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E Lin

Showing results (931-940 of 998) with videos related to

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Human & Experimental Toxicology|August 8, 2008
Iron-generated hydroxyl radicals kill retinal cells in vivo: effect of ferulic acidH M Chao, Y H Chen, J H Liu, et al.
American Journal of Human Genetics|January 10, 2006
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlationSeema R Lalani, Arsalan M Safiullah, Susan D Fernbach, et al.
Cell|October 20, 2020
SARS-CoV-2 Disrupts Splicing, Translation, and Protein Trafficking to Suppress Host DefensesAbhik K Banerjee, Mario R Blanco, Emily A Bruce, et al.
American Journal of Human Genetics|August 8, 2024
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germlineKatherine A Wood, R Spencer Tong, Marialetizia Motta, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Molecular aspects, clinical aspects and possible treatment modalities for Costello syndrome: Proceedings from the 1st International Costello Syndrome Research Symposium 2007Katherine A Rauen, Erin Hefner, Kristin Carrillo, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|October 23, 2025
Exploring Centiloid Robustness: Impact of Sample Size and Image Resolution on Centiloid Conversion AccuracyJiaxiuxiu Zhang, David N Soleimani-Meigooni, Robert Koeppe, et al.
American Journal of Medical Genetics. Part A|August 17, 2019
Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior yearsAngela E Lin, Siddharth K Prakash, Niels H Andersen, et al.
European Heart Journal|November 12, 2023
Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmiasArt Schuermans, Caitlyn Vlasschaert, Victor Nauffal, et al.
Nature Cardiovascular Research|August 28, 2024
Loss-of-function mutations in Dnmt3a and Tet2 lead to accelerated atherosclerosis and concordant macrophage phenotypesPhilipp J Rauch, Jayakrishnan Gopakumar, Alexander J Silver, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Clinical, pathological, and molecular analyses of cardiovascular abnormalities in Costello syndrome: a Ras/MAPK pathway syndromeAngela E Lin, Mark E Alexander, Steven D Colan, et al.
Pageof 100

Showing results (931-940 of 998) with videos related to

Sort By:
Pageof 100
Human & Experimental Toxicology|August 8, 2008
Iron-generated hydroxyl radicals kill retinal cells in vivo: effect of ferulic acidH M Chao, Y H Chen, J H Liu, et al.
American Journal of Human Genetics|January 10, 2006
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlationSeema R Lalani, Arsalan M Safiullah, Susan D Fernbach, et al.
Cell|October 20, 2020
SARS-CoV-2 Disrupts Splicing, Translation, and Protein Trafficking to Suppress Host DefensesAbhik K Banerjee, Mario R Blanco, Emily A Bruce, et al.
American Journal of Human Genetics|August 8, 2024
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germlineKatherine A Wood, R Spencer Tong, Marialetizia Motta, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Molecular aspects, clinical aspects and possible treatment modalities for Costello syndrome: Proceedings from the 1st International Costello Syndrome Research Symposium 2007Katherine A Rauen, Erin Hefner, Kristin Carrillo, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|October 23, 2025
Exploring Centiloid Robustness: Impact of Sample Size and Image Resolution on Centiloid Conversion AccuracyJiaxiuxiu Zhang, David N Soleimani-Meigooni, Robert Koeppe, et al.
American Journal of Medical Genetics. Part A|August 17, 2019
Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior yearsAngela E Lin, Siddharth K Prakash, Niels H Andersen, et al.
European Heart Journal|November 12, 2023
Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmiasArt Schuermans, Caitlyn Vlasschaert, Victor Nauffal, et al.
Nature Cardiovascular Research|August 28, 2024
Loss-of-function mutations in Dnmt3a and Tet2 lead to accelerated atherosclerosis and concordant macrophage phenotypesPhilipp J Rauch, Jayakrishnan Gopakumar, Alexander J Silver, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Clinical, pathological, and molecular analyses of cardiovascular abnormalities in Costello syndrome: a Ras/MAPK pathway syndromeAngela E Lin, Mark E Alexander, Steven D Colan, et al.
Pageof 100