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International Journal of Molecular Sciences
|
August 29, 2024
Is Exon Skipping a Viable Therapeutic Approach for Vascular Ehlers-Danlos Syndrome with Mutations in <i>COL3A1</i> Exon 10 or 15?
Sasiwimon Utama, Jessica M Cale, Chalermchai Mitrpant, et al.
Methods and Protocols
|
June 25, 2025
Expression and Site-Specific Biotinylation of Human Cytosolic 5'-Nucleotidase 1A in <i>Escherichia coli</i>
Nataliya Slater, Anuradha Sooda, Frank L Mastaglia, et al.
Frontiers in Public Health
|
September 30, 2017
Comprehending the Health Informatics Spectrum: Grappling with System Entropy and Advancing Quality Clinical Research
Matthew I Bellgard, Nigel Chartres, Gerald F Watts, et al.
BMC Molecular Biology
|
July 3, 2007
Antisense oligonucleotide induced exon skipping and the dystrophin gene transcript: cocktails and chemistries
Abbie M Adams, Penny L Harding, Patrick L Iversen, et al.
Frontiers in Pharmacology
|
April 8, 2022
Investigating the Implications of <i>CFTR</i> Exon Skipping Using a <i>Cftr</i> Exon 9 Deleted Mouse Model
Kelly M Martinovich, Anthony Kicic, Stephen M Stick, et al.
BMC Medical Genetics
|
October 22, 2011
Mismatched single stranded antisense oligonucleotides can induce efficient dystrophin splice switching
Clayton T Fragall, Abbie M Adams, Russell D Johnsen, et al.
Molecular Genetics & Genomic Medicine
|
February 6, 2014
Antisense suppression of donor splice site mutations in the dystrophin gene transcript
Sue Fletcher, Penny L Meloni, Russell D Johnsen, et al.
Autism : the International Journal of Research and Practice
|
February 7, 2020
A framework of evidence-based practice for digital support, co-developed with and for the autism community
Vanessa Zervogianni, Sue Fletcher-Watson, Gerardo Herrera, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 22, 2009
Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping
Aurélie Goyenvalle, Arran Babbs, Dave Powell, et al.
Frontiers in Neuroscience
|
December 24, 2019
ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?
Rita Mejzini, Loren L Flynn, Ianthe L Pitout, et al.
Page
of 18
Search research articles
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Showing results (91-100 of 173) with videos related to
Sort By:
Page
of 18
International Journal of Molecular Sciences
|
August 29, 2024
Is Exon Skipping a Viable Therapeutic Approach for Vascular Ehlers-Danlos Syndrome with Mutations in <i>COL3A1</i> Exon 10 or 15?
Sasiwimon Utama, Jessica M Cale, Chalermchai Mitrpant, et al.
Methods and Protocols
|
June 25, 2025
Expression and Site-Specific Biotinylation of Human Cytosolic 5'-Nucleotidase 1A in <i>Escherichia coli</i>
Nataliya Slater, Anuradha Sooda, Frank L Mastaglia, et al.
Frontiers in Public Health
|
September 30, 2017
Comprehending the Health Informatics Spectrum: Grappling with System Entropy and Advancing Quality Clinical Research
Matthew I Bellgard, Nigel Chartres, Gerald F Watts, et al.
BMC Molecular Biology
|
July 3, 2007
Antisense oligonucleotide induced exon skipping and the dystrophin gene transcript: cocktails and chemistries
Abbie M Adams, Penny L Harding, Patrick L Iversen, et al.
Frontiers in Pharmacology
|
April 8, 2022
Investigating the Implications of <i>CFTR</i> Exon Skipping Using a <i>Cftr</i> Exon 9 Deleted Mouse Model
Kelly M Martinovich, Anthony Kicic, Stephen M Stick, et al.
BMC Medical Genetics
|
October 22, 2011
Mismatched single stranded antisense oligonucleotides can induce efficient dystrophin splice switching
Clayton T Fragall, Abbie M Adams, Russell D Johnsen, et al.
Molecular Genetics & Genomic Medicine
|
February 6, 2014
Antisense suppression of donor splice site mutations in the dystrophin gene transcript
Sue Fletcher, Penny L Meloni, Russell D Johnsen, et al.
Autism : the International Journal of Research and Practice
|
February 7, 2020
A framework of evidence-based practice for digital support, co-developed with and for the autism community
Vanessa Zervogianni, Sue Fletcher-Watson, Gerardo Herrera, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 22, 2009
Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping
Aurélie Goyenvalle, Arran Babbs, Dave Powell, et al.
Frontiers in Neuroscience
|
December 24, 2019
ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?
Rita Mejzini, Loren L Flynn, Ianthe L Pitout, et al.
Page
of 18