Biophysical Research Communications|December 3, 1999
An important von Hippel-Lindau tumor suppressor domain mediates Sp1-binding and self-associationH T Cohen, M Zhou, A M Welsh, et al.
Pageof 3