Homozygous deletions within human chromosome band 9p21 in melanoma. - Wikidata - awgldk - TriplyDB

Homozygous deletions within human chromosome band 9p21 in melanoma.

Homozygous deletions within human chromosome band 9p21 in melanoma.

http://www.wikidata.org/entity/Q37286548

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Genomic cloning of methylthioadenosine phosphorylase: a purine metabolic enzyme deficient in multiple different cancers Frizzled homolog proteins, microRNAs and Wnt signaling in cancer Antioncogenes and human cancer.Problems in the interpretation of apparent "radial growth phase" malignant melanomas that metastasize.Molecular clonality of in-transit melanoma metastasis.Melanoma epidemiology, biology and prognosis.Tumor progression, early diagnosis and prognosis of melanoma.Copy number loss of the interferon gene cluster in melanomas is linked to reduced T cell infiltrate and poor patient prognosis Ladder-like amplification of the type I interferon gene cluster in the human osteosarcoma cell line MG63 Two distinct pathways of p16 gene inactivation in gallbladder cancer.Collateral Lethality: A new therapeutic strategy in oncology Molecular aspects of melanocytic dysplastic nevi Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).Confirmation of chromosome 9p linkage in familial melanoma.Allelotyping of butadiene-induced lung and mammary adenocarcinomas of B6C3F1 mice: frequent losses of heterozygosity in regions homologous to human tumor-suppressor genes.Chromosome 9p deletions in cutaneous malignant melanoma tumors: the minimal deleted region involves markers outside the p16 (CDKN2) gene.Localization of a putative tumor suppressor gene by using homozygous deletions in melanomas CDKNA2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas: evidence for a second tumor suppressor gene proximal to CDKN2A.MTS1/p16/CDKN2 lesions in primary glioblastoma multiforme.Low-frequency loss of heterozygosity in Moloney murine leukemia virus-induced tumors in BRAKF1/J mice.Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity.Homozygous deletions on the short arm of chromosome 9 in ovarian adenocarcinoma cell lines and loss of heterozygosity in sporadic tumors Mutations and altered expression of p16INK4 in human cancer.Recurrent DNA copy number changes in 1q, 4q, 6q, 9p, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesothelioma High frequency of chromosome 9 deletion in ovarian cancer: evidence for three tumour-suppressor loci.Involvement of the pRb/p16/cdk4/cyclin D1 pathway in the tumorigenesis of sporadic malignant melanomas.The CDKN2A (p16) gene and human cancer.p53 cooperates with DNA methylation and a suicidal interferon response to maintain epigenetic silencing of repeats and noncoding RNAs Transgenic mouse model of malignant skin melanoma Genetics of melanoma Deletions of the region 17p11-13 in advanced melanoma revealed by cytogenetic analysis and fluorescence in situ hybridization Role of p16/MTS1, cyclin D1 and RB in primary oral cancer and oral cancer cell lines Definition of the role of chromosome 9p21 in sporadic melanoma through genetic analysis of primary tumours and their metastases. The Melanoma Cooperative Group.Breakpoint junctions of chromosome 9p deletions in two human glioma cell lines.Augmentation of effects of interferon-stimulated genes by reversal of epigenetic silencing: potential application to melanoma.Loss of heterozygosity on chromosome 1 and 9 and hormone receptor analysis of metastatic malignant melanoma presenting in breast.Chromosomal and genetic alterations of 7,12-dimethylbenz[a]anthracene-induced melanoma from TP-ras transgenic mice.PTPLAD2 is a tumor suppressor in esophageal squamous cell carcinogenesis.Uncovering the immunotherapeutic cycle initiated by p19Arf and interferon-β gene transfer to cancer cells: An inducer of immunogenic cell death.p53 gene mutations and photocarcinogenesis.

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P2860

Homozygous deletions within human chromosome band 9p21 in melanoma.

http://www.wikidata.org/entity/Q37286548

description

1992 nî lūn-bûn

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1992年の論文

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1992年学术文章

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1992年学术文章

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1992年学术文章

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1992年学术文章

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1992年學術文章

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1992年學術文章

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1992年學術文章

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name

Homozygous deletions within human chromosome band 9p21 in melanoma.

@en

Homozygous deletions within human chromosome band 9p21 in melanoma.

@nl

type

label

Homozygous deletions within human chromosome band 9p21 in melanoma.

@en

Homozygous deletions within human chromosome band 9p21 in melanoma.

@nl

prefLabel

Homozygous deletions within human chromosome band 9p21 in melanoma.

@en

Homozygous deletions within human chromosome band 9p21 in melanoma.

@nl

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PNAS.89.21.10557

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Proceedings of the National Academy of Sciences of the United States of America

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Homozygous deletions within human chromosome band 9p21 in melanoma.

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A N Houghton

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B Bouchard

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D R Vlock

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J Lahti

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J M Kirkwood

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J W Fountain

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L Titus-Ernstoff

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M Karayiorgou

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M S Ernstoff

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S Vijayasaradhi

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P2860

Nucleotide sequence of the cDNA encoding human tyrosinase-related protein

The melanoma antigen gp75 is the human homologue of the mouse b (brown) locus gene product

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

Assignment of the human TYRP (brown) locus to chromosome region 9p23 by nonradioactive in situ hybridization

The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4

Loss of heterozygosity for loci on the long arm of chromosome 6 in human malignant melanoma

Identification of a chromosome 18q gene that is altered in colorectal cancers

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

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

Homozygous deletion of the alpha- and beta 1-interferon genes in human leukemia and derived cell lines

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