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1دورية أكاديمية
المؤلفون: Charalambos Demetriou, Sayeda Abu-Amero, Anna C Thomas, Miho Ishida, Reena Aggarwal, Lara Al-Olabi, Lydia J Leon, Jaime L Stafford, Argyro Syngelaki, Donald Peebles, Kypros H Nicolaides, Lesley Regan, Philip Stanier, Gudrun E Moore
المصدر: PLoS ONE, Vol 9, Iss 1, p e85454 (2014)
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Jennifer M Frost, Dave Monk, Taita Stojilkovic-Mikic, Kathryn Woodfine, Lyn S Chitty, Adele Murrell, Philip Stanier, Gudrun E Moore
المصدر: PLoS ONE, Vol 5, Iss 10, p e13556 (2010)
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Jennifer M Frost, Ramya Udayashankar, Harry D Moore, Gudrun E Moore
المصدر: PLoS ONE, Vol 5, Iss 7, p e11595 (2010)
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Jennifer M Frost, Gudrun E Moore
المصدر: PLoS Genetics, Vol 6, Iss 7, p e1001015 (2010)
وصف الملف: electronic resource
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5دورية أكاديمية
المؤلفون: Layla Parker-Katiraee, Andrew R Carson, Takahiro Yamada, Philippe Arnaud, Robert Feil, Sayeda N Abu-Amero, Gudrun E Moore, Masahiro Kaneda, George H Perry, Anne C Stone, Charles Lee, Makiko Meguro-Horike, Hiroyuki Sasaki, Keiko Kobayashi, Kazuhiko Nakabayashi, Stephen W Scherer
المصدر: PLoS Genetics, Vol 3, Iss 5, p e65 (2007)
وصف الملف: electronic resource
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6دورية أكاديمية
المؤلفون: Andrew J Wood, Roland G Roberts, David Monk, Gudrun E Moore, Reiner Schulz, Rebecca J Oakey
المصدر: PLoS Genetics, Vol 3, Iss 2, p e20 (2007)
وصف الملف: electronic resource
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7دورية أكاديمية
المؤلفون: Jenifer P. Suntharalingham, Miho Ishida, Ignacio Del Valle, Susanne E. Stalman, Nita Solanky, Emma Wakeling, Gudrun E. Moore, John C. Achermann, Federica Buonocore
المصدر: Frontiers in Endocrinology, Vol 13 (2022)
مصطلحات موضوعية: SAMD9, FGR, NGS, adrenal insufficiency, endocrinopathies, myelodysplastic syndrome (MDS), Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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8
المؤلفون: Maria Derakhshan, Noah J Kessler, Miho Ishida, Charalambos Demetriou, Nicolas Brucato, Gudrun E Moore, Caroline H D Fall, Giriraj R Chandak, Francois-Xavier Ricaut, Andrew M Prentice, Garrett Hellenthal, Matt J Silver
المساهمون: Evolution et Diversité Biologique (EDB), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Medical Research Council, Human Genetics Division [Singapore], Genome Institute of Singapore (GIS), University College of London [London] (UCL)
المصدر: Nucleic Acids Research
Nucleic Acids Research, 2022, 50 (12), pp.6735-6752. ⟨10.1093/nar/gkac503⟩مصطلحات موضوعية: Tissue-and ethnicity-independent, Illumina 450K array, Hypervariable DNA methylation, Genetics, Early embryo, Humans, Reproducibility of Results, Systemic inter-individual variation, [SDE.BE]Environmental Sciences/Biodiversity and Ecology, DNA Methylation
وصف الملف: application/pdf; text
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bae458740f23f467577d189ea55c9238
https://pubmed.ncbi.nlm.nih.gov/35713545 -
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المؤلفون: Daniël A. Lionarons, Davide Zecchin, Jeffrey R. MacDonald, Wei-Li Di, Hui Chen, Miriam Molina, Stuart Horswell, Gemma Tell, Véronique Bataille, Dale Bryant, Julia Newton-Bishop, Philip Stanier, Gudrun E. Moore, Kiran Parmar, Josep Malvehy, Catherine A. Harwood, Satyamaanasa Polubothu, Cristina Carrera, Jérémie Nsengimana, Veronica A. Kinsler, Julian Downward, Nathan Wlodarchak, Alan Pittman, Susana Puig, Yongna Xing, Neil J. Sebire, Anna C. Thomas, Mark Harland, L. Al-Olabi, Mehdi Zarrei, Michael Howell, Sarah Brand, Paulina Stadnik, Stephen W. Scherer, Lilian Hunt, Eugene Healy, Dale Moulding, Paula Aguilera, J.A. Puig-Butillé, Deborah Morrogh, Vanessa Martins da Silva, Sam Loughlin, Regula Waelchli, Sara Martin Barberan, Greg Elgar, Lionel Larue
المساهمون: Oncology, CCA - Cancer biology and immunology, CCA - Cancer Treatment and Quality of Life
المصدر: Genetics in medicine, 23(9), 1636-1647. Lippincott Williams and Wilkins
Genetics in Medicineمصطلحات موضوعية: 0301 basic medicine, Model organisms, Skin Neoplasms, Gene Expression, Biology, Germline, Article, 030207 dermatology & venereal diseases, 03 medical and health sciences, Signalling & Oncogenes, 0302 clinical medicine, Congenital melanocytic nevus, medicine, Genetic predisposition, Nevus, Humans, Gene, Melanoma, Genetics (clinical), Computational & Systems Biology, Chemical Biology & High Throughput, Genome Integrity & Repair, Tumour Biology, Microphthalmia-associated transcription factor, medicine.disease, Phenotype, Immunohistochemistry, 030104 developmental biology, Cancer research, Genetics & Genomics, Developmental Biology
وصف الملف: text; spreadsheet; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cf020b972091ef0da9c25d686d2a0a5
https://pure.amc.nl/en/publications/inherited-duplications-of-ppp2r3b-predispose-to-nevi-and-melanoma-via-a-c21orf91driven-proliferative-phenotype(c7c1481a-d0e0-4090-8d51-8c03bd58e817).html -
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المؤلفون: Emma Wakeling, Jenny Child, Deborah J G Mackay, Miho Ishida, Christopher D. Byrne, Justin H Davies, I. Karen Temple, Oluwakemi Lokulo-Sodipe, Hazel Inskip, Gudrun E. Moore, Angela Fenwick, Lisa Marie Ballard
المصدر: Journal of Medical Genetics
مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, Adolescent, uniparental disomy, Short stature, Epigenesis, Genetic, Impaired glucose tolerance, Genomic Imprinting, Young Adult, Insulin-Like Growth Factor II, parasitic diseases, Genetics, medicine, Humans, Genetics (clinical), Aged, Chromosome 7 (human), business.industry, Silver Russell syndrome, Silver–Russell syndrome, Genotype-Phenotype Correlations, Retrospective cohort study, DNA Methylation, Middle Aged, medicine.disease, Uniparental disomy, Growth hormone treatment, short stature, Silver-Russell Syndrome, Phenotype, Cohort, Quality of Life, Female, RNA, Long Noncoding, medicine.symptom, imprinting, business
وصف الملف: text; image
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4fcf40152ba1c5a1d9381d94b71adf0
https://eprints.soton.ac.uk/437350/