Resultats de la cerca - Anwar, Saima

Drosophila GAGA factor polyglutamine domains exhibit prion-like behavior per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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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