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Epilepsia
|
May 8, 2013
Exome sequencing reveals new causal mutations in children with epileptic encephalopathies
Krishna 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 formation
Maia 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 milk
Genevieve 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 Lange
J 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 clefting
Irfan 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 mutations
Robert 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 region
Jonathan 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 Models
Kevin O Saunders, Laurent K Verkoczy, Chuancang Jiang, et al.
Page
of 70
Search research articles
Search
Showing results (691-700 of 698) with videos related to
Sort By:
Page
of 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 encephalopathies
Krishna 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 formation
Maia 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 milk
Genevieve 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 Lange
J 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 clefting
Irfan 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 mutations
Robert 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 region
Jonathan 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 Models
Kevin O Saunders, Laurent K Verkoczy, Chuancang Jiang, et al.
Page
of 70