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J H Smith

Showing results (481-490 of 588) with videos related to

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American Journal of Human Genetics|July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locusSadaf Naz, Chantal M Giguere, David C Kohrman, et al.
Plos One|March 9, 2017
Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approachDenise Yan, Guangxin Xiang, Xingping Chai, et al.
Molecular Immunology|April 7, 2015
Atypical aHUS: State of the artCarla M Nester, Thomas Barbour, Santiago Rodriquez de Cordoba, et al.
Developmental Cell|January 2, 2018
A Human IPS Model Implicates Embryonic B-Myeloid Fate Restriction as Developmental Susceptibility to B Acute Lymphoblastic Leukemia-Associated ETV6-RUNX1Charlotta Böiers, Simon E Richardson, Emma Laycock, et al.
Human Genetics|April 22, 2023
Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteomeMallory R Tollefson, Rose A Gogal, A Monique Weaver, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2008
A catechol-O-methyltransferase that is essential for auditory function in mice and humansXin Du, Martin Schwander, Eva Marie Y Moresco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37Kevin T Booth, James W Askew, Zohreh Talebizadeh, et al.
Frontiers in Immunology|May 27, 2022
Complement Factor I Variants in Complement-Mediated Renal DiseasesYuzhou Zhang, Renee X Goodfellow, Nicolo Ghiringhelli Borsa, et al.
Kidney International|December 20, 2016
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies ConferenceTimothy H J Goodship, H Terence Cook, Fadi Fakhouri, et al.
Nature|May 2, 2008
Angiogenesis selectively requires the p110alpha isoform of PI3K to control endothelial cell migrationMariona Graupera, Julie Guillermet-Guibert, Lazaros C Foukas, et al.
Pageof 59

Showing results (481-490 of 588) with videos related to

Sort By:
Pageof 59
American Journal of Human Genetics|July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locusSadaf Naz, Chantal M Giguere, David C Kohrman, et al.
Plos One|March 9, 2017
Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approachDenise Yan, Guangxin Xiang, Xingping Chai, et al.
Molecular Immunology|April 7, 2015
Atypical aHUS: State of the artCarla M Nester, Thomas Barbour, Santiago Rodriquez de Cordoba, et al.
Developmental Cell|January 2, 2018
A Human IPS Model Implicates Embryonic B-Myeloid Fate Restriction as Developmental Susceptibility to B Acute Lymphoblastic Leukemia-Associated ETV6-RUNX1Charlotta Böiers, Simon E Richardson, Emma Laycock, et al.
Human Genetics|April 22, 2023
Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteomeMallory R Tollefson, Rose A Gogal, A Monique Weaver, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2008
A catechol-O-methyltransferase that is essential for auditory function in mice and humansXin Du, Martin Schwander, Eva Marie Y Moresco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37Kevin T Booth, James W Askew, Zohreh Talebizadeh, et al.
Frontiers in Immunology|May 27, 2022
Complement Factor I Variants in Complement-Mediated Renal DiseasesYuzhou Zhang, Renee X Goodfellow, Nicolo Ghiringhelli Borsa, et al.
Kidney International|December 20, 2016
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies ConferenceTimothy H J Goodship, H Terence Cook, Fadi Fakhouri, et al.
Nature|May 2, 2008
Angiogenesis selectively requires the p110alpha isoform of PI3K to control endothelial cell migrationMariona Graupera, Julie Guillermet-Guibert, Lazaros C Foukas, et al.
Pageof 59