Showing results (521-530 of 704) with videos related to

Sort By:
Pageof 71
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
CFH and CFHR Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative GlomerulonephritisRossella Piras, Matteo Breno, Elisabetta Valoti, et al.
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.
Pageof 71