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Results: 21 to 30 of 37

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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
Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocation.
Lovett BD, Lo Nigro L, Rappaport EF, Blair IA, Osheroff N, Zheng N, Megonigal MD, Williams WR, Nowell PC, Felix CA
(2001) Proc Natl Acad Sci U S A 98: 9802-7
MeSH Terms: Antigens, Neoplasm, Antineoplastic Combined Chemotherapy Protocols, Catechols, Child, Chromosome Breakage, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 4, Combined Modality Therapy, Cyclophosphamide, DNA Topoisomerases, Type II, DNA, Neoplasm, DNA-Binding Proteins, Dactinomycin, Etoposide, Female, Histone-Lysine N-Methyltransferase, Humans, Ifosfamide, Isoenzymes, Models, Genetic, Molecular Sequence Data, Myeloid-Lymphoid Leukemia Protein, Neoplasm Proteins, Neoplasms, Second Primary, Nuclear Proteins, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Proto-Oncogenes, Radiotherapy, Adjuvant, Recombination, Genetic, Rhabdomyosarcoma, Alveolar, Soft Tissue Neoplasms, Transcription Factors, Transcriptional Elongation Factors, Translocation, Genetic, Vincristine
Added March 5, 2014
0 Communities
1 Members
0 Resources
35 MeSH Terms
Lack of defective expression of the ATM gene in sporadic breast cancer tissues and cell lines.
Kovalev S, Mateen A, Zaika AI, O'Hea BJ, Moll UM
(2000) Int J Oncol 16: 825-31
MeSH Terms: Ataxia Telangiectasia, Ataxia Telangiectasia Mutated Proteins, Breast, Breast Neoplasms, Cell Cycle Proteins, Chromosomes, Human, Pair 11, DNA-Binding Proteins, Female, Gene Expression Regulation, Neoplastic, Humans, Loss of Heterozygosity, Mutation, Protein Serine-Threonine Kinases, Reverse Transcriptase Polymerase Chain Reaction, Tumor Cells, Cultured, Tumor Suppressor Proteins
Added March 5, 2014
0 Communities
1 Members
0 Resources
16 MeSH Terms
Discontinuous deletions at 11q23 in B cell chronic lymphocytic leukemia.
Zhu Y, Monni O, El-Rifai W, Siitonen SM, Vilpo L, Vilpo J, Knuutila S
(1999) Leukemia 13: 708-12
MeSH Terms: Aged, Chromosome Deletion, Chromosomes, Human, Pair 11, Female, Humans, In Situ Hybridization, Fluorescence, Leukemia, Lymphocytic, Chronic, B-Cell, Male, Middle Aged
Added March 5, 2014
0 Communities
1 Members
0 Resources
9 MeSH Terms
Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.
Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP
(1999) Proc Natl Acad Sci U S A 96: 5203-8
MeSH Terms: Beckwith-Wiedemann Syndrome, Chromosomes, Human, Pair 11, Gene Expression Regulation, Genomic Imprinting, Humans, Insulin-Like Growth Factor II, KCNQ Potassium Channels, KCNQ1 Potassium Channel, Membrane Proteins, Potassium Channels, Potassium Channels, Voltage-Gated, Transcription, Genetic, Wilms Tumor
Added November 27, 2013
1 Communities
1 Members
0 Resources
13 MeSH Terms
Hemihypertrophy and a poorly differentiated embryonal rhabdomyosarcoma of the pelvis.
Samuel DP, Tsokos M, DeBaun MR
(1999) Med Pediatr Oncol 32: 38-43
MeSH Terms: Adolescent, Chromosomes, Human, Pair 11, Fatal Outcome, Foot Deformities, Congenital, Humans, Hypertrophy, Immunohistochemistry, Leg, Loss of Heterozygosity, Lung Neoplasms, Male, MyoD Protein, Pelvic Neoplasms, Rhabdomyosarcoma, Embryonal, Trans-Activators
Added November 27, 2013
1 Communities
0 Members
0 Resources
15 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
The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships.
Lindner T, Gragnoli C, Schulze J, Rietzsch H, Petzold C, Schröder HE, Cox NJ, Bell GI
(1997) Diabetes 46: 1227-9
MeSH Terms: ATP-Binding Cassette Transporters, Aged, Base Sequence, Chicago, Chromosomes, Human, Pair 11, Diabetes Mellitus, Type 2, Family, Genetic Linkage, Genetic Markers, Genotype, Germany, Humans, Middle Aged, Obesity, Potassium Channels, Potassium Channels, Inwardly Rectifying, Receptors, Drug, Sulfonylurea Receptors, Whites
Added February 22, 2016
0 Communities
1 Members
0 Resources
19 MeSH Terms
The human HNP36 gene is localized to chromosome 11q13 and produces alternative transcripts that are not mutated in multiple endocrine neoplasia, type 1 (MEN I) syndrome.
Williams JB, Rexer B, Sirripurapu S, John S, Goldstein R, Phillips JA, Haley LL, Sait SN, Shows TB, Smith CM, Gerhard DS
(1997) Genomics 42: 325-30
MeSH Terms: Alternative Splicing, Base Sequence, Chromosome Mapping, Chromosomes, Human, Pair 11, DNA Primers, DNA, Complementary, Equilibrative-Nucleoside Transporter 2, Humans, In Situ Hybridization, Fluorescence, Molecular Sequence Data, Multiple Endocrine Neoplasia Type 1, Mutation, Nuclear Proteins, Polymerase Chain Reaction, RNA, Messenger, Sequence Homology, Amino Acid, Tissue Distribution
Added March 10, 2014
0 Communities
1 Members
0 Resources
17 MeSH Terms
Spontaneous DNA lesions poison human topoisomerase IIalpha and stimulate cleavage proximal to leukemic 11q23 chromosomal breakpoints.
Kingma PS, Greider CA, Osheroff N
(1997) Biochemistry 36: 5934-9
MeSH Terms: Base Sequence, Chromosomes, Human, Pair 11, DNA, DNA Damage, DNA Topoisomerases, Type II, Humans, Leukemia, Molecular Sequence Data, Recombinant Proteins, Topoisomerase II Inhibitors, Translocation, Genetic
Added March 5, 2014
0 Communities
1 Members
0 Resources
11 MeSH Terms