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NARA Subscribed Scholarly Literature Discovery
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The role of CDHR3 in susceptibility to otitis mediaNARA Subscribed
Journal of Molecular Medicine · 2021 · Vol. 99 · Issue 11 · Springer
Scott D. Hirsch; Christina L. Elling; Tori C. Bootpetch; Melissa A. Scholes; Lena Hafrén; Sven-Olrik Streubel; Harold S. Pine; Todd M. Wine; Wasyl Szeremeta; Jeremy D. Prager; Elisabet Einarsdottir; Ayesha Yousaf; Erin E. Baschal; Sakina Rehman; Michael J. Bamshad; Deborah A. Nickerson; Saima Riazuddin; Suzanne M. Leal; Zubair M. Ahmed; Patricia J. Yoon; Juha Kere; Kenny H. Chan; Petri S. Mattila; Norman R. Friedman; Tasnee Chonmaitree; Daniel N. Frank; Allen F. Ryan; Regie Lyn P. Santos-Cortez
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A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomesNARA Subscribed
Human Genetics · 2021 · Vol. 140 · Issue 4 · Springer
Muhammad Ali; Shahid Y. Khan; Tony A. Rodrigues; Tânia Francisco; Xiaodong Jiao; Hang Qi; Firoz Kabir; Bushra Irum; Bushra Rauf; Asma A. Khan; Azra Mehmood; Muhammad Asif Naeem; Muhammad Zaman Assir; Muhammad Hassaan Ali; Mohsin Shahzad; Khaled K. Abu-Amero; Shehla Javed Akram; Javed Akram; Sheikh Riazuddin; Saima Riazuddin; Michael L. Robinson; Myriam Baes; Jorge E. Azevedo; J. Fielding Hejtmancik; S. Amer Riazuddin
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IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesisNARA Subscribed
Human Genetics · 2018 · Vol. 137 · Issue 6-7 · Springer
Anil Chekuri; Aditya A. Guru; Pooja Biswas; Kari Branham; Shyamanga Borooah; Angel Soto-Hermida; Michael Hicks; Naheed W. Khan; Hiroko Matsui; Akhila Alapati; Pongali B. Raghavendra; Susanne Roosing; Sripriya Sarangapani; Sinnakaruppan Mathavan; Amalio Telenti; John R. Heckenlively; S. Amer Riazuddin; Kelly A. Frazer; Paul A. Sieving; Radha Ayyagari
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Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing lossNARA Subscribed
Human Genetics · 2015 · Vol. 134 · Issue 4 · Springer
Gowri Nayak; Lukas Varga; Claire Trincot; Mohsin Shahzad; Penelope L. Friedman; Iwar Klimes; John H. Greinwald; S. Amer Riazuddin; Ivica Masindova; Milan Profant; Shaheen N. Khan; Thomas B. Friedman; Zubair M. Ahmed; Daniela Gasperikova; Sheikh Riazuddin; Saima Riazuddin
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New approaches to generate disease-resistant GladiolusNARA Subscribed
World Journal of Microbiology and Biotechnology · 2008 · Vol. 24 · Issue 3 · Springer
Idrees Ahmad Nasir; S. Riazuddin
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The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3NARA Subscribed
Human Genetics · 2007 · Vol. 122 · Issue 5 · Springer
Quratul Ain; Sabiha Nazli; Saima Riazuddin; Ateeq-ul Jaleel; S. Amer Riazuddin; Ahmad U. Zafar; Shaheen N. Khan; Tayyab Husnain; Andrew J. Griffith; Zubair M. Ahmed; Thomas B. Friedman; Sheikh Riazuddin
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Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 geneNARA Subscribed
Human Genetics · 2007 · Vol. 122 · Issue 3-4 · Springer
Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; S. Amer Riazuddin; Zahoor Ahmad; Raphael Caruso; Ian MacDonald; Paul Sieving; Sheikh Riazuddin; J. Fielding Hejtmancik
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Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3NARA Subscribed
Human Genetics · 2007 · Vol. 120 · Issue 6 · Springer
Shahid Y. Khan; Saima Riazuddin; Muhammad Tariq; Saima Anwar; Muhammad I. Shabbir; S. Amer Riazuddin; Shaheen N. Khan; Tayyab Husnain; Zubair M. Ahmed; Thomas B. Friedman; Sheikh Riazuddin
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Somatic embryogenesis in wild relatives of cotton (Gossypium Spp.)NARA Subscribed
Journal of Zhejiang University-SCIENCE B · 2006 · Vol. 7 · Issue 4 · Springer
Abdul Qayyum Rao; S. Sarfraz Hussain; M. Saqib Shahzad; S. Yassir Abbas Bokhari; M. Hashim Raza; Allah Rakha; A. Majeed; A. Ali Shahid; Zafar Saleem; Tayyab Husnain; S. Riazuddin
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Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3–p21.2 between D1S2896 and D1S457 but outside ABCA4NARA Subscribed
Human Genetics · 2005 · Vol. 118 · Issue 3-4 · Springer
Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; S. Amer Riazuddin; Radha Ayyagari; Farooq Sabar; Raphael Caruso; Paul A. Sieving; Sheikh Riazuddin; J. Fielding Hejtmancik
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A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1NARA Subscribed
Human Genetics · 2005 · Vol. 116 · Issue 1-2 · Springer
Khushnooda Ramzan; Rehan S. Shaikh; Jamil Ahmad; Shaheen N. Khan; Saima Riazuddin; Zubair M. Ahmed; Thomas B. Friedman; Edward R. Wilcox; Sheikh Riazuddin
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Variability in expression of insecticidal Cry1Ab gene in Indica Basmati riceNARA Subscribed
Euphytica · 2002 · Vol. 128 · Issue 1 · Springer
Tayyab Husnain; Jan Asad; Shahina B. Maqbool; Swapan K. Datta; S. Riazuddin
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Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICNARA Subscribed
Human Genetics · 2002 · Vol. 110 · Issue 6 · Springer
Zubair M. Ahmed; Tenesha N. Smith; Saima Riazuddin; Tomoko Makishima; Manju Ghosh; Sirosh Bokhari; Puthezhath S. Menon; Dilip Deshmukh; Andrew J. Griffith; Sheikh Riazuddin; Thomas B. Friedman; Edward R. Wilcox
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Mini-scale Genomic DNA Extraction from CottonNARA Subscribed
Plant Molecular Biology Reporter · 1999 · Vol. 17 · Issue 3 · Springer
Bushra Chaudhry; Afshan Yasmin; Tayyib Husnain; S. Riazuddin
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