Showing results (581-590 of 674) with videos related to

Sort By:
Pageof 68
Human Molecular Genetics|October 23, 2003
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Zubair M Ahmed, Saima Riazuddin, Jamil Ahmad, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 29, 1999
Dosimetry-based therapy in metastatic breast cancer patients using 90Y monoclonal antibody 170H.82 with autologous stem cell support and cyclosporin AC M Richman, S J DeNardo, R T O'Donnell, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 4, 2017
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Plos Genetics|October 8, 2011
A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler miceKiyoto Kurima, Ronna Hertzano, Oksana Gavrilova, et al.
Human Genetics|September 5, 2023
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueductIsabelle Roux, Cristina Fenollar-Ferrer, Hyun Jae Lee, et al.
Medical Physics|May 13, 2020
Characterization of an organic semiconductor diode for dosimetry in radiotherapyJessie A Posar, Jeremy Davis, Matthew J Large, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
The New England Journal of Medicine|April 15, 2005
Modification of human hearing loss by plasma-membrane calcium pump PMCA2Julie M Schultz, Yandan Yang, Ariel J Caride, et al.
Pageof 68