(Q24317589)

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

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scholarly article

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

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Forkhead box F1

1 reference

GOA release 2020-03-11

Stimulated by retinoic acid 6

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GOA release 2020-03-11

ductus arteriosus closure

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GOA release 2020-03-11

alveolar capillary dysplasia

1 reference

based on heuristic

inferred from title

3

object named as

Samarth S Bhatt

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Tomas W Fitzgerald

object named as

Tomas Fitzgerald

35

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Donna M McDonald-McGinn

14

object named as

Donna McDonald-McGinn

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26

object named as

Usha Kini

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Pawel Stankiewicz

1

object named as

Paweł Stankiewicz

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38

object named as

Ankita Patel

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author name string

Partha Sen

2

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Mekayla Storer

4

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Zhilian Xia

5

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Bassem A Bejjani

6

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Zhishuo Ou

7

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Joanna Wiszniewska

8

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Daniel J Driscoll

9

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Melissa K Maisenbacher

10

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Juan Bolivar

11

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Mislen Bauer

12

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Elaine H Zackai

13

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Małgorzata M J Nowaczyk

15

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Mitzi Murray

16

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Virginia Hustead

17

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Kristin Mascotti

18

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Regina Schultz

19

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Lavinia Hallam

20

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Duncan McRae

21

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Andrew G Nicholson

22

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Robert Newbury

23

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Jane Durham-O'Donnell

24

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Gail Knight

25

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Tamim H Shaikh

27

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Vicki Martin

28

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Matthew Tyreman

29

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Ingrid Simonic

30

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Lionel Willatt

31

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Joan Paterson

32

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Sarju Mehta

33

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Diana Rajan

34

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Susan Gribble

36

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Elena Prigmore

37

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Lisa G Shaffer

39

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Nigel P Carter

40

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Sau Wai Cheung

41

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Claire Langston

42

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Charles Shaw-Smith

43

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language of work or name

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publication date

June 2009

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American Journal of Human Genetics

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84

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6

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780-91

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Computational and experimental identification of novel human imprinted genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Haploinsufficiency of the forkhead gene Foxf1, a target for sonic hedgehog signaling, causes lung and foregut malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Differential activation of lung-specific genes by two forkhead proteins, FREAC-1 and FREAC-2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Hedgehog induction of murine vasculogenesis is mediated by Foxf1 and Bmp4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Roles of forkhead transcription factor Foxc2 (MFH-1) and endothelin receptor A in cardiovascular morphogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Mesenchymal expression of Foxl1, a winged helix transcriptional factor, regulates generation and maintenance of gut-associated lymphoid organs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Defects in pulmonary vasculature and perinatal lung hemorrhage in mice heterozygous null for the Forkhead Box f1 transcription factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

19 March 2017

Mechanisms for human genomic rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Transcriptional control of lung morphogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Alveolar capillary dysplasia: a logical approach to a fatal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

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=2694971

27 September 2017

Foxf1haploinsufficiency reduces Notch-2 signaling during mouse lung development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Structural characterization of the mouse Foxf1a gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Differential expression of forkhead box transcription factors following butylated hydroxytoluene lung injury

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Congenital alveolar capillary dysplasia with misalignment of pulmonary veins associated with hypoplastic left heart syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Mesenchymal transcription factor Fkh6 is essential for the development and differentiation of parietal cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Alveolar capillary dysplasia. Report of a case of prolonged life without extracorporeal membrane oxygenation (ECMO) and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Familial persistent pulmonary hypertension of the newborn resulting from misalignment of the pulmonary vessels (congenital alveolar capillary dysplasia)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

Misalignment of pulmonary veins with alveolar capillary dysplasia: affected siblings and variable phenotypic expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

27 September 2017

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=2694971

29 November 2018

Alveolar capillary dysplasia: a six-year single center experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

29 November 2018

Function and regulation of FoxF1 during Xenopus gut development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

29 November 2018

Fusion of lung lobes and vessels in mouse embryos heterozygous for the forkhead box f1 targeted allele.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694971

29 November 2018

Inhaled nitric oxide enhances oxygenation but not survival in infants with alveolar capillary dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19500772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Foxl1-deficient mice exhibit aberrant epithelial cell positioning resulting from dysregulated EphB/EphrinB expression in the small intestine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19500772

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/19500772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of lymphoedema-distichiasis families forFOXC2 mutations reveals small insertions and deletions throughout the gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19500772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19500772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First confirmed case with paternal uniparental disomy of chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/19500772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital misalignment of pulmonary veins with alveolar capillary dysplasia causing persistent neonatal pulmonary hypertension: report of two affected siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/19500772

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/19500772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJHG.2009.05.005

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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