(Q40827716)

24 September 2017

Functional evidence for an ovarian cancer tumor suppressor gene on chromosome 22 by microcell-mediated chromosome transfer (English)

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24 September 2017

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11

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24 September 2017

10

Mills GB

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24 September 2017

Kruzelock RP

1

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24 September 2017

Cuevas BD

2

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24 September 2017

Wiener JR

3

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24 September 2017

Xu FJ

4

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24 September 2017

Yu Y

5

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24 September 2017

Cabeza-Arvelaiz Y

6

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24 September 2017

Pershouse M

7

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24 September 2017

Lovell MM

8

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24 September 2017

Killary AM

9

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24 September 2017

language of work or name

English

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publication date

1 December 2000

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24 September 2017

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24 September 2017

19

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24 September 2017

54

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24 September 2017

6277-6285

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1204013

24 September 2017

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cites work

Chromosome translocation t(14;22) and oncogene (c-sis) variant in a pedigree with familial meningioma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Potential role of the inactivated X chromosome in ovarian epithelial tumor development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Loss of heterozygosity for chromosome 22 DNA sequences in human meningioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Overexpression of the p53 protein and allele loss at 17p13 in ovarian carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Loss of heterozygosity on chromosome 22 in ovarian carcinoma is distal to and is not accompanied by mutations in NF2 at 22q12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Evidence for a unifocal origin in familial ovarian cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Ovarian cancer has frequent loss of heterozygosity at chromosome 12p12.3-13.1 (region of TEL and Kip1 loci) and chromosome 12q23-ter: evidence for two new tumour-suppressor genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuroma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Allele loss at the retinoblastoma locus in human ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

New vector for transfer of yeast artificial chromosomes to mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Rapid screening of a YAC library by pulsed-field gel Southern blot analysis of pooled YAC clones

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Combined molecular genetic studies of chromosome 22q and the neurofibromatosis type 2 gene in central nervous system tumors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Transfer of a yeast artificial chromosome carrying human DNA from Saccharomyces cerevisiae into mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Mutations of the E-cadherin gene in human gynecologic cancers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Search for putative suppressor genes in meningioma: significance of chromosome 22

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Deletion of Alu sequences in the fifth c-sis intron in individuals with meningiomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Analysis of malignancy in human cells: malignant and transformed phenotypes are under separate genetic control

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Loss of heterozygosity on chromosome 5 in sporadic ovarian carcinoma is a late event and is not associated with mutations in APC at 5q21-22

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

Deletion mapping of the long arm of chromosome 22 in human meningiomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Simultaneous identification of chromatid replication and of human chromosomes in metaphases of man-mouse somatic cell hybrids

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Tumor suppressor genes studied by cell hybridization and chromosome transfer.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Narrowing the critical region for a rhabdoid tumor locus in 22q11

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

The biology of ovarian cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Transformation of yeast spheroplasts without cell fusion

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Molecular genetic changes in human epithelial ovarian malignancies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Frequency and distribution of NF2 mutations in schwannomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

A gene for neurofibromatosis 2

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Pulmonary hypertension and polymorphonuclear leukocyte elastase after esophageal cancer operations.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Two tumor suppressive loci on chromosome 10 involved in human glioblastomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Frequent loss of heterozygosity on chromosome 22 in hepatocellular carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Frequent loss of heterozygosity at telomeric loci on 22q in sporadic colorectal cancers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204013

7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1204013

1 reference

Dimensions Publication ID

24 September 2017

0 references

1 reference