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Safdar Abbas

Showing results (41-50 of 57) with videos related to

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Frontiers in Genetics|September 5, 2022
Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesiclesKhalid Al Hawsawi, Mazin Al Jabri, Mazen S Dajam, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|December 17, 2022
A novel homozygous truncating variant in PPFIBP1 further delineates PPFIBP1-associated neurodevelopmental disorderAhmed Waqas, Romana Liaqat, Sidrah Shaheen, et al.
JPMA. the Journal of the Pakistan Medical Association|December 20, 2019
Genetic study of Khyber-Pukhtunkhwa resident Pakistani families presenting primary microcephaly with intellectual disabilityJamshaid Ahmed, Christian Windpassinger, Muhammad Salim, et al.
Genetics and Molecular Biology|February 13, 2026
A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani familySana Fatima, Dong Sun, Jianguo Han, et al.
Neurogenetics|December 26, 2025
Mutation screening of the ASPM gene in multiple Pashtun origin MCPH families revealed the recurrent nonsense mutation p.Trp1326*: A step towards the development of a genetic diagnostic testHamna Batool Hashmi, Muhammad Muzammal, Aiman Saleem, et al.
Plos One|June 2, 2026
Synergistic interfacial engineering of mesoporous magnetic metal oxide TiO2 nanocomposites for sustainable visible-light photocatalysis: Experimental insights and ML-based performance predictionSafdar Abbas Kazmi, Muhammad Saqib Khan, Muhammad Bilal, et al.
Frontiers in Endocrinology|March 24, 2023
A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani familySafeer Ahmad, Muhammad Zeeshan Ali, Sumra Wajid Abbasi, et al.
Plos One|February 13, 2025
Prevalence and chemotherapy of Staphylococcus aureus mastitis in dairy cattleAsjad Umair Shah, Jawaria Ali Khan, Muhammad Avais, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2023
Basis for high-affinity ethylene binding by the ethylene receptor ETR1 of ArabidopsisBeenish J Azhar, Safdar Abbas, Sitwat Aman, et al.
Genetics and Molecular Biology|January 23, 2025
Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome)Majid Alfadhel, Bashayr S Alhubayshi, Muhammad Umair, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Frontiers in Genetics|September 5, 2022
Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesiclesKhalid Al Hawsawi, Mazin Al Jabri, Mazen S Dajam, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|December 17, 2022
A novel homozygous truncating variant in PPFIBP1 further delineates PPFIBP1-associated neurodevelopmental disorderAhmed Waqas, Romana Liaqat, Sidrah Shaheen, et al.
JPMA. the Journal of the Pakistan Medical Association|December 20, 2019
Genetic study of Khyber-Pukhtunkhwa resident Pakistani families presenting primary microcephaly with intellectual disabilityJamshaid Ahmed, Christian Windpassinger, Muhammad Salim, et al.
Genetics and Molecular Biology|February 13, 2026
A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani familySana Fatima, Dong Sun, Jianguo Han, et al.
Neurogenetics|December 26, 2025
Mutation screening of the ASPM gene in multiple Pashtun origin MCPH families revealed the recurrent nonsense mutation p.Trp1326*: A step towards the development of a genetic diagnostic testHamna Batool Hashmi, Muhammad Muzammal, Aiman Saleem, et al.
Plos One|June 2, 2026
Synergistic interfacial engineering of mesoporous magnetic metal oxide TiO2 nanocomposites for sustainable visible-light photocatalysis: Experimental insights and ML-based performance predictionSafdar Abbas Kazmi, Muhammad Saqib Khan, Muhammad Bilal, et al.
Frontiers in Endocrinology|March 24, 2023
A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani familySafeer Ahmad, Muhammad Zeeshan Ali, Sumra Wajid Abbasi, et al.
Plos One|February 13, 2025
Prevalence and chemotherapy of Staphylococcus aureus mastitis in dairy cattleAsjad Umair Shah, Jawaria Ali Khan, Muhammad Avais, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2023
Basis for high-affinity ethylene binding by the ethylene receptor ETR1 of ArabidopsisBeenish J Azhar, Safdar Abbas, Sitwat Aman, et al.
Genetics and Molecular Biology|January 23, 2025
Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome)Majid Alfadhel, Bashayr S Alhubayshi, Muhammad Umair, et al.
Pageof 6