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W Klinger

Showing results (221-230 of 251) with videos related to

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Genomics|June 25, 2002
Canine PKD1 is a single-copy gene: genomic organization and comparative analysisWilliam R Dackowski, Hilary F Luderer, Partha Manavalan, et al.
Experimental and Toxicologic Pathology : Official Journal of the Gesellschaft Fur Toxikologische Pathologie|October 23, 1998
Ciprofibrate--racemate and enantiomers: effects of a four-week treatment on male inbred Fischer rats. A biochemical and morphological studyW Klinger, A Lupp, E Karge, et al.
American Journal of Human Genetics|May 1, 1993
Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimensB E Ward, S L Gersen, M P Carelli, et al.
Human Molecular Genetics|March 1, 1997
High throughput parallel analysis of hundreds of patient samples for more than 100 mutations in multiple disease genesA P Shuber, L A Michalowsky, G S Nass, et al.
The American Journal of Physiology|December 1, 1990
Expression of normal and cystic fibrosis phenotypes by continuous airway epithelial cell linesD M Jefferson, J D Valentich, F C Marini, et al.
The Journal of Clinical Investigation|March 18, 2010
CNS-targeted gene therapy improves survival and motor function in a mouse model of spinal muscular atrophyMarco A Passini, Jie Bu, Eric M Roskelley, et al.
Nature|September 27, 1990
Expression and characterization of the cystic fibrosis transmembrane conductance regulatorR J Gregory, S H Cheng, D P Rich, et al.
American Journal of Human Genetics|March 1, 1993
Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite populationJ Zielenski, T M Fujiwara, D Markiewicz, et al.
Annals of Neurology|September 11, 1999
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsionsH Lerche, C Biervert, A K Alekov, et al.
Nature|September 27, 1990
Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cellsD P Rich, M P Anderson, R J Gregory, et al.
Pageof 26

Showing results (221-230 of 251) with videos related to

Sort By:
Pageof 26
Genomics|June 25, 2002
Canine PKD1 is a single-copy gene: genomic organization and comparative analysisWilliam R Dackowski, Hilary F Luderer, Partha Manavalan, et al.
Experimental and Toxicologic Pathology : Official Journal of the Gesellschaft Fur Toxikologische Pathologie|October 23, 1998
Ciprofibrate--racemate and enantiomers: effects of a four-week treatment on male inbred Fischer rats. A biochemical and morphological studyW Klinger, A Lupp, E Karge, et al.
American Journal of Human Genetics|May 1, 1993
Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimensB E Ward, S L Gersen, M P Carelli, et al.
Human Molecular Genetics|March 1, 1997
High throughput parallel analysis of hundreds of patient samples for more than 100 mutations in multiple disease genesA P Shuber, L A Michalowsky, G S Nass, et al.
The American Journal of Physiology|December 1, 1990
Expression of normal and cystic fibrosis phenotypes by continuous airway epithelial cell linesD M Jefferson, J D Valentich, F C Marini, et al.
The Journal of Clinical Investigation|March 18, 2010
CNS-targeted gene therapy improves survival and motor function in a mouse model of spinal muscular atrophyMarco A Passini, Jie Bu, Eric M Roskelley, et al.
Nature|September 27, 1990
Expression and characterization of the cystic fibrosis transmembrane conductance regulatorR J Gregory, S H Cheng, D P Rich, et al.
American Journal of Human Genetics|March 1, 1993
Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite populationJ Zielenski, T M Fujiwara, D Markiewicz, et al.
Annals of Neurology|September 11, 1999
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsionsH Lerche, C Biervert, A K Alekov, et al.
Nature|September 27, 1990
Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cellsD P Rich, M P Anderson, R J Gregory, et al.
Pageof 26