Page last updated: 2024-08-18

isomethyleugenol and Beckwith-Wiedemann Syndrome

isomethyleugenol has been researched along with Beckwith-Wiedemann Syndrome in 18 studies

Research

Studies (18)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	10 (55.56)	18.2507
2000's	5 (27.78)	29.6817
2010's	3 (16.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bliek, J; Bouc, YL; Brioude, F; Coze, C; Eggermann, T; Ferrero, GB; Hennekam, R; Kratz, C; Maas, SM; Mackay, DJG; Maher, ER; Mussa, A; Netchine, I	1
Baiocchi, M; Hussain, K; Yousuf, FS	1
DeBaun, MR; Feinberg, AP; Grange, DK; Lennerz, JK; Timmerman, RJ; Zehnbauer, BA	1
Bliek, J; Gaston, V; Gicquel, C; Le Bouc, Y; Maas, S; Mannens, M	1
Agosti, M; Bonati, MT; Cogliati, F; Dalla Bernardina, B; Ferraiuolo, S; Finelli, P; Larizza, L; Recalcati, MP; Russo, S; Sala, M; Tibiletti, MG	1
Algar, E; Bennetts, B; McGillivray, G; Peters, G; Poon, C; Wilson, M; Wu, ZH	1
Deal, CL	1
Bliek, J; Boavida, M; Coad, N; Feinberg, AP; Hoovers, JM; Little, P; Mannens, M; Redeker, E; Steenman, M; Verjaal, M	1
Brown, KW; Elliott, M; Maher, ER; Reik, W; Sartori, P; Slatter, RE	1
Polychronakos, C	1
Cabrol, S; Gourmelen, M; Le Bouc, Y; Schneid, H; Seurin, D; Vazquez, MP	1
DeBaun, MR; Feinberg, AP; Rainier, S	1
Becroft, DM; Morison, IM; Reeve, AE; Taniguchi, T; Woods, CG	1
Bickmore, W; Brown, KW; Le Bouc, Y; Maher, ER; Reik, W; Schneid, H	1
Reik, W	1
Greally, JM	1
Algar, E; Amor, D; Brickell, S; Deeble, G; Smith, P	1
Ainscough, JF; Barton, SC; John, RM; Surani, MA	1

Reviews

5 review(s) available for isomethyleugenol and Beckwith-Wiedemann Syndrome

Article	Year
Parental genomic imprinting. Current opinion in pediatrics, 1995, Volume: 7, Issue:4 Topics: Angelman Syndrome; Animals; Beckwith-Wiedemann Syndrome; Diabetes Mellitus, Type 1; Genomic Imprinting; Humans; Insulin-Like Growth Factor II; Kidney Neoplasms; Methylation; Mice; Muscle Proteins; Neoplasms; Prader-Willi Syndrome; RNA, Long Noncoding; RNA, Untranslated; Transcription, Genetic; Wilms Tumor	1995
Parental imprinting of the genes for IGF-II and its receptor. Advances in experimental medicine and biology, 1993, Volume: 343 Topics: Animals; Beckwith-Wiedemann Syndrome; Chromosomes, Human, Pair 11; DNA; Female; Humans; Insulin-Like Growth Factor II; Kidney Neoplasms; Male; Methylation; Mice; Mice, Transgenic; Placenta; Pregnancy; Receptor, IGF Type 2; Wilms Tumor	1993
Genomic imprinting, DNA methylation, and cancer. Journal of the National Cancer Institute. Monographs, 1995, Issue:17 Topics: Animals; Beckwith-Wiedemann Syndrome; DNA, Neoplasm; Genomic Imprinting; Humans; Methylation; Models, Genetic; Neoplasms; Neoplasms, Experimental; Pedigree	1995
The Wellcome Prize Lecture. Genetic imprinting: the battle of the sexes rages on. Experimental physiology, 1996, Volume: 81, Issue:2 Topics: Animals; Beckwith-Wiedemann Syndrome; Biological Evolution; Chromosomes; DNA; Gene Expression Regulation, Developmental; Genomic Imprinting; Humans; Mammals; Methylation; Sex Factors	1996
Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome. Molecular biotechnology, 1999, Volume: 11, Issue:2 Topics: Beckwith-Wiedemann Syndrome; Chromatin; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, Pair 11; CpG Islands; Genomic Imprinting; Heterochromatin; Humans; Insulin-Like Growth Factor II; Methylation; Models, Genetic; Muscle Proteins; RNA, Long Noncoding; RNA, Untranslated	1999

Other Studies

13 other study(ies) available for isomethyleugenol and Beckwith-Wiedemann Syndrome

Article	Year
Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply. European journal of human genetics : EJHG, 2018, Volume: 26, Issue:4 Topics: Beckwith-Wiedemann Syndrome; DNA Methylation; Genomic Imprinting; Humans; Methylation; Wilms Tumor	2018
Hypopituitarism in a patient with Beckwith-Wiedemann syndrome due to hypomethylation of KvDMR1. Pediatrics, 2014, Volume: 133, Issue:4 Topics: Beckwith-Wiedemann Syndrome; Child, Preschool; Follow-Up Studies; Humans; Hypopituitarism; Infant, Newborn; Methylation; Potassium Channels, Voltage-Gated	2014
Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield. The Journal of molecular diagnostics : JMD, 2010, Volume: 12, Issue:5 Topics: Autoradiography; Base Sequence; Beckwith-Wiedemann Syndrome; Blotting, Southern; DNA Primers; Electrophoresis, Agar Gel; Humans; Methylation; RNA, Long Noncoding; RNA, Untranslated	2010
Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS). The Journal of pediatrics, 2004, Volume: 145, Issue:6 Topics: Beckwith-Wiedemann Syndrome; Child, Preschool; France; Genes, Wilms Tumor; Genotype; Humans; Incidence; Kidney Neoplasms; Membrane Proteins; Methylation; Neoplasms; Netherlands; Potassium Channels, Voltage-Gated; Predictive Value of Tests; Risk Factors; Wilms Tumor	2004
Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region. Journal of medical genetics, 2006, Volume: 43, Issue:8 Topics: Beckwith-Wiedemann Syndrome; Child; Chromosome Aberrations; Chromosome Segregation; Chromosomes, Human, Pair 11; Female; Gene Duplication; Genome, Human; Histones; Humans; In Situ Hybridization, Fluorescence; Infant; Infant, Newborn; Male; Membrane Proteins; Methylation; Microsatellite Repeats; Pedigree; Physical Chromosome Mapping; Potassium Channels, Voltage-Gated	2006
The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports. American journal of medical genetics. Part A, 2008, Jan-15, Volume: 146A, Issue:2 Topics: Beckwith-Wiedemann Syndrome; Child; Child, Preschool; Female; Genome, Human; Genotype; Humans; Methylation; Microsatellite Repeats; Mosaicism; Phenotype; Polymorphism, Single Nucleotide; Uniparental Disomy	2008
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. European journal of human genetics : EJHG, 1994, Volume: 2, Issue:1 Topics: Beckwith-Wiedemann Syndrome; Child; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Human, Pair 11; DNA; Female; Gene Expression; Genes, Tumor Suppressor; Humans; In Situ Hybridization, Fluorescence; Insulin; Insulin-Like Growth Factor II; Karyotyping; Male; Methylation; Neoplastic Syndromes, Hereditary; Parents; Pedigree; Polymorphism, Restriction Fragment Length; Sex Factors; Translocation, Genetic; Trisomy; Wilms Tumor	1994
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome. Human molecular genetics, 1994, Volume: 3, Issue:8 Topics: Alleles; Beckwith-Wiedemann Syndrome; Chromosomes, Human, Pair 11; DNA; Humans; Methylation; Polymerase Chain Reaction; Restriction Mapping	1994
Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome. Journal of medical genetics, 1993, Volume: 30, Issue:5 Topics: Adult; Alleles; Beckwith-Wiedemann Syndrome; Blotting, Northern; Blotting, Southern; Calcitonin; Child; Chromosomes, Human, Pair 11; DNA; Fathers; Female; Gene Expression Regulation; Gene Frequency; Humans; Immunoblotting; Insulin; Insulin-Like Growth Factor II; Leukocytes; Male; Methylation; Mothers; Restriction Mapping; RNA, Messenger	1993
Somatic overgrowth associated with overexpression of insulin-like growth factor II. Nature medicine, 1996, Volume: 2, Issue:3 Topics: Base Sequence; Beckwith-Wiedemann Syndrome; Child; Child, Preschool; DNA Primers; Female; Gene Expression; Genomic Imprinting; Growth Disorders; Humans; Infant; Insulin-Like Growth Factor II; Kidney; Kidney Neoplasms; Male; Methylation; Molecular Sequence Data; Mosaicism; Muscle Proteins; Promoter Regions, Genetic; RNA, Long Noncoding; RNA, Untranslated; Wilms Tumor	1996
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain. Human molecular genetics, 1995, Volume: 4, Issue:12 Topics: Base Sequence; Beckwith-Wiedemann Syndrome; Cells, Cultured; DNA Primers; DNA Replication; Female; Genomic Imprinting; Humans; Insulin-Like Growth Factor II; Male; Methylation; Molecular Sequence Data; Muscle Proteins; RNA, Long Noncoding; RNA, Untranslated	1995
Analysis of CDKN1C in Beckwith Wiedemann syndrome. Human mutation, 2000, Volume: 15, Issue:6 Topics: Alleles; Beckwith-Wiedemann Syndrome; Chromosomes, Human, Pair 11; Cyclin-Dependent Kinase Inhibitor p57; DNA Mutational Analysis; Family Health; Fetal Blood; Gene Frequency; Genetic Markers; Genomic Imprinting; Genotype; Humans; Insulin-Like Growth Factor II; Kidney; Lymphocytes; Methylation; Models, Genetic; Mutation; Nuclear Proteins; Phenotype; Polymorphism, Genetic; Reverse Transcriptase Polymerase Chain Reaction	2000
Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome. Human molecular genetics, 2001, Jul-15, Volume: 10, Issue:15 Topics: Animals; Beckwith-Wiedemann Syndrome; Cartilage; Chromosome Mapping; Contig Mapping; CpG Islands; Cyclin-Dependent Kinase Inhibitor p57; Enhancer Elements, Genetic; Female; Genomic Imprinting; Genotype; Humans; In Situ Hybridization; Male; Methylation; Mice; Mice, Transgenic; Models, Genetic; Muscle, Skeletal; Mutation; Nuclear Proteins; Phenotype; Promoter Regions, Genetic; Tissue Distribution; Transgenes; Translocation, Genetic	2001