Human chromosome 11 contains two different growth suppressor genes for embryonal rhabdomyosarcoma - Wikidata - wikimedia - TriplyDB

Human chromosome 11 contains two different growth suppressor genes for embryonal rhabdomyosarcoma

Human chromosome 11 contains two different growth suppressor genes for embryonal rhabdomyosarcoma

http://www.wikidata.org/entity/Q36858083

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Mrvi1, a common MRV integration site in BXH2 myeloid leukemias, encodes a protein with homology to a lymphoid-restricted membrane protein Jaw1 Chromosome 7 suppresses indefinite division of nontumorigenic immortalized human fibroblast cell lines KMST-6 and SUSM-1 Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11 FOXO1-FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma.Caveolin-1 is down-regulated in alveolar rhabdomyosarcomas and negatively regulates tumor growth.Functional cloning of a tumor suppressor gene, TSLC1, in human non-small cell lung cancer.Senescence of immortal human fibroblasts by the introduction of normal human chromosome 6 In vitro loss of heterozygosity targets the PTEN/MMAC1 gene in melanoma.Microsatellite instability in childhood rhabdomyosarcoma is locus specific and correlates with fractional allelic loss.Selecting multimodal therapy for rhabdomyosarcoma.Caveolins in rhabdomyosarcoma Rhabdomyosarcomas: an overview on the experimental animal models.RETRACTED: Association of ataxia telangiectasia mutated (ATM) gene mutation/deletion with rhabdomyosarcoma.The role of insulin-like growth factor system in soft tissue sarcomas: from physiopathology to targeted therapeutic approaches.Optimization of rhabdomyosarcoma disseminated disease assessment by flow cytometry.Identification of candidate liver tumor suppressor genes from human 11p11.2-p12.Subchromosomal mapping of a putative transformation suppressor gene on human chromosome 1.Complementation of a DNA repair deficiency in six human tumor cell lines by chromosome 11.Embryonal Rhabdomyosarcoma of the Adult's Vocal Cord: A Case Report.Hypermethylation of the WT1 and calcitonin gene promoter regions at chromosome 11p in human colorectal cancer.Notch, wnt, and hedgehog pathways in rhabdomyosarcoma: from single pathways to an integrated network.Hedgehog Pathway Inhibition Hampers Sphere and Holoclone Formation in Rhabdomyosarcoma.Ligand-dependent Hedgehog pathway activation in Rhabdomyosarcoma: the oncogenic role of the ligands.A review of soft-tissue sarcomas: translation of biological advances into treatment measures.

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P2860

Human chromosome 11 contains two different growth suppressor genes for embryonal rhabdomyosarcoma

http://www.wikidata.org/entity/Q36858083

description

1992 nî lūn-bûn

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1992年の論文

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1992年論文

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1992年論文

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1992年論文

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1992年論文

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1992年論文

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1992年论文

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1992年论文

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1992年论文

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name

Human chromosome 11 contains t ...... for embryonal rhabdomyosarcoma

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type

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Human chromosome 11 contains t ...... for embryonal rhabdomyosarcoma

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Human chromosome 11 contains t ...... for embryonal rhabdomyosarcoma

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

P1476

Human chromosome 11 contains t ...... for embryonal rhabdomyosarcoma

@en

P2093

B E Weissman

http://www.w3.org/2001/XMLSchema#string

E Livanos

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H J Scrable

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M J Arboleda

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M Oshimura

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W E Loh

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W K Cavenee

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P2860

Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers

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

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

Isolation of a transforming sequence from a human bladder carcinoma cell line

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

Suppression of human colorectal carcinoma cell growth by wild-type p53

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

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

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

P304

1755-1759

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scholarly article

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10.1073/PNAS.89.5.1755

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5

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89

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1992-03-01T00:00:00Z

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21809135

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1347425

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48531

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