نتائج البحث - Layal Abi Farraj
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Mutational Analysis of<i>MIR184</i>in Sporadic Keratoconus and Myopia حسب Judith Lechner, Ha Ae Bae, Jasenka Guduric‐Fuchs, Aine Rice, Gowthaman Govindarajan, Salina Siddiqui, Layal Abi Farraj, Shea Ping Yip, Maurice Yap, Manoranjan Das, Emmanuelle Souzeau, D J Coster, Richard Mills, Richard Lindsay, Tony Phillips, Paul Mitchell, Manir Ali, Chris F. Inglehearn, Periasamy Sundaresan, Jamie E. Craig, David Simpson, Kathryn P. Burdon, Colin E. Willoughby
منشور في 2013Artigo -
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A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus حسب Alison J. Hardcastle, Petra Lišková, Yelena Bykhovskaya, Bennet J. McComish, Alice E. Davidson, Chris F. Inglehearn, Xiaohui Li, Hélène Choquet, Mahmoud Habeeb, Sionne E. M. Lucas, Srujana Sahebjada, Nikolas Pontikos, Karla E. Rojas López, Anthony P. Khawaja, Manir Ali, Ľubica Ďuďáková, Pavlína Skalická, Bart T. H. van Dooren, Annette J.M. Geerards, Christoph Haudum, Valeria Lo Faro, Abi Tenen, Mark Simcoe, Karina Patasova, Darioush Yarrand, Jie Yin, Salina Siddiqui, Aine Rice, Layal Abi Farraj, Yii-Der Ida Chen, Jugnoo S. Rahi, Ronald M. Krauss, Elizabeth Theusch, Jac Charlesworth, Loretta Szczotka‐Flynn, Carmel Toomes, Magda A. Meester‐Smoor, Andrea J. Richardson, Paul A. Mitchell, Kent D. Taylor, Ronald B. Melles, Anthony J. Aldave, Richard Mills, Ke Cao, Elsie Chan, Mark Daniell, Jie Jin Wang, Jerome I. Rotter, Alex W. Hewitt, Stuart MacGregor, Caroline C. W. Klaver, Wishal D. Ramdas, Jamie E. Craig, Sudha K. Iyengar, David O’Brart, Eric Jorgenson, Paul N. Baird, Yaron S. Rabinowitz, Kathryn P. Burdon, Christopher J. Hammond, Stephen J. Tuft, Pirro G. Hysi
منشور في 2021Revisão
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Medicine
Cornea
Extracellular matrix
Keratoconus
Mutation
Ophthalmology
Ameloblast
Amelogenesis
Amelogenesis imperfecta
Amelogenin
Anatomy
Cell biology
Dentinogenesis imperfecta
Dentistry
Disease
Enamel paint
Genetic association
Genome-wide association study
Genotype
Missense mutation
Molecular biology
Osteogenesis imperfecta
Pathology
Phenotype
Single-nucleotide polymorphism