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

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

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

http://www.wikidata.org/entity/Q33858202

about

Mutually exclusive expression of a helix-loop-helix gene and N-myc in human neuroblastomas and in normal development Intrachromosomal rearrangements fusing L-myc and rlf in small-cell lung cancer Expression of the receptor-linked protein tyrosine phosphatase LAR: proteolytic cleavage and shedding of the CAM-like extracellular region A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3 miR-34a repression of SIRT1 regulates apoptosis cDNA array-CGH profiling identifies genomic alterations specific to stage and MYCN-amplification in neuroblastoma Epigenetic deregulation of microRNAs in rhabdomyosarcoma and neuroblastoma and translational perspectives Role of CHD5 in human cancers: 10 years later Neuroblastoma: issues in transplantation PPAR Gamma in Neuroblastoma: The Translational Perspectives of Hypoglycemic Drugs Genomic structure and mutational analysis of the human KIF1B gene which is homozygously deleted in neuroblastoma at chromosome 1p36.2 Therapeutic activity of CPT-11, a DNA-topoisomerase I inhibitor, against peripheral primitive neuroectodermal tumour and neuroblastoma xenografts Olfactory neuroblastoma is a peripheral primitive neuroectodermal tumor related to Ewing sarcoma Molecular genetics of neurological tumours Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression.Aberrant expression of RAB1A in human tongue cancer.Diagnosis and classification of the small round-cell tumors of childhood.Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma.Evidence for mitotic recombination in Wei/+ heterozygous mice.Pediatric oncology.Autoantibody signature differentiates Wilms tumor patients from neuroblastoma patients.3T3 cell lines stably expressing Pax6 or Pax6(5a)--a new tool used for identification of common and isoform specific target genes Clinical categories of neuroblastoma are associated with different patterns of loss of heterozygosity on chromosome arm 1p.Genetic characterization of large parathyroid adenomas A unique role of the DNA fragmentation factor in maintaining genomic stability.Neuroblastoma tumour genetics: clinical and biological aspects.Constitutional 1p36 deletion in a child with neuroblastoma.Loss of heterozygosity for alleles on chromosome II in cervical carcinoma.Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV Dominant and recessive molecular changes in neuroblastomas.Molecular biology in the diagnosis and prognosis of solid and lymphoid tumors.Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology.Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas.The tumour suppressor CHD5 forms a NuRD-type chromatin remodelling complex.Mechanisms of CHD5 Inactivation in neuroblastomas.Allelic imbalance on chromosome 5q predicts long-term survival in neuroblastoma An increased NM23H1 copy number may be a poor prognostic factor independent of LOH on 1p in neuroblastomas A dominant-negative mutant of Max that inhibits sequence-specific DNA binding by Myc proteins.

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P2860

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

http://www.wikidata.org/entity/Q33858202

description

1989 nî lūn-bûn

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1989 թուականի Մայիսին հրատարակուած գիտական յօդուած

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1989 թվականի մայիսին հրատարակված գիտական հոդված

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

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Loss of heterozygosity for the ...... tion with N-myc amplification.

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C T Fong

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P2860

The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity

Human renin gene: structure and sequence analysis

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

Corrected sequences of cDNAs for human salivary and pancreatic alpha-amylases [corrected]

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

Clonal analysis of human colorectal tumors

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

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma

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