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Muhammad Ansar

Showing results (51-60 of 191) with videos related to

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The Journal of Investigative Dermatology|June 12, 2004
A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosisMuhammad Arshad Rafiq, Muhammad Ansar, Saqib Mahmood, et al.
Polymers|August 26, 2022
Rheological, Aging, and Microstructural Properties of Polycarbonate and Polytetrafluoroethylene Modified BitumenMuhammad Ansar, Muhammad Ali Sikandar, Fadi Althoey, et al.
BMC Plant Biology|March 13, 2023
Shattering and yield expression of sesame (Sesamum indicum L) genotypes influenced by paclobutrazol concentration under rainfed conditions of PothwarJahangir Ahmed, Ghulam Qadir, Muhammad Ansar, et al.
Clinical Imaging|October 26, 2024
Ultrasound shear wave elastography of the placenta: a potential tool for early detection of fetal growth restrictionMuhammad Ansar, Muhammad Arsam Ali, Noraiz Ali, et al.
Virology Journal|May 4, 2011
Inhibition of full length hepatitis C virus particles of 1a genotype through small interference RNAMuhammad Ansar, Usman Ali Ashfaq, Imran Shahid, et al.
Journal of Human Genetics|February 21, 2009
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3Muhammad Salman Chishti, Kwanghyuk Lee, Merry-Lynn McDonald, et al.
Scientific Reports|January 31, 2025
Long-term impact of different prevalent cropping systems on soil physico-chemical characteristics under subtropical climate conditions of Punjab, PakistanFahad Ali Fayyaz, Irfan Aziz, Muhammad Ansar, et al.
Genetics Research International|May 9, 2012
Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX GeneKwanghyuk Lee, Mohammad Amin Ud Din, Muhammad Ansar, et al.
Genes|July 30, 2016
Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from PakistanChristeen Ramane J Pedurupillay, Erlend Christoffer Sommer Landsend, Magnus Dehli Vigeland, et al.
Archives of Dermatological Research|June 14, 2006
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi originsPeter John, Muhammad Tariq, Muhammad Arshad Rafiq, et al.
Pageof 20

Showing results (51-60 of 191) with videos related to

Sort By:
Pageof 20
The Journal of Investigative Dermatology|June 12, 2004
A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosisMuhammad Arshad Rafiq, Muhammad Ansar, Saqib Mahmood, et al.
Polymers|August 26, 2022
Rheological, Aging, and Microstructural Properties of Polycarbonate and Polytetrafluoroethylene Modified BitumenMuhammad Ansar, Muhammad Ali Sikandar, Fadi Althoey, et al.
BMC Plant Biology|March 13, 2023
Shattering and yield expression of sesame (Sesamum indicum L) genotypes influenced by paclobutrazol concentration under rainfed conditions of PothwarJahangir Ahmed, Ghulam Qadir, Muhammad Ansar, et al.
Clinical Imaging|October 26, 2024
Ultrasound shear wave elastography of the placenta: a potential tool for early detection of fetal growth restrictionMuhammad Ansar, Muhammad Arsam Ali, Noraiz Ali, et al.
Virology Journal|May 4, 2011
Inhibition of full length hepatitis C virus particles of 1a genotype through small interference RNAMuhammad Ansar, Usman Ali Ashfaq, Imran Shahid, et al.
Journal of Human Genetics|February 21, 2009
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3Muhammad Salman Chishti, Kwanghyuk Lee, Merry-Lynn McDonald, et al.
Scientific Reports|January 31, 2025
Long-term impact of different prevalent cropping systems on soil physico-chemical characteristics under subtropical climate conditions of Punjab, PakistanFahad Ali Fayyaz, Irfan Aziz, Muhammad Ansar, et al.
Genetics Research International|May 9, 2012
Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX GeneKwanghyuk Lee, Mohammad Amin Ud Din, Muhammad Ansar, et al.
Genes|July 30, 2016
Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from PakistanChristeen Ramane J Pedurupillay, Erlend Christoffer Sommer Landsend, Magnus Dehli Vigeland, et al.
Archives of Dermatological Research|June 14, 2006
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi originsPeter John, Muhammad Tariq, Muhammad Arshad Rafiq, et al.
Pageof 20