Deletion mapping of chromosome 1p and 22q in pheochromocytoma. - Wikidata - wikimedia - TriplyDB

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

http://www.wikidata.org/entity/Q55037406

about

5' flanking sequence of the human immediate early responsive gene ccn1 (cyr61) and mapping of polymorphic CA repeat sequence motifs in the human ccn1 (cyr61) locus.Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology.Overexpression of ERBB-2 was more frequently detected in malignant than benign pheochromocytomas by multiplex ligation-dependent probe amplification and immunohistochemistry.Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.Functional evidence for an ovarian cancer tumor suppressor gene on chromosome 22 by microcell-mediated chromosome transfer.Chromosome 22q a frequent site of allele loss in head and neck carcinoma.Quantitative real-time PCR identifies a critical region of deletion on 22q13 related to prognosis in oral cancer.Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.Predominant occurrence of somatic mutations of theNF2 gene in meningiomas and schwannomas

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P2860

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

http://www.wikidata.org/entity/Q55037406

description

1993 nî lūn-bûn

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1993年の論文

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1993年学术文章

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1993年学术文章

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1993年学术文章

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1993年学术文章

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1993年学术文章

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1993年學術文章

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1993年學術文章

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1993年學術文章

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name

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

@en

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

@nl

type

label

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

@en

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

@nl

prefLabel

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

@en

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

@nl

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J.1349-7006.1993.TB00150.X

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Japanese Journal of Cancer Research

P1476

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

@en

P2093

E Shin

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H Kurahashi

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I Nishisho

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K Takami

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S Fujita

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S Takai

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T Kobayashi

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T Mori

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Y Kurita

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P2860

The isolation of a human Ig V lambda gene from a recombinant library of chromosome 22 and estimation of its copy number

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

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

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

The CEPH consortium linkage map of human chromosome 1

Gel electrophoresis of restriction fragments

Genetic alterations during colorectal-tumor development

Identification of FAP locus genes from chromosome 5q21

Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients

Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.

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402-408

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10.1111/J.1349-7006.1993.TB00150.X

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phaeochromocytoma

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5919302

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