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J H Smith

Showing results (401-410 of 588) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|March 7, 2015
USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptomsHideaki Moteki, Hidekane Yoshimura, Hela Azaiez, et al.
Plos Genetics|August 22, 2009
A claudin-9-based ion permeability barrier is essential for hearingYoko Nakano, Sung H Kim, Hyoung-Mi Kim, et al.
European Journal of Human Genetics : EJHG|July 22, 2010
Genetic male infertility and mutation of CATSPER ion channelsMichael S Hildebrand, Matthew R Avenarius, Marc Fellous, et al.
Journal of Nephrology|July 19, 2015
C3 glomerulonephritis and autoimmune disease: more than a fortuitous association?Mariam P Alexander, Fernando C Fervenza, An S De Vriese, et al.
Molecular Biology Reports|August 6, 2004
Refining the DFNB17 interval in consanguineous Indian familiesYingshi Guo, Valentina Pilipenko, Lynne H Y Lim, et al.
Science (New York, N.Y.)|July 20, 2002
Impaired B and T cell antigen receptor signaling in p110delta PI 3-kinase mutant miceKlaus Okkenhaug, Antonio Bilancio, Géraldine Farjot, et al.
Plos Genetics|November 11, 2011
Foxn1 regulates lineage progression in cortical and medullary thymic epithelial cells but is dispensable for medullary sublineage divergenceCraig S Nowell, Nicholas Bredenkamp, Stéphanie Tetélin, et al.
International Journal of Pediatric Otorhinolaryngology|December 17, 2011
Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing lossBehzad Davarnia, Mojgan Babanejad, Zohreh Fattahi, et al.
Blood|June 30, 2021
Functional characterization of 105 factor H variants associated with aHUS: lessons for variant classificationHector Martín Merinero, Yuzhou Zhang, Emilia Arjona, et al.
Frontiers in Genetics|July 2, 2021
<i>CFH</i> and <i>CFHR</i> Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative GlomerulonephritisRossella Piras, Matteo Breno, Elisabetta Valoti, et al.
Pageof 59

Showing results (401-410 of 588) with videos related to

Sort By:
Pageof 59
The Annals of Otology, Rhinology, and Laryngology|March 7, 2015
USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptomsHideaki Moteki, Hidekane Yoshimura, Hela Azaiez, et al.
Plos Genetics|August 22, 2009
A claudin-9-based ion permeability barrier is essential for hearingYoko Nakano, Sung H Kim, Hyoung-Mi Kim, et al.
European Journal of Human Genetics : EJHG|July 22, 2010
Genetic male infertility and mutation of CATSPER ion channelsMichael S Hildebrand, Matthew R Avenarius, Marc Fellous, et al.
Journal of Nephrology|July 19, 2015
C3 glomerulonephritis and autoimmune disease: more than a fortuitous association?Mariam P Alexander, Fernando C Fervenza, An S De Vriese, et al.
Molecular Biology Reports|August 6, 2004
Refining the DFNB17 interval in consanguineous Indian familiesYingshi Guo, Valentina Pilipenko, Lynne H Y Lim, et al.
Science (New York, N.Y.)|July 20, 2002
Impaired B and T cell antigen receptor signaling in p110delta PI 3-kinase mutant miceKlaus Okkenhaug, Antonio Bilancio, Géraldine Farjot, et al.
Plos Genetics|November 11, 2011
Foxn1 regulates lineage progression in cortical and medullary thymic epithelial cells but is dispensable for medullary sublineage divergenceCraig S Nowell, Nicholas Bredenkamp, Stéphanie Tetélin, et al.
International Journal of Pediatric Otorhinolaryngology|December 17, 2011
Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing lossBehzad Davarnia, Mojgan Babanejad, Zohreh Fattahi, et al.
Blood|June 30, 2021
Functional characterization of 105 factor H variants associated with aHUS: lessons for variant classificationHector Martín Merinero, Yuzhou Zhang, Emilia Arjona, et al.
Frontiers in Genetics|July 2, 2021
<i>CFH</i> and <i>CFHR</i> Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative GlomerulonephritisRossella Piras, Matteo Breno, Elisabetta Valoti, et al.
Pageof 59