(Q34686027)

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Cytogenetically normal uterine leiomyomas without MED12-mutations - a source to identify unknown mechanisms of the development of uterine smooth muscle tumors.

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25506394%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Cytogenetically normal uterine leiomyomas without MED12-mutations - a source to identify unknown mechanisms of the development of uterine smooth muscle tumors (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25506394%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Carsten Holzmann

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25506394%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

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Dominique Nadine Markowski

2

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Europe PubMed Central

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25 February 2020

Dirk Koczan

3

1 reference

Europe PubMed Central

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25 February 2020

Wolfgang Küpker

4

1 reference

Europe PubMed Central

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25 February 2020

Burkhard Maria Helmke

5

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Europe PubMed Central

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25 February 2020

Jörn Bullerdiek

6

1 reference

Europe PubMed Central

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25 February 2020

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29 November 2014

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Europe PubMed Central

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25 February 2020

Molecular Cytogenetics

1 reference

Europe PubMed Central

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25 February 2020

7

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Europe PubMed Central

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25 February 2020

1

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25 February 2020

88

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Europe PubMed Central

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25 February 2020

copyright license

Creative Commons Attribution 4.0 International

29 November 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Genome-wide acquired uniparental disomy as well as chromosomal gains and losses in an uterine epithelioid leiomyoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Cell cultures in uterine leiomyomas: rapid disappearance of cells carrying MED12 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

MED12 exon 2 mutations in histopathological uterine leiomyoma variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Chromothripsis and cancer: causes and consequences of chromosome shattering

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

MED12 alterations in both human benign and malignant uterine soft tissue tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Chromothripsis identifies a rare and aggressive entity among newly diagnosed multiple myeloma patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Massive genomic rearrangement acquired in a single catastrophic event during cancer development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Novel patterns of genome rearrangement and their association with survival in breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

A novel Cys212Tyr founder mutation in parkin and allelic heterogeneity of juvenile Parkinsonism in a population from North West Colombia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264251

7 July 2018

Characterization of uterine leiomyomas by whole-genome sequencing.

1 reference

https://api.crossref.org/works/10.1186%2FS13039-014-0088-1

21 January 2018

MED12 mutations in leiomyosarcoma and extrauterine leiomyoma.

1 reference

https://api.crossref.org/works/10.1186%2FS13039-014-0088-1

21 January 2018

Molecular topography of the MED12-deleted region in smooth muscle tumors: a possible link between non-B DNA structures and hypermutability

1 reference

https://api.crossref.org/works/10.1186%2FS13039-014-0088-1

21 January 2018

MED12 exon 2 mutations in uterine and extrauterine smooth muscle tumors.

1 reference

https://api.crossref.org/works/10.1186%2FS13039-014-0088-1

21 January 2018

Uterine fibroids: do we deal with more than one disease?

1 reference

https://api.crossref.org/works/10.1186%2FS13039-014-0088-1

21 January 2018

Overexpression of HMGA2 in uterine leiomyomas points to its general role for the pathogenesis of the disease.

1 reference

https://api.crossref.org/works/10.1186%2FS13039-014-0088-1

21 January 2018

HMGA2 and the p19Arf-TP53-CDKN1A axis: a delicate balance in the growth of uterine leiomyomas.

1 reference

https://api.crossref.org/works/10.1186%2FS13039-014-0088-1

21 January 2018

MED12 mutations in uterine fibroids--their relationship to cytogenetic subgroups

1 reference

https://pubmed.ncbi.nlm.nih.gov/25506394

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analyses of 6 different types of uterine smooth muscle tumors: Emphasis in atypical leiomyoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/25506394

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/S13039-014-0088-1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25506394%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25506394%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25506394%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

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