(Q28237518)

Angel M Carcaboso

11

0 references

Jaume Mora

Jaume Mora

14

0 references

Darren Hargrave

Darren Hargrave

18

0 references

Mara Vinci

Maria Vinci

9

0 references

Olena Morozova

Olena Morozova

5

0 references

David Castel

David Castel

7

0 references

Jacques Grill

23

Jacques Grill

0 references

Michelle Monje

17

Michelle Monje

0 references

Chris Jones

Chris Jones

22

0 references

S Puget

20

Stéphanie Puget

0 references

author name string

Kathryn R Taylor

1

0 references

Alan Mackay

2

0 references

Nathalène Truffaux

3

0 references

Yaron S Butterfield

4

0 references

Cathy Philippe

6

0 references

Catherine S Grasso

8

0 references

Diana Carvalho

10

0 references

Carmen de Torres

12

0 references

Ofelia Cruz

13

0 references

Natacha Entz-Werle

15

0 references

Alex N Bullock

19

0 references

Stephen Yip

Structure of the bone morphogenetic protein receptor ALK2 and implications for fibrodysplasia ossificans progressiva

21

0 references

language of work or name

English

0 references

publication date

May 2014

0 references

published in

Nature Genetics

0 references

volume

46

0 references

issue

5

0 references

page(s)

457-61

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=4018681

Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

BMP type I receptor inhibition reduces heterotopic [corrected] ossification

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Inhibition of PRC2 activity by a gain-of-function H3 mutation found in pediatric glioblastoma

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

CNS demyelination in fibrodysplasia ossificans progressiva

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Paediatric and adult malignant glioma: close relatives or distant cousins?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Mesenchymal transition and PDGFRA amplification/mutation are key distinct oncogenic events in pediatric diffuse intrinsic pontine gliomas

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Genome-wide analyses identify recurrent amplifications of receptor tyrosine kinases and cell-cycle regulatory genes in diffuse intrinsic pontine glioma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Inherited human diseases of heterotopic bone formation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Anaesthetic management of a child with fibrodysplasia ossificans progressiva

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

Prospective study of awake craniotomy used routinely and nonselectively for supratentorial tumors

29 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2925

A unique mutation of ALK2, G356D, found in a patient with fibrodysplasia ossificans progressiva is a moderately activated BMP type I receptor

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2925

Stereotactic biopsy of diffuse pontine lesions in children

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4018681

27 November 2018

Identifiers

DOI

10.1038/NG.2925

1 reference

1 reference

1 reference

PubMed publication ID

24705252

1 reference