Resultados de procura - Anwar, Saima

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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Novel approaches to circumvent the devastating effects of pests on sugarcane por 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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome por 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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin por 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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Mutations in CIB2, a calcium and integrin binding protein, cause Usher syndrome type 1J and nonsyndromic deafness DFNB48 por 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.

Ligazón do recurso Ligazón do recurso Ligazón do recurso