(Q84567847)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Two candidate tumor suppressor genes, MEOX2 and SOSTDC1, identified in a 7p21 homozygous deletion region in a Wilms tumor (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Fumio Kasai

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

author name string

Junjiro Ohshima

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Masayuki Haruta

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Yuiko Fujiwara

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Tadashi Ariga

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Hajime Okita

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Masahiro Fukuzawa

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Jun-Ichi Hata

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Hiroshi Horie

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Yasuhiko Kaneko

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

publication date

1 December 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

Genes, Chromosomes and Cancer

7 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

volume

48

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

page(s)

1037-1050

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

Derivation and characterization of a Wilms' tumour cell line, WiT 49.

7 February 2020

cites work

1 reference

7 January 2021

Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor study

1 reference

7 January 2021

A human bone morphogenetic protein antagonist is down-regulated in renal cancer

1 reference

7 January 2021

Correlative gene expression and DNA methylation profiling in lung development nominate new biomarkers in lung cancer.

1 reference

7 January 2021

Treatment of Wilms' tumor. Results of the Third National Wilms' Tumor Study

1 reference

7 January 2021

Sequential WT1 and CTNNB1 mutations and alterations of beta-catenin localisation in intralobar nephrogenic rests and associated Wilms tumours: two case studies

1 reference

7 January 2021

Canonical WNT signalling determines lineage specificity in Wilms tumour

1 reference

7 January 2021

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1 reference

7 January 2021

Molecular cloning of a diverged homeobox gene that is rapidly down-regulated during the G0/G1 transition in vascular smooth muscle cells

1 reference

7 January 2021

Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour.

1 reference

7 January 2021

Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities

1 reference

7 January 2021

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

1 reference

7 January 2021

Wise, a context-dependent activator and inhibitor of Wnt signalling

1 reference

7 January 2021

Regulation of mammalian tooth cusp patterning by ectodin

1 reference

7 January 2021

Identification of a secreted BMP antagonist, ectodin, integrating BMP, FGF, and SHH signals from the tooth enamel knot

1 reference

7 January 2021

CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in WT1-mutant Wilms' tumors

1 reference

7 January 2021

Wilms tumor suppressor WTX negatively regulates WNT/beta-catenin signaling

1 reference

7 January 2021

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

1 reference

7 January 2021

Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma

1 reference

7 January 2021

The homeobox gene Gax inhibits angiogenesis through inhibition of nuclear factor-kappaB-dependent endothelial cell gene expression

1 reference

7 January 2021

Bax-mediated cell death by the Gax homeoprotein requires mitogen activation but is independent of cell cycle activity

1 reference

7 January 2021

Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14.

1 reference

7 January 2021

Functional inactivation of the WTX gene is not a frequent event in Wilms' tumors

1 reference

7 January 2021

Loss of heterozygosity at 7p in Wilms' tumour development

1 reference

7 January 2021

Loss of Imprinting of Insulin-Like Growth Factor-II (IGF2) Gene in Distinguishing Specific Biologic Subtypes of Wilms Tumor

1 reference

7 January 2021

The murine Pou6f2 gene is temporally and spatially regulated during kidney embryogenesis and its human homolog is overexpressed in a subset of Wilms tumors.

1 reference

7 January 2021

Wilms' tumour: connecting tumorigenesis and organ development in the kidney

1 reference

7 January 2021

An X chromosome gene, WTX, is commonly inactivated in Wilms tumor

1 reference

7 January 2021

Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors

1 reference

7 January 2021

p21CIP1-mediated inhibition of cell proliferation by overexpression of the gax homeodomain gene

1 reference

7 January 2021

Molecular characterization of a 7p15-21 homozygous deletion in a Wilms tumor

1 reference

7 January 2021

Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma

1 reference

7 January 2021

The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour

1 reference

7 January 2021

Perilobar nephrogenic rests are nonobligate molecular genetic precursor lesions of insulin-like growth factor-II-associated Wilms tumors

1 reference

7 January 2021

Uterine sensitization-associated gene-1 (USAG-1), a novel BMP antagonist expressed in the kidney, accelerates tubular injury.

1 reference

7 January 2021

Genomic profiling maps loss of heterozygosity and defines the timing and stage dependence of epigenetic and genetic events in Wilms' tumors.

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20705

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19760604%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference