Výsledky vyhledávání - S. Qasim Mehdi

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  1. 1
    Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database information

    Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database information Autor Qasim Ayub, Aisha Mohyuddin, Raheel Qamar, Kehkashan Mazhar, Tatiana Zerjal, S. Qasim Mehdi, Chris Tyler‐Smith

    Vydáno 2000
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  2. 2
    Induced Pluripotent Stem Cells: Next Generation Cells for Tissue Regeneration

    Induced Pluripotent Stem Cells: Next Generation Cells for Tissue Regeneration Autor Ayman Yousif Ibrahim, Mohammad Qasim Mehdi, Abbas Omar Abbas, Abdulrahman H. Alashkar, Kh.H. Haider

    Vydáno 2016
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  3. 3
    The Kalash Genetic Isolate: Ancient Divergence, Drift, and Selection

    The Kalash Genetic Isolate: Ancient Divergence, Drift, and Selection Autor Qasim Ayub, Massimo Mezzavilla, Luca Pagani, Marc Haber, Aisha Mohyuddin, Shagufta Khaliq, S. Qasim Mehdi, Chris Tyler‐Smith

    Vydáno 2015
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  4. 4
    Detection of Numerous Y Chromosome Biallelic Polymorphisms by Denaturing High-Performance Liquid Chromatography

    Detection of Numerous Y Chromosome Biallelic Polymorphisms by Denaturing High-Performance Liquid Chromatography Autor Peter A. Underhill, Jin Li, Alice Lin, S. Qasim Mehdi, Trefor Jenkins, Douglas Vollrath, Ronald W. Davis, L. Luca Cavalli-Sforza, Peter J. Oefner

    Vydáno 1997
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    Carta
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  5. 5
    Impact of Congenital Cardiac Catheterization Project on Outcomes-Quality Improvement (C3PO-QI) in LMICs

    Impact of Congenital Cardiac Catheterization Project on Outcomes-Quality Improvement (C3PO-QI) in LMICs Autor Ali, Fatima, Qasim Mehdi, Mohammad, Akhtar, Saleem, Aslam, Nadeem, Abbas, Rashid, Shah, Izat, Abidi, Jabbir, Arthur, Sajid, Nizar, Zeenat, Goodmann, Andrea, Bergersen, Lisa, Hasan, Babar

    Vydáno 2019
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  6. 6
    Geographically Separate Increases in the Frequency of the Derived ADH1B*47His Allele in Eastern and Western Asia

    Geographically Separate Increases in the Frequency of the Derived ADH1B*47His Allele in Eastern and Western Asia Autor Hui Li, Namita Mukherjee, Usha Soundararajan, Zsanett Tárnok, Csaba Barta, Shagufta Khaliq, Aisha Mohyuddin, Sylvester L.B. Kajuna, S. Qasim Mehdi, Judith R. Kidd, Kenneth K. Kídd

    Vydáno 2007
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  7. 7
    Ethiopian Genetic Diversity Reveals Linguistic Stratification and Complex Influences on the Ethiopian Gene Pool

    Ethiopian Genetic Diversity Reveals Linguistic Stratification and Complex Influences on the Ethiopian Gene Pool Autor Luca Pagani, Toomas Kivisild, Ayele Tarekegn, Rosemary Ekong, Chris Plaster, Irene Gallego Romero, Qasim Ayub, S. Qasim Mehdi, Mark Thomas, Donata Luiselli, Endashaw Bekele, Neil Bradman, David J. Balding, Chris Tyler‐Smith

    Vydáno 2012
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  8. 8
    ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous

    ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous Autor Lev Prasov, Tehmina Masud, Shagufta Khaliq, S. Qasim Mehdi, Aiysha Abid, Edward R. Oliver, Eduardo Silva, Amy Lewanda, Michael C. Brodsky, Mark Borchert, Daniel Kelberman, Jane C. Sowden, Mehul Dattani, Tom Glaser

    Vydáno 2012
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  9. 9
    Y-Chromosome Lineages Trace Diffusion of People and Languages in Southwestern Asia

    Y-Chromosome Lineages Trace Diffusion of People and Languages in Southwestern Asia Autor Lluı́s Quintana-Murci, Csilla Krausz, Tatiana Zerjal, S.Hamid Sayar, Michael F. Hammer, S. Qasim Mehdi, Qasim Ayub, Raheel Qamar, Aisha Mohyuddin, Uppala Radhakrishna, Mark A. Jobling, Chris Tyler‐Smith, Ken McElreavey

    Vydáno 2001
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  10. 10
    Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

    Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis Autor Melanie M. Sohocki, Sara J. Bowne, Lori S. Sullivan, Seth Blackshaw, Constance L. Cepko, Annette Payne, Shomi Bhattacharya, Shagufta Khaliq, S. Qasim Mehdi, David G. Birch, Wilbur R. Harrison, F.F.B. Elder, John R. Heckenlively, Stephen P. Daiger

    Vydáno 2000
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  11. 11
    Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asian Pastoralists

    Polarity and Temporality of High-Resolution Y-Chromosome Distributions in India Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence of Central Asia... Autor Sanghamitra Sengupta, Lev A. Zhivotovsky, Roy King, S. Qasim Mehdi, Christopher A. Edmonds, Cheryl‐Emiliane T. Chow, Alice Lin, Mitashree Mitra, Samir Kumar Sil, A. Ramesh, Monika Rani, Chitra Thakur, L. L. Cavalli‐Sforza, Partha P. Majumder, Peter A. Underhill

    Vydáno 2006
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  12. 12
    Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome

    Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome Autor Olga S. Koutsopoulos, Christine Kretz, Claudia M Weller, Aurélien Roux, Halina Mojzisova, Johann Böhm, Catherine Koch, Anne Toussaint, Émilie Heckel, Daphne Stemkens, Simone A. J. ter Horst, Christelle Thibault-Carpentier, Muriel Koch, S. Qasim Mehdi, Emilia K. Bijlsma, Jean‐Louis Mandel, Julien Vermot, Jocelyn Laporte

    Vydáno 2012
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  13. 13
    Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor

    Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor Autor Lluís Quintana‐Murci, Raphaëlle Chaix, R. Spencer Wells, Doron M. Behar, Hamid Sayar, Rosaria Scozzari, Chiara Rengo, Nadia Al-Zahery, Ornella Semino, A. Silvana Santachiara‐Benerecetti, Alfredo Coppa, Qasim Ayub, Aisha Mohyuddin, Chris Tyler‐Smith, S. Qasim Mehdi, Antonio Torroni, Ken McElreavey

    Vydáno 2004
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  14. 14
    Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor

    Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor Autor Quintana-Murci, Lluís, Chaix, Raphaëlle, Wells, R. Spencer, Behar, Doron M., Sayar, Hamid, Scozzari, Rosaria, Rengo, Chiara, Al-Zahery, Nadia, Semino, Ornella, Santachiara-Benerecetti, A. Silvana, Coppa, Alfredo, Ayub, Qasim, Mohyuddin, Aisha, Tyler-Smith, Chris, Qasim Mehdi, S., Torroni, Antonio, McElreavey, Ken

    Vydáno 2004
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  15. 15
    Refined Geographic Distribution of the Oriental <i>ALDH2*504Lys</i> (nee <i>487Lys</i>) Variant

    Refined Geographic Distribution of the Oriental <i>ALDH2*504Lys</i> (nee <i>487Lys</i>) Variant Autor Hui Li, S. A. Borinskaya, Kimio Yoshimura, N. R. Kal’ina, Andrey Marusin, В. А. Степанов, Zhendong Qin, Shagufta Khaliq, Mi‐Young Lee, Yajun Yang, Aisha Mohyuddin, David Gurwitz, S. Qasim Mehdi, Е. И. Рогаев, Jin Li, N. K. Yankovsky, Judith R. Kidd, Kenneth K. Kídd

    Vydáno 2009
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  16. 16
    Differential Structuring of Human Populations for Homologous X and Y Microsatellite Loci

    Differential Structuring of Human Populations for Homologous X and Y Microsatellite Loci Autor Rosaria Scozzari, Fulvio Cruciani, Patrizia Malaspina, P. Santolamazza, Bianca Maria Ciminelli, Antonio Torroni, David Modiano, Douglas C. Wallace, Kenneth K. Kídd, Antonel Olckers, Pedro Moral, L. Terrenato, Nejat Akar, Raheel Qamar, Atika Mansoor, S. Qasim Mehdi, Tullio Meloni, Giuseppe Vona, David E.C. Cole, Wangwei Cai, Andrea Novelletto

    Vydáno 1997
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  17. 17
    Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

    Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness Autor Hamish S. Scott, Jun Kudoh, Marie Wattenhofer‐Donzé, Kazunori Shibuya, Asher Berry, Roman Chrast, Michel Guipponi, Jun Wang, Kazuhiko Kawasaki, Shuichi Asakawa, Satoshi Minoshima, Farah Younus, S. Qasim Mehdi, Uppala Radhakrishna, Marie-Pierre Papasavvas, Corinne Gehrig, Colette Rossier, Michael Korostishevsky, Andreas Gal, Nobuyoshi Shimizu, Batsheva Bonné‐Tamir, Stylianos E. Antonarakis

    Vydáno 2001
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  18. 18
    Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture

    Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture Autor Nabil Enattah, Tine G.K. Jensen, Mette Ødegaard Nielsen, Rikke Lewinski, Mikko Kuokkanen, Heli Rasinperä, Hatem El‐Shanti, Jeong Kee Seo, Michael Alifrangis, Insaf F. Khalil, Abdrazak Natah, Ahmed Ali, Sirajedin Natah, David Comas, S. Qasim Mehdi, Leif Groop, Else Marie Vestergaard, Faiqa Imtiaz, Mohamed S. Rashed, Brian F. Meyer, Jesper T. Troelsen, Leena Peltonen

    Vydáno 2008
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  19. 19
    A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

    A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia Autor Perundurai S. Dhandapany, Sakthivel Sadayappan, Yali Xue, Gareth T. Powell, Deepa Selvi Rani, Prathiba Nallari, Taranjit Singh, Madhu Khullar, Pedro Soares, Ajay Bahl, Jagan Mohan Tharkan, Pradeep Vaideeswar, Andiappan Rathinavel, Calambur Narasimhan, Dharma Rakshak Ayapati, Qasim Ayub, S. Qasim Mehdi, Stephen Oppenheimer, Martin Richards, Alkes L. Price, Nick Patterson, David Reich, Lalji Singh, Chris Tyler‐Smith, Kumarasamy Thangaraj

    Vydáno 2009
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  20. 20
    Evidence of Still-Ongoing Convergence Evolution of the Lactase Persistence T-13910 Alleles in Humans

    Evidence of Still-Ongoing Convergence Evolution of the Lactase Persistence T-13910 Alleles in Humans Autor Nabil Enattah, Aimée Trudeau, Ville N. Pimenoff, Luigi Maiuri, Salvatore Auricchio, Luigi Greco, Mauro Rossi, Michael J. Lentze, Jieun Seo, Soheila Rahgozar, Insaf F. Khalil, Michael Alifrangis, Sirajedin Natah, Leif Groop, Nael Shaat, Andrew Kozlov, Galina Verschubskaya, David Comas, Kazima Bulayeva, S. Qasim Mehdi, Joseph D. Terwilliger, Timo Sahi, Erkki Savilahti, Markus Perola, Antti Sajantila, Irma Järvelä, Leena Peltonen

    Vydáno 2007
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