Sökresultat - Shahzad, Mohsin

Modeling the enablers of online consumer engagement and platform preference in online food delivery platforms during COVID-19 av Habib, Aqib, Irfan, Muhammad, Shahzad, Mohsin

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Towards Automatic License Plate Detection av Mahmood, Zahid, Khan, Khurram, Khan, Uzair, Adil, Syed Hasan, Ali, Syed Saad Azhar, Shahzad, Mohsin

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Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss av Zafar, Saba, Shahzad, Mohsin, Ishaq, Rafaqat, Yousaf, Ayesha, Shaikh, Rehan S., Akram, Javed, Ahmed, Zubair M., Riazuddin, Saima

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In silico screening, SAR and kinetic studies of naturally occurring flavonoids against SARS CoV-2 main protease av Imran, Muhammad, Iqbal, Sana, Hussain, Ajaz, Uddin, Jalal, Shahzad, Mohsin, Khaliq, Tanwir, Razzaq Ahmed, Abdul, Mushtaq, Laiba, Kashif, Muhammad, Mahmood, Khalid

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A novel CHST3 allele associated with Spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred av Waryah, Ali M., Shahzad, Mohsin, Shaikh, Hina, Sheikh, Shakeel A., Channa, Naseem A., Hufnagel, Robert B., Makhdoom, Asadullah, Riazuddin, Saima, Ahmed, Zubair M.

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Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani population av Yousaf, Sairah, Shahzad, Mohsin, Tasleem, Kausar, Sheikh, Shakeel A., Tariq, Nabeela, Shabbir, Asra S., Ali, Muhammad, Waryah, Ali M., Shaikh, Rehan S., Riazuddin, Saima, Ahmed, Zubair M.

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Genome sequencing and analysis of genomic diversity in the locally transmitted SARS‐CoV‐2 in Pakistan av Shakeel, Muhammad, Irfan, Muhammad, Nisa, Zaib un, Farooq, Saba, Ain, Noor ul, Iqbal, Waseem, Kakar, Niamatullah, Jahan, Shah, Shahzad, Mohsin, Siddiqi, Saima, Khan, Ishtiaq Ahmad

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Molecular and Clinical Studies of X-linked Deafness Among Pakistani Families av Waryah, Ali M., Ahmed, Zubair M., Choo, Daniel I., Sisk, Robert A., Binder, Munir A., Shahzad, Mohsin, Khan, Shaheen N., Friedman, Thomas B., Riazuddin, Sheikh, Riazuddin, Saima

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DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3 av Khan, Shahid Yar, Riazuddin, Saima, Shahzad, Mohsin, Ahmed, Nazir, Zafar, Ahmad Usman, Rehman, Atteeq Ur, Morell, Robert J, Griffith, Andrew J, Ahmed, Zubair M, Riazuddin, Sheikh, Friedman, Thomas B

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Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79 av Rehman, Atteeq Ur, Morell, Robert J., Belyantseva, Inna A., Khan, Shahid Y., Boger, Erich T., Shahzad, Mohsin, Ahmed, Zubair M., Riazuddin, Saima, Khan, Shaheen N., Riazuddin, Sheikh, Friedman, Thomas B.

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Mutations in FYCO1 identified in families with congenital cataracts av Iqbal, Hira, Khan, Shahid Y., Zhou, Lin, Irum, Bushra, Ali, Muhammad, Ahmed, Mariya R., Shahzad, Mohsin, Ali, Muhammad Hassaan, Naeem, Muhammad Asif, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer

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Novel Loss-of-Function Mutations in COCH Cause Autosomal Recessive Nonsyndromic Hearing Loss av Booth, Kevin T, Ghaffar, Amama, Rashid, Muhammad, Hovey, Luke T, Hussain, Mureed, Frees, Kathy, Renkes, Erika M, Nishimura, Carla J, Shahzad, Mohsin, Smith, Richard J, Ahmed, Zubair, Azaiez, Hela, Riazuddin, Saima

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Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population av Shahzad, Mohsin, Yousaf, Sairah, Waryah, Yar M., Gul, Hadia, Kausar, Tasleem, Tariq, Nabeela, Mahmood, Umair, Ali, Muhammad, Khan, Muzammil A., Waryah, Ali M., Shaikh, Rehan S., Riazuddin, Saima, Ahmed, Zubair M.

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Genetic Causes of Oculocutaneous Albinism in Pakistani Population av Sajid, Zureesha, Yousaf, Sairah, Waryah, Yar M., Mughal, Tauqeer A., Kausar, Tasleem, Shahzad, Mohsin, Rao, Ali R., Abbasi, Ansar A., Shaikh, Rehan S., Waryah, Ali M., Riazuddin, Saima, Ahmed, Zubair M.

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Isolation of phytochemicals from Malva neglecta Wallr and their quantum chemical, molecular docking exploration as active drugs against COVID-19 av Irfan, Ahmad, Imran, Muhammad, Khalid, Noreen, Hussain, Riaz, Basra, Muhammad Asim Raza, Khaliq, Tanwir, Shahzad, Mohsin, Hussien, Mohamed, Shah, Asma Tufail, Qayyum, Muhammad Abdul, Al-Sehemi, Abdullah G., Assiri, Mohammed A.

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Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness av Tona, Risa, Lopez, Ivan A., Fenollar-Ferrer, Cristina, Faridi, Rabia, Anselmi, Claudio, Khan, Asma A., Shahzad, Mohsin, Morell, Robert J., Gu, Shoujun, Hoa, Michael, Dong, Lijin, Ishiyama, Akira, Belyantseva, Inna A., Riazuddin, Sheikh, Friedman, Thomas B.

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Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss av Nayak, Gowri, Varga, Lukas, Trincot, Claire, Shahzad, Mohsin, Friedman, Penelope L., Klimes, Iwar, Greinwald, John H., Riazuddin, S Amer, Masindova, Ivica, Profant, Milan, Khan, Shaheen N., Friedman, Thomas B., Ahmed, Zubair M., Gasperikova, Daniela, Riazuddin, Sheikh, Riazuddin, Saima

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Genetic Analysis through OtoSeq of Pakistani Families Segregating Prelingual Hearing Loss av Shahzad, Mohsin, Sivakumaran, Theru A, Qaiser, Tanveer A., Schultz, Julie M., Hussain, Zawar, Flanagan, Megan, Bhinder, Munir A., Kissell, Diane, Greinwald, John H, Khan, Shaheen N., Friedman, Thomas B., Zhang, Kejian, Riazuddin, Saima, Riazuddin, Sheikh, Ahmed, Zubair M.

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Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness av Rehman, Atteeq U., Bird, Jonathan E., Faridi, Rabia, Shahzad, Mohsin, Shah, Sujay, Lee, Kwanghyuk, Khan, Shaheen N., Imtiaz, Ayesha, Ahmed, Zubair M., Riazuddin, Saima, Santos-Cortez, Regie Lyn P., Ahmad, Wasim, Leal, Suzanne M., Riazuddin, Sheikh, Friedman, Thomas B.

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A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype av Iqbal, Zafar, Shahzad, Mohsin, Vissers, Lisenka E L M, van Scherpenzeel, Monique, Gilissen, Christian, Razzaq, Attia, Zahoor, Muhammad Yasir, Khan, Shaheen N, Kleefstra, Tjitske, Veltman, Joris A, de Brouwer, Arjan P M, Lefeber, Dirk J, van Bokhoven, Hans, Riazuddin, Sheikh

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