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Journal of Child Neurology|October 8, 2009
Mutation analysis of the ASPM gene in 18 Pakistani families with autosomal recessive primary microcephalyRizwana Kousar, Hira Nawaz, Maryam Khurshid, et al.
Human Genetics|December 25, 2010
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2Sulman Basit, Kwanghyuk Lee, Rabia Habib, et al.
Current Pharmaceutical Design|July 1, 2025
Elucidating the Complex Etiology of Schizophrenia: Comprehensive Insights into the Therapeutic Roles of Natural Compounds and Pharmacological InterventionsMd Ali Mujtaba, Purushottam Gangane, Mohammed Kaleem, et al.
The Journal of Investigative Dermatology|January 29, 2005
A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1Muhammad Arshad Rafiq, Mohammad Faiyaz-Ul-Haque, Mohammad Amin Ud Din, et al.
Molecules (Basel, Switzerland)|January 21, 2023
An Attention towards the Prophylactic and Therapeutic Options of Phytochemicals for SARS-CoV-2: A Molecular InsightShoaib Shoaib, Mohammad Azam Ansari, Geetha Kandasamy, et al.
Frontiers in Pharmacology|May 3, 2021
Pharmacological Evaluation of Safoof-e-Pathar Phori- A Polyherbal Unani Formulation for UrolithiasisWasim Ahmad, Mohammad Ahmed Khan, Kamran Ashraf, et al.
Pharmaceuticals (Basel, Switzerland)|November 10, 2022
In Vitro, Molecular Docking and In Silico ADME/Tox Studies of Emodin and Chrysophanol against Human Colorectal and Cervical CarcinomaWasim Ahmad, Mohammad Azam Ansari, Abdulrhman Alsayari, et al.
Cancers|February 11, 2023
Prospective Epigenetic Actions of Organo-Sulfur Compounds against Cancer: Perspectives and Molecular MechanismsShoaib Shoaib, Mohammad Azam Ansari, Mohammed Ghazwani, et al.
Journal of Surgical Case Reports|March 18, 2024
Pseudoaneurysm of cystic artery stump after laparoscopic cholecystectomy managed successfully with branch hepatic artery embolization using jail techniqueKhizer Masroor Anns, Faheemullah Khan, Muhammad Aman, et al.
Genetic Testing and Molecular Biomarkers|August 9, 2020
Sequence Variants in the <i>WNT10B</i> and <i>TP63</i> Genes Underlying Isolated Split-Hand/Split-Foot MalformationMuhammad Bilal, Amir Hayat, Muhammad Umair, et al.
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