(Q34754714)

English

Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma

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scholarly article

1 reference

Europe PubMed Central

4 August 2017

Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma (English)

1 reference

Europe PubMed Central

4 August 2017

congenital disorder

0 references

congenital mesoblastic nephroma

1 reference

based on heuristic

inferred from title

mesoblastic nephroma

1 reference

based on heuristic

inferred from title

author name string

B P Rubin

1

1 reference

Europe PubMed Central

4 August 2017

C J Chen

2

1 reference

Europe PubMed Central

4 August 2017

T W Morgan

3

1 reference

Europe PubMed Central

4 August 2017

S Xiao

4

1 reference

Europe PubMed Central

4 August 2017

H E Grier

5

1 reference

Europe PubMed Central

4 August 2017

H P Kozakewich

6

1 reference

Europe PubMed Central

4 August 2017

A R Perez-Atayde

7

1 reference

Europe PubMed Central

4 August 2017

J A Fletcher

8

1 reference

Europe PubMed Central

4 August 2017

language of work or name

0 references

publication date

1 November 1998

1 reference

Europe PubMed Central

4 August 2017

The American Journal of Pathology

1 reference

Europe PubMed Central

4 August 2017

153

1 reference

Europe PubMed Central

4 August 2017

1451-1458

1 reference

Europe PubMed Central

4 August 2017

5

1 reference

Europe PubMed Central

4 August 2017

A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

The TEL/platelet-derived growth factor beta receptor (PDGF beta R) fusion in chronic myelomonocytic leukemia is a transforming protein that self-associates and activates PDGF beta R kinase-dependent signaling pathways

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

p210BCR/ABL, p190BCR/ABL, and TEL/ABL activate similar signal transduction pathways in hematopoietic cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Oligomerization of the ABL tyrosine kinase by the Ets protein TEL in human leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Consistent numerical chromosome aberrations in congenital fibrosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Chromosome aberrations in mesoblastic nephroma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Fibrosarcoma in infants and children. Application of new techniques.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Trk receptors use redundant signal transduction pathways involving SHC and PLC-gamma 1 to mediate NGF responses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Human trks: molecular cloning, tissue distribution, and expression of extracellular domain immunoadhesins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

The novel activation of ABL by fusion to an ets-related gene, TEL.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Novel fluorescence in situ hybridization approaches in solid tumors. Characterization of frozen specimens, touch preparations, and cytological preparations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Primary renal tumours in the first year of life. A population based review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Fibrosarcoma in early infancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Congenital mesoblastic nephroma of infancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Congenital mesoblastic nephroma: a clinicoradiologic study of 17 cases representing the pathologic spectrum of the disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Mesoblastic nephromas: a study of 29 tumours from the SIOP nephroblastoma file.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Cytogenetic investigation of a case of congenital fibrosarcoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Deletion of part of the short arm of chromosome 17 in a congenital fibrosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Cytogenetic analysis of a congenital fibrosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

trkC, a new member of the trk family of tyrosine protein kinases, is a receptor for neurotrophin-3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Ultrastructural, immunocytochemical, and cytogenetic characterization of a large congenital fibrosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Infantile fibrosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Infantile and adult fibrosarcomas of the soft tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

7 July 2018

Trisomy 11 and other nonrandom trisomies in congenital fibrosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

26 October 2018

Chromosomal translocations in human cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

26 October 2018

Congenital mesoblastic nephroma of infancy. A report of eight cases and the relationship to Wilms' tumor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

26 October 2018

The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853403

9 December 2018

Neonatal renal tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Fetal hamartoma of kidney. A benign, symptomatic, congenital tumor, not a form of Wilms' tumor

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Therapy and outcome in 51 children with mesoblastic nephroma: A report of the national Wilms' tumor study

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Malignant mesenchymal nephroma of infancy: report of a case with pulmonary metastases

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Fibrosarcoma in infants and children

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

So-called congenital-infantile fibrosarcoma: does it exist and what is it?

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Cytogenetic characterization of congenital or infantile fibrosarcoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Nonrandom numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Presence or absence of trisomy 11 is correlated with histologic subtype in congenital mesoblastic nephroma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Congenital fibrosarcoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Fibrosarcomas in infants and children

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965732-X

7 January 2021

Atypical mesoblastic nephroma. Pathologic characterization of a potentially aggressive variant of conventional congenital mesoblastic nephroma

1 reference

https://pubmed.ncbi.nlm.nih.gov/9811336

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S0002-9440(10)65732-X

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

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