Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans (Q24635323)

14

0 references

Stanislas Lyonnet

15

0 references

Jeanne Amiel

18

0 references

Laurence Faivre

4

0 references

Arnold Munnich

12

0 references

Alice Goldenberg

9

0 references

Joana Alves Vidigal

object named as

Joana Alves Vidigal

13

0 references

Andrea Ventura

object named as

Andrea Ventura

17

0 references

Evelyn Yao

2

object named as

Evelyn Yao

0 references

author name string

Loïc de Pontual

1

0 references

Patrick Callier

3

0 references

Valérie Drouin

5

0 references

Sandra Cariou

6

0 references

Arie Van Haeringen

7

0 references

David Geneviève

8

0 references

Myriam Oufadem

10

0 references

Sylvie Manouvrier

11

0 references

Alexandra Henrion-Caude

miR-19 is a key oncogenic component of mir-17-92

16

0 references

language of work or name

English

0 references

publication date

October 2011

0 references

published in

Nature Genetics

0 references

volume

43

0 references

issue

10

0 references

page(s)

1026-30

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Genetic dissection of the miR-17~92 cluster of microRNAs in Myc-induced B-cell lymphomas

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

The miR-17/92 polycistron is up-regulated in sonic hedgehog-driven medulloblastomas and induced by N-myc in sonic hedgehog-treated cerebellar neural precursors

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

The miR-17~92 cluster collaborates with the Sonic Hedgehog pathway in medulloblastoma

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Mapping and sequencing of structural variation from eight human genomes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

A microRNA expression signature of human solid tumors defines cancer gene targets

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

c-Myc-regulated microRNAs modulate E2F1 expression

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

A microRNA polycistron as a potential human oncogene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Detection of large-scale variation in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

The myc-miR-17~92 axis blunts TGF{beta} signaling and production of multiple TGF{beta}-dependent antiangiogenic factors

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

A polycistronic microRNA cluster, miR-17-92, is overexpressed in human lung cancers and enhances cell proliferation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Identification and characterization of a novel gene, C13orf25, as a target for 13q31-q32 amplification in malignant lymphoma

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Feingold syndrome: clinical review and genetic mapping

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Activities of N-Myc in the developing limb link control of skeletal size with digit separation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Integration of external signaling pathways with the core transcriptional network in embryonic stem cells

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Augmentation of tumor angiogenesis by a Myc-activated microRNA cluster

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

The miR-17-92 microRNA cluster regulates multiple components of the TGF-β pathway in neuroblastoma

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Delineation of 15q13.3 microdeletions.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

MYCN-regulated microRNAs repress estrogen receptor-alpha (ESR1) expression and neuronal differentiation in human neuroblastoma

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Antagomir-17-5p abolishes the growth of therapy-resistant neuroblastoma through p21 and BIM

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Genotype-phenotype correlations in MYCN-related Feingold syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

MYCN regulates oncogenic MicroRNAs in neuroblastoma

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Interstitial deletion of 13q22-->q31: case report and review of the literature.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

A targeted mutation reveals a role for N-myc in branching morphogenesis in the embryonic mouse lung

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184212

A microRNA cluster as a target of genomic amplification in malignant lymphoma.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.915

Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.915

Dissecting the role of N-myc in development using a single targeting vector to generate a series of alleles.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.915

Defects of embryonic organogenesis resulting from targeted disruption of the N-myc gene in the mouse

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21892160

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Loss of N-myc function results in embryonic lethality and failure of the epithelial component of the embryo to develop

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21892160

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.915

1 reference

Dimensions Publication ID

1430449

1052685738

0 references

1430449

1 reference

1 reference

1 reference