(Q55037406)

16 June 2018

title

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

1 reference

16 June 2018

1 reference

E Shin

1

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16 June 2018

S Fujita

2

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16 June 2018

K Takami

3

1 reference

16 June 2018

H Kurahashi

4

1 reference

16 June 2018

Y Kurita

5

1 reference

16 June 2018

T Kobayashi

6

1 reference

16 June 2018

T Mori

7

1 reference

16 June 2018

I Nishisho

8

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16 June 2018

S Takai

9

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16 June 2018

publication date

1 April 1993

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16 June 2018

number of pages

7

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Japanese Journal of Cancer Research

inferred from page(s)

published in

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16 June 2018

volume

84

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16 June 2018

page(s)

402-408

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16 June 2018

issue

4

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16 June 2018

Occurrence of pheochromocytoma in Rochester, Minnesota, 1950 through 1979.

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Structural gene for beta-nerve growth factor not defective in familial dysautonomia

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Human immunoglobulin C lambda 6 gene encodes the Kern+Oz-lambda chain and C lambda 4 and C lambda 5 are pseudogenes

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Twenty-eight loci form a continuous linkage map of markers for human chromosome 1.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Isolation and mapping of a polymorphic DNA sequence (pCMM8.1) on chromosome 1p [D1S63]

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Isolation and mapping of a polymorphic DNA sequence (pMCT118) on chromosome 1p [D1S80]

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Isolation and mapping of a polymorphic DNA sequence (pEFZ31) on chromosome 22 [D22S32]

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Isolation and mapping of a polymorphic DNA sequence (pHHH106) on chromosome 1 [D1S67]

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Isolation and mapping of a polymorphic DNA sequence (pEFD53.2) on chromosome 1 [D1S73]

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Isolation and mapping of a polymorphic DNA sequence for NRAS pMCR3 on chromosome 1.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

RFLP detected with a 5'-bcr-gene-sequence (HGM8 provisional no. D22S11).

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

XhoI polymorphism at the human pronatriodilatin (hPND) gene locus

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Genetic alterations during colorectal-tumor development

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Report of the committee on the genetic constitution of chromosome 22.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

A genetic linkage map of the long arm of human chromosome 22.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

The p53 proto-oncogene can act as a suppressor of transformation

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Isolation and mapping of a polymorphic DNA sequence (pEFZ13) on chromosome 1p [D1S64].

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Mapping of human chromosome 22 with a panel of somatic cell hybrids

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

A t(4;22) in a meningioma points to the localization of a putative tumor-suppressor gene

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Identification of FAP locus genes from chromosome 5q21

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Three distinct regions involved in 3p deletion in human lung cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Adrenal medullary disease in multiple endocrine neoplasia, type 2: pheochromocytoma and its precursors

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Clonal origin of inherited medullary thyroid carcinoma and pheochromocytoma

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Gel electrophoresis of restriction fragments

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Allele loss on chromosome 10 and point mutation of ras oncogenes are infrequent in tumors of MEN 2A.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5919302

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

13 August 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1993.TB00150.X

Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1993.TB00150.X

Deletion of genes on chromosome 1 in endocrine neoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1993.TB00150.X

The CEPH consortium linkage map of human chromosome 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1993.TB00150.X

Accumulation of genetic alterations and progression of primary breast cancer

21 January 2018

1 reference

12 December 2020

Loss of genes on chromosome 22 in medullary thyroid carcinoma and pheochromocytoma

1 reference

12 December 2020

Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer

1 reference

12 December 2020

Close linkage of MEN2A with RBP3 locus in Japanese kindreds

1 reference

12 December 2020

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

12 December 2020

Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma

1 reference

12 December 2020

Isolation of DNA clones revealing restriction fragment length polymorphisms in the human genome

1 reference

12 December 2020

Chromosomal deletion and retinoblastoma

1 reference

12 December 2020

Localization of the FGR protooncogene on the genetic linkage map of human chromosome 1p

1 reference

12 December 2020

The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus

1 reference

12 December 2020

Concordant deletions of chromosome 3p and loss of heterozygosity for chromosomes 13 and 17 in small cell lung carcinoma.

1 reference

12 December 2020

10.1111/J.1349-7006.1993.TB00150.X

Identifiers

DOI

1 reference

16 June 2018

PMCID

5919302

1 reference

16 June 2018

PubMed ID

8514606

1 reference

16 June 2018