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Muhammad Ismail Khan

Showing results (11-20 of 38) with videos related to

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Scientifica|September 16, 2025
Fresh Record of Family Cyprinidae From River Kurram at Bannu, Khyber Pakhtunkhwa, Pakistan: A Statistical AnalysisAbdul Haseeb, Ali Muhammad Yousafzai, Latif Ahmad, et al.
Biological Trace Element Research|May 7, 2024
Comet Assay and Micronucleus Test in Circulating Erythrocytes of Ctenopharyngodon idella Exposed to Nickel Oxide NanoparticlesJamshid Khan, Nazish Shah, Farmanullah Dawar, et al.
Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders|April 14, 2011
Hydroxyl radical modification of immunoglobulin g generated cross-reactive antibodies: its potential role in systemic lupus erythematosusHani A Al-Shobaili, Ahmad A Al Robaee, Abdullateef Alzolibani, et al.
Scientific Reports|July 22, 2025
Anomaly detection in encrypted network traffic using self-supervised learningSadaf Sattar, Shumaila Khan, Muhammad Ismail Khan, et al.
Microbial Pathogenesis|November 6, 2025
Isolation and characterization of a potent bacteriophage KA targeting an antibiotic-resistant human pathogenic strain of Klebsiella pneumoniae KP1Aneela Nawaz, Nauman Ahmed Khalid, Sidra Zaheer, et al.
BMC Medical Genetics|December 14, 2019
Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10Amjad Khan, Rongrong Wang, Shirui Han, et al.
BMC Medical Genetics|October 31, 2019
Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10Amjad Khan, Rongrong Wang, Shirui Han, et al.
Disease Markers|August 18, 2011
Immunological functions of oxidized human immunoglobulin G in type 1diabetes mellitus: its potential role in diabetic smokers as a biomarker of elevated oxidative stressZafar Rasheed, Hani A Al-Shobaili, Abdullateef A Alzolibani, et al.
Human Genome Variation|December 10, 2020
Novel homozygous variant in the TPO gene associated with congenital hypothyroidism and mild-intellectual disabilityAmjad Khan, Muhammad Umair, Rania Abdulfattah Sharaf, et al.
The Journal of Gene Medicine|September 29, 2020
Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun familyMuhammad Ismail Khan, Muhammad Latif, Maria Saif, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Scientifica|September 16, 2025
Fresh Record of Family Cyprinidae From River Kurram at Bannu, Khyber Pakhtunkhwa, Pakistan: A Statistical AnalysisAbdul Haseeb, Ali Muhammad Yousafzai, Latif Ahmad, et al.
Biological Trace Element Research|May 7, 2024
Comet Assay and Micronucleus Test in Circulating Erythrocytes of Ctenopharyngodon idella Exposed to Nickel Oxide NanoparticlesJamshid Khan, Nazish Shah, Farmanullah Dawar, et al.
Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders|April 14, 2011
Hydroxyl radical modification of immunoglobulin g generated cross-reactive antibodies: its potential role in systemic lupus erythematosusHani A Al-Shobaili, Ahmad A Al Robaee, Abdullateef Alzolibani, et al.
Scientific Reports|July 22, 2025
Anomaly detection in encrypted network traffic using self-supervised learningSadaf Sattar, Shumaila Khan, Muhammad Ismail Khan, et al.
Microbial Pathogenesis|November 6, 2025
Isolation and characterization of a potent bacteriophage KA targeting an antibiotic-resistant human pathogenic strain of Klebsiella pneumoniae KP1Aneela Nawaz, Nauman Ahmed Khalid, Sidra Zaheer, et al.
BMC Medical Genetics|December 14, 2019
Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10Amjad Khan, Rongrong Wang, Shirui Han, et al.
BMC Medical Genetics|October 31, 2019
Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10Amjad Khan, Rongrong Wang, Shirui Han, et al.
Disease Markers|August 18, 2011
Immunological functions of oxidized human immunoglobulin G in type 1diabetes mellitus: its potential role in diabetic smokers as a biomarker of elevated oxidative stressZafar Rasheed, Hani A Al-Shobaili, Abdullateef A Alzolibani, et al.
Human Genome Variation|December 10, 2020
Novel homozygous variant in the TPO gene associated with congenital hypothyroidism and mild-intellectual disabilityAmjad Khan, Muhammad Umair, Rania Abdulfattah Sharaf, et al.
The Journal of Gene Medicine|September 29, 2020
Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun familyMuhammad Ismail Khan, Muhammad Latif, Maria Saif, et al.
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