المؤلفون: Kamal K E Gadalla, Paul D Ross, John S Riddell, Mark E S Bailey, Stuart R Cobb

المصدر: PLoS ONE, Vol 9, Iss 11, p e112889 (2014)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC4231076?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/fbd81503313d477bb13f07d3700029f2

المؤلفون: Kamal K.E. Gadalla, Paul D. Ross, Mark E.S. Bailey, Ralph D. Hector, Stuart Cobb, Noha Gamal Bahey

المصدر: Future Neurology. 10:467-484

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Genetic enhancement, Rett syndrome, Neurological disorder, Biology, medicine.disease_cause, medicine.disease, MECP2, Neurology, medicine, Neurology (clinical), Gene, Adeno-associated virus, X chromosome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d48b62b2221bc624f9535a67040db09e
https://doi.org/10.2217/fnl.15.29

المؤلفون: R. C. Spike, Paul D. Ross, Kenton T. Woodard, Sahana Nagabhushan Kalburgi, Mark E.S. Bailey, Stuart Cobb, Anne E. West, Kamal Ke Gadalla, R. Jude Samulski, Jie V. Deng, Steven J. Gray, Lavanya Bachaboina

المصدر: Molecular Therapy. 21(1):18-30

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Rett syndrome, Biology, Virus, MECP2, Green fluorescent protein, Andrology, Mice, mental disorders, Drug Discovery, medicine, Rett Syndrome, Genetics, Animals, Gene, Survival rate, Molecular Biology, Mice, Knockout, Pharmacology, Gene Transfer Techniques, Brain, Genetic Therapy, Dependovirus, medicine.disease, Phenotype, nervous system diseases, Survival Rate, Animals, Newborn, Immunology, Knockout mouse, Molecular Medicine, Original Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1ffe00d1f7c3f206fd17eb6727dac52

المؤلفون: K. Elizabeth Tanner, Bushra Kamal, Stuart Cobb, Jim Selfridge, Christopher M. Loughrey, Jacky Guy, Charlotte S. McCarroll, Thomas H. Gillingwater, Adrian Bird, Ross A. Jones, Paul D. Ross, Noha Gamal Bahey, Mark E.S. Bailey

المصدر: Human Molecular Genetics
Ross, P D, Guy, J, Selfridge, J, Kamal, B, Bahey, N, Tanner, E, Gillingwater, T, Jones, R, Loughrey, C M, McCarroll, C S, Bailey, M E S, Bird, A & Cobb, S 2016, ' Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddw269

مصطلحات موضوعية: 0301 basic medicine, Nervous system, congenital, hereditary, and neonatal diseases and abnormalities, Methyl-CpG-Binding Protein 2, Central nervous system, Rett syndrome, Neurological disorder, Biology, Bioinformatics, MECP2, 03 medical and health sciences, Mice, Genetics, medicine, Rett Syndrome, Animals, Molecular Biology, Genetics (clinical), Mice, Knockout, Genetic disorder, Wild type, Brain, General Medicine, Articles, medicine.disease, Phenotype, 3. Good health, Disease Models, Animal, 030104 developmental biology, medicine.anatomical_structure, Organ Specificity, Neuroscience

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be652e382544678f2133c1d397ecd7ac
https://pubmed.ncbi.nlm.nih.gov/28173151