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Cell Reports
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November 14, 2019
Anti-CRISPR AcrIIA5 Potently Inhibits All Cas9 Homologs Used for Genome Editing
Bianca Garcia, Jooyoung Lee, Alireza Edraki, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 20, 2011
Identification and characterization of a functional mitochondrial angiotensin system
Peter M Abadir, D Brian Foster, Michael Crow, et al.
EMBO Molecular Medicine
|
March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expression
Eleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Pediatrics
|
July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation
Ronald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Nature Communications
|
August 4, 2015
Clinically relevant copy number variations detected in cerebral palsy
Maryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature
|
July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene
Dwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Plos One
|
November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrels
Eva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
BMC Genomics
|
April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
Christian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Nature Medicine
|
January 24, 2007
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states
Ronald D Cohn, Christel van Erp, Jennifer P Habashi, et al.
Nature Medicine
|
July 18, 2017
Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism
Dwi U Kemaladewi, Eleonora Maino, Elzbieta Hyatt, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 100) with videos related to
Sort By:
Page
of 10
Cell Reports
|
November 14, 2019
Anti-CRISPR AcrIIA5 Potently Inhibits All Cas9 Homologs Used for Genome Editing
Bianca Garcia, Jooyoung Lee, Alireza Edraki, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 20, 2011
Identification and characterization of a functional mitochondrial angiotensin system
Peter M Abadir, D Brian Foster, Michael Crow, et al.
EMBO Molecular Medicine
|
March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expression
Eleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Pediatrics
|
July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation
Ronald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Nature Communications
|
August 4, 2015
Clinically relevant copy number variations detected in cerebral palsy
Maryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature
|
July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene
Dwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Plos One
|
November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrels
Eva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
BMC Genomics
|
April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
Christian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Nature Medicine
|
January 24, 2007
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states
Ronald D Cohn, Christel van Erp, Jennifer P Habashi, et al.
Nature Medicine
|
July 18, 2017
Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism
Dwi U Kemaladewi, Eleonora Maino, Elzbieta Hyatt, et al.
Page
of 10