Search research articles
Contact Us
Filters
Showing results (81-90 of 103) with videos related to
Page
of 11
Sort By:
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 11, 2016
Exosome-mediated Delivery of Hydrophobically Modified siRNA for Huntingtin mRNA Silencing
Marie-Cécile Didiot, Lauren M Hall, Andrew H Coles, et al.
Nature Communications
|
October 3, 2022
Chemical engineering of therapeutic siRNAs for allele-specific gene silencing in Huntington's disease models
Faith Conroy, Rachael Miller, Julia F Alterman, et al.
Molecular and Cellular Biology
|
September 16, 2009
Mutant huntingtin impairs vesicle formation from recycling endosomes by interfering with Rab11 activity
Xueyi Li, Clive Standley, Ellen Sapp, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 13, 2023
Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington's disease
Daniel O'Reilly, Jillian Belgrad, Chantal Ferguson, et al.
Human Molecular Genetics
|
August 8, 2002
Increased huntingtin protein length reduces the number of polyglutamine-induced gene expression changes in mouse models of Huntington's disease
Edmond Y W Chan, Ruth Luthi-Carter, Andrew Strand, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 25, 2015
Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas
Rodrigo A Toledo, Yuejuan Qin, Zi-Ming Cheng, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 29, 2015
Widespread Central Nervous System Gene Transfer and Silencing After Systemic Delivery of Novel AAV-AS Vector
Sourav R Choudhury, Anne F Harris, Damien J Cabral, et al.
Nature Genetics
|
February 16, 2010
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma
Yuejuan Qin, Li Yao, Elizabeth E King, et al.
Molecular Therapy. Methods & Clinical Development
|
November 3, 2023
Awake intracerebroventricular delivery and safety assessment of oligonucleotides in a large animal model
Hector Ribeiro Benatti, Rachel D Prestigiacomo, Toloo Taghian, et al.
JCI Insight
|
December 22, 2021
Comparative route of administration studies using therapeutic siRNAs show widespread gene modulation in Dorset sheep
Chantal M Ferguson, Bruno Mdc Godinho, Julia F Alterman, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 103) with videos related to
Sort By:
Page
of 11
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 11, 2016
Exosome-mediated Delivery of Hydrophobically Modified siRNA for Huntingtin mRNA Silencing
Marie-Cécile Didiot, Lauren M Hall, Andrew H Coles, et al.
Nature Communications
|
October 3, 2022
Chemical engineering of therapeutic siRNAs for allele-specific gene silencing in Huntington's disease models
Faith Conroy, Rachael Miller, Julia F Alterman, et al.
Molecular and Cellular Biology
|
September 16, 2009
Mutant huntingtin impairs vesicle formation from recycling endosomes by interfering with Rab11 activity
Xueyi Li, Clive Standley, Ellen Sapp, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 13, 2023
Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington's disease
Daniel O'Reilly, Jillian Belgrad, Chantal Ferguson, et al.
Human Molecular Genetics
|
August 8, 2002
Increased huntingtin protein length reduces the number of polyglutamine-induced gene expression changes in mouse models of Huntington's disease
Edmond Y W Chan, Ruth Luthi-Carter, Andrew Strand, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 25, 2015
Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas
Rodrigo A Toledo, Yuejuan Qin, Zi-Ming Cheng, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 29, 2015
Widespread Central Nervous System Gene Transfer and Silencing After Systemic Delivery of Novel AAV-AS Vector
Sourav R Choudhury, Anne F Harris, Damien J Cabral, et al.
Nature Genetics
|
February 16, 2010
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma
Yuejuan Qin, Li Yao, Elizabeth E King, et al.
Molecular Therapy. Methods & Clinical Development
|
November 3, 2023
Awake intracerebroventricular delivery and safety assessment of oligonucleotides in a large animal model
Hector Ribeiro Benatti, Rachel D Prestigiacomo, Toloo Taghian, et al.
JCI Insight
|
December 22, 2021
Comparative route of administration studies using therapeutic siRNAs show widespread gene modulation in Dorset sheep
Chantal M Ferguson, Bruno Mdc Godinho, Julia F Alterman, et al.
Page
of 11