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Rafiullah Rafiullah

Showing results (1-10 of 14) with videos related to

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Human Molecular Genetics|February 17, 2017
Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalizationHenning Fröhlich, Rafiullah Rafiullah, Nathalie Schmitt, et al.
Pharmacotherapy|January 28, 2026
Association of Serotonin Transporter Gene 5HTTLPR rs25531 Polymorphism With Escitalopram Efficacy in Patients With Major Depressive DisorderMuhammad Faisal Afridi, Shahbaz Ahmad Zakki, Rafiullah Rafiullah, et al.
Endocrine|October 12, 2021
Controversy on the management of patients carrying RET p.V804M mutationAli S Alzahrani, Meshael Alswailem, Balgees Alghamdi, et al.
Experimental Oncology|October 8, 2025
IDENTIFICATION AND FUNCTIONAL CHARACTERIZATION OF MICRORNAS REGULATING HTERTMaham Ansari, Rafiullah Rafiullah, Abdul Wali, et al.
Journal of Neurogenetics|December 12, 2022
An expansion of phenotype: novel homozygous variant in the <i>MED17</i> identified in patients with progressive microcephaly and global developmental delayRafiullah Rafiullah, Alia M Albalawi, Sultan R Alaradi, et al.
Frontiers in Molecular Neuroscience|October 16, 2018
Sex Hormones Regulate <i>SHANK</i> ExpressionSimone Berkel, Ahmed Eltokhi, Henning Fröhlich, et al.
Journal of Medical Genetics|November 15, 2015
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani familyRafiullah Rafiullah, Muhammad Aslamkhan, Nagarajan Paramasivam, et al.
Medicina (Kaunas, Lithuania)|January 21, 2023
Identification and <i>In Silico</i> Analysis of a Homozygous Nonsense Variant in <i>TGM1</i> Gene Segregating with Congenital Ichthyosis in a Consanguineous FamilyAbdulhadi Almazroea, Ambreen Ijaz, Abdul Aziz, et al.
Journal of Human Genetics|June 17, 2016
Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disabilityKirti Mittal, Muhammad A Rafiq, Rafiullah Rafiullah, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activityRafiullah Rafiullah, Alyssa B Long, Anna A Ivanova, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|February 17, 2017
Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalizationHenning Fröhlich, Rafiullah Rafiullah, Nathalie Schmitt, et al.
Pharmacotherapy|January 28, 2026
Association of Serotonin Transporter Gene 5HTTLPR rs25531 Polymorphism With Escitalopram Efficacy in Patients With Major Depressive DisorderMuhammad Faisal Afridi, Shahbaz Ahmad Zakki, Rafiullah Rafiullah, et al.
Endocrine|October 12, 2021
Controversy on the management of patients carrying RET p.V804M mutationAli S Alzahrani, Meshael Alswailem, Balgees Alghamdi, et al.
Experimental Oncology|October 8, 2025
IDENTIFICATION AND FUNCTIONAL CHARACTERIZATION OF MICRORNAS REGULATING HTERTMaham Ansari, Rafiullah Rafiullah, Abdul Wali, et al.
Journal of Neurogenetics|December 12, 2022
An expansion of phenotype: novel homozygous variant in the <i>MED17</i> identified in patients with progressive microcephaly and global developmental delayRafiullah Rafiullah, Alia M Albalawi, Sultan R Alaradi, et al.
Frontiers in Molecular Neuroscience|October 16, 2018
Sex Hormones Regulate <i>SHANK</i> ExpressionSimone Berkel, Ahmed Eltokhi, Henning Fröhlich, et al.
Journal of Medical Genetics|November 15, 2015
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani familyRafiullah Rafiullah, Muhammad Aslamkhan, Nagarajan Paramasivam, et al.
Medicina (Kaunas, Lithuania)|January 21, 2023
Identification and <i>In Silico</i> Analysis of a Homozygous Nonsense Variant in <i>TGM1</i> Gene Segregating with Congenital Ichthyosis in a Consanguineous FamilyAbdulhadi Almazroea, Ambreen Ijaz, Abdul Aziz, et al.
Journal of Human Genetics|June 17, 2016
Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disabilityKirti Mittal, Muhammad A Rafiq, Rafiullah Rafiullah, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activityRafiullah Rafiullah, Alyssa B Long, Anna A Ivanova, et al.
Pageof 2