Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Griffith

Showing results (681-690 of 786) with videos related to

Pageof 79
Sort By:
Human Genetics|July 11, 2002
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICZubair M Ahmed, Tenesha N Smith, Saima Riazuddin, et al.
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hereditary hearing loss with thyroid abnormalitiesByung Yoon Choi, Julie Muskett, Kelly A King, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 22, 2022
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Chemistry of Materials : a Publication of the American Chemical Society|August 28, 2023
Rapid and Reversible Lithium Insertion in the Wadsley-Roth-Derived Phase NaNb<sub>13</sub>O<sub>33</sub>Ashlea R Patterson, Rodrigo Elizalde-Segovia, Kira E Wyckoff, et al.
Ear and Hearing|August 19, 2003
Recent advances in the understanding of syndromic forms of hearing lossThomas B Friedman, Julie M Schultz, Tamar Ben-Yosef, et al.
Journal of Synchrotron Radiation|September 3, 2021
Towards high spatial resolution tissue-equivalent dosimetry for microbeam radiation therapy using organic semiconductorsJessie A Posar, Matthew Large, Saree Alnaghy, et al.
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.
Pageof 79

Showing results (681-690 of 786) with videos related to

Sort By:
Pageof 79
Human Genetics|July 11, 2002
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICZubair M Ahmed, Tenesha N Smith, Saima Riazuddin, et al.
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hereditary hearing loss with thyroid abnormalitiesByung Yoon Choi, Julie Muskett, Kelly A King, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 22, 2022
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Chemistry of Materials : a Publication of the American Chemical Society|August 28, 2023
Rapid and Reversible Lithium Insertion in the Wadsley-Roth-Derived Phase NaNb<sub>13</sub>O<sub>33</sub>Ashlea R Patterson, Rodrigo Elizalde-Segovia, Kira E Wyckoff, et al.
Ear and Hearing|August 19, 2003
Recent advances in the understanding of syndromic forms of hearing lossThomas B Friedman, Julie M Schultz, Tamar Ben-Yosef, et al.
Journal of Synchrotron Radiation|September 3, 2021
Towards high spatial resolution tissue-equivalent dosimetry for microbeam radiation therapy using organic semiconductorsJessie A Posar, Matthew Large, Saree Alnaghy, et al.
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.
Pageof 79