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Saima Riazuddin

Showing results (21-30 of 134) with videos related to

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American Journal of Medical Genetics. Part A|September 15, 2005
A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12Rehan Sadiq Shaikh, Khushnooda Ramzan, Sabiha Nazli, et al.
Molecular Genetics & Genomic Medicine|September 20, 2024
Identification of rare missense variants in the BSN gene co-segregating with chronic otitis media in a consanguineous Pakistani familyAyesha Yousaf, Sairah Yousaf, Asra S Shabbir, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 21, 2023
Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1FSehar Riaz, Saumil Sethna, Todd Duncan, et al.
Human Genetics|November 13, 2004
A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1Khushnooda Ramzan, Rehan S Shaikh, Jamil Ahmad, et al.
Journal of Human Genetics|March 17, 2009
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in PakistanisSaima Anwar, Saima Riazuddin, Zubair M Ahmed, et al.
Human Genetics|February 16, 2005
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1Jamil Ahmad, Shaheen N Khan, Shahid Y Khan, et al.
The International Journal of Biochemistry & Cell Biology|June 15, 2020
Retraction notice to "PP2ACα deficiency impairs early cortical development through inducing DNA damage in neuroprojenitor cells" [Int. J. Biochem. Cell Biol. 109C (2019) 40-58]Bo Liu, Lin Lin, Saima Riazuddin, et al.
Human Genetics|August 23, 2008
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndromeZubair M Ahmed, Saima Riazuddin, Sandar Aye, et al.
Disease Models & Mechanisms|August 19, 2025
MSRB3 antioxidant activity is necessary for inner ear cuticular plate structure and hair bundle integrityGowri Nayak, Elodie M Richard, Byung Cheon Lee, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2024
CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase patternArnaud P J Giese, Andrew Parker, Sakina Rehman, et al.
Pageof 14

Showing results (21-30 of 134) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part A|September 15, 2005
A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12Rehan Sadiq Shaikh, Khushnooda Ramzan, Sabiha Nazli, et al.
Molecular Genetics & Genomic Medicine|September 20, 2024
Identification of rare missense variants in the BSN gene co-segregating with chronic otitis media in a consanguineous Pakistani familyAyesha Yousaf, Sairah Yousaf, Asra S Shabbir, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 21, 2023
Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1FSehar Riaz, Saumil Sethna, Todd Duncan, et al.
Human Genetics|November 13, 2004
A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1Khushnooda Ramzan, Rehan S Shaikh, Jamil Ahmad, et al.
Journal of Human Genetics|March 17, 2009
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in PakistanisSaima Anwar, Saima Riazuddin, Zubair M Ahmed, et al.
Human Genetics|February 16, 2005
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1Jamil Ahmad, Shaheen N Khan, Shahid Y Khan, et al.
The International Journal of Biochemistry & Cell Biology|June 15, 2020
Retraction notice to "PP2ACα deficiency impairs early cortical development through inducing DNA damage in neuroprojenitor cells" [Int. J. Biochem. Cell Biol. 109C (2019) 40-58]Bo Liu, Lin Lin, Saima Riazuddin, et al.
Human Genetics|August 23, 2008
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndromeZubair M Ahmed, Saima Riazuddin, Sandar Aye, et al.
Disease Models & Mechanisms|August 19, 2025
MSRB3 antioxidant activity is necessary for inner ear cuticular plate structure and hair bundle integrityGowri Nayak, Elodie M Richard, Byung Cheon Lee, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2024
CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase patternArnaud P J Giese, Andrew Parker, Sakina Rehman, et al.
Pageof 14