检索结果 - Anwar, Saima

Drosophila GAGA factor polyglutamine domains exhibit prion-like behavior 由 Tariq, Muhammad, Wegrzyn, Renee, Anwar, Saima, Bukau, Bernd, Paro, Renato

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Deciphering the impact of novel coronavirus pandemic on agricultural sustainability, food security, and socio-economic sectors—a review 由 Mumtaz, Mehvish, Hussain, Nazim, Baqar, Zulqarnain, Anwar, Saima, Bilal, Muhammad

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Genome-wide RNAi screen in Drosophila reveals Enok as a novel trithorax group regulator 由 Umer, Zain, Akhtar, Jawad, Khan, Muhammad Haider Farooq, Shaheen, Najma, Haseeb, Muhammad Abdul, Mazhar, Khalida, Mithani, Aziz, Anwar, Saima, Tariq, Muhammad

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Kinome-Wide RNAi Screen Uncovers Role of Ballchen in Maintenance of Gene Activation by Trithorax Group in Drosophila 由 Khan, Muhammad Haider Farooq, Akhtar, Jawad, Umer, Zain, Shaheen, Najma, Shaukat, Ammad, Munir, Muhammad Shahbaz, Mithani, Aziz, Anwar, Saima, Tariq, Muhammad

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Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome 由 Ahmed, Zubair M., Riazuddin, Saima, Aye, Sandar, Ali, Rana A., Venselaar, Hanka, Anwar, Saima, Belyantseva, Polina P., Qasim, Muhammad, Riazuddin, Sheikh, Friedman, Thomas B.

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Novel approaches to circumvent the devastating effects of pests on sugarcane 由 Qamar, Zahida, Nasir, Idrees Ahmad, Abouhaidar, Mounir G., Hefferon, Kathleen L., Rao, Abdul Qayyum, Latif, Ayesha, Ali, Qurban, Anwar, Saima, Rashid, Bushra, Shahid, Ahmad Ali

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Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome 由 Riazuddin, Saima, Anwar, Saima, Fischer, Martin, Ahmed, Zubair M., Khan, Shahid Y., Janssen, Audrey G.H., Zafar, Ahmad U., Scholl, Ute, Husnain, Tayyab, Belyantseva, Inna A., Friedman, Penelope L., Riazuddin, Sheikh, Friedman, Thomas B., Fahlke, Christoph

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MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin 由 Mašindová, Ivica, Šoltýsová, Andrea, Varga, Lukáš, Mátyás, Petra, Ficek, Andrej, Hučková, Miloslava, Sůrová, Martina, Šafka-Brožková, Dana, Anwar, Saima, Bene, Judit, Straka, Slavomír, Janicsek, Ingrid, Ahmed, Zubair M., Seeman, Pavel, Melegh, Béla, Profant, Milan, Klimeš, Iwar, Riazuddin, Saima, Kádasi, Ľudevít, Gašperíková, Daniela

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Mutations in CIB2, a calcium and integrin binding protein, cause Usher syndrome type 1J and nonsyndromic deafness DFNB48 由 Riazuddin, Saima, Belyantseva, Inna A., Giese, Arnaud, Lee, Kwanghyuk, Indzhykulian, Artur A., Nandamuri, Sri Pratima, Yousaf, Rizwan, Sinha, Ghanshyam P., Lee, Sue, Terrell, David, Hegde, Rashmi S., Ali, Rana A., Anwar, Saima, Andrade-Elizondo, Paula B., Sirmaci, Asli, Parise, Leslie V., Basit, Sulman, Wali, Abdul, Ayub, Muhammad, Ansar, Muhammad, Ahmad, Wasim, Khan, Shaheen N., Akram, Javed, Tekin, Mustafa, Riazuddin, Sheikh, Cook, Tiffany, Buschbeck, Elke K., Frolenkov, Gregory I., Leal, Suzanne M., Friedman, Thomas B., Ahmed, Zubair M.

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