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Photodiagnosis and Photodynamic Therapy
|
December 16, 2020
Cost effective and efficient screening of tuberculosis disease with Raman spectroscopy and machine learning algorithms
Rahat Ullah, Saranjam Khan, Iqra Ishtiaq Chaudhary, et al.
American Journal of Medical Genetics. Part A
|
May 26, 2021
An intrafamilial phenotypic variability in Ellis-Van Creveld syndrome due to a novel 27 bps deletion mutation
Ayesha Zaka, Shaheen Shahzad, Hadi Zahid Rao, et al.
Scientific Reports
|
May 2, 2026
Synergistic Effects of Laser-synthesized Silver Nanoparticles and Photosensitizers for enhanced Antibacterial and Anticancer activity
Saira Israr, Irfa Zafeer, Ifrah Shafqat, et al.
Journal of Biomolecular Structure & Dynamics
|
June 22, 2023
Structural and functional insights into a novel homozygous missense pathogenic variant in <i>CUL7</i> identified in consanguineous Pakistani family
Ayesha Zaka, Maha Yousaf, Shaheen Shahzad, et al.
Breast Cancer (Tokyo, Japan)
|
July 25, 2018
CDKN2A/P16INK4A variants association with breast cancer and their in-silico analysis
Ayesha Aftab, Shaheen Shahzad, Hafiz Muhammad Jafar Hussain, et al.
American Journal of Stem Cells
|
May 22, 2025
Investigating nanoparticle's utilization in stem cell therapy for neurological disorders
Sadia Aziz, Sundus Anbreen, Shaheen Shahzad, et al.
Applied Spectroscopy
|
July 18, 2017
Raman Spectroscopy Combined with Principal Component Analysis for Screening Nasopharyngeal Cancer in Human Blood Sera
Saranjam Khan, Rahat Ullah, Samina Javaid, et al.
Plos One
|
November 28, 2023
Characterization and applications of glutaminase free L-asparaginase from indigenous Bacillus halotolerans ASN9
Ifrah Shafqat, Shaheen Shahzad, Azra Yasmin, et al.
Journal of Biomolecular Structure & Dynamics
|
October 14, 2025
Novel Filamin genes variants implicated in skeletal dysplasias: integrated structural modeling and <i>in silico</i> functional characterization
Maha Yousaf, Ayesha Zaka, Shaheen Shahzad, et al.
European Journal of Dermatology : EJD
|
April 4, 2018
A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
Farooq Ahmad, Ishtaiq Ahmed, Abdul Nasir, et al.
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Search research articles
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Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Photodiagnosis and Photodynamic Therapy
|
December 16, 2020
Cost effective and efficient screening of tuberculosis disease with Raman spectroscopy and machine learning algorithms
Rahat Ullah, Saranjam Khan, Iqra Ishtiaq Chaudhary, et al.
American Journal of Medical Genetics. Part A
|
May 26, 2021
An intrafamilial phenotypic variability in Ellis-Van Creveld syndrome due to a novel 27 bps deletion mutation
Ayesha Zaka, Shaheen Shahzad, Hadi Zahid Rao, et al.
Scientific Reports
|
May 2, 2026
Synergistic Effects of Laser-synthesized Silver Nanoparticles and Photosensitizers for enhanced Antibacterial and Anticancer activity
Saira Israr, Irfa Zafeer, Ifrah Shafqat, et al.
Journal of Biomolecular Structure & Dynamics
|
June 22, 2023
Structural and functional insights into a novel homozygous missense pathogenic variant in <i>CUL7</i> identified in consanguineous Pakistani family
Ayesha Zaka, Maha Yousaf, Shaheen Shahzad, et al.
Breast Cancer (Tokyo, Japan)
|
July 25, 2018
CDKN2A/P16INK4A variants association with breast cancer and their in-silico analysis
Ayesha Aftab, Shaheen Shahzad, Hafiz Muhammad Jafar Hussain, et al.
American Journal of Stem Cells
|
May 22, 2025
Investigating nanoparticle's utilization in stem cell therapy for neurological disorders
Sadia Aziz, Sundus Anbreen, Shaheen Shahzad, et al.
Applied Spectroscopy
|
July 18, 2017
Raman Spectroscopy Combined with Principal Component Analysis for Screening Nasopharyngeal Cancer in Human Blood Sera
Saranjam Khan, Rahat Ullah, Samina Javaid, et al.
Plos One
|
November 28, 2023
Characterization and applications of glutaminase free L-asparaginase from indigenous Bacillus halotolerans ASN9
Ifrah Shafqat, Shaheen Shahzad, Azra Yasmin, et al.
Journal of Biomolecular Structure & Dynamics
|
October 14, 2025
Novel Filamin genes variants implicated in skeletal dysplasias: integrated structural modeling and <i>in silico</i> functional characterization
Maha Yousaf, Ayesha Zaka, Shaheen Shahzad, et al.
European Journal of Dermatology : EJD
|
April 4, 2018
A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
Farooq Ahmad, Ishtaiq Ahmed, Abdul Nasir, et al.
Page
of 3