(Q52650343)

English

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

scientific article published on 19 May 2014

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scholarly article

1 reference

Europe PubMed Central

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18 March 2020

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

1 reference

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18 March 2020

alveolar capillary dysplasia

1 reference

based on heuristic

inferred from title

Avinash V Dharmadhikari

2

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18 March 2020

Pawel Stankiewicz

11

object named as

Paweł Stankiewicz

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18 March 2020

author name string

Przemyslaw Szafranski

1

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18 March 2020

Jennifer A Wambach

3

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18 March 2020

Chris T Towe

4

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18 March 2020

Frances V White

5

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18 March 2020

R Mark Grady

6

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18 March 2020

Pirooz Eghtesady

7

1 reference

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18 March 2020

F Sessions Cole

8

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18 March 2020

Gail Deutsch

9

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18 March 2020

Partha Sen

10

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18 March 2020

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publication date

19 May 2014

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18 March 2020

American Journal of Medical Genetics

1 reference

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18 March 2020

164A

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18 March 2020

8

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18 March 2020

2013-2019

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18 March 2020

Long noncoding RNAs: fresh perspectives into the RNA world

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Novel FOXF1 deep intronic deletion causes lethal lung developmental disorder, alveolar capillary dysplasia with misalignment of pulmonary veins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Alveolar capillary dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Long noncoding RNAs with enhancer-like function in human cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Long noncoding RNA as modular scaffold of histone modification complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Mechanisms of change in gene copy number

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Expanding the phenotype of alveolar capillary dysplasia (ACD).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

22 May 2018

Profound hypoxemia and pulmonary hypertension in a 7-month-old infant: late presentation of alveolar capillary dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

13 August 2018

Late presentation of alveolar capillary dysplasia in an infant.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107046

13 August 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36606

21 January 2018

Inversion upstream of FOXF1 in a case of lethal alveolar capillary dysplasia with misalignment of pulmonary veins

1 reference

https://pubmed.ncbi.nlm.nih.gov/24842713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prolonged survival in alveolar capillary dysplasia syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24842713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Misalignment of pulmonary veins and alveolar capillary dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24842713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late presentation of misalignment of lung vessels with alveolar capillary dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24842713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.A.36606

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24842713%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24842713%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

1 reference

Europe PubMed Central

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18 March 2020

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