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Muhammad Ismail Khan

Showing results (31-40 of 38) with videos related to

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Frontiers in Psychiatry|July 23, 2020
Highly Recurrent Copy Number Variations in <i>GABRB2</i> Associated With Schizophrenia and Premenstrual Dysphoric DisorderAta Ullah, Xi Long, Wai-Kin Mat, et al.
Nucleosides, Nucleotides & Nucleic Acids|February 6, 2024
Novel mutation in alpha-spectrin gene in Saudi patients with hereditary spherocytosisAhmad Alshomar, Ahmed A Ahmed, Zafar Rasheed, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 28, 2023
Effect of Cypermethrin on Blood Hematology and Biochemical Parameters in Fresh Water Fish Ctenopharyngodon idella (Grass Carp)Mujeeb Ullah, Ali Muhammad Yousafzai, Ijaz Muhammad, et al.
Immunological Investigations|July 11, 2020
Absence of CD74 Isoform at 41kDa Prevents the Heterotypic Associations between CD74 and CD44 in Human Lung Adenocarcinoma-derived CellsWaleed Al Abdulmonem, Zafar Rasheed, Abdullah S M Aljohani, et al.
American Journal of Medical Genetics. Part A|June 15, 2022
Whole exome sequencing identifies a novel compound heterozygous GFM1 variant underlying developmental delay, dystonia, polymicrogyria, and severe intellectual disability in a Pakhtun familyAtta Ullah Khan, Ibrar Khan, Muhammad Ismail Khan, et al.
Brain : a Journal of Neurology|April 11, 2019
A mutation in the major autophagy gene, WIPI2, associated with global developmental abnormalitiesMusharraf Jelani, Hannah C Dooley, Andrea Gubas, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|March 23, 2021
Clinical Characteristics, Mortality and Associated risk factors in COVID-19 patients reported in ten major hospitals of Khyber Pakhtunkhwa, PakistanZia UlHaq, Muhammad Shahzad, Maria Ishaq Khattak, et al.
Gene|November 13, 2023
Unveiling genetics of non-syndromic albinism using whole exome sequencing: A comprehensive study of TYR, TYRP1, OCA2 and MC1R genes in 17 familiesQaiser Zaman, Jamshid Khan, Mashal Ahmad, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Frontiers in Psychiatry|July 23, 2020
Highly Recurrent Copy Number Variations in <i>GABRB2</i> Associated With Schizophrenia and Premenstrual Dysphoric DisorderAta Ullah, Xi Long, Wai-Kin Mat, et al.
Nucleosides, Nucleotides & Nucleic Acids|February 6, 2024
Novel mutation in alpha-spectrin gene in Saudi patients with hereditary spherocytosisAhmad Alshomar, Ahmed A Ahmed, Zafar Rasheed, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 28, 2023
Effect of Cypermethrin on Blood Hematology and Biochemical Parameters in Fresh Water Fish Ctenopharyngodon idella (Grass Carp)Mujeeb Ullah, Ali Muhammad Yousafzai, Ijaz Muhammad, et al.
Immunological Investigations|July 11, 2020
Absence of CD74 Isoform at 41kDa Prevents the Heterotypic Associations between CD74 and CD44 in Human Lung Adenocarcinoma-derived CellsWaleed Al Abdulmonem, Zafar Rasheed, Abdullah S M Aljohani, et al.
American Journal of Medical Genetics. Part A|June 15, 2022
Whole exome sequencing identifies a novel compound heterozygous GFM1 variant underlying developmental delay, dystonia, polymicrogyria, and severe intellectual disability in a Pakhtun familyAtta Ullah Khan, Ibrar Khan, Muhammad Ismail Khan, et al.
Brain : a Journal of Neurology|April 11, 2019
A mutation in the major autophagy gene, WIPI2, associated with global developmental abnormalitiesMusharraf Jelani, Hannah C Dooley, Andrea Gubas, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|March 23, 2021
Clinical Characteristics, Mortality and Associated risk factors in COVID-19 patients reported in ten major hospitals of Khyber Pakhtunkhwa, PakistanZia UlHaq, Muhammad Shahzad, Maria Ishaq Khattak, et al.
Gene|November 13, 2023
Unveiling genetics of non-syndromic albinism using whole exome sequencing: A comprehensive study of TYR, TYRP1, OCA2 and MC1R genes in 17 familiesQaiser Zaman, Jamshid Khan, Mashal Ahmad, et al.
Pageof 4