Suchergebnisse - Shahzad, Mohsin

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

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Towards Automatic License Plate Detection von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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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