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Brian C Lin

Showing results (1-10 of 8) with videos related to

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Journal of Virology|November 20, 2009
Multimerization of hepatitis delta antigen is a critical determinant of RNA binding specificityBrian C Lin, Dawn A Defenbaugh, John L Casey
Trends in Pharmacological Sciences|October 28, 2022
Implementing computational methods in tandem with synonymous gene recoding for therapeutic developmentBrian C Lin, Nayiri M Kaissarian, Chava Kimchi-Sarfaty
Journal of Neuromuscular Diseases|June 13, 2026
Meeting report: 2025 muscular dystrophy association summit on 'safety and challenges in gene therapy of neuromuscular diseases'Brian C Lin, Angela Lek, Carsten G Bönnemann, et al.
The FEBS Journal|July 17, 2021
UBQLN proteins in health and disease with a focus on UBQLN2 in ALS/FTDBrian C Lin, Nicole R Higgins, Trong H Phung, et al.
Genome Biology|May 22, 2023
In silico methods for predicting functional synonymous variantsBrian C Lin, Upendra Katneni, Katarzyna I Jankowska, et al.
Human Molecular Genetics|April 23, 2021
ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein importBrian C Lin, Trong H Phung, Nicole R Higgins, et al.
Journal of Medical Genetics|December 24, 2016
Single synonymous mutation in factor IX alters protein properties and underlies haemophilia BVijaya L Simhadri, Nobuko Hamasaki-Katagiri, Brian C Lin, et al.
Protein & Cell|May 25, 2025
Therapeutic implications of synonymous gene recoding: Insights into mechanisms controlling protein biogenesis and activityBrian C Lin, Katarzyna I Jankowska, Upendra K Katneni, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Virology|November 20, 2009
Multimerization of hepatitis delta antigen is a critical determinant of RNA binding specificityBrian C Lin, Dawn A Defenbaugh, John L Casey
Trends in Pharmacological Sciences|October 28, 2022
Implementing computational methods in tandem with synonymous gene recoding for therapeutic developmentBrian C Lin, Nayiri M Kaissarian, Chava Kimchi-Sarfaty
Journal of Neuromuscular Diseases|June 13, 2026
Meeting report: 2025 muscular dystrophy association summit on 'safety and challenges in gene therapy of neuromuscular diseases'Brian C Lin, Angela Lek, Carsten G Bönnemann, et al.
The FEBS Journal|July 17, 2021
UBQLN proteins in health and disease with a focus on UBQLN2 in ALS/FTDBrian C Lin, Nicole R Higgins, Trong H Phung, et al.
Genome Biology|May 22, 2023
In silico methods for predicting functional synonymous variantsBrian C Lin, Upendra Katneni, Katarzyna I Jankowska, et al.
Human Molecular Genetics|April 23, 2021
ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein importBrian C Lin, Trong H Phung, Nicole R Higgins, et al.
Journal of Medical Genetics|December 24, 2016
Single synonymous mutation in factor IX alters protein properties and underlies haemophilia BVijaya L Simhadri, Nobuko Hamasaki-Katagiri, Brian C Lin, et al.
Protein & Cell|May 25, 2025
Therapeutic implications of synonymous gene recoding: Insights into mechanisms controlling protein biogenesis and activityBrian C Lin, Katarzyna I Jankowska, Upendra K Katneni, et al.
Pageof 1