Search research articles
Contact Us
Filters
Showing results (61-70 of 169) with videos related to
Page
of 17
Sort By:
Nature Medicine
|
May 11, 2023
Personalized antisense oligonucleotides 'for free, for life' - the n-Lorem Foundation
Joseph G Gleeson, C Frank Bennett, Jeffrey B Carroll, et al.
Clinical Pharmacology in Drug Development
|
August 16, 2022
Preclinical and Phase 1 Assessment of Antisense Oligonucleotide Bepirovirsen in Hepatitis B Virus-Transgenic Mice and Healthy Human Volunteers: Support for Clinical Dose Selection and Evaluation of Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses
Kelong Han, Dickens Theodore, Gina McMullen, et al.
American Journal of Human Genetics
|
June 25, 2019
NCALD Antisense Oligonucleotide Therapy in Addition to Nusinersen further Ameliorates Spinal Muscular Atrophy in Mice
Laura Torres-Benito, Svenja Schneider, Roman Rombo, et al.
Cell Reports
|
September 30, 2016
Mammary Tumor-Associated RNAs Impact Tumor Cell Proliferation, Invasion, and Migration
Sarah D Diermeier, Kung-Chi Chang, Susan M Freier, et al.
Human Molecular Genetics
|
June 5, 2015
DICER/AGO-dependent epigenetic silencing of D4Z4 repeats enhanced by exogenous siRNA suggests mechanisms and therapies for FSHD
Jong-Won Lim, Lauren Snider, Zizhen Yao, et al.
Nucleic Acids Research
|
May 19, 2004
Identification and functional validation of PNAs that inhibit murine CD40 expression by redirection of splicing
Andrew M Siwkowski, Leila Malik, Christine C Esau, et al.
Gene Therapy
|
January 25, 2022
Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1
Siham Ait Benichou, Dominic Jauvin, Thiéry De Serres-Bérard, et al.
Nature Communications
|
March 28, 2026
Restoring early postnatal synaptic dysregulation rescues motor neuron degeneration in a mouse model of Spinal and Bulbar Muscular Atrophy
Tomoki Hirunagi, Kentaro Sahashi, Madoka Iida, et al.
Nucleic Acids Research
|
November 19, 2008
Potent inhibition of microRNA in vivo without degradation
Scott Davis, Stephanie Propp, Susan M Freier, et al.
Journal of Huntington'S Disease
|
July 27, 2014
Antisense oligonucleotide-mediated correction of transcriptional dysregulation is correlated with behavioral benefits in the YAC128 mouse model of Huntington's disease
Lisa M Stanek, Wendy Yang, Stuart Angus, et al.
Page
of 17
Search research articles
Search
Showing results (61-70 of 169) with videos related to
Sort By:
Page
of 17
Nature Medicine
|
May 11, 2023
Personalized antisense oligonucleotides 'for free, for life' - the n-Lorem Foundation
Joseph G Gleeson, C Frank Bennett, Jeffrey B Carroll, et al.
Clinical Pharmacology in Drug Development
|
August 16, 2022
Preclinical and Phase 1 Assessment of Antisense Oligonucleotide Bepirovirsen in Hepatitis B Virus-Transgenic Mice and Healthy Human Volunteers: Support for Clinical Dose Selection and Evaluation of Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses
Kelong Han, Dickens Theodore, Gina McMullen, et al.
American Journal of Human Genetics
|
June 25, 2019
NCALD Antisense Oligonucleotide Therapy in Addition to Nusinersen further Ameliorates Spinal Muscular Atrophy in Mice
Laura Torres-Benito, Svenja Schneider, Roman Rombo, et al.
Cell Reports
|
September 30, 2016
Mammary Tumor-Associated RNAs Impact Tumor Cell Proliferation, Invasion, and Migration
Sarah D Diermeier, Kung-Chi Chang, Susan M Freier, et al.
Human Molecular Genetics
|
June 5, 2015
DICER/AGO-dependent epigenetic silencing of D4Z4 repeats enhanced by exogenous siRNA suggests mechanisms and therapies for FSHD
Jong-Won Lim, Lauren Snider, Zizhen Yao, et al.
Nucleic Acids Research
|
May 19, 2004
Identification and functional validation of PNAs that inhibit murine CD40 expression by redirection of splicing
Andrew M Siwkowski, Leila Malik, Christine C Esau, et al.
Gene Therapy
|
January 25, 2022
Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1
Siham Ait Benichou, Dominic Jauvin, Thiéry De Serres-Bérard, et al.
Nature Communications
|
March 28, 2026
Restoring early postnatal synaptic dysregulation rescues motor neuron degeneration in a mouse model of Spinal and Bulbar Muscular Atrophy
Tomoki Hirunagi, Kentaro Sahashi, Madoka Iida, et al.
Nucleic Acids Research
|
November 19, 2008
Potent inhibition of microRNA in vivo without degradation
Scott Davis, Stephanie Propp, Susan M Freier, et al.
Journal of Huntington'S Disease
|
July 27, 2014
Antisense oligonucleotide-mediated correction of transcriptional dysregulation is correlated with behavioral benefits in the YAC128 mouse model of Huntington's disease
Lisa M Stanek, Wendy Yang, Stuart Angus, et al.
Page
of 17