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Nucleic Acids Research
|
March 29, 2025
Mechanism-based approach in designing patient-specific combination therapies for nonsense mutation diseases
Saleem Y Bhat, Arpan Bhattacharya, Hong Li, et al.
American Journal of Physiology. Cell Physiology
|
December 1, 2006
Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1
John D Lueck, Codrin Lungu, Ami Mankodi, et al.
Science (New York, N.Y.)
|
July 18, 2009
Reversal of RNA dominance by displacement of protein sequestered on triplet repeat RNA
Thurman M Wheeler, Krzysztof Sobczak, John D Lueck, et al.
Elife
|
October 7, 2016
Atomic mutagenesis in ion channels with engineered stoichiometry
John D Lueck, Adam L Mackey, Daniel T Infield, et al.
Elife
|
December 13, 2016
Cellular encoding of Cy dyes for single-molecule imaging
Lilia Leisle, Rahul Chadda, John D Lueck, et al.
Scientific Reports
|
December 31, 2024
Engineered tRNAs efficiently suppress CDKL5 premature termination codons
Stefano Pezzini, Aurora Mustaccia, Pierre Aboa, et al.
Cell Calcium
|
January 10, 2009
Alternative splicing of RyR1 alters the efficacy of skeletal EC coupling
Takashi Kimura, John D Lueck, Peta J Harvey, et al.
The Journal of Clinical Investigation
|
August 28, 2012
Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy
Aaron M Beedle, Amy J Turner, Yoshiaki Saito, et al.
Human Molecular Genetics
|
June 24, 2005
Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1
Takashi Kimura, Masayuki Nakamori, John D Lueck, et al.
Nature Communications
|
July 8, 2026
Elimination of myotonia improves myopathy in a muscleblind-like knockout model of myotonic dystrophy
Matthew T Sipple, Sakura A Hamazaki, Vanessa Todorow, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Nucleic Acids Research
|
March 29, 2025
Mechanism-based approach in designing patient-specific combination therapies for nonsense mutation diseases
Saleem Y Bhat, Arpan Bhattacharya, Hong Li, et al.
American Journal of Physiology. Cell Physiology
|
December 1, 2006
Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1
John D Lueck, Codrin Lungu, Ami Mankodi, et al.
Science (New York, N.Y.)
|
July 18, 2009
Reversal of RNA dominance by displacement of protein sequestered on triplet repeat RNA
Thurman M Wheeler, Krzysztof Sobczak, John D Lueck, et al.
Elife
|
October 7, 2016
Atomic mutagenesis in ion channels with engineered stoichiometry
John D Lueck, Adam L Mackey, Daniel T Infield, et al.
Elife
|
December 13, 2016
Cellular encoding of Cy dyes for single-molecule imaging
Lilia Leisle, Rahul Chadda, John D Lueck, et al.
Scientific Reports
|
December 31, 2024
Engineered tRNAs efficiently suppress CDKL5 premature termination codons
Stefano Pezzini, Aurora Mustaccia, Pierre Aboa, et al.
Cell Calcium
|
January 10, 2009
Alternative splicing of RyR1 alters the efficacy of skeletal EC coupling
Takashi Kimura, John D Lueck, Peta J Harvey, et al.
The Journal of Clinical Investigation
|
August 28, 2012
Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy
Aaron M Beedle, Amy J Turner, Yoshiaki Saito, et al.
Human Molecular Genetics
|
June 24, 2005
Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1
Takashi Kimura, Masayuki Nakamori, John D Lueck, et al.
Nature Communications
|
July 8, 2026
Elimination of myotonia improves myopathy in a muscleblind-like knockout model of myotonic dystrophy
Matthew T Sipple, Sakura A Hamazaki, Vanessa Todorow, et al.
Page
of 4