-
1
المساهمون: Monk, David, Mackay, Deborah J. G., Eggermann, Thoma, Maher, Eamonn R., Riccio, Andrea
المصدر: Nature reviews. Genetics (Online) 20 (2019): 235–248. doi:10.1038/s41576-018-0092-0
info:cnr-pdr/source/autori:Monk D.; Mackay D.J.G.; Eggermann T.; Maher E.R.; Riccio A./titolo:Genomic imprinting disorders: lessons on how genome, epigenome and environment interact/doi:10.1038%2Fs41576-018-0092-0/rivista:Nature reviews. Genetics (Online)/anno:2019/pagina_da:235/pagina_a:248/intervallo_pagine:235–248/volume:20
Dipòsit Digital de la UB
Universidad de Barcelonaمصطلحات موضوعية: Biology, Genome, Germline, Genomic Imprinting, 03 medical and health sciences, 0302 clinical medicine, Genetic, Genetics, Animals, Humans, Epigenetics, Imprinting (psychology), genome, Molecular Biology, Gene, Genetics (clinical), 030304 developmental biology, 0303 health sciences, Genome, Human, Genetic Diseases, Inborn, Genomics, Epigenome, DNA Methylation, Epigenètica, epigenome and environment interact, Genòmica, DNA methylation, Genomic imprinting, 030217 neurology & neurosurgery
وصف الملف: application/pdf; text
-
2
المؤلفون: Robert J. Grimer, Elena Arrigoni, Abdullah Alholle, Anna T. Brini, Ashraf Dallol, Seley Gharanei, Eamonn R. Maher, Smadar Avigad, Dean Gentle, Takeshi Kishida, Sumathi Vaiyapuri, Farida Latif, Toru Hiruma
المصدر: Epigenetics. 8:1198-1204
مصطلحات موضوعية: Cancer Research, Candidate gene, Bone Neoplasms, Sarcoma, Ewing, Biology, medicine.disease_cause, Epigenesis, Genetic, chemistry.chemical_compound, Cell Line, Tumor, medicine, Humans, Gene silencing, Gene Silencing, Epigenetics, Molecular Biology, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling, Mesenchymal Stem Cells, Methylation, DNA Methylation, Molecular biology, Demethylating agent, Survival Rate, Gene expression profiling, chemistry, DNA methylation, Transcriptome, Carcinogenesis
-
3
المؤلفون: Gabriele Schackert, Dietmar Krex, Dean Gentle, Eamonn R. Maher, Wenbin Wei, Farida Latif, Victoria K. Hill, Thoraia Shinawi, Garth Cruickshank, Mark R. Morris
المصدر: Epigenetics. 8:149-156
مصطلحات موضوعية: Cancer Research, IDH1, Brain tumor, Biology, medicine.disease_cause, Bioinformatics, Central Nervous System Neoplasms, medicine, Humans, Survivors, Epigenetics, Molecular Biology, Mutation, Brief Report, Methylation, DNA Methylation, Prognosis, medicine.disease, Phenotype, Isocitrate Dehydrogenase, CpG site, DNA methylation, Cancer research, CpG Islands, Glioblastoma
-
4
المؤلفون: Emma L. Baple, Deborah J G Mackay, Louise E. Docherty, Lukas Soellner, Claire L. S. Turner, Emma Kivuva, Karin Buiting, Thomas Eggermann, Matthias Begemann, Rebecca L. Poole, Sarah F. Smithson, I. Karen Temple, Michal Patalan, Eamonn R. Maher, Julian P Hamilton-Shield, Bernhard Horsthemke, Jasmin Beygo, Jarosław Peregud-Pogorzelski, Sahar Mansour, Faisal I. Rezwan, Maria Gizewska
المساهمون: Mackay, Deborah JG [0000-0003-3088-4401], Apollo - University of Cambridge Repository
المصدر: Nature Communications
Nature Communications 6, 8086 (2015). doi:10.1038/ncomms9086مصطلحات موضوعية: Male, Beckwith-Wiedemann Syndrome, medicine.medical_treatment, Medizin, General Physics and Astronomy, Monozygotic twin, Autoantigens, Polymerase Chain Reaction, Infant, Newborn, Diseases, Epigenesis, Genetic, Diabetes mellitus genetics, Pregnancy, Imprinting (psychology), Genetics, Multidisciplinary, Nuclear Proteins, Hydatidiform Mole, 3. Good health, Uterine Neoplasms, DNA methylation, Female, Biologie, Infertility, Female, Adult, Adolescent, DNA Copy Number Variations, Mothers, Biology, Article, General Biochemistry, Genetics and Molecular Biology, Mitochondrial Proteins, Genomic Imprinting, Young Adult, Diabetes Mellitus, medicine, Humans, Computer Simulation, Obesity, Epigenetics, Autistic Disorder, Assisted reproductive technology, Silver–Russell syndrome, Sequence Analysis, DNA, Twins, Monozygotic, General Chemistry, DNA Methylation, medicine.disease, Abortion, Spontaneous, Silver-Russell Syndrome, Mutation, Genomic imprinting
وصف الملف: text; spreadsheet; application/pdf
-
5
المؤلفون: Eamonn R. Maher, Derek Lim
المصدر: The Obstetrician & Gynaecologist. 12:37-42
مصطلحات موضوعية: Regulation of gene expression, Genetics, business.industry, DNA methylation, Gene expression, Medicine, Reproductive technology, Epigenetics, Genomic imprinting, business, Gene, Epigenomics
-
6
المؤلفون: Wolf Reik, Derek Lim, Eamonn R. Maher, Louise Brueton, Sarah Bowdin, Edward Blair, Alan Fryer, Wayne Lam, Gail Kirby, Fiona Macdonald, Trevor Cole, Louise Tee, Christine Oley
المصدر: Human Reproduction. 24:741-747
مصطلحات موضوعية: Male, Beckwith-Wiedemann Syndrome, Reproductive Techniques, Assisted, Beckwith–Wiedemann syndrome, Fertilization in Vitro, Reproductive technology, Biology, Epigenesis, Genetic, Genomic Imprinting, medicine, Humans, Sperm Injections, Intracytoplasmic, Epigenetics, Allele, Imprinting (psychology), Child, Alleles, Genetics, Rehabilitation, Obstetrics and Gynecology, Genomics, DNA Methylation, medicine.disease, Phenotype, Differentially methylated regions, Reproductive Medicine, Child, Preschool, Mutation, Female, Genomic imprinting
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::985941c49b9377180e9cc1646781934a
https://doi.org/10.1093/humrep/den406 -
7
المؤلفون: Farida Latif, Caroline D E Margetts, Mark R. Morris, Fiona E. McRonald, Daniel Catchpoole, Dewi Astuti, Alberto Cascón, Mercedes Robledo, Hartmut P. H. Neumann, Eamonn R. Maher, Dean Gentle
المصدر: Endocrine-Related Cancer
مصطلحات موضوعية: Adult, endocrine system, Cancer Research, Candidate gene, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Adrenal Gland Neoplasms, Pheochromocytoma, Biology, Epigenesis, Genetic, Neuroblastoma, chemistry.chemical_compound, Endocrinology, Cell Line, Tumor, medicine, Humans, Genes, Tumor Suppressor, Epigenetics, Promoter Regions, Genetic, Oligonucleotide Array Sequence Analysis, Research, Gene Expression Profiling, Promoter, Sequence Analysis, DNA, Methylation, DNA Methylation, medicine.disease, Demethylating agent, homeobox A9, Oncology, chemistry, Neural Crest, DNA methylation, Cancer research, CpG Islands
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bbe1d42f17e37728cdb112a3d82e74e
https://doi.org/10.1677/erc-08-0072 -
8
المؤلفون: Peter Selby, Patricia Harnden, Margaret A. Knowles, Rosamonde E. Banks, Dewi Astuti, Eamonn R. Maher, Dena Cohen, P. Tirukonda, Anthea J. Stanley, Nick Hornigold, Claire Taylor, Adrian D. Joyce
المصدر: Cancer Research. 66:2000-2011
مصطلحات موضوعية: Adult, Male, Cancer Research, Tumor suppressor gene, Loss of Heterozygosity, Biology, Epigenesis, Genetic, Loss of heterozygosity, Carcinoma, medicine, Humans, Clinical significance, Epigenetics, Promoter Regions, Genetic, Carcinoma, Renal Cell, Aged, Neoplasm Staging, Aged, 80 and over, Genetics, Cancer, Methylation, DNA Methylation, Middle Aged, medicine.disease, Kidney Neoplasms, Oncology, Von Hippel-Lindau Tumor Suppressor Protein, Mutation, DNA methylation, Cancer research, Female
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51fb1641e3092c9997e3e421f5ae4655
https://doi.org/10.1158/0008-5472.can-05-3074 -
9
المؤلفون: Wolf Reik, Gianfranco Sebastio, Gail A Evans, Hussain Raza, Sarah Bowdin, Jet Bliek, Wendy N. Cooper, Antonita C Haire, Andrea Riccio, Anita Luharia, Fiona Macdonald, Paul N. Schofield, Richard Grundy, Eamonn R. Maher
المساهمون: Human Genetics, Cooper, Wn, Luharia, A, Evans, Ga, Raza, H, Haire, Ac, Grundy, R, Bowdin, Sc, Riccio, Andrea, Sebastio, G, Bliek, J, Schofield, Pn, Reik, W, Macdonald, F, Maher, Er
المصدر: European journal of human genetics, 13(9), 1025-1032. Nature Publishing Group
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Beckwith-Wiedemann Syndrome, Genotype, Beckwith, Beckwith–Wiedemann syndrome, Biology, Wilms Tumor, Genomic Imprinting, Wiedemann, Neoplasms, Genetics, medicine, Humans, Epigenetics, Imprinting (psychology), Child, Hemihypertrophy, Alleles, Genetics (clinical), Base Sequence, KCNQ1OT1, Imprinting, Uniparental Disomy, medicine.disease, Uniparental disomy, Phenotype, DNA methylation, Cancer research, Female, Genomic imprinting
-
10
المؤلفون: Dean Gentle, Hartmut P. H. Neumann, Dewi Astuti, Mercedes Robledo, Wendy N. Cooper, C D E Margetts, Daniel Catchpoole, Eamonn R. Maher, A Cascón, Farida Latif
المصدر: Endocrine-Related Cancer. 12:161-172
مصطلحات موضوعية: Male, Cancer Research, RNA, Untranslated, von Hippel-Lindau Disease, endocrine system diseases, SDHB, Endocrinology, Diabetes and Metabolism, Loss of Heterozygosity, Multiple endocrine neoplasia type 2, Pheochromocytoma, Biology, GPI-Linked Proteins, Receptors, Tumor Necrosis Factor, Germline, Epigenesis, Genetic, Thrombospondin 1, Loss of heterozygosity, Genomic Imprinting, Endocrinology, Receptors, Tumor Necrosis Factor, Member 10c, Tumor Cells, Cultured, medicine, Humans, Genes, Tumor Suppressor, Epigenetics, Adaptor Proteins, Signal Transducing, Genetics, Caspase 8, Chromosomes, Human, Pair 11, Proteins, DNA Methylation, medicine.disease, Receptors, TNF-Related Apoptosis-Inducing Ligand, Tumor Necrosis Factor Decoy Receptors, Oncology, Caspases, DNA methylation, Female, RNA, Long Noncoding, SDHD, Genomic imprinting
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90327a66dd57ff76c3f5f80db00e2e0b
https://doi.org/10.1677/erc.1.00865
إعادة تعيين المنقحات
عرض المنقحات (%%عد%%)
Find this article in full text from Springer Verlag. 
PDF full text from Publisher