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Biorxiv : the Preprint Server for Biology|March 3, 2023
LRRC23 truncation impairs radial spoke 3 head assembly and sperm motility underlying male infertilityJae Yeon Hwang, Pengxin Chai, Shoaib Nawaz, et al.Elife|December 13, 2023
LRRC23 truncation impairs radial spoke 3 head assembly and sperm motility underlying male infertilityJae Yeon Hwang, Pengxin Chai, Shoaib Nawaz, et al.Genes|February 25, 2023
A Novel Homozygous Nonsense Variant in the <i>DYM</i> Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous FamilyAbu Bakar, Sulaiman Shams, Nousheen Bibi, et al.Molecular Syndromology|July 14, 2025
A Novel Variant in the Cyto-Tail of <i>SMO</i> Gene Underlying Isolated Postaxial PolydactylyMuhammad Javed Khan, Abdullah, Hammal Khan, et al.American Journal of Medical Genetics. Part A|August 30, 2016
Hypomorphic MKS1 mutation in a Pakistani family with mild Joubert syndrome and atypical features: Expanding the phenotypic spectrum of MKS1-related ciliopathies, Saadullah Khan, Imran Ullah, et al.Journal of Fungi (Basel, Switzerland)|February 25, 2023
Trichoderma-Mediated ZnO Nanoparticles and Their Antibiofilm and Antibacterial ActivitiesBalagangadharaswamy Shobha, Bagepalli Shivaram Ashwini, Mohammed Ghazwani, et al.American Journal of Medical Genetics|July 19, 2002
Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasiaMuhammad Faiyaz-Ul-Haque, Wasim Ahmad, Abdul Wahab, et al.Plants (Basel, Switzerland)|September 23, 2022
Antibacterial, Anticandidal, and Antibiofilm Potential of Fenchone: In Vitro, Molecular Docking and In Silico/ADMET StudyWasim Ahmad, Mohammad Azam Ansari, Mohammad Yusuf, et al.Journal of Fungi (Basel, Switzerland)|April 25, 2025
Correction: Shobha et al. Trichoderma-Mediated ZnO Nanoparticles and Their Antibiofilm and Antibacterial Activities. <i>J. Fungi</i> 2023, <i>9</i>, 133Balagangadharaswamy Shobha, Bagepalli Shivaram Ashwini, Mohammed Ghazwani, et al.Annals of Human Genetics|June 8, 2019
BBS5 and INPP5E mutations associated with ciliopathy disorders in families from PakistanShazia Khan, Siying Lin, Gaurav V Harlalka, et al.Pageof 34