A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosis (Q35805104)

10 August 2017

A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosis (English)

1 reference

10 August 2017

0 references

Federica Baldan

0 references

Patrizia Dello Russo

1 reference

10 August 2017

Alessandra Franzoni

1 reference

10 August 2017

Cinzia Puppin

1 reference

10 August 2017

Giovanna De Maglio

1 reference

10 August 2017

Carla Pittini

1 reference

10 August 2017

Luigi Cattarossi

1 reference

10 August 2017

Stefano Pizzolitto

1 reference

10 August 2017

Giuseppe Damante

1 reference

10 August 2017

13 October 2015

1 reference

10 August 2017

1 reference

10 August 2017

1 reference

10 August 2017

1 reference

FOXF1 mediates mesenchymal stem cell fusion-induced reprogramming of lung cancer cells

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Forkhead transcription factor FOXF1 is a novel target gene of the p53 family and regulates cancer cell migration and invasiveness.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Familial pulmonary capillary hemangiomatosis early in life

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Epigenetic inactivation of the potential tumor suppressor gene FOXF1 in breast cancer

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Expanding the phenotype of alveolar capillary dysplasia (ACD).

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Congenital pulmonary capillary hemangiomatosis: Report of two cases and review of the literature

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Two deletions overlapping a distant FOXF1 enhancer unravel the role of lncRNA LINC01081 in etiology of alveolar capillary dysplasia with misalignment of pulmonary veins.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Pulmonary capillary hemangiomatosis: the puzzle takes shape.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Updated Clinical Classification of Pulmonary Hypertension

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

EIF2AK4 mutations in pulmonary capillary hemangiomatosis

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Congenital pulmonary lymphangiectasis: an unusual cause of respiratory distress in neonates

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Alveolar capillary dysplasia: a logical approach to a fatal disease

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4605103

Misalignment of lung vessels and alveolar capillary dysplasia: a case report with autopsy

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26462560

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Misalignment of lung vessels: a syndrome causing persistent neonatal pulmonary hypertension

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26462560

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Capillary haemangiomatosis of the lungs

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26462560

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S12881-015-0241-7

1 reference

Dimensions Publication ID

10 August 2017

0 references

1 reference

10 August 2017

PubMed publication ID

26462560

1 reference