Risultati della ricerca - Muhammad Ansar

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  1. 1
    Board diversity and financial statement comparability: evidence from China

    Board diversity and financial statement comparability: evidence from China di Ning, Ding, Irfan-Ullah, Majeed, Muhammad Ansar, Zeb, Aurang

    Pubblicazione 2022
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  2. 2
    Silicon-induced reversibility of cadmium toxicity in rice

    Silicon-induced reversibility of cadmium toxicity in rice di Farooq, Muhammad Ansar, Detterbeck, Amelie, Clemens, Stephan, Dietz, Karl-Josef

    Pubblicazione 2016
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  3. 3
    Potassium and Humic Acid Synergistically Increase Salt Tolerance and Nutrient Uptake in Contrasting Wheat Genotypes through Ionic Homeostasis and Activation of Antioxidant Enzymes

    Potassium and Humic Acid Synergistically Increase Salt Tolerance and Nutrient Uptake in Contrasting Wheat Genotypes through Ionic Homeostasis and Activation of Antioxidant Enzymes di Abbas, Ghulam, Rehman, Sadia, Siddiqui, Manzer H., Ali, Hayssam M., Farooq, Muhammad Ansar, Chen, Yinglong

    Pubblicazione 2022
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  4. 4
    Exogenous melatonin induces salt and drought stress tolerance in rice by promoting plant growth and defense system

    Exogenous melatonin induces salt and drought stress tolerance in rice by promoting plant growth and defense system di Zakirullah Khan, Rahmatullah Jan, Saleem Asif, Muhammad Ansar Farooq, Yoon‐Hee Jang, Eun‐Gyeong Kim, Nari Kim, Kyung‐Min Kim

    Pubblicazione 2024
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  5. 5
    Comparative Genome-wide Analysis and Expression Profiling of Histone Acetyltransferase (HAT) Gene Family in Response to Hormonal Applications, Metal and Abiotic Stresses in Cotton

    Comparative Genome-wide Analysis and Expression Profiling of Histone Acetyltransferase (HAT) Gene Family in Response to Hormonal Applications, Metal and Abiotic Stresses in Cotton di Imran, Muhammad, Shafiq, Sarfraz, Farooq, Muhammad Ansar, Naeem, Muhammad Kashif, Widemann, Emilie, Bakhsh, Ali, Jensen, Kevin B., Wang, Richard R.-C.

    Pubblicazione 2019
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  6. 6
    Effect of Sulphur Application on Photosynthesis and Biomass Accumulation of Sesame Varieties under Rainfed Conditions

    Effect of Sulphur Application on Photosynthesis and Biomass Accumulation of Sesame Varieties under Rainfed Conditions di 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

    Pubblicazione 2018
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  7. 7
    Sulphur application increases seed yield and oil content in sesame seeds under rainfed conditions

    Sulphur application increases seed yield and oil content in sesame seeds under rainfed conditions di 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

    Pubblicazione 2018
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  8. 8
    Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance

    Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance di 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

    Pubblicazione 2018
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  9. 9
    A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family

    A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family di 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

    Pubblicazione 2014
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  10. 10
    A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort

    A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort di 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

    Pubblicazione 2025
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  11. 11
    WDR62 is associated with the spindle pole and is mutated in human microcephaly

    WDR62 is associated with the spindle pole and is mutated in human microcephaly di 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

    Pubblicazione 2010
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  12. 12
    Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

    Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74 di 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

    Pubblicazione 2010
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  13. 13
    Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

    Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability di 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

    Pubblicazione 2012
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  14. 14
    Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

    Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment di 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

    Pubblicazione 2010
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  15. 15
    Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish

    Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish di 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

    Pubblicazione 2014
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  16. 16
    FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice

    FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice di 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

    Pubblicazione 2018
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  17. 17
    Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency

    Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency di 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

    Pubblicazione 2019
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  18. 18
    Mutation of ATF6 causes autosomal recessive achromatopsia

    Mutation of ATF6 causes autosomal recessive achromatopsia di 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

    Pubblicazione 2015
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  19. 19
    Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability

    Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability di 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

    Pubblicazione 2014
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  20. 20
    Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

    Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability di 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

    Pubblicazione 2011
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