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1دورية أكاديمية
المؤلفون: Azizi, S., Asadi, E., Howard, S., Muir, B.W., O'Shea, R., Bab-Hadiashar, A.
المصدر: IEEE Transactions on Automation Science and Engineering IEEE Trans. Automat. Sci. Eng. Automation Science and Engineering, IEEE Transactions on. PP(99):1-12
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المؤلفون: Terri McVeigh, Duff M, Carroll C, O'Shea R, Bradley L, Farrell M, Dj, Gallagher, Clabby C, Aj, Green
المصدر: Europe PubMed Central
مصطلحات موضوعية: Phenotype, Adenomatous Polyposis Coli, Genotype, Incidence, Mutation, Humans, Intestinal Polyps, Genetic Predisposition to Disease, Colorectal Neoplasms, Ireland, DNA Glycosylases, Retrospective Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fd6f6392c16546415fc93a42390a4e6a
https://pubmed.ncbi.nlm.nih.gov/28644590 -
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المؤلفون: O'Shea, R, Collins, A, Howe, C
المصدر: Environmental Challenges. 8:100559
مصطلحات موضوعية: History, Global and Planetary Change, Environmental Engineering, Polymers and Plastics, Business and International Management, Management, Monitoring, Policy and Law, Pollution, Waste Management and Disposal, Industrial and Manufacturing Engineering
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::879fbe67fd63e20db627daf86fbb627b
https://doi.org/10.1016/j.envc.2022.100559 -
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المؤلفون: Gray, S A, O'Shea, R, Petty, M E, Loonsk, J
مصطلحات موضوعية: New York, Database Management Systems, Health Resources, Humans, Health Education, Online Systems, United States, Research Article, Information Systems
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::ea6437f0cd61d3395e0fc97cc4df5a46
https://europepmc.org/articles/PMC226379/ -
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المؤلفون: Terri McVeigh, Duff, M., Carroll, C., Cody, N., O’shea, R., Bradley, L., Farrell, M., Gallagher, D. J., Clabby, C., Green, A. J.
المصدر: University College Dublin
Scopus-ElsevierURL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5f5eae106dce0d670884914cd16545e6
https://app.dimensions.ai/details/publication/pub.1086135449 -
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المساهمون: Aymé S., Rodwell C., eds.
مصطلحات موضوعية: EUCERD Rare Diseases Orphanet
وصف الملف: 92 page(s); text; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2295::7612162728552deccbf7fc7c0dc6a325
http://www.manchester.ac.uk/escholar/uk-ac-man-scw:268884 -
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المؤلفون: Fitzgerald, T.W., Gerety, S.S., Jones, W.D., van Kogelenberg, M., King, D.A., McRae, J., Morley, K.I., Parthiban, V., Al-Turki, S., Ambridge, K., Barrett, D.M., Bayzetinova, T., Clayton, S., Coomber, E.L., Gribble, S., Jones, P., Krishnappa, N., Mason, L.E., Middleton, A., Miller, R., Prigmore, E., Rajan, D., Sifrim, A., Tivey, A.R., Ahmed, M., Akawi, N., Andrews, R., Anjum, U., Archer, H., Armstrong, R., Balasubramanian, M., Banerjee, R., Baralle, D., Batstone, P., Baty, D., Bennett, C., Berg, J., Bernhard, B., Bevan, A.P., Blair, E., Blyth, M., Bohanna, D., Bourdon, L., Bourn, D., Brady, A., Bragin, E., Brewer, C., Brueton, L., Brunstrom, K., Bumpstead, S.J., Bunyan, D.J., Burn, J., Burton, J., Canham, N., Castle, B., Chandler, K., Clasper, S., Clayton-Smith, J., Cole, T., Collins, A., Collinson, M.N., Connell, F., Cooper, N., Cox, H., Cresswell, L., Cross, G., Crow, Y., D'Alessandro, M., Dabir, T., Davidson, R., Davies, S., Dean, J., Deshpande, C., Devlin, G., Dixit, A., Dominiczak, A., Donnelly, C., Donnelly, D., Douglas, A., Duncan, A., Eason, J., Edkins, S., Ellard, S., Ellis, P., Elmslie, F., Evans, K., Everest, S., Fendick, T., Fisher, R., Flinter, F., Foulds, N., Fryer, A., Fu, B., Gardiner, C., Gaunt, L., Ghali, N., Gibbons, R., Pereira, S.L.G., Goodship, J., Goudie, D., Gray, E., Greene, P., Greenhalgh, L., Harrison, L., Hawkins, R., Hellens, S., Henderson, A., Hobson, E., Holden, S., Holder, S., Hollingsworth, G., Homfray, T., Humphreys, M., Hurst, J., Ingram, S., Irving, M., Jarvis, J., Jenkins, L., Johnson, D., Jones, D., Jones, E., Josifova, D., Joss, S., Kaemba, B., Kazembe, S., Kerr, B., Kini, U., Kinning, E., Kirby, G., Kirk, C., Kivuva, E., Kraus, A., Kumar, D., Lachlan, K., Lam, W., Lampe, A., Langman, C., Lees, M., Lim, D., Lowther, G., Lynch, S.A., Magee, A., Maher, E., Mansour, S., Marks, K., Martin, K., Maye, U., McCann, E., McConnell, V., McEntagart, M., McGowan, R., McKay, K., McKee, S., McMullan, D.J., McNerlan, S., Mehta, S., Metcalfe, K., Miles, E., Mohammed, S., Montgomery, T., Moore, D., Morgan, S., Morris, A., Morton, J., Mugalaasi, H., Murday, V., Nevitt, L., Newbury-Ecob, R., Norman, A., O'Shea, R., Ogilvie, C., Park, S., Parker, M.J., Patel, C., Paterson, J., Payne, S., Phipps, J., Pilz, D.T., Porteous, D., Pratt, N., Prescott, K., Price, S., Pridham, A., Procter, A., Purnell, H., Ragge, N., Rankin, J., Raymond, L., Rice, D., Robert, L., Roberts, E., Roberts, G., Roberts, J., Roberts, P., Ross, A., Rosser, E., Saggar, A., Samant, S., Sandford, R., Sarkar, A., Schweier, S., Scott, C., Scott, R., Selby, A., Seller, A., Sequeira, C., Shannon, N., Shanrif, S., Shaw-Smith, C., Shearing, E., Shears, D., Simonic, I., Simpkin, D., Singzon, R., Skitt, Z., Smith, A., Smith, B., Smith, K., Smithson, S., Sneddon, L., Splitt, M., Squires, M., Stewart, F., Stewart, H., Suri, M., Sutton, V., Swaminathan, G.J., Sweeney, E., Tatton-Brown, K., Taylor, C., Taylor, R., Tein, M., Temple, I.K., Thomson, J., Tolmie, J., Torokwa, A., Treacy, B., Turner, C., Turnpenny, P., Tysoe, C., Vandersteen, A., Vasudevan, P., Vogt, J., Wakeling, E., Walker, D., Waters, J., Weber, A., Wellesley, D., Whiteford, M., Widaa, S., Wilcox, S., Williams, D., Williams, N., Woods, G., Wragg, C., Wright, M., Yang, F., Yau, M., Carter, N.P., Parker, M., Firth, H.V., FitzPatrick, D.R., Wright, C.F., Barrett, J.C., Hurles, M.E., The Deciphering Developmental Disorders Study, .
المصدر: Nature
مصطلحات موضوعية: Male, Parents, Chromosomal Proteins, Non-Histone, Developmental Disabilities, Transposases, SYNGAP1, medicine.disease_cause, Bioinformatics, DEAD-box RNA Helicases, 0302 clinical medicine, Guanine Nucleotide Exchange Factors, Missense mutation, Exome, Protein Phosphatase 2, Child, Dynamin I, Zebrafish, Exome sequencing, Genes, Dominant, Polycomb Repressive Complex 1, 0303 health sciences, Mutation, Multidisciplinary, Gene Expression Regulation, Developmental, Nuclear Proteins, DNA-Binding Proteins, Child, Preschool, Female, Adolescent, Mutation, Missense, Nerve Tissue Proteins, Protein Serine-Threonine Kinases, Biology, Article, 03 medical and health sciences, Rare Diseases, medicine, Animals, Humans, 030304 developmental biology, Chromosome Aberrations, Homeodomain Proteins, Genome, Human, Mechanism (biology), Infant, Newborn, Infant, Phosphoproteins, United Kingdom, Human genetics, Repressor Proteins, Human genome, Carrier Proteins, 030217 neurology & neurosurgery, Transcription Factors
وصف الملف: application/pdf; text
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المؤلفون: Stockner T, Alexander F. Hoffman, Schwazer J, Sandtner W, Pollak D, Harald H. Sitte, Kathrin Jäntsch, O'Shea R, Marco Niello, Gradisch R, Carl R. Lupica, Julian Maier, Sideromenos S, Michael H. Baumann
مصطلحات موضوعية: Drug, Psychomotor learning, biology, Chemistry, media_common.quotation_subject, medicine.medical_treatment, Pharmacology, Receptor–ligand kinetics, Stimulant, medicine, biology.protein, Enantiomer, media_common, Dopamine transporter
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::04ff8c99e37200267fb60307eb328dc1
https://doi.org/10.21203/rs.3.rs-612345/v1 -
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المؤلفون: Rosenbaum, P, O'Shea, R
مصطلحات موضوعية: Adult, Male, Adolescent, behavior and behavior mechanisms, Humans, Social Support, Female, Smoking Cessation, Middle Aged, Research Article, Aged
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::bb054162db708f82724c9058cdf1b028
https://europepmc.org/articles/PMC1403623/