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Showing results (691-700 of 698) with videos related to

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Epilepsia|May 8, 2013
Exome sequencing reveals new causal mutations in children with epileptic encephalopathiesKrishna R Veeramah, Laurel Johnstone, Tatiana M Karafet, et al.
Frontiers in Physiology|October 30, 2024
Cancer and lymphatic marker FOXC2 drives wound healing and fibrotic tissue formationMaia B Granoski, Katharina S Fischer, William W Hahn, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2013
Tenascin-C is an innate broad-spectrum, HIV-1-neutralizing protein in breast milkGenevieve G Fouda, Frederick H Jaeger, Joshua D Amos, et al.
Journal of Medical Genetics|December 5, 2008
Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de LangeJ Yan, F Zhang, E Brundage, et al.
American Journal of Human Genetics|June 28, 2011
Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial cleftingIrfan Saadi, Fowzan S Alkuraya, Stephen S Gisselbrecht, et al.
Human Molecular Genetics|November 4, 2011
A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutationsRobert A Maue, Robert W Burgess, Bing Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome regionJonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, et al.
Cell Reports|December 28, 2017
Vaccine Induction of Heterologous Tier 2 HIV-1 Neutralizing Antibodies in Animal ModelsKevin O Saunders, Laurent K Verkoczy, Chuancang Jiang, et al.
Pageof 70

Showing results (691-700 of 698) with videos related to

Sort By:
Pageof 70
You have reached the last page of results.This site can display upto 698 results.
Epilepsia|May 8, 2013
Exome sequencing reveals new causal mutations in children with epileptic encephalopathiesKrishna R Veeramah, Laurel Johnstone, Tatiana M Karafet, et al.
Frontiers in Physiology|October 30, 2024
Cancer and lymphatic marker FOXC2 drives wound healing and fibrotic tissue formationMaia B Granoski, Katharina S Fischer, William W Hahn, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2013
Tenascin-C is an innate broad-spectrum, HIV-1-neutralizing protein in breast milkGenevieve G Fouda, Frederick H Jaeger, Joshua D Amos, et al.
Journal of Medical Genetics|December 5, 2008
Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de LangeJ Yan, F Zhang, E Brundage, et al.
American Journal of Human Genetics|June 28, 2011
Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial cleftingIrfan Saadi, Fowzan S Alkuraya, Stephen S Gisselbrecht, et al.
Human Molecular Genetics|November 4, 2011
A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutationsRobert A Maue, Robert W Burgess, Bing Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome regionJonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, et al.
Cell Reports|December 28, 2017
Vaccine Induction of Heterologous Tier 2 HIV-1 Neutralizing Antibodies in Animal ModelsKevin O Saunders, Laurent K Verkoczy, Chuancang Jiang, et al.
Pageof 70