Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer

Paul Rozen, Ruth Shomrat, Hana Strul, +4

Gastroenterology

Cancer RiskCancer EpidemiologyMedicineGeneticsGenetic Epidemiology +11

Expression of the cDNA for the beta subunit of human casein kinase II confers partial UV resistance on xeroderma pigmentosum cells

Tal Teitz, Dalia Eli, Michal Penner, +6

Mutation Research/DNA Repair

Molecular PhysiologyCell SignalingXeroderma Pigmentosum CellsNatural SciencesPhotocarcinogenesis +8

Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCR

Mira Malcov, Tova Naiman, Dalit Ben Yosef, +5

Reproductive BioMedicine Online

Fragile X SyndromeGenetic TestingXenotransplantationMendelian DisorderGenetic Disorder +7

Immortalization of xeroderma pigmentosum cells by simian virus 40 DNA having a defective origin of DNA replication

Dan Canaani, Tova Naiman, Tal Teitz, +1

Somatic Cell and Molecular Genetics

Viral ReplicationMolecular VirologyNatural SciencesGeneticsMolecular Biology +9

Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia

Paul Rozen, Tova Naiman, Hana Strul, +6

Cancer

Molecular Cloning of a Novel Human Gene Encoding a 63-kDa Protein and Its Sublocalization within the 11q13 Locus

Boris Perelman, N. Dafni, Tova Naiman, +9

Genomics

MECP2 Mutations in Israel: Implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome

Yuval Yaron, Bruria Ben Zeev, Ruth Shomrat, +3

Human Mutation

Gross RearrangementsMendelian DisorderGenetic DisorderRett SyndromeGenetics +11

Assignment of the Human Casein Kinase II α′ Subunit Gene (CSNK2A1) to Chromosome 16p13.2-p13.3

Teresa L. Yang‐Feng, Tova Naiman, Idit Kopatz, +3

Genomics

ChromatinChromatin StructureCell DivisionCytogeneticsChromosomal Localization +13

The Risk of Fragile X Premutation Expansion Is Lower in Carriers Detected by General Prenatal Screening Than in Carriers from Known Fragile X Families

Eli Geva, Yuval Yaron, Ruth Shomrat, +6

Genetic Testing

Genetic TestingFertilityGeneticsGenetic EpidemiologyGynecology +18

Complementation of the UV-sensitive phenotype of a xeroderma pigmentosum human cell line by transfection with a cDNA clone library.

Tal Teitz, Tova Naiman, Sofia Avissar, +3

Proceedings of the National Academy of Sciences

Reverse GeneticsGeneticsMolecular BiologyCdna Clone LibraryMolecular Genetics +17