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Donglin Bai

Showing results (61-70 of 67) with videos related to

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Frontiers in Cell and Developmental Biology|March 2, 2023
<i>GJB4</i> variants linked to skin disease exhibit a trafficking deficiency en route to gap junction formation that can be restored by co-expression of select connexinsSergiu A Lucaciu, Rhett Figliuzzi, Ruth Neumann, et al.
The Journal of Physiology|January 16, 2025
Skin disease-associated GJB4 variants differentially influence connexin stability, cell viability and channel functionSergiu A Lucaciu, Stephanie E Leighton, Robert S Wong, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 13, 2026
Human pannexin mutations and their implications in erosive osteoarthritisJustin Tang, Jason Lu, Danielle Johnston, et al.
Biology|March 29, 2023
Discovery of <i>GJC1</i> (Cx45) as a New Gene Underlying Congenital Heart Disease and ArrhythmiasYan-Jie Li, Juan Wang, Willy G Ye, et al.
The New England Journal of Medicine|June 23, 2006
Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillationMichael H Gollob, Douglas L Jones, Andrew D Krahn, et al.
Development (Cambridge, England)|September 13, 2005
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasiaAnn M Flenniken, Lucy R Osborne, Nicole Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 23, 2025
ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over timeKezang C Tshering, Marina T DiStefano, Andrea M Oza, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
Frontiers in Cell and Developmental Biology|March 2, 2023
<i>GJB4</i> variants linked to skin disease exhibit a trafficking deficiency en route to gap junction formation that can be restored by co-expression of select connexinsSergiu A Lucaciu, Rhett Figliuzzi, Ruth Neumann, et al.
The Journal of Physiology|January 16, 2025
Skin disease-associated GJB4 variants differentially influence connexin stability, cell viability and channel functionSergiu A Lucaciu, Stephanie E Leighton, Robert S Wong, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 13, 2026
Human pannexin mutations and their implications in erosive osteoarthritisJustin Tang, Jason Lu, Danielle Johnston, et al.
Biology|March 29, 2023
Discovery of <i>GJC1</i> (Cx45) as a New Gene Underlying Congenital Heart Disease and ArrhythmiasYan-Jie Li, Juan Wang, Willy G Ye, et al.
The New England Journal of Medicine|June 23, 2006
Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillationMichael H Gollob, Douglas L Jones, Andrew D Krahn, et al.
Development (Cambridge, England)|September 13, 2005
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasiaAnn M Flenniken, Lucy R Osborne, Nicole Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 23, 2025
ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over timeKezang C Tshering, Marina T DiStefano, Andrea M Oza, et al.
Pageof 7