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Advances in Experimental Medicine and Biology
|
August 26, 2017
Gene Therapy in the Nervous System: Failures and Successes
Jayanth S Chandran, Joseph M Scarrott, Pamela J Shaw, et al.
Expert Opinion on Biological Therapy
|
May 12, 2015
Current developments in gene therapy for amyotrophic lateral sclerosis
Joseph M Scarrott, Saúl Herranz-Martín, Aziza R Alrafiah, et al.
Biotechnology Journal
|
December 10, 2022
Increased recombinant adeno-associated virus production by HEK293 cells using small molecule chemical additives
Joseph M Scarrott, Yusuf B Johari, Thilo H Pohle, et al.
Biotechnology Journal
|
June 20, 2024
Molecular design of controllable recombinant adeno-associated virus (AAV) expression systems for enhanced vector production
Yusuf B Johari, Thilo H Pohle, Jared Whitehead, et al.
Biotechnology Journal
|
April 28, 2022
Engineering of the CMV promoter for controlled expression of recombinant genes in HEK293 cells
Yusuf B Johari, Joseph M Scarrott, Thilo H Pohle, et al.
Brain Communications
|
January 12, 2023
Ap4b1-knockout mouse model of hereditary spastic paraplegia type 47 displays motor dysfunction, aberrant brain morphology and ATG9A mislocalization
Joseph M Scarrott, João Alves-Cruzeiro, Paolo M Marchi, et al.
Molecular Therapy. Nucleic Acids
|
September 10, 2018
Translating SOD1 Gene Silencing toward the Clinic: A Highly Efficacious, Off-Target-free, and Biomarker-Supported Strategy for fALS
Tommaso Iannitti, Joseph M Scarrott, Shibi Likhite, et al.
Biotechnology and Bioengineering
|
October 31, 2020
Production of trimeric SARS-CoV-2 spike protein by CHO cells for serological COVID-19 testing
Yusuf B Johari, Stephen R P Jaffé, Joseph M Scarrott, et al.
EMBO Molecular Medicine
|
October 2, 2024
Pre-clinical development of AP4B1 gene replacement therapy for hereditary spastic paraplegia type 47
Jessica P Wiseman, Joseph M Scarrott, João Alves-Cruzeiro, et al.
Human Molecular Genetics
|
January 10, 2020
Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking
Robert Behne, Julian Teinert, Miriam Wimmer, et al.
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Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Advances in Experimental Medicine and Biology
|
August 26, 2017
Gene Therapy in the Nervous System: Failures and Successes
Jayanth S Chandran, Joseph M Scarrott, Pamela J Shaw, et al.
Expert Opinion on Biological Therapy
|
May 12, 2015
Current developments in gene therapy for amyotrophic lateral sclerosis
Joseph M Scarrott, Saúl Herranz-Martín, Aziza R Alrafiah, et al.
Biotechnology Journal
|
December 10, 2022
Increased recombinant adeno-associated virus production by HEK293 cells using small molecule chemical additives
Joseph M Scarrott, Yusuf B Johari, Thilo H Pohle, et al.
Biotechnology Journal
|
June 20, 2024
Molecular design of controllable recombinant adeno-associated virus (AAV) expression systems for enhanced vector production
Yusuf B Johari, Thilo H Pohle, Jared Whitehead, et al.
Biotechnology Journal
|
April 28, 2022
Engineering of the CMV promoter for controlled expression of recombinant genes in HEK293 cells
Yusuf B Johari, Joseph M Scarrott, Thilo H Pohle, et al.
Brain Communications
|
January 12, 2023
Ap4b1-knockout mouse model of hereditary spastic paraplegia type 47 displays motor dysfunction, aberrant brain morphology and ATG9A mislocalization
Joseph M Scarrott, João Alves-Cruzeiro, Paolo M Marchi, et al.
Molecular Therapy. Nucleic Acids
|
September 10, 2018
Translating SOD1 Gene Silencing toward the Clinic: A Highly Efficacious, Off-Target-free, and Biomarker-Supported Strategy for fALS
Tommaso Iannitti, Joseph M Scarrott, Shibi Likhite, et al.
Biotechnology and Bioengineering
|
October 31, 2020
Production of trimeric SARS-CoV-2 spike protein by CHO cells for serological COVID-19 testing
Yusuf B Johari, Stephen R P Jaffé, Joseph M Scarrott, et al.
EMBO Molecular Medicine
|
October 2, 2024
Pre-clinical development of AP4B1 gene replacement therapy for hereditary spastic paraplegia type 47
Jessica P Wiseman, Joseph M Scarrott, João Alves-Cruzeiro, et al.
Human Molecular Genetics
|
January 10, 2020
Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking
Robert Behne, Julian Teinert, Miriam Wimmer, et al.
Page
of 1