نتائج البحث - "Eamonn R. Maher"

41

Genetic and epigenetic analysis of recurrent hydatidiform mole

المؤلفون: Bruce E. Hayward, Eamonn R. Maher, Eamonn Sheridan, Hussain Jafri, Graham R. Taylor, M. Reza Abdollahi, Michel De Vos, Nargese Talati, Kausar Nazir, Yasmin Rashid, David T. Bonthron, Denise Williams, Esther Meyer, Faridon Setna, Shahnaz Hussaini

المصدر: Human mutation. 30(5)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b770d7daef7a071a59a243f32f6d7f65
https://pubmed.ncbi.nlm.nih.gov/19309689

View record at Wiley

42

Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinoma

المؤلفون: Takeshi Kishida, Bin Tean Teh, Farida Latif, Eamonn R. Maher, Mark R. Morris, Mahera Abdulrahman, Dean Gentle, Noel W. Clarke, Masahiro Yao, Michael D Brown

المصدر: Morris, M R, Gentle, D, Abdulrahman, M, Clarke, N, Brown, M, Kishida, T, Yao, M, Teh, B T, Latif, F & Maher, E R 2008, ' Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinoma ', British Journal of Cancer, vol. 98, no. 2, pp. 496-501 . https://doi.org/10.1038/sj.bjc.6604180
British Journal of Cancer

مصطلحات موضوعية: renal cell carcinoma, Candidate gene, Cancer Research, Tumor suppressor gene, Biology, Transfection, urologic and male genital diseases, Methylation, Epigenesis, Genetic, chemistry.chemical_compound, Cell Line, Tumor, Humans, Genes, Tumor Suppressor, Epigenetics, Promoter Regions, Genetic, Carcinoma, Renal Cell, neoplasms, Epigenomics, Receptors, Scavenger, Genetics, Regulation of gene expression, epigenetics, Genetics and Genomics, Chemokine CXCL16, Genomics, DNA Methylation, Kidney Neoplasms, female genital diseases and pregnancy complications, Renal cell carcinoma, Demethylating agent, Gene Expression Regulation, Neoplastic, chemistry, Oncology, DNA methylation, Neoplastic Stem Cells, Cancer research, methylation, Chemokines, CXC, Genes, Neoplasm

وصف الملف: application/octet-stream; text; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ffed3610be66e3aeaecffdade434267
https://www.research.manchester.ac.uk/portal/en/publications/functional-epigenomics-approach-to-identify-methylated-candidate-tumour-suppressor-genes-in-renal-cell-carcinoma(76247102-640c-4622-b3dd-1d0591f977ca).html

43

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour

المؤلفون: Gianfranco Sebastio, Paola Collini, Gaetano Verde, Maria Vittoria Cubellis, Maria Michela Rinaldi, Valentina Citro, Andrea Riccio, Cinzia Magnani, Agostina De Crescenzo, Angela Sparago, Luigi Boccuto, Daniela Perotti, Flavia Cerrato, Paolo D'Angelo, Eamonn R. Maher, Giovanni Neri

المساهمون: Cerrato, Flavia, Sparago, A., Verde, G., DE CRESCENZO, A., Citro, V., Cubellis, M., Rinaldi, M., Boccuto, L., Neri, G., Magnani, C., D'Angelo, P., Collini, P., Perrotti, D., Sebastio, G., Maher, E., Riccio, Andrea, Cerrato, F, Sparago, A, Verde, G, DE CRESCENZO, A, Citro, V, Cubellis, MARIA VITTORIA, Rinaldi, Mm, Boccuto, L, Neri, G, Magnani, C, Dangelo, P, Collini, P, Perotti, D, Sebastio, G, Maher, E. AND RICCIO A.

المصدر: Human molecular genetics
17 (2008): 1427–1435. doi:10.1093/hmg/ddn031
info:cnr-pdr/source/autori:Cerrato F.; Sparago A.; Verde G.; De Crescenzo A.; Citro V.; Cubellis M.V.; Rinaldi M.M.; Boccuto L.; Neri G.; Magnani C.; D'Angelo P.; Collini P.; Perotti D.; Sebastio G.; Maher E.R.; Riccio A./titolo:Different mechanisms cause imprinting defects at the IGF2%2FH19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour/doi:10.1093%2Fhmg%2Fddn031/rivista:Human molecular genetics (Print)/anno:2008/pagina_da:1427/pagina_a:1435/intervallo_pagine:1427–1435/volume:17

مصطلحات موضوعية: Male, CCCTC-Binding Factor, Beckwith-Wiedemann Syndrome, RNA, Untranslated, Beckwith–Wiedemann syndrome, Locus (genetics), Biology, Settore MED/03 - GENETICA MEDICA, Wilms Tumor, Insulin-Like Growth Factor II, Chromosome Segregation, Genetics, medicine, Humans, Epigenetics, Allele, Imprinting (psychology), Molecular Biology, Alleles, Genetics (clinical), Chromosomes, Human, Pair 11, human cancer, BWS syndrome, Wilms' tumor, General Medicine, DNA Methylation, medicine.disease, Pedigree, genomic imprinting, DNA-Binding Proteins, Repressor Proteins, Haplotypes, Italy, Mutation, DNA methylation, Female, RNA, Long Noncoding, imprinting, Genomic imprinting, Gene Deletion, epigenetic