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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 37 of 37

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The gene encoding p120cas, a novel catenin, localizes on human chromosome 11q11 (CTNND) and mouse chromosome 2 (Catns).
Reynolds AB, Jenkins NA, Gilbert DJ, Copeland NG, Shapiro DN, Wu J, Daniel JM
(1996) Genomics 31: 127-9
MeSH Terms: Animals, Base Sequence, Catenins, Cell Adhesion Molecules, Chromosome Mapping, Chromosomes, Human, Pair 11, DNA, Complementary, Female, Humans, In Situ Hybridization, Fluorescence, Male, Mice, Mice, Inbred C57BL, Molecular Sequence Data, Muridae, Neoplasms, Phenotype, Phosphoproteins, Species Specificity
Added March 5, 2014
1 Communities
1 Members
0 Resources
19 MeSH Terms
Lack of microsatellite instability in giant cell tumor of bone.
Scheiner M, Hedges L, Schwartz HS, Butler MG
(1996) Cancer Genet Cytogenet 88: 35-8
MeSH Terms: Adult, Bone Neoplasms, Carcinoma, Giant Cell, Chromosome Aberrations, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 17, Chromosomes, Human, Pair 18, Chromosomes, Human, Pair 19, Chromosomes, Human, Pair 5, Female, Heterozygote, Humans, Male, Microsatellite Repeats, Middle Aged, Polymerase Chain Reaction, Telomerase, Telomere
Added March 5, 2014
0 Communities
1 Members
0 Resources
19 MeSH Terms
Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
Glaser B, Chiu KC, Liu L, Anker R, Nestorowicz A, Cox NJ, Landau H, Kaiser N, Thornton PS, Stanley CA
(1995) Hum Mol Genet 4: 879-86
MeSH Terms: Alleles, Chromosome Mapping, Chromosomes, Human, Pair 11, Female, Founder Effect, Genes, Recessive, Genetic Linkage, Genetic Markers, Haplotypes, Humans, Hyperinsulinism, Jews, Male, Pedigree, Polymorphism, Genetic, Recombination, Genetic
Added February 22, 2016
0 Communities
1 Members
0 Resources
16 MeSH Terms
Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.
Cox NJ, Bell GI, Xiang KS
(1988) Am J Hum Genet 43: 495-501
MeSH Terms: Alleles, Chromosome Mapping, Chromosomes, Human, Pair 11, Gene Frequency, Genetic Linkage, Haplotypes, Humans, Insulin, Insulin-Like Growth Factor II, Polymorphism, Restriction Fragment Length, Somatomedins
Added February 22, 2016
0 Communities
1 Members
0 Resources
11 MeSH Terms
Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.
Xiang K, Cox NJ, Bell GI
(1988) Nucleic Acids Res 16: 3599
MeSH Terms: Chromosomes, Human, Pair 11, DNA Restriction Enzymes, Deoxyribonucleases, Type II Site-Specific, Genetic Linkage, Humans, Insulin-Like Growth Factor II, Polymorphism, Genetic, Polymorphism, Restriction Fragment Length, Somatomedins
Added February 22, 2016
0 Communities
1 Members
0 Resources
9 MeSH Terms
Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: the GAW5 data.
Cox NJ, Gogolin KJ, Horvath VJ, Barker DF, Wright E, Tran T, Skolnick MH, Boehm BO, Fehsel K, Bertrams J
(1989) Genet Epidemiol 6: 21-6
MeSH Terms: Chromosome Mapping, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 6, Diabetes Mellitus, Type 1, Epidemiologic Methods, Europe, Genes, Regulator, HLA-DQ Antigens, HLA-DR Antigens, Humans, Insulin, Multicenter Studies as Topic, North America, Polymorphism, Restriction Fragment Length
Added February 22, 2016
0 Communities
1 Members
0 Resources
14 MeSH Terms
Cytogenetic abnormalities in a rare case of giant cell osteogenic sarcoma.
Schwartz HS, Allen GA, Chudoba I, Butler MG
(1992) Cancer Genet Cytogenet 58: 60-5
MeSH Terms: Adolescent, Bone Neoplasms, Chromosome Aberrations, Chromosomes, Human, Pair 11, Female, Femur, Giant Cell Tumors, Humans, Monosomy, Osteosarcoma, Telomere
Added March 5, 2014
0 Communities
1 Members
0 Resources
11 MeSH Terms