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

S Riazuddin

Showing results (41-50 of 60) with videos related to

Pageof 6
Sort By:
Osteoarthritis and Cartilage|October 4, 2016
Vitamin E protects rat mesenchymal stem cells against hydrogen peroxide-induced oxidative stress in vitro and improves their therapeutic potential in surgically-induced rat model of osteoarthritisF U Bhatti, A Mehmood, N Latief, et al.
Biotechnology Advances|June 22, 2019
RETRACTED: The myth of plant transformationAbdul Qayyum Rao, Allah Bakhsh, Sarfraz Kiani, et al.
Biotechnology Advances|June 11, 2009
The myth of plant transformationAbdul Qayyum Rao, Allah Bakhsh, Sarfraz Kiani, et al.
Molekuliarnaia Biologiia|October 17, 2008
[Identification and expression of six drought responsive transcripts through differential display in desi cottion (Gossypium aroreum)]A Maqbool, M Zahur, M Irfan, et al.
Human Genetics|December 6, 2001
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeN Liburd, M Ghosh, S Riazuddin, et al.
Cell|February 13, 2001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.
Journal of Medical Genetics|June 27, 2001
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessT Ben-Yosef, M Wattenhofer, S Riazuddin, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlationThomas B Friedman, John T Hinnant, Manju Ghosh, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Clinical Genetics|November 18, 2015
A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindredA M Waryah, M Shahzad, H Shaikh, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Osteoarthritis and Cartilage|October 4, 2016
Vitamin E protects rat mesenchymal stem cells against hydrogen peroxide-induced oxidative stress in vitro and improves their therapeutic potential in surgically-induced rat model of osteoarthritisF U Bhatti, A Mehmood, N Latief, et al.
Biotechnology Advances|June 22, 2019
RETRACTED: The myth of plant transformationAbdul Qayyum Rao, Allah Bakhsh, Sarfraz Kiani, et al.
Biotechnology Advances|June 11, 2009
The myth of plant transformationAbdul Qayyum Rao, Allah Bakhsh, Sarfraz Kiani, et al.
Molekuliarnaia Biologiia|October 17, 2008
[Identification and expression of six drought responsive transcripts through differential display in desi cottion (Gossypium aroreum)]A Maqbool, M Zahur, M Irfan, et al.
Human Genetics|December 6, 2001
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeN Liburd, M Ghosh, S Riazuddin, et al.
Cell|February 13, 2001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.
Journal of Medical Genetics|June 27, 2001
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessT Ben-Yosef, M Wattenhofer, S Riazuddin, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlationThomas B Friedman, John T Hinnant, Manju Ghosh, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Clinical Genetics|November 18, 2015
A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindredA M Waryah, M Shahzad, H Shaikh, et al.
Pageof 6