Søgeresultater - Muhammad Ansar
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Potassium and Humic Acid Synergistically Increase Salt Tolerance and Nutrient Uptake in Contrasting Wheat Genotypes through Ionic Homeostasis and Activation of Antioxidant Enzymes af Abbas, Ghulam, Rehman, Sadia, Siddiqui, Manzer H., Ali, Hayssam M., Farooq, Muhammad Ansar, Chen, Yinglong
Udgivet 2022Text -
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Comparative Genome-wide Analysis and Expression Profiling of Histone Acetyltransferase (HAT) Gene Family in Response to Hormonal Applications, Metal and Abiotic Stresses in Cotton af Imran, Muhammad, Shafiq, Sarfraz, Farooq, Muhammad Ansar, Naeem, Muhammad Kashif, Widemann, Emilie, Bakhsh, Ali, Jensen, Kevin B., Wang, Richard R.-C.
Udgivet 2019Text -
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Effect of Sulphur Application on Photosynthesis and Biomass Accumulation of Sesame Varieties under Rainfed Conditions af Muhammad Ali Raza, Ling Feng, Nasır Iqbal, Abdul Manaf, Muhammad Hayder Bin Khalid, Sana Rehman, Allah Wasaya, Muhammad Ansar, Masum Billah, Feng Yang, Wenyu Yang
Udgivet 2018Artigo -
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Sulphur application increases seed yield and oil content in sesame seeds under rainfed conditions af Muhammad Ali Raza, Ling Feng, Abdul Manaf, Allah Wasaya, Muhammad Ansar, Anwaar Hussain, Muhammad Hayder Bin Khalid, Nasır Iqbal, Zeng Jin Xi, Yuan Kai Chen, Jun Xu Chen, Feng Yang, Wenyu Yang
Udgivet 2018Artigo -
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Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance af Khurram Liaqat, Isabelle Schrauwen, Syed Irfan Raza, Kwanghyuk Lee, Shabir Hussain, Imen Chakchouk, Abdul Nasır, Anushree Acharya, Izoduwa Abbe, Muhammad Umair, Muhammad Ansar, Irfan Ullah, Khadim Shah, Michael J. Bamshad, Deborah A. Nickerson, Wasim Ahmad, Suzanne M. Leal
Udgivet 2018Artigo -
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A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family af Muzammil Ahmad Khan, Verena Rupp, Meritxell Orpinell, Muhammad Sajid Hussain, Janine Altmüller, Michel O. Steinmetz, Christian Enzinger, Hölger Thiele, Wolfgang Höhne, Gudrun Nürnberg, Shahid Mahmood Baig, Muhammad Ansar, Peter Nürnberg, John B. Vincent, Michael R. Speicher, Pierre Gönczy, Christian Windpassinger
Udgivet 2014Artigo -
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A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort af Mukhtar Ullah, Atta Ur Rehman, Mathieu Quinodoz, Abdur Rashid, Francesca Cancellieri, Asad Munir, Karolina Kamińska, Afia Iqbal, Samra Javed, Muhammad Dawood, Hafiz Muhammad Azhar Baig, Shamim Saleha, Shagufta Naz, Humera Kausar, Ali Muhammad Waryah, Andrea Superti‐Furga, Muhammad Ansar, Carlo Rivolta
Udgivet 2025Artigo -
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WDR62 is associated with the spindle pole and is mutated in human microcephaly af Adeline K. Nicholas, Maryam Khurshid, Julie Désir, Ofélia P. Carvalho, James J. Cox, Gemma Thornton, Rizwana Kausar, Muhammad Ansar, Wasim Ahmad, Alain Verloès, Sandrine Passemard, Jean-Paul Misson, Susan Lindsay, Fanni Gergely, William B. Dobyns, Emma Roberts, Marc Abramowicz, C. Geoffrey Woods
Udgivet 2010Artigo -
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Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74 af Zubair M. Ahmed, Rizwan Yousaf, Byung Cheon Lee, Shaheen N. Khan, Sue Lee, Kwanghyuk Lee, Tayyab Husnain, Atteeq U. Rehman, Sarah Bonneux, Muhammad Ansar, Wasim Ahmad, Suzanne M. Leal, Vadim N. Gladyshev, Inna A. Belyantseva, Guy Van Camp, Sheikh Riazuddin, Thomas B. Friedman, Saima Riazuddin
Udgivet 2010Artigo -
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Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability af Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor, Shobbir Hussain, Joana V. Flores, Verena Rupp, Akshita K. Vincent, Roland Malli, Ghazanfar Ali, Falak Sher Khan, Gisele E. Ishak, Dan Doherty, Rosanna Weksberg, Muhammad Ayub, Christian Windpassinger, Shahnaz Ibrahim, Michaela Frye, Muhammad Ansar, John B. Vincent
Udgivet 2012Artigo -
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Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment af Margit Schraders, Kwanghyuk Lee, Jaap Oostrik, P.L.M. Huygen, Ghazanfar Ali, Lies H. Hoefsloot, Joris A. Veltman, Frans P.M. Cremers, Sulman Basit, Muhammad Ansar, Cor W. R. J. Cremers, Henricus P. M. Kunst, Wasim Ahmad, R.J.C. Admiraal, Suzanne M. Leal, Hannie Kremer
Udgivet 2010Artigo -
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Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish af Regie Lyn P. Santos‐Cortez, Kwanghyuk Lee, Arnaud P. J. Giese, Muhammad Ansar, Muhammad Aminuddin, K. Rehn, Xin Wang, Abdul Aziz, I. Chiu, Raja Hussain Ali, Joshua D. Smith, Jay Shendure, M. Bamshad, Deborah A. Nickerson, Zubair M. Ahmed, Wasim Ahmad, Saima Riazuddin, Suzanne M. Leal
Udgivet 2014Artigo -
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FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice af Isabelle Schrauwen, Arnaud P. J. Giese, Abdul Aziz, David Lafont, Imen Chakchouk, Regie Lyn P. Santos‐Cortez, Kwanghyuk Lee, Anushree Acharya, Falak Sher Khan, Asmat Ullah, Deborah A. Nickerson, Michael J. Bamshad, Ghazanfar Ali, Saima Riazuddin, Muhammad Ansar, Wasim Ahmad, Zubair M. Ahmed, Suzanne M. Leal
Udgivet 2018Artigo -
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Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency af Muhammad Ansar, Emmanuelle Ranza, Madhur Shetty, Sohail Aziz Paracha, Maleeha Azam, Ilse Kern, Justyna Iwaszkiewicz, Omer Farooq, Constantin J. Pournaras, Ariane Malclès, Mateusz Kecik, Carlo Rivolta, Waqar Muzaffar, Aziz Qurban, Liaqat Ali, Yacine Aggoun, Federico Santoni, Periklis Makrythanasis, Jawad Ahmed, Raheel Qamar, Muhammad Tahir Sarwar, L. Keith Henry, Stylianos E. Antonarakis
Udgivet 2019Artigo -
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Mutation of ATF6 causes autosomal recessive achromatopsia af Muhammad Ansar, Regie Lyn P. Santos‐Cortez, Muhammad Arif Nadeem Saqib, Fareeha Zulfiqar, Kwanghyuk Lee, Naeem Mahmood Ashraf, Ehsan Ullah, Xin Wang, Sundus Sajid, Falak Sher Khan, Muhammad Aminuddin, Joshua D. Smith, Jay Shendure, Michael J. Bamshad, Deborah A. Nickerson, Abdul Hameed, Saima Riazuddin, Zubair M. Ahmed, Wasim Ahmad, Suzanne M. Leal
Udgivet 2015Artigo -
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Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability af Rosalind Law, Tracy Dixon‐Salazar, Julie Jerber, Na Cai, Ansar Ahmed Abbasi, Maha S. Zaki, Kirti Mittal, Stacey Gabriel, Muhammad Rafiq, Valeed Khan, Maria Nguyen, Ghazanfar Ali, Brett Copeland, Eric Scott, Nasim Vasli, Anna Mikhailov, Muhammad Nasim Khan, Danielle M. Andrade, Muhammad Ayaz, Muhammad Ansar, Muhammad Ayub, John B. Vincent, Joseph G. Gleeson
Udgivet 2014Artigo -
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Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability af Muhammad Rafiq, Andreas W. Kuß, Lucia Puettmann, Abdul Noor, Annapoorani Ramiah, Ghazanfar Ali, Hao Hu, Nadir Ali Kerio, Yong Xiang, Masoud Garshasbi, Muzammil Ahmad Khan, Gisele E. Ishak, Rosanna Weksberg, Reinhard Ullmann, Andreas Tzschach, Kimia Kahrizi, Khalid Mahmood, Farooq Naeem, Muhammad Ayub, Kelley W. Moremen, John B. Vincent, Hans Hilger Ropers, Muhammad Ansar, Hossein Najmabadi
Udgivet 2011Artigo
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Biology
Gene
Genetics
Mutation
Medicine
Phenotype
Exome sequencing
Audiology
Hearing loss
Missense mutation
Disease gene identification
Exome
Allele
Internal medicine
Microcephaly
Anatomy
Candidate gene
Consanguinity
Endocrinology
Genetic heterogeneity
Locus (genetics)
Pedigree chart
Sanger sequencing
Agronomy
Biochemistry
Cell biology
Environmental health
Frameshift mutation
Genotype
Horticulture