Selective transfer of individual human chromosomes to recipient cells.
about
The isolation and characterization of a novel cDNA demonstrating an altered mRNA level in nontumorigenic Wilms' microcell hybrid cellsMicrocell-mediated chromosome transfer identifies EPB41L3 as a functional suppressor of epithelial ovarian cancers.Tumor suppressive role of a 2.4 Mb 9q33-q34 critical region and DEC1 in esophageal squamous cell carcinoma.Construction of gene libraries for each human chromosome.Progression of colorectal cancer is associated with multiple tumor suppressor gene defects but inhibition of tumorigenicity is accomplished by correction of any single defect via chromosome transfer.Microcell-mediated transfer of a single human chromosome complements xeroderma pigmentosum group A fibroblastsDirect gene transfer into human cultured cells facilitated by laser micropuncture of the cell membrane.Growth of Chlamydia trachomatis in enucleated cells.A recombination event that redefines the Huntington disease region.Localization of HeLa cell tumor-suppressor gene to the long arm of chromosome II.Suppression of tumorigenicity with continued expression of the c-Ha-ras oncogene in EJ bladder carcinoma-human fibroblast hybrid cells.Isolation of polymorphic DNA fragments from human chromosome 4.The manipulation of chromosomes by mankind: the uses of microcell-mediated chromosome transfer.Human immunodeficiency virus type 1 Rev-responsive element RNA binds to host cell-specific proteins.Functional evidence for a second tumor suppressor gene on human chromosome 17.Human chromosome 12 encodes a species-specific factor which increases human immunodeficiency virus type 1 tat-mediated trans activation in rodent cellsSuppression of deregulated c-MYC expression in human colon carcinoma cells by chromosome 5 transfer.Isolation of microcell hybrid clones containing retroviral vector insertions into specific human chromosomesSelection against expression of the Escherichia coli gene gpt in hprt+ mouse teratocarcinoma and hybrid cellsLoss of oncogenic ras expression does not correlate with loss of tumorigenicity in human cells.Frontiers in mammalian cell culture.Differential elimination of 3p and retention of 3q segments in human/mouse microcell hybrids during tumor growth.Oncoprotein BMI-1 induces the malignant transformation of HaCaT cells.Functional evidence of decreased tumorigenicity associated with monochromosome transfer of chromosome 14 in esophageal cancer and the mapping of tumor-suppressive regions to 14q32.Monochromosome transfer provides functional evidence for growth-suppressive genes on chromosome 14 in nasopharyngeal carcinoma.Chromosome 18 suppresses the tumorigenicity of prostate cancer cells.The gene as theme in the paradigm of cancer.Malignant transformation of human diploid fibroblasts and suppression of their anchorage independence by introduction of chromosome 13.Transchromosomal mouse embryonic stem cell lines and chimeric mice that contain freely segregating segments of human chromosome 21.The Janeway Lecture 1992. Nine decades of radiobiology: is radiation therapy any the better for it?Sustained nontumorigenic phenotype correlates with a largely stable chromosome content during long-term culture of the human keratinocyte line HaCaT.Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay.Normal human chromosome 2 induces cellular senescence in the human cervical carcinoma cell line SiHa.Suppression of the tumorigenic phenotype of a rat liver epithelial tumor cell line by the p11.2-p12 region of human chromosome 11.Simple purification of human chromosomes to homogeneity using muntjac hybrid cells.Evidence that wild-type TP53, and not genes on either chromosome 1 or 11, controls the tumorigenic phenotype of the human fibrosarcoma HT1080.Chromosome 13 transfer provides evidence for regulation of RB1 protein expression.Correlation of the inability to sustain growth in defined serum-free medium with the suppression of tumorigenicity in Wilms' nephroblastoma.Irradiation microcell-mediated chromosome transfer (XMMCT): the generation of specific chromosomal arm deletions.Transfer of a normal human chromosome 11 suppresses tumorigenicity of some but not all tumor cell lines.
P2860
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P2860
Selective transfer of individual human chromosomes to recipient cells.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh
1985年學術文章
@zh-hant
name
Selective transfer of individual human chromosomes to recipient cells.
@ast
Selective transfer of individual human chromosomes to recipient cells.
@en
type
label
Selective transfer of individual human chromosomes to recipient cells.
@ast
Selective transfer of individual human chromosomes to recipient cells.
@en
prefLabel
Selective transfer of individual human chromosomes to recipient cells.
@ast
Selective transfer of individual human chromosomes to recipient cells.
@en
P2093
P2860
P356
P1476
Selective transfer of individual human chromosomes to recipient cells.
@en
P2093
E J Stanbridge
E S Srivatsan
G V Leipzig
J H Sameshima
P2860
P304
P356
10.1128/MCB.5.1.140
P407
P577
1985-01-01T00:00:00Z