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

Muhammad Amin

Showing results (341-350 of 352) with videos related to

Pageof 36
Sort By:
Human Molecular Genetics|February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafishRegie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.
BMC Microbiology|August 23, 2025
Metagenomic insights into host-specific gastroenteritis bacteria in forest rodents of Sarawak, Borneo: implications for one health surveillance of rodent-borne pathogensMuhammad Amin Iman Azmi, Julius William-Dee, Muhd Amsyari Morni, et al.
Molecular Vision|March 25, 2015
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani originZeinab Ravesh, Mohammed E El Asrag, Nicole Weisschuh, et al.
Advances in Therapy|June 14, 2024
APPaRENT 3: Asthma Patients' and Physicians' Perspectives on the Burden and Management of Asthma in Seven CountriesBhumika Aggarwal, Mohamed Al-Moamary, Riyad Allehebi, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
Scientific Reports|July 16, 2024
Post-discharge spirometry evaluation in patients recovering from moderate-to-critical COVID-19: a cross-sectional studyChee-Shee Chai, Muhammad Amin Bin Ibrahim, Nur Amira Binti Azhar, et al.
BMC Medical Genetics|June 25, 2015
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like FeaturesMuhammad Arshad Rafiq, Claire S Leblond, Muhammad Arif Nadeem Saqib, et al.
Bjpsych Open|July 10, 2023
Afghan mental health and psychosocial well-being: thematic review of four decades of research and interventionsQais Alemi, Catherine Panter-Brick, Spozhmay Oriya, et al.
Nature Communications|February 21, 2024
Structure-guided engineering of immunotherapies targeting TRBC1 and TRBC2 in T cell malignanciesMathieu Ferrari, Matteo Righi, Vania Baldan, et al.
Archives of Osteoporosis|April 2, 2024
Survey of awareness and attitudes to the management of fragility fractures among the membership of the Asia Pacific Orthopaedic AssociationJoon Kiong Lee, Paul James Mitchell, Seng Bin Ang, et al.
Pageof 36

Showing results (341-350 of 352) with videos related to

Sort By:
Pageof 36
Human Molecular Genetics|February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafishRegie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.
BMC Microbiology|August 23, 2025
Metagenomic insights into host-specific gastroenteritis bacteria in forest rodents of Sarawak, Borneo: implications for one health surveillance of rodent-borne pathogensMuhammad Amin Iman Azmi, Julius William-Dee, Muhd Amsyari Morni, et al.
Molecular Vision|March 25, 2015
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani originZeinab Ravesh, Mohammed E El Asrag, Nicole Weisschuh, et al.
Advances in Therapy|June 14, 2024
APPaRENT 3: Asthma Patients' and Physicians' Perspectives on the Burden and Management of Asthma in Seven CountriesBhumika Aggarwal, Mohamed Al-Moamary, Riyad Allehebi, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
Scientific Reports|July 16, 2024
Post-discharge spirometry evaluation in patients recovering from moderate-to-critical COVID-19: a cross-sectional studyChee-Shee Chai, Muhammad Amin Bin Ibrahim, Nur Amira Binti Azhar, et al.
BMC Medical Genetics|June 25, 2015
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like FeaturesMuhammad Arshad Rafiq, Claire S Leblond, Muhammad Arif Nadeem Saqib, et al.
Bjpsych Open|July 10, 2023
Afghan mental health and psychosocial well-being: thematic review of four decades of research and interventionsQais Alemi, Catherine Panter-Brick, Spozhmay Oriya, et al.
Nature Communications|February 21, 2024
Structure-guided engineering of immunotherapies targeting TRBC1 and TRBC2 in T cell malignanciesMathieu Ferrari, Matteo Righi, Vania Baldan, et al.
Archives of Osteoporosis|April 2, 2024
Survey of awareness and attitudes to the management of fragility fractures among the membership of the Asia Pacific Orthopaedic AssociationJoon Kiong Lee, Paul James Mitchell, Seng Bin Ang, et al.
Pageof 36