Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis (Q57252309)

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15 October 2019

title

Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis (English)

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15 October 2019

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7

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15 October 2019

Cécile Jeanpierre

9

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15 October 2019

author name string

Austruy E

1

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15 October 2019

Candon S

2

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15 October 2019

Henry I

3

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15 October 2019

Gyapay G

4

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15 October 2019

Tournade MF

5

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15 October 2019

Mannens M

6

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15 October 2019

Junien C

8

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15 October 2019

publication date

1 December 1995

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Genes, Chromosomes and Cancer

15 October 2019

published in

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15 October 2019

volume

14

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15 October 2019

issue

4

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15 October 2019

page(s)

285-294

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Acceleration of nucleic acid hybridization rate by polyethylene glycol

15 October 2019

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Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

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Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor.

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7 January 2021

Subregional physical mapping of an alpha B-crystallin sequence and of a new expressed sequence D11S877E to human 11q.

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7 January 2021

Genetics of Wilms' tumor: a blend of aberrant development and genomic imprinting

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7 January 2021

Further chromosome studies on Wilms' tumor cells of patients without aniridia

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Allelic loss on chromosome 11p is a less frequent event in bilateral than in unilateral Wilms' tumours

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Chromosome 1 studies in Wilms' tumor

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7 January 2021

Epigenetic lesions at the H19 locus in Wilms' tumour patients

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7 January 2021

Testing genomic imprinting in Wilm's tumor.

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7 January 2021

A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors

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7 January 2021

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

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7 January 2021

Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour

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7 January 2021

Mapping of the 12q12-q22 region with respect to tumor translocation breakpoints

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7 January 2021

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

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7 January 2021

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour

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7 January 2021

Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.

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7 January 2021

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7 January 2021

Four dinucleotide repeat polymorphisms on human chromosome 16 at D16S289, D16S318, D16S319 and D16S320

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7 January 2021

The cytogenetics of Wilms' tumor

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Bilateral nephroblastoma associated with a 3;17 translocation

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7 January 2021

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

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7 January 2021

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Identifiers

DOI

10.1002/GCC.2870140407

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8605117%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

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