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International Immunopharmacology|January 15, 2022
Commonly expressed key transcriptomic profiles of sepsis in the human circulation and brain via integrated analysisHuiyin Deng, Jiuyi Li, Abid Ali Shah, et al.
Molecular Biology Reports|April 25, 2024
Mutational spectrum of CFTR in cystic fibrosis patients with gastrointestinal and hepatobiliary manifestationsNadia Waheed, Rehmana Waris, Maryam Naseer, et al.
BMC Medical Genomics|January 5, 2021
A splice-site variant (c.3289-1G>T) in OTOF underlies profound hearing loss in a Pakistani kindredAshfaque Ahmed, Meng Wang, Rizwan Khan, et al.
Frontiers in Pediatrics|October 30, 2023
Truncated DNM1 variant underlines developmental delay and epileptic encephalopathyTayyaba Afsar, Xiaoyun Huang, Abid Ali Shah, et al.
Journal of Biomolecular Structure & Dynamics|July 12, 2023
Structural and dynamics insights into the GBA variants associated with Parkinson's diseaseArif Mahmood, Abdus Samad, Shazia Bano, et al.
Medicina (Kaunas, Lithuania)|February 25, 2023
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in <i>CYB5R3</i> Gene in Patients with MethemoglobinemiaAsmat Ullah, Abid Ali Shah, Fibhaa Syed, 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.
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