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Saima Mohsin

Verified
United Kingdom
As seen in: Sky News Daily, CNN, CNN International, Nature, Sky News, MDPI, Arizona Daily Star, WCVB-TV (Boston, MA), WDIV-TV (Detroit, MI), KSAT-TV (San Antonio, TX), Courrier International and
Presenter @SkyNews | Kathy Gannon Legacy Award 2024 | Patron @PalaceForLife @cpfc | prev CNN International Correspondent | Hidden Disability |@saimamohsininsta
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Articles

Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource

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By Christopher Koch, Shruthi Bandyadka, Brian R Doyon, Daniel Denning, Muhammad Jahanzaib, Muhammad Mian, Muhammad Bilal Liaqat, Lubna Kamani, Nazish Butt, Anjum Jalal, Riffat Sultana, Shahid Abbas, Musfireh Siddiqeh, Muhammad Bilal, Asadullah Khan, Khalid Parvez Babar, Javed Iqbal, Umar Usman, Muhammad Bajwa, Ali Hyder, Muhammad Sadik Memon, Nauman Hashmani, Ambreen Muddassir, Mateen Akram, MUHAMMAD HUSSAIN, Saima Mohsin Verified, Tariq Mehmood, Shahid Mukhtar, Adil Mahmood, Sheraz Khan, Muhammad Khan, Noor ul Hadi, Roshina Anjum, Rehan Abdullah, Muhammad Usman Musharraf, Muhammad Bashir, Muhammad Shoaib Ali, Irfan Majeed, Shahzad Ali Khan, Ikuyo Kou, Wataru Morii, Katherine Smith, Kousik Kundu, Stewart MacArthur, Sebastian Wasilewski, Slavé Petrovski, Juan L Rodriguez-Flores, Moeen Riaz, Manav Kapoor, Joshua Backman, Alan R. Shuldiner, James E. Bradner, Asif Rasheed, John E. Dominy, Allan M Gurtan, Danish Saleheen, Wafa Gul, Aneeqa Bano, Marium Dahar, Namra Saqib, Aflak Rasheed, Faizan Aslam, Mohsin Iqbal Haroon, Samreen Bugti, Abdul Lateef Rodeni, Tahir Rasool, Muhammad Noor Wazir, Rahmat Ghaffar, Sanaullah Jan, Chihiro Hata, Makoto Asaumi, Kieren Lythgow, Igor Splawski
| Nature Verified
Abstract Naturally occurring loss-of-function variants in human genes enable drug target discovery because they mimic pharmacological inhibition of proteins. However, the study of these genetic variants is constrained by their rarity. Sequencing of diverse populations, particularly those enriched in familial relatedness, has been postulated to promote discovery of rare genetic variants1,2,3.
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Unraveling the physiological impact of ANGPTL8 loss-of-function variants in humans

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By Yan Chen, Kylia Williams, Eugene Y. Zhen, Hongxia Li, Thomas Beyer, Muhammad Jahanzaib, Muhammad Mian, Riffat Sultana, Anjum Jalal, Shahid Abbas, Saima Mohsin Verified, Shahid Mukhtar, Adil Mahmood, Timothy Ryan, Laura Michael, Giacomo Ruotolo, Danish Saleheen, Yi Wen, Robert Konrad, Pallav Bhatnagar, Arkan Abadi, Maryalice Hartley, Danisha DeBowles, Yue-Wei Qian, Asif Rahseed, Ambreen Muddassir
| Nature Verified
Abstract Angiopoietin-like 8 (ANGPTL8) is a calorically responsive regulator of lipoprotein lipase (LPL). It does this by forming complexes with ANGPTL3 or ANGPTL4 that either inhibit LPL in oxidative tissues or preserve LPL activity in adipose tissue, respectively. Human heterozygous (reference allele/alternate allele, R/A) carriers of rs145464906/p.Q121X and rs760351239/p.Q131X ANGPTL8 protein truncating variants (PTVs) have favorable lipid profiles and decreased cardiovascular risk.
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IJMS | Free Full-Text | Inhibiting Intracellular α2C-Adrenoceptor Surface Translocation Using Decoy Peptides: Identification of an Essential Role of the C-Terminus in Receptor Trafficking

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By Saima Mohsin Verified, Fasiha Saeed, Syed Ali, Aisha Raza
| MDPI
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
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