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Kim M Keeling

Showing results (11-20 of 33) with videos related to

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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 4, 2023
Discovery of dysregulated circular RNAs in whole blood transcriptomes from cystic fibrosis patients - implication of a role for cellular senescence in cystic fibrosisEdward A Salinas, Victor Macauley, Kim M Keeling, et al.
Heliyon|December 4, 2023
RNA binding proteins PTBP1 and HNRNPL regulate <i>CFTR</i> mRNA decayAmna Siddiqui, Arpit Saxena, Joshua Echols, et al.
Disease Models & Mechanisms|August 2, 2020
A regulated NMD mouse model supports NMD inhibition as a viable therapeutic option to treat genetic diseasesJosh Echols, Amna Siddiqui, Yanying Dai, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 20, 2022
Ataluren suppresses a premature termination codon in an MPS I-H mouseDan Wang, Xiaojiao Xue, Gwen Gunn, et al.
Nature Communications|March 21, 2024
Extended stop codon context predicts nonsense codon readthrough efficiency in human cellsKotchaphorn Mangkalaphiban, Lianwu Fu, Ming Du, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 17, 2006
Clinical doses of amikacin provide more effective suppression of the human CFTR-G542X stop mutation than gentamicin in a transgenic CF mouse modelMing Du, Kim M Keeling, Liming Fan, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|July 12, 2011
Enhancement of alveolar epithelial sodium channel activity with decreased cystic fibrosis transmembrane conductance regulator expression in mouse lungAhmed Lazrak, Asta Jurkuvenaite, Lan Chen, et al.
RNA (New York, N.Y.)|March 24, 2004
Leaky termination at premature stop codons antagonizes nonsense-mediated mRNA decay in S. cerevisiaeKim M Keeling, Jessica Lanier, Ming Du, et al.
Molecular Genetics and Metabolism|September 16, 2009
Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutationDan Wang, Charu Shukla, Xiaoli Liu, et al.
Human Molecular Genetics|June 3, 2017
Identification of the amino acids inserted during suppression of CFTR nonsense mutations and determination of their functional consequencesXiaojiao Xue, Venkateshwar Mutyam, Amita Thakerar, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 4, 2023
Discovery of dysregulated circular RNAs in whole blood transcriptomes from cystic fibrosis patients - implication of a role for cellular senescence in cystic fibrosisEdward A Salinas, Victor Macauley, Kim M Keeling, et al.
Heliyon|December 4, 2023
RNA binding proteins PTBP1 and HNRNPL regulate <i>CFTR</i> mRNA decayAmna Siddiqui, Arpit Saxena, Joshua Echols, et al.
Disease Models & Mechanisms|August 2, 2020
A regulated NMD mouse model supports NMD inhibition as a viable therapeutic option to treat genetic diseasesJosh Echols, Amna Siddiqui, Yanying Dai, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 20, 2022
Ataluren suppresses a premature termination codon in an MPS I-H mouseDan Wang, Xiaojiao Xue, Gwen Gunn, et al.
Nature Communications|March 21, 2024
Extended stop codon context predicts nonsense codon readthrough efficiency in human cellsKotchaphorn Mangkalaphiban, Lianwu Fu, Ming Du, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 17, 2006
Clinical doses of amikacin provide more effective suppression of the human CFTR-G542X stop mutation than gentamicin in a transgenic CF mouse modelMing Du, Kim M Keeling, Liming Fan, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|July 12, 2011
Enhancement of alveolar epithelial sodium channel activity with decreased cystic fibrosis transmembrane conductance regulator expression in mouse lungAhmed Lazrak, Asta Jurkuvenaite, Lan Chen, et al.
RNA (New York, N.Y.)|March 24, 2004
Leaky termination at premature stop codons antagonizes nonsense-mediated mRNA decay in S. cerevisiaeKim M Keeling, Jessica Lanier, Ming Du, et al.
Molecular Genetics and Metabolism|September 16, 2009
Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutationDan Wang, Charu Shukla, Xiaoli Liu, et al.
Human Molecular Genetics|June 3, 2017
Identification of the amino acids inserted during suppression of CFTR nonsense mutations and determination of their functional consequencesXiaojiao Xue, Venkateshwar Mutyam, Amita Thakerar, et al.
Pageof 4