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The Australasian Journal of Dermatology|March 18, 2014
Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hairSabba Mehmood, Abid Jan, Dost Muhammad, et al.
Ecotoxicology and Environmental Safety|June 26, 2017
Role of Streptomyces pactum in phytoremediation of trace elements by Brassica juncea in mine polluted soilsAmjad Ali, Di Guo, Amanullah Mahar, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|November 28, 2025
Predisposition of an Intronic Duplication in CHEK2 Gene in the Cases of Breast Cancer from BalochistanAbdul Hameed Baloch, Jamila Shuja, Nasrullah Bangulzai, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|November 30, 2018
Prevalence of Epstein–Barr Virus Genotypes in Pakistani Lymphoma PatientsSadia Salahuddin, Jabbar Khan, Joharia Azhar, 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 familyFarooq Ahmad, Ishtaiq Ahmed, Abdul Nasir, et al.
International Journal of Phytoremediation|March 26, 2026
Elucidating the phytoremediation potential of aquatic macrophytes for Cd, Cr, and Pb under varying pH and salinityMaria Mussarat, Waqar Ahmad, Dost Muhammad, et al.
Computational and Mathematical Methods in Medicine|April 18, 2019
Bayesian Analysis of Three-Parameter Frechet Distribution with Medical ApplicationsKamran Abbas, Nosheen Yousaf Abbasi, Amjad Ali, et al.
Frontiers in Plant Science|September 23, 2022
Tandem application of endophytic fungus <i>Serendipita indica</i> and phosphorus synergistically recuperate arsenic induced stress in riceShafaque Sehar, Qidong Feng, Muhammad Faheem Adil, et al.
Ergonomics|September 8, 2024
A systems approach to managing the risk of healthcare acquired infection in an acute hospital setting supported by human factors ergonomics, data science, data governance and AIMarie E Ward, Una Geary, Rob Brennan, et al.
Human Genetics|July 16, 2011
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood groupGuntram Borck, Naseebullah Kakar, Jochen Hoch, et al.
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