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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: 31 to 34 of 34

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Functional characterization of a testis-specific DNA binding activity at the H19/Igf2 imprinting control region.
Bowman AB, Levorse JM, Ingram RS, Tilghman SM
(2003) Mol Cell Biol 23: 8345-51
MeSH Terms: Animals, Animals, Newborn, Base Sequence, Binding Sites, DNA, DNA Methylation, Female, Genomic Imprinting, Insulin-Like Growth Factor II, Male, Mice, Mice, Mutant Strains, Ovary, RNA, Long Noncoding, RNA, Untranslated, Testis
Added June 9, 2010
1 Communities
1 Members
0 Resources
16 MeSH Terms
Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19.
DeBaun MR, Niemitz EL, Feinberg AP
(2003) Am J Hum Genet 72: 156-60
MeSH Terms: Adult, Beckwith-Wiedemann Syndrome, Child, CpG Islands, DNA Methylation, Female, Fertilization in Vitro, Genomic Imprinting, Humans, Male, Membrane Proteins, Molecular Sequence Data, Phenotype, Potassium Channels, Voltage-Gated, RNA, Long Noncoding, RNA, Untranslated
Added November 27, 2013
1 Communities
1 Members
0 Resources
16 MeSH Terms
Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects.
DeBaun MR, Niemitz EL, McNeil DE, Brandenburg SA, Lee MP, Feinberg AP
(2002) Am J Hum Genet 70: 604-11
MeSH Terms: Abdomen, Beckwith-Wiedemann Syndrome, Chromosomes, Human, Pair 11, Cohort Studies, DNA Methylation, Female, Fetal Macrosomia, Gene Frequency, Genetic Predisposition to Disease, Genomic Imprinting, Humans, Hypertrophy, Hypoglycemia, Male, Membrane Proteins, Molecular Sequence Data, Neoplasms, Phenotype, Potassium Channels, Voltage-Gated, RNA, Long Noncoding, RNA, Untranslated, Registries, Uniparental Disomy
Added November 27, 2013
1 Communities
1 Members
0 Resources
23 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