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Muhammad Ayub

Showing results (191-200 of 261) with videos related to

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Journal of Medicine and Life|December 4, 2024
A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosaMuhammad Ayub, Xing Xiong, Saima Anwer, et al.
Toxicology|March 24, 2018
The critical role of p16/Rb pathway in the inhibition of GH3 cell cycle induced by T-2 toxinZainab Fatima, Pu Guo, Deyu Huang, et al.
Journal of Autism and Developmental Disorders|March 7, 2026
Identifying Neurodevelopmental Domain Subgroups in Autism and ADHDAneta D Krakowski, Katherine Tombeau Cost, Marlee Vandewouw, et al.
Cognitive Behaviour Therapy|February 17, 2026
Effectiveness and outcomes of digital telehealth third-wave cognitive behavioral therapy for depression and anxiety: a systematic review and meta-analysisVanessa Ip, Santhija Jegatheeswaran, Aaima Akbar Cheema, et al.
International Journal of Environmental Research and Public Health|February 11, 2023
Groundwater Quality, Health Risk Assessment, and Source Distribution of Heavy Metals Contamination around Chromite Mines: Application of GIS, Sustainable Groundwater Management, Geostatistics, PCAMLR, and PMF Receptor ModelAbdur Rashid, Muhammad Ayub, Zahid Ullah, et al.
Human Genetics|May 8, 2008
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)Zahid Azeem, Musharraf Jelani, Gul Naz, et al.
JAMA Network Open|March 13, 2023
Identifying Replicable Subgroups in Neurodevelopmental Conditions Using Resting-State Functional Magnetic Resonance Imaging DataMarlee M Vandewouw, Jessica Brian, Jennifer Crosbie, et al.
Clinical and Experimental Dermatology|February 7, 2023
A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani familyXing Xiong, Syed Ashraf Uddin, Sobia Munir, et al.
Human Genetics|August 8, 2014
Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorderIltaf Ahmed, Kirti Mittal, Taimoor I Sheikh, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|February 18, 2021
The adaptation and feasibility of dialectical behaviour therapy for adults with intellectual developmental disabilities and transdiagnoses: A pilot community-based randomized controlled trialJessica Jones, Ashleigh Blinkhorn, Meg McQueen, et al.
Pageof 27

Showing results (191-200 of 261) with videos related to

Sort By:
Pageof 27
Journal of Medicine and Life|December 4, 2024
A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosaMuhammad Ayub, Xing Xiong, Saima Anwer, et al.
Toxicology|March 24, 2018
The critical role of p16/Rb pathway in the inhibition of GH3 cell cycle induced by T-2 toxinZainab Fatima, Pu Guo, Deyu Huang, et al.
Journal of Autism and Developmental Disorders|March 7, 2026
Identifying Neurodevelopmental Domain Subgroups in Autism and ADHDAneta D Krakowski, Katherine Tombeau Cost, Marlee Vandewouw, et al.
Cognitive Behaviour Therapy|February 17, 2026
Effectiveness and outcomes of digital telehealth third-wave cognitive behavioral therapy for depression and anxiety: a systematic review and meta-analysisVanessa Ip, Santhija Jegatheeswaran, Aaima Akbar Cheema, et al.
International Journal of Environmental Research and Public Health|February 11, 2023
Groundwater Quality, Health Risk Assessment, and Source Distribution of Heavy Metals Contamination around Chromite Mines: Application of GIS, Sustainable Groundwater Management, Geostatistics, PCAMLR, and PMF Receptor ModelAbdur Rashid, Muhammad Ayub, Zahid Ullah, et al.
Human Genetics|May 8, 2008
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)Zahid Azeem, Musharraf Jelani, Gul Naz, et al.
JAMA Network Open|March 13, 2023
Identifying Replicable Subgroups in Neurodevelopmental Conditions Using Resting-State Functional Magnetic Resonance Imaging DataMarlee M Vandewouw, Jessica Brian, Jennifer Crosbie, et al.
Clinical and Experimental Dermatology|February 7, 2023
A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani familyXing Xiong, Syed Ashraf Uddin, Sobia Munir, et al.
Human Genetics|August 8, 2014
Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorderIltaf Ahmed, Kirti Mittal, Taimoor I Sheikh, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|February 18, 2021
The adaptation and feasibility of dialectical behaviour therapy for adults with intellectual developmental disabilities and transdiagnoses: A pilot community-based randomized controlled trialJessica Jones, Ashleigh Blinkhorn, Meg McQueen, et al.
Pageof 27