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Sher Alam

Showing results (1-10 of 32) with videos related to

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Human Genome Variation|May 23, 2023
A novel frameshift variant in UBA2 causing split-hand/foot malformations in a Pakistani familyAsia Parveen, Muhammad Tariq, Sher Alam Khan, et al.
Chemical Communications (Cambridge, England)|April 11, 2008
Nanostructured microspheres of MnO2 formed by room temperature solution processingJonathan P Hill, Sher Alam, Katsuhiko Ariga, et al.
Journal of Nursing Management|April 14, 2025
Professional Quality of Life and Psychological Impact on Frontline Healthcare Worker during the Fourth Wave of COVID-19Hanif Ullah, Safia Arbab, Chang-Qing Liu, et al.
Frontiers in Plant Science|August 23, 2021
Effect of Pyrazosulfuron-Methyl on the Photosynthetic Characteristics and Antioxidant Systems of Foxtail MilletKe Ma, Weili Zhang, Liguang Zhang, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 14, 2008
Three-dimensional ultralarge-pore ia3d mesoporous silica with various pore diameters and their application in biomolecule immobilizationAjayan Vinu, Narasimhan Gokulakrishnan, Veerappan V Balasubramanian, et al.
Journal of Nursing Management|July 25, 2025
Work-Related Stress, Professional Respect, and Psychological Counseling Among Nurses: A Cross-Sectional StudyHanif Ullah, Safia Arbab, Sher Alam Khan, et al.
Chemistry, an Asian Journal|February 24, 2011
Iron oxide nanoparticles embedded onto 3D mesochannels of KIT-6 with different pore diameters and their excellent magnetic propertiesSher Alam, Chokkalingam Anand, S M J Zaidi, et al.
Journal of Clinical Laboratory Analysis|December 8, 2021
Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous familyFozia Fozia, Khadim Shah, Rubina Nazli, et al.
Frontiers in Pediatrics|August 20, 2021
Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis BullosaFozia Fozia, Rubina Nazli, Nousheen Bibi, et al.
BMC Medical Genetics|April 14, 2017
A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani familyAnwar Kamal Khan, Noor Muhammad, Abdul Aziz, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Human Genome Variation|May 23, 2023
A novel frameshift variant in UBA2 causing split-hand/foot malformations in a Pakistani familyAsia Parveen, Muhammad Tariq, Sher Alam Khan, et al.
Chemical Communications (Cambridge, England)|April 11, 2008
Nanostructured microspheres of MnO2 formed by room temperature solution processingJonathan P Hill, Sher Alam, Katsuhiko Ariga, et al.
Journal of Nursing Management|April 14, 2025
Professional Quality of Life and Psychological Impact on Frontline Healthcare Worker during the Fourth Wave of COVID-19Hanif Ullah, Safia Arbab, Chang-Qing Liu, et al.
Frontiers in Plant Science|August 23, 2021
Effect of Pyrazosulfuron-Methyl on the Photosynthetic Characteristics and Antioxidant Systems of Foxtail MilletKe Ma, Weili Zhang, Liguang Zhang, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 14, 2008
Three-dimensional ultralarge-pore ia3d mesoporous silica with various pore diameters and their application in biomolecule immobilizationAjayan Vinu, Narasimhan Gokulakrishnan, Veerappan V Balasubramanian, et al.
Journal of Nursing Management|July 25, 2025
Work-Related Stress, Professional Respect, and Psychological Counseling Among Nurses: A Cross-Sectional StudyHanif Ullah, Safia Arbab, Sher Alam Khan, et al.
Chemistry, an Asian Journal|February 24, 2011
Iron oxide nanoparticles embedded onto 3D mesochannels of KIT-6 with different pore diameters and their excellent magnetic propertiesSher Alam, Chokkalingam Anand, S M J Zaidi, et al.
Journal of Clinical Laboratory Analysis|December 8, 2021
Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous familyFozia Fozia, Khadim Shah, Rubina Nazli, et al.
Frontiers in Pediatrics|August 20, 2021
Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis BullosaFozia Fozia, Rubina Nazli, Nousheen Bibi, et al.
BMC Medical Genetics|April 14, 2017
A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani familyAnwar Kamal Khan, Noor Muhammad, Abdul Aziz, et al.
Pageof 4