Search research articles
Contact Us
Filters
Showing results (881-890 of 968) with videos related to
Page
of 97
Sort By:
The Journal of Clinical Investigation
|
February 7, 2020
Exosomes mediate sensory hair cell protection in the inner ear
Andrew M Breglio, Lindsey A May, Melanie Barzik, et al.
Women'S Health Issues : Official Publication of the Jacobs Institute of Women'S Health
|
May 6, 2023
Neighborhood Socioeconomic Status, Green Space, and Walkability and Risk for Falls Among Postmenopausal Women: The Women's Health Initiative
Marilyn E Wende, Matthew C Lohman, Daniela B Friedman, et al.
Molecular Therapy. Methods & Clinical Development
|
September 11, 2023
Dual-AAV vector-mediated expression of <i>MYO7A</i> improves vestibular function in a mouse model of Usher syndrome 1B
Samantha C Lau, Mhamed Grati, Kevin Isgrig, 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 syndrome
N Liburd, M Ghosh, S Riazuddin, et al.
Breast Cancer Research : BCR
|
May 13, 2020
Insulin resistance contributes to racial disparities in breast cancer prognosis in US women
Emily J Gallagher, Kezhen Fei, Sheldon M Feldman, et al.
Current Biology : CB
|
January 5, 2021
Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin
Jamis McGrath, Chun-Yu Tung, Xiayi Liao, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
June 18, 2013
Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss
Mohsin Shahzad, Theru A Sivakumaran, Tanveer A Qaiser, et al.
Human Genetics
|
February 11, 2015
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss
Gowri Nayak, Lukas Varga, Claire Trincot, et al.
Frontiers in Aging
|
May 22, 2023
Highlighting the value of Alzheimer's disease-focused registries: lessons learned from cancer surveillance
Margaret C Miller, Rana Bayakly, Bernard G Schreurs, et al.
American Journal of Human Genetics
|
April 11, 2003
Mutations of MYO6 are associated with recessive deafness, DFNB37
Zubair M Ahmed, Robert J Morell, Saima Riazuddin, et al.
Page
of 97
Search research articles
Search
Showing results (881-890 of 968) with videos related to
Sort By:
Page
of 97
The Journal of Clinical Investigation
|
February 7, 2020
Exosomes mediate sensory hair cell protection in the inner ear
Andrew M Breglio, Lindsey A May, Melanie Barzik, et al.
Women'S Health Issues : Official Publication of the Jacobs Institute of Women'S Health
|
May 6, 2023
Neighborhood Socioeconomic Status, Green Space, and Walkability and Risk for Falls Among Postmenopausal Women: The Women's Health Initiative
Marilyn E Wende, Matthew C Lohman, Daniela B Friedman, et al.
Molecular Therapy. Methods & Clinical Development
|
September 11, 2023
Dual-AAV vector-mediated expression of <i>MYO7A</i> improves vestibular function in a mouse model of Usher syndrome 1B
Samantha C Lau, Mhamed Grati, Kevin Isgrig, 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 syndrome
N Liburd, M Ghosh, S Riazuddin, et al.
Breast Cancer Research : BCR
|
May 13, 2020
Insulin resistance contributes to racial disparities in breast cancer prognosis in US women
Emily J Gallagher, Kezhen Fei, Sheldon M Feldman, et al.
Current Biology : CB
|
January 5, 2021
Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin
Jamis McGrath, Chun-Yu Tung, Xiayi Liao, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
June 18, 2013
Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss
Mohsin Shahzad, Theru A Sivakumaran, Tanveer A Qaiser, et al.
Human Genetics
|
February 11, 2015
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss
Gowri Nayak, Lukas Varga, Claire Trincot, et al.
Frontiers in Aging
|
May 22, 2023
Highlighting the value of Alzheimer's disease-focused registries: lessons learned from cancer surveillance
Margaret C Miller, Rana Bayakly, Bernard G Schreurs, et al.
American Journal of Human Genetics
|
April 11, 2003
Mutations of MYO6 are associated with recessive deafness, DFNB37
Zubair M Ahmed, Robert J Morell, Saima Riazuddin, et al.
Page
of 97