Showing results (441-450 of 704) with videos related to

Sort By:
Pageof 71
Current Biology : CB|January 25, 2006
Inactivation of NADPH oxidase organizer 1 results in severe imbalancePéter J Kiss, Judit Knisz, Yuzhou Zhang, et al.
Cell Reports|February 12, 2013
Tcf15 primes pluripotent cells for differentiationOwen R Davies, Chia-Yi Lin, Aliaksandra Radzisheuskaya, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 11, 2016
Characterization of C3 in C3 glomerulopathySanjeev Sethi, Julie A Vrana, Fernando C Fervenza, et al.
Hearing Research|May 3, 2011
Viral vector tropism for supporting cells in the developing murine cochleaAbraham M Sheffield, Samuel P Gubbels, Michael S Hildebrand, et al.
The Laryngoscope|December 10, 2020
Rigid Video Laryngoscopy for Intubation in Severe Pierre Robin Sequence: A Retrospective ReviewJoseph D Peterson, Michael D Puricelli, Ahmed Alkhateeb, et al.
BMJ Case Reports|June 21, 2011
Sensorineural deafness and male infertility: a contiguous gene deletion syndromeYuzhou Zhang, Mahdi Malekpour, Navid Al-Madani, et al.
American Journal of Human Genetics|April 7, 2009
Human male infertility caused by mutations in the CATSPER1 channel proteinMatthew R Avenarius, Michael S Hildebrand, Yuzhou Zhang, et al.
Auris, Nasus, Larynx|August 9, 2002
High-throughput screening for GJB2 mutations--its clinical application to genetic testing in prelingual deafness screening for GJB2 mutationsAkemi Sugata, Kunihiro Fukushima, Ken-ichi Sugata, et al.
Human Mutation|March 12, 2008
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BORAmit Kochhar, Dana J Orten, Jessica L Sorensen, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
Mutations in LOXHD1 gene cause various types and severities of hearing lossKentaro Mori, Hideaki Moteki, Yumiko Kobayashi, et al.
Pageof 71