Homozygous deletion on the chromosomal region 5q12.3 in human lines of small-cell lung cancers
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2002-07-01
著者
-
MIWA Wataru
Oncogene Division, National Cancer Center Research Institute
-
SEKIYA Takao
Oncogene Division, National Cancer Center Research Institute
-
MURAKAMI Yoshinori
Oncogene Division, National Cancer Center Research Institute
-
Murakami Y
Tumor Suppression & Functional Genomics Project Natl. Cancer Cent. Res. Inst.
-
MARUYAMA Tomoko
Tumor Suppression and the Functional Genomics Project, National Cancer Center Research Institute
-
TAMURA Kenji
Oncogene Division, National Cancer Center Research Institute
-
MARUYAMA Tomoko
Oncogene Division, National Cancer Center Research Institute
-
Murakami Yoshinori
Tumor Suppression And Functional Genomics Project National Cancer Center Research Institute
-
Miwa Wataru
Oncogene Division National Cancer Center Research Institute
-
Sekiya T
Faculty Of Engineering Yokohama National University
-
Maruyama Tomoko
Tumor Suppression & Functional Genomics Project National Cancer Center Research Institute
-
Murakami Yoshinori
Oncogene Division National Cancer Center Research Institute
-
Sekiya Takao
Oncogene Division National Cancer Center Research Institute
-
Tamura K
Oncogene Division National Cancer Center Research Institute
-
Tamura Kenji
Oncogene Division National Cancer Center Research Institute
-
SEKIYA Takao
Oncogene Div. Natl. Cancer Ctr. Res. Inst.
関連論文
- Outpatient clinic for genetic counseling and gene testing of retinoblastoma
- Absence of a Mutation of the p21/WAF1 Gene in Human Lung and Pancreatic Cancers
- Association of p53 Gene Mutations with Short Survival in Pancreatic Adenocarcinoma
- Detection of allelic imbalance in the gene expression of hMSH2 or RB1 in lymphocytes from pedigrees of hereditary, nonpolyposis, colorectal cancer and retinoblastoma by an RNA difference plot
- P-13. Comparative assignments of the TSLC1 and TSLC1-like tumor suppressor genes, TSLL1 and TSLL2, to rat chromosomes by fluorescence in situ hybridization(Abstracts of the oral and poster presentations, Abstracts of the 54th Annual Meeting of the Society
- Homozygous deletion on the chromosomal region 5q12.3 in human lines of small-cell lung cancers
- Promoter Methylation of TSLC1 and Tumor Suppression by Its Gene Product in Human Prostate Cancer
- Four single-nucleotide polymorphisms in the human BUB1 gene
- Construction of human-rodent hybrid cells containing single transferable fragments of human chromosome 10p
- Deletion Mapping of Chromosome 10 in Human Glioma
- Involvement of a cell adhesion molecule, TSLC1/IGSF4, in human oncogenesis
- Nonsense Mutation at Codon 63 of the BRCA1 Gene in Japanese Breast Cancer Patients
- Isolation of CpG island fragments from P1 clones of human chromosome 11q13 on the basis of thermal stability of DNA fragments
- Nemo-like kinase suppresses a wide range of transcription factors, including nuclear factor-кB
- Defects in Anatase TiO_2 Single Crystal Controlled by Heat Treatments (Condensed Matter: Electronic Structure, Electrical, Magnetic and Optical Properties)
- Multiple gastrinoma successfully resected with the aid of intraoperative arterial secretin injection test
- Alterations of p53 gene and Ha-ras gene are independent events in solar keratosis and squamous cell carcinoma
- Low Incidence of a Nucleotide Sequence Alteration of the Neurofibromatosis 2 Gene in Human Breast Cancers
- Decay Processes of a Photo-Excited State in a Strong Electron-Phonon Coupling System Trans-[Pt(en)_2Cl_2](CIO_4)_2
- Luminescence Spectrum of a Strong Electron-Phonon Coupling System trans-[PtCl_2(en)_2](ClO_4)_2 : Condensed Matter: Electronic Properties, etc.
- Genetic alterations in human pancreatic cancer
- Nucleotide sequence of the remaining allele of c-H-ras-1 in a human lung carcinoma having loss of heterozygosity at the HRAS1 locus.
- Isolation of CpG Island Fragments: a Putative Promoter Region of the Human Prostacyclin Synthase Gene.:a Putative Promoter Region of the Human Prostacyclin Synthase Gene