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Asmat Ullah

Showing results (101-110 of 192) with videos related to

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Klinische Padiatrie|May 10, 2021
Correction: Tay-Sachs Disease: Two Novel Rare HEXA Mutations from Pakistan and MoroccoFarah Bibi, Asmat Ullah, Thomas Bourinaris, et al.
Journal of Cellular and Molecular Medicine|February 18, 2020
Sanguinarine disrupts the colocalization and interaction of HIF-1α with tyrosine and serine phosphorylated-STAT3 in breast cancerQi Su, Jingjing Wang, Mengying Fan, et al.
Klinische Padiatrie|April 8, 2021
Tay-Sachs Disease: Two Novel Rare HEXA Mutations from Pakistan and MoroccoFarah Bibi, Asmat Ullah, Thomas Bourinaris, et al.
The Journal of Gene Medicine|September 27, 2023
Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmiaWarda Akbar, Asmat Ullah, Nighat Haider, et al.
Current Protein & Peptide Science|November 1, 2023
Biological Significance of EphB4 Expression in CancerAsmat Ullah, Anam Razzaq, Chuanzan Zhou, et al.
Medicina (Kaunas, Lithuania)|December 23, 2022
Exome Sequencing Revealed a Novel Splice Site Variant in the <i>CRB2</i> Gene Underlying Nephrotic SyndromeAnam Simaab, Jai Krishin, Sultan Rashid Alaradi, et al.
European Journal of Medical Genetics|August 15, 2018
A novel insertion and deletion mutation in the BHLHA9 underlies polydactyly and mesoaxial synostotic syndactyly with phalangeal reductionAsmat Ullah, Raja Hussain Ali, Ayesha Isani Majeed, et al.
Current Molecular Pharmacology|February 23, 2024
Sanguinarine Attenuates Lung Cancer Progression via Oxidative Stress-induced Cell ApoptosisAsmat Ullah, Anum Razzaq, Mohammad Y Alfaifi, et al.
Cureus|April 14, 2025
Beyond Routine Monitoring: A Comprehensive Review of Direct Oral Anticoagulants and the Role of Coagulation Profiles in Their ManagementJayalekshmi Jayakumar, Fiqe Khan, Meher Ayyazuddin, et al.
Reproduction in Domestic Animals = Zuchthygiene|March 18, 2023
Association of genotypes at rs438228855 in bovine SLC35A3 receptor gene of Pakistani cattle with the susceptibility to develop complex vertebral malformationAmbar Rafiq, Gul Zareen, Sana Akbar, et al.
Pageof 20

Showing results (101-110 of 192) with videos related to

Sort By:
Pageof 20
Klinische Padiatrie|May 10, 2021
Correction: Tay-Sachs Disease: Two Novel Rare HEXA Mutations from Pakistan and MoroccoFarah Bibi, Asmat Ullah, Thomas Bourinaris, et al.
Journal of Cellular and Molecular Medicine|February 18, 2020
Sanguinarine disrupts the colocalization and interaction of HIF-1α with tyrosine and serine phosphorylated-STAT3 in breast cancerQi Su, Jingjing Wang, Mengying Fan, et al.
Klinische Padiatrie|April 8, 2021
Tay-Sachs Disease: Two Novel Rare HEXA Mutations from Pakistan and MoroccoFarah Bibi, Asmat Ullah, Thomas Bourinaris, et al.
The Journal of Gene Medicine|September 27, 2023
Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmiaWarda Akbar, Asmat Ullah, Nighat Haider, et al.
Current Protein & Peptide Science|November 1, 2023
Biological Significance of EphB4 Expression in CancerAsmat Ullah, Anam Razzaq, Chuanzan Zhou, et al.
Medicina (Kaunas, Lithuania)|December 23, 2022
Exome Sequencing Revealed a Novel Splice Site Variant in the <i>CRB2</i> Gene Underlying Nephrotic SyndromeAnam Simaab, Jai Krishin, Sultan Rashid Alaradi, et al.
European Journal of Medical Genetics|August 15, 2018
A novel insertion and deletion mutation in the BHLHA9 underlies polydactyly and mesoaxial synostotic syndactyly with phalangeal reductionAsmat Ullah, Raja Hussain Ali, Ayesha Isani Majeed, et al.
Current Molecular Pharmacology|February 23, 2024
Sanguinarine Attenuates Lung Cancer Progression via Oxidative Stress-induced Cell ApoptosisAsmat Ullah, Anum Razzaq, Mohammad Y Alfaifi, et al.
Cureus|April 14, 2025
Beyond Routine Monitoring: A Comprehensive Review of Direct Oral Anticoagulants and the Role of Coagulation Profiles in Their ManagementJayalekshmi Jayakumar, Fiqe Khan, Meher Ayyazuddin, et al.
Reproduction in Domestic Animals = Zuchthygiene|March 18, 2023
Association of genotypes at rs438228855 in bovine SLC35A3 receptor gene of Pakistani cattle with the susceptibility to develop complex vertebral malformationAmbar Rafiq, Gul Zareen, Sana Akbar, et al.
Pageof 20