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J H Smith

Showing results (411-420 of 588) with videos related to

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Hearing Research|March 31, 2004
Characterisation of DRASIC in the mouse inner earMichael S Hildebrand, Michelle G de Silva, Tuomas Klockars, et al.
Japanese Journal of Pharmacology|February 28, 2002
Effect of protease-activated receptor-2 deficiency on allergic dermatitis in the mouse earJunichi Kawagoe, Toshiaki Takizawa, Jiro Matsumoto, et al.
Human Genetics|October 23, 2009
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populationsIsabelle Schrauwen, Megan Ealy, Erik Fransen, et al.
Human Molecular Genetics|May 13, 2005
A mouse model of tuberous sclerosis 1 showing background specific early post-natal mortality and metastatic renal cell carcinomaCatherine Wilson, Shelley Idziaszczyk, Lee Parry, et al.
Hepatology (Baltimore, Md.)|November 30, 2006
Reg2 inactivation increases sensitivity to Fas hepatotoxicity and delays liver regeneration post-hepatectomy in miceHanh-Tu Lieu, Marie-Thérèse Simon, Thao Nguyen-Khoa, et al.
The Laryngoscope|November 4, 2010
A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing lossMichael S Hildebrand, Luke Gandolfo, A Eliot Shearer, et al.
Nature Reviews. Disease Primers|January 13, 2017
Congenital hearing lossAnna M H Korver, Richard J H Smith, Guy Van Camp, et al.
American Journal of Human Genetics|September 19, 2003
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)M Zhu, T Yang, S Wei, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in IranMojgan Babanejad, Zohreh Fattahi, Niloofar Bazazzadegan, et al.
Neuron|December 13, 2005
Neurofascins are required to establish axonal domains for saltatory conductionDiane L Sherman, Steven Tait, Shona Melrose, et al.
Pageof 59

Showing results (411-420 of 588) with videos related to

Sort By:
Pageof 59
Hearing Research|March 31, 2004
Characterisation of DRASIC in the mouse inner earMichael S Hildebrand, Michelle G de Silva, Tuomas Klockars, et al.
Japanese Journal of Pharmacology|February 28, 2002
Effect of protease-activated receptor-2 deficiency on allergic dermatitis in the mouse earJunichi Kawagoe, Toshiaki Takizawa, Jiro Matsumoto, et al.
Human Genetics|October 23, 2009
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populationsIsabelle Schrauwen, Megan Ealy, Erik Fransen, et al.
Human Molecular Genetics|May 13, 2005
A mouse model of tuberous sclerosis 1 showing background specific early post-natal mortality and metastatic renal cell carcinomaCatherine Wilson, Shelley Idziaszczyk, Lee Parry, et al.
Hepatology (Baltimore, Md.)|November 30, 2006
Reg2 inactivation increases sensitivity to Fas hepatotoxicity and delays liver regeneration post-hepatectomy in miceHanh-Tu Lieu, Marie-Thérèse Simon, Thao Nguyen-Khoa, et al.
The Laryngoscope|November 4, 2010
A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing lossMichael S Hildebrand, Luke Gandolfo, A Eliot Shearer, et al.
Nature Reviews. Disease Primers|January 13, 2017
Congenital hearing lossAnna M H Korver, Richard J H Smith, Guy Van Camp, et al.
American Journal of Human Genetics|September 19, 2003
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)M Zhu, T Yang, S Wei, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in IranMojgan Babanejad, Zohreh Fattahi, Niloofar Bazazzadegan, et al.
Neuron|December 13, 2005
Neurofascins are required to establish axonal domains for saltatory conductionDiane L Sherman, Steven Tait, Shona Melrose, et al.
Pageof 59