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The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

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Results: 181 to 186 of 186

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The Helicobacter pylori genome is modified at CATG by the product of hpyIM.
Xu Q, Peek RM, Miller GG, Blaser MJ
(1997) J Bacteriol 179: 6807-15
MeSH Terms: Amino Acid Sequence, Bacterial Proteins, Base Sequence, Blotting, Southern, Cloning, Molecular, Conserved Sequence, DNA Methylation, DNA, Bacterial, Databases, Factual, Genes, Bacterial, Genome, Bacterial, Helicobacter pylori, Molecular Sequence Data, Mutagenesis, Phylogeny, Polymerase Chain Reaction, Sequence Analysis, DNA, Sequence Homology, Amino Acid, Site-Specific DNA-Methyltransferase (Adenine-Specific), Substrate Specificity
Added March 5, 2014
0 Communities
1 Members
0 Resources
20 MeSH Terms
Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.
Lee MP, DeBaun M, Randhawa G, Reichard BA, Elledge SJ, Feinberg AP
(1997) Am J Hum Genet 61: 304-9
MeSH Terms: Beckwith-Wiedemann Syndrome, Chromosomes, Human, Pair 11, CpG Islands, Cyclin-Dependent Kinase Inhibitor p57, Cyclin-Dependent Kinases, DNA Methylation, DNA Mutational Analysis, Dinucleoside Phosphates, Female, Frameshift Mutation, Gene Frequency, Genetic Heterogeneity, Genomic Imprinting, Humans, Infant, KCNQ Potassium Channels, KCNQ1 Potassium Channel, Male, Nuclear Proteins, Pedigree, Potassium Channels, Potassium Channels, Voltage-Gated
Added September 19, 2013
0 Communities
1 Members
0 Resources
22 MeSH Terms
Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity.
Huq AH, Sutcliffe JS, Nakao M, Shen Y, Gibbs RA, Beaudet AL
(1997) Genome Res 7: 642-8
MeSH Terms: Alleles, Autoantigens, Cells, Cultured, Chromosomes, Human, Pair 15, Cloning, Molecular, CpG Islands, DNA Methylation, DNA-Cytosine Methylases, Exons, Gene Expression, HeLa Cells, Humans, Methylation, Molecular Sequence Data, Polymerase Chain Reaction, Prader-Willi Syndrome, Promoter Regions, Genetic, Repetitive Sequences, Nucleic Acid, Ribonucleoproteins, Small Nuclear, Sequence Analysis, DNA, Transfection, snRNP Core Proteins
Added February 20, 2014
0 Communities
1 Members
0 Resources
22 MeSH Terms
Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
Kubota T, Sutcliffe JS, Aradhya S, Gillessen-Kaesbach G, Christian SL, Horsthemke B, Beaudet AL, Ledbetter DH
(1996) Am J Med Genet 66: 77-80
MeSH Terms: Autoantigens, DNA Methylation, Exons, Female, Genetic Markers, Genomic Imprinting, Humans, Male, Prader-Willi Syndrome, Ribonucleoproteins, Small Nuclear, snRNP Core Proteins
Added February 20, 2014
0 Communities
1 Members
0 Resources
11 MeSH Terms
Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus.
Jinno Y, Sengoku K, Nakao M, Tamate K, Miyamoto T, Matsuzaka T, Sutcliffe JS, Anan T, Takuma N, Nishiwaki K, Ikeda Y, Ishimaru T, Ishikawa M, Niikawa N
(1996) Hum Mol Genet 5: 1155-61
MeSH Terms: Alleles, Animals, Base Sequence, CpG Islands, DNA, DNA Methylation, DNA Primers, Embryonic Development, Evolution, Molecular, Female, Genes, Tumor Suppressor, Genomic Imprinting, Humans, Male, Mice, Molecular Sequence Data, Muscle Proteins, Placenta, Polymerase Chain Reaction, Pregnancy, RNA, Long Noncoding, RNA, Untranslated, Species Specificity
Added February 20, 2014
0 Communities
1 Members
0 Resources
23 MeSH Terms
Detection of imprinting mutations in Angelman syndrome using a probe for exon alpha of SNRPN.
Beuten J, Sutcliffe JS, Casey BM, Beaudet AL, Hennekam RC, Willems PJ
(1996) Am J Med Genet 63: 414-5
MeSH Terms: Angelman Syndrome, Autoantigens, Blotting, Southern, CpG Islands, DNA Methylation, DNA Probes, Exons, Genomic Imprinting, Humans, Mutation, Prader-Willi Syndrome, Ribonucleoproteins, Small Nuclear, snRNP Core Proteins
Added February 20, 2014
0 Communities
1 Members
0 Resources
13 MeSH Terms