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Leslie B Gordon

Showing results (41-50 of 55) with videos related to

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The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|August 20, 2011
Age-dependent loss of MMP-3 in Hutchinson-Gilford progeria syndromeIngrid A Harten, Rima S Zahr, Joan M Lemire, et al.
Geroscience|June 25, 2022
Clonal hematopoiesis is not prevalent in Hutchinson-Gilford progeria syndromeMiriam Díez-Díez, Marta Amorós-Pérez, Jorge de la Barrera, et al.
Nature Medicine|March 12, 2021
A targeted antisense therapeutic approach for Hutchinson-Gilford progeria syndromeMichael R Erdos, Wayne A Cabral, Urraca L Tavarez, et al.
Med (New York, N.Y.)|July 1, 2026
AI-driven therapeutic antisense oligonucleotide for processing-deficient progeroid laminopathiesLin Lv, Chang Liu, Lidan Hu, et al.
Nature|April 26, 2003
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndromeMaria Eriksson, W Ted Brown, Leslie B Gordon, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 28, 2010
Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of agingMichelle Olive, Ingrid Harten, Richard Mitchell, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2006
Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson-Gilford progeria syndromeRenee Varga, Maria Eriksson, Michael R Erdos, et al.
Human Genetics|November 20, 2018
Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutationsDavor Lessel, Ayse Bilge Ozel, Susan E Campbell, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2016
Cardiac electrical defects in progeroid mice and Hutchinson-Gilford progeria syndrome patients with nuclear lamina alterationsJosé Rivera-Torres, Conrado J Calvo, Anna Llach, et al.
Medicine|March 18, 2008
Predictors of acquired lipodystrophy in juvenile-onset dermatomyositis and a gradient of severityApril Bingham, Gulnara Mamyrova, Kristina I Rother, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|August 20, 2011
Age-dependent loss of MMP-3 in Hutchinson-Gilford progeria syndromeIngrid A Harten, Rima S Zahr, Joan M Lemire, et al.
Geroscience|June 25, 2022
Clonal hematopoiesis is not prevalent in Hutchinson-Gilford progeria syndromeMiriam Díez-Díez, Marta Amorós-Pérez, Jorge de la Barrera, et al.
Nature Medicine|March 12, 2021
A targeted antisense therapeutic approach for Hutchinson-Gilford progeria syndromeMichael R Erdos, Wayne A Cabral, Urraca L Tavarez, et al.
Med (New York, N.Y.)|July 1, 2026
AI-driven therapeutic antisense oligonucleotide for processing-deficient progeroid laminopathiesLin Lv, Chang Liu, Lidan Hu, et al.
Nature|April 26, 2003
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndromeMaria Eriksson, W Ted Brown, Leslie B Gordon, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 28, 2010
Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of agingMichelle Olive, Ingrid Harten, Richard Mitchell, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2006
Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson-Gilford progeria syndromeRenee Varga, Maria Eriksson, Michael R Erdos, et al.
Human Genetics|November 20, 2018
Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutationsDavor Lessel, Ayse Bilge Ozel, Susan E Campbell, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2016
Cardiac electrical defects in progeroid mice and Hutchinson-Gilford progeria syndrome patients with nuclear lamina alterationsJosé Rivera-Torres, Conrado J Calvo, Anna Llach, et al.
Medicine|March 18, 2008
Predictors of acquired lipodystrophy in juvenile-onset dermatomyositis and a gradient of severityApril Bingham, Gulnara Mamyrova, Kristina I Rother, et al.
Pageof 6