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Asim Ali

Showing results (241-250 of 258) with videos related to

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JAMA Ophthalmology|December 21, 2023
Definition and Diagnostic Criteria for Pediatric BlepharokeratoconjunctivitisNallely R Morales-Mancillas, Fabiola Velazquez-Valenzuela, Shigeru Kinoshita, et al.
Clinical Genetics|October 18, 2020
Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and miceBeibei Zhang, Ihsan Khan, Chunyu Liu, et al.
American Journal of Human Genetics|July 8, 2022
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humansSuixing Fan, Yuying Jiao, Ranjha Khan, et al.
American Journal of Human Genetics|January 28, 2021
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humansSuixing Fan, Yuying Jiao, Ranjha Khan, et al.
Journal of the American College of Cardiology|September 2, 2025
Twice-A-Day CLOpidogrel vs Ticagrelor to Reduce Short-Term MACE after Primary PCI: The TADCLOT TrialAbdul Hakeem, Jehangir Ali Shah, Rajesh Kumar, et al.
American Heart Journal|April 14, 2025
Rationale and design of the TADCLOT trial: A double blind randomized controlled trial comparing twice a day clopidogrel vs ticagrelor in reducing major cardiac events in patients with acute STEMI undergoing primary percutaneous coronary interventionAbdul Hakeem, Jehangir Ali Shah, Rajesh Kumar, et al.
Scientific Reports|July 27, 2025
Pediatric gastrointestinal basidiobolomycosis: descriptive bicenteric retrospective studyNabil S Dhayhi, Alanoud Zaid Aljarbou, Abdulaziz H Alhazmi, et al.
Science Bulletin|February 3, 2023
A TOP6BL mutation abolishes meiotic DNA double-strand break formation and causes human infertilityYuying Jiao, Suixing Fan, Nazish Jabeen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Correction: A homozygous FANCM frameshift pathogenic variant causes male infertilityHao Yin, Hui Ma, Sajjad Hussain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2018
A homozygous FANCM frameshift pathogenic variant causes male infertilityHao Yin, Hui Ma, Sajjad Hussain, et al.
Pageof 26

Showing results (241-250 of 258) with videos related to

Sort By:
Pageof 26
JAMA Ophthalmology|December 21, 2023
Definition and Diagnostic Criteria for Pediatric BlepharokeratoconjunctivitisNallely R Morales-Mancillas, Fabiola Velazquez-Valenzuela, Shigeru Kinoshita, et al.
Clinical Genetics|October 18, 2020
Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and miceBeibei Zhang, Ihsan Khan, Chunyu Liu, et al.
American Journal of Human Genetics|July 8, 2022
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humansSuixing Fan, Yuying Jiao, Ranjha Khan, et al.
American Journal of Human Genetics|January 28, 2021
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humansSuixing Fan, Yuying Jiao, Ranjha Khan, et al.
Journal of the American College of Cardiology|September 2, 2025
Twice-A-Day CLOpidogrel vs Ticagrelor to Reduce Short-Term MACE after Primary PCI: The TADCLOT TrialAbdul Hakeem, Jehangir Ali Shah, Rajesh Kumar, et al.
American Heart Journal|April 14, 2025
Rationale and design of the TADCLOT trial: A double blind randomized controlled trial comparing twice a day clopidogrel vs ticagrelor in reducing major cardiac events in patients with acute STEMI undergoing primary percutaneous coronary interventionAbdul Hakeem, Jehangir Ali Shah, Rajesh Kumar, et al.
Scientific Reports|July 27, 2025
Pediatric gastrointestinal basidiobolomycosis: descriptive bicenteric retrospective studyNabil S Dhayhi, Alanoud Zaid Aljarbou, Abdulaziz H Alhazmi, et al.
Science Bulletin|February 3, 2023
A TOP6BL mutation abolishes meiotic DNA double-strand break formation and causes human infertilityYuying Jiao, Suixing Fan, Nazish Jabeen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Correction: A homozygous FANCM frameshift pathogenic variant causes male infertilityHao Yin, Hui Ma, Sajjad Hussain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2018
A homozygous FANCM frameshift pathogenic variant causes male infertilityHao Yin, Hui Ma, Sajjad Hussain, et al.
Pageof 26