Evaluation of candidate tumour suppressor genes on chromosome 18 in colorectal cancers

Sam Thiagalingam, Christoph Lengauer, Frederick S. Leach, +9

Nature Genetics

Tumor BiologyChromatinColorectal CancersMedicineGenetics +9

Non-function of a Moloney murine leukaemia virus regulatory sequence in F9 embryonal carcinoma cells

Elwood Linney, Brian R. Davis, Joan Overhauser, +2

Nature

Tumor BiologyOncogenic AgentPathologyAdult T-cell Leukemia-lymphomaGene Expression +5

Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation

Mainardi Pc, Chiara Perfumo, Gabriella Coucourde, +6

Journal of Medical Genetics

Gene Deletion DataMolecular CharacterisationItalian Cdcs RegisterCytogeneticsGenetic Disorder +9

Hemizygosity of δ-Catenin (CTNND2) Is Associated with Severe Mental Retardation in Cri-du-Chat Syndrome

Miguel Medina, R. Catrinel Marinescu, Joan Overhauser, +1

Genomics

Severe Mental RetardationCri-du-chat SyndromeMolecular NeurosciencePsychiatryGenetic Disorder +5

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome

Joan Overhauser, Xlaogu Huang, Meryl Gersh, +6

Human Molecular Genetics

CytogeneticsGeneticsPathologyMolecular GeneticsEpigenetics +17

Human exonuclease I interacts with the mismatch repair protein hMSH2.

Christoph Schmütte, R. Catrinel Marinescu, Margaret M. Sadoff, +3

PubMed

ChromatinGenome InstabilityHuman ExonucleaseSomatic VariantNatural Sciences +12

A Microsatellite Genetic Linkage Map of Human Chromosome 18

Richard E. Straub, Marcy C. Speer, Ying Luo, +4

Genomics

CytogeneticsGeneticsLinkage AnalysisHuman Chromosome 18Genetic Variation +1

Transformation properties of type 5 adenovirus mutants that differentially express the E1A gene products.

Keri Haley, Joan Overhauser, Lee E. Babiss, +2

Proceedings of the National Academy of Sciences

Transformation PropertiesBaby Rat KidneyViral ReplicationNatural SciencesAdenovirus Mutants +13

Molecular analysis of the 18q- syndrome--and correlation with phenotype.

Antonie D. Kline, Mary E. White, Ronald J. Wapner, +7

PubMed

Evidence for a distinct region causing a cat-like cry in patients with 5p deletions.

Meryl Gersh, Sheryl A. Goodart, Linda M. Pasztor, +3

PubMed