Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression. - Wikidata - awgldk - TriplyDB

Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression.

Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression.

http://www.wikidata.org/entity/Q30502324

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Detection of three novel translocation and specific common chromosomal break sites in malignant melanoma by spectral karyotyping Molecular clonality of in-transit melanoma metastasis.A modifying locus for familial adenomatous polyposis may be present on chromosome 1p35-p36 Tumor progression, early diagnosis and prognosis of melanoma.Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma.Malignancy: Tumor Suppressor Gene Aberrations in Acute Myelogenous Leukemia.A ubiquitin ligase, skeletrophin, is a negative regulator of melanoma invasion.Oncogenes in melanomas.Molecular biology in the diagnosis and prognosis of solid and lymphoid tumors.Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer Neuroblastoma--clinical applications of molecular parameters.Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival.Association of specific chromosome alterations with tumour phenotype in posterior uveal melanoma.Homozygous deletions within human chromosome band 9p21 in melanoma.Tumor suppressor genes and cancer of the human nervous system.Liquid Biopsies for Assessing Metastatic Melanoma Progression.PLA2 (group IIA phospholipase A2) as a prognostic determinant in stage II colorectal carcinoma.Loss of heterozygosity on chromosome 1 and 9 and hormone receptor analysis of metastatic malignant melanoma presenting in breast.Chromosomal imbalances in primary and metastatic melanomas revealed by comparative genomic hybridization.Characterization of chromosome 1 abnormalities in malignant melanomas.p73-Binding Partners and Their Functional Significance.PITSLRE protein kinase activity is associated with apoptosis.Regulation of the p53 homolog p73 by adenoviral oncogene E1A.Frequent allelic imbalance suggests involvement of a tumor suppressor gene at 1p36 in the pathogenesis of human lung cancers.Genetics of risk factors for melanoma: an adult twin study of nevi and freckles.TTC4, a novel candidate tumor suppressor gene at 1p31 is often mutated in malignant melanoma of the skin.Lack of phospholipase A2 mutations in neuroblastoma, melanoma and colon-cancer cell lines.Genomic instability in 1p and human malignancies.Metastasis suppressed, but tumorigenicity and local invasiveness unaffected, in the human melanoma cell line MelJuSo after introduction of human chromosomes 1 or 6.Biologic, immunocytochemical, and cytogenetic characterization of two new human melanoma cell lines: IIB-MEL-LES and IIB-MEL-IAN.Decreased RIZ1 expression but not RIZ2 in hepatoma and suppression of hepatoma tumorigenicity by RIZ1.Transformation of murine melanocytes by basic fibroblast growth factor cDNA and oncogenes and selective suppression of the transformed phenotype in a reconstituted cutaneous environment The tumor suppressor Chd5 is induced during neuronal differentiation in the developing mouse brain.Genetic alterations in hepatocellular carcinomas: association between loss of chromosome 4q and p53 gene mutations.The biology of perlecan: the multifaceted heparan sulphate proteoglycan of basement membranes and pericellular matrices.The PR domain of the Rb-binding zinc finger protein RIZ1 is a protein binding interface and is related to the SET domain functioning in chromatin-mediated gene expression.Tumor suppressor gene methylation on the short arm of chromosome 1 in chronic myelogenous leukemia.Preliminary evidence for involvement of the tumour suppressor gene CHD5 in a family with cutaneous melanoma.Molecular genetic analysis of malignant melanomas for aberrations of the WNT signaling pathway genes CTNNB1, APC, ICAT and BTRC.

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P2860

Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression.

http://www.wikidata.org/entity/Q30502324

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1989 nî lūn-bûn

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1989 թուականի Յունիսին հրատարակուած գիտական յօդուած

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1989年の論文

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1989年論文

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1989年論文

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1989年論文

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1989年論文

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1989年论文

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Loss of alleles from the dista ...... in melanoma tumor progression.

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Loss of alleles from the dista ...... in melanoma tumor progression.

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Loss of alleles from the dista ...... in melanoma tumor progression.

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Loss of alleles from the dista ...... in melanoma tumor progression.

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Loss of alleles from the dista ...... in melanoma tumor progression.

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Loss of alleles from the dista ...... in melanoma tumor progression.

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Loss of alleles from the dista ...... in melanoma tumor progression.

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P2860

Identification of a single chromosome in the normal human genome essential for suppression of hamster cell transformation

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage

A general method for isolation of high molecular weight DNA from eukaryotes

Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.

Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p.

Variable number of tandem repeat (VNTR) markers for human gene mapping.

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.

Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene

Cutaneous malignant melanoma and familial dysplastic nevi: evidence for autosomal dominance and pleiotropy.

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