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Muhammad Ansar

Showing results (71-80 of 191) with videos related to

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Ecotoxicology and Environmental Safety|November 15, 2025
Nitrogen-doped carbon quantum dots enhance rice seedlings growth and antioxidant defense system under arsenic stressAyesha Batool, Muhammad Ansar Farooq, Muhammad Mubashar Iqbal, et al.
Frontiers in Plant Science|October 27, 2022
Silicon-nanoparticles doped biochar is more effective than biochar for mitigation of arsenic and salinity stress in Quinoa: Insight to human health risk assessmentHameed Alsamadany, Hesham F Alharby, Hassan S Al-Zahrani, et al.
The Australasian Journal of Dermatology|March 18, 2014
Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hairSabba Mehmood, Abid Jan, Dost Muhammad, et al.
Frontiers in Plant Science|August 22, 2022
Comparative efficiency of silica gel, biochar, and plant growth promoting bacteria on Cr and Pb availability to <i>Solanum melongena</i> L. in contaminated soil irrigated with wastewaterUmm E Rabiya, Muhammad Ali, Muhammad Ansar Farooq, et al.
International Journal of Molecular Sciences|November 17, 2019
Comparative Genome-wide Analysis and Expression Profiling of Histone Acetyltransferase (HAT) Gene Family in Response to Hormonal Applications, Metal and Abiotic Stresses in CottonMuhammad Imran, Sarfraz Shafiq, Muhammad Ansar Farooq, et al.
Ophthalmic Research|April 24, 2023
A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA SplicingMukhtar Ullah, Atta Ur Rehman, Marc Folcher, et al.
The International Journal of Neuroscience|October 25, 2022
<i>KIF1A</i> novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IICSaima Ghafoor, Muhammad Arshad Rafiq, Syed Tahir Abbas Shah, et al.
Genes|April 23, 2022
Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani FamilyKhurram Liaqat, Shabir Hussain, Anushree Acharya, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from PakistanMuhammad Ansar, Mohammad Amin ud Din, Muhammad Arshad, et al.
Archives of Medical Research|May 14, 2011
A novel deletion mutation in proteoglycan-4 underlies camptodactyly-arthropathy-coxa-vara-pericarditis syndrome in a consanguineous pakistani familySulman Basit, Zafar Iqbal, Masha Umicevic-Mirkov, et al.
Pageof 20

Showing results (71-80 of 191) with videos related to

Sort By:
Pageof 20
Ecotoxicology and Environmental Safety|November 15, 2025
Nitrogen-doped carbon quantum dots enhance rice seedlings growth and antioxidant defense system under arsenic stressAyesha Batool, Muhammad Ansar Farooq, Muhammad Mubashar Iqbal, et al.
Frontiers in Plant Science|October 27, 2022
Silicon-nanoparticles doped biochar is more effective than biochar for mitigation of arsenic and salinity stress in Quinoa: Insight to human health risk assessmentHameed Alsamadany, Hesham F Alharby, Hassan S Al-Zahrani, et al.
The Australasian Journal of Dermatology|March 18, 2014
Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hairSabba Mehmood, Abid Jan, Dost Muhammad, et al.
Frontiers in Plant Science|August 22, 2022
Comparative efficiency of silica gel, biochar, and plant growth promoting bacteria on Cr and Pb availability to <i>Solanum melongena</i> L. in contaminated soil irrigated with wastewaterUmm E Rabiya, Muhammad Ali, Muhammad Ansar Farooq, et al.
International Journal of Molecular Sciences|November 17, 2019
Comparative Genome-wide Analysis and Expression Profiling of Histone Acetyltransferase (HAT) Gene Family in Response to Hormonal Applications, Metal and Abiotic Stresses in CottonMuhammad Imran, Sarfraz Shafiq, Muhammad Ansar Farooq, et al.
Ophthalmic Research|April 24, 2023
A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA SplicingMukhtar Ullah, Atta Ur Rehman, Marc Folcher, et al.
The International Journal of Neuroscience|October 25, 2022
<i>KIF1A</i> novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IICSaima Ghafoor, Muhammad Arshad Rafiq, Syed Tahir Abbas Shah, et al.
Genes|April 23, 2022
Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani FamilyKhurram Liaqat, Shabir Hussain, Anushree Acharya, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from PakistanMuhammad Ansar, Mohammad Amin ud Din, Muhammad Arshad, et al.
Archives of Medical Research|May 14, 2011
A novel deletion mutation in proteoglycan-4 underlies camptodactyly-arthropathy-coxa-vara-pericarditis syndrome in a consanguineous pakistani familySulman Basit, Zafar Iqbal, Masha Umicevic-Mirkov, et al.
Pageof 20