(Q50959564)

English

Heterozygous ABCA3 mutation associated with non-fatal evolution of respiratory distress.

scientific article published on 6 July 2007

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scholarly article

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

Heterozygous ABCA3 mutation associated with non-fatal evolution of respiratory distress. (English)

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

1 reference

based on heuristic

inferred from title

5

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

author name string

Takuya Yokota

1

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

Yoshihiro Matsumura

2

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

Nobuhiro Ban

3

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

Tadashi Matsubayashi

4

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

publication date

6 July 2007

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

European Journal of Pediatrics

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

167

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

691-693

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

6

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

https://scigraph.springernature.com/pub.10.1007/s00431-007-0542-8

0 references

Serum and bronchoalveolar fluid KL-6 levels in patients with pulmonary alveolar proteinosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17618459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ABCA3 gene mutations in newborns with fatal surfactant deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/17618459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization and classification of ATP-binding cassette transporter ABCA3 mutants in fatal surfactant deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17618459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/17618459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alteration of the Pulmonary Surfactant System in Full-Term Infants with Hereditary ABCA3 Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/17618459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human ABCA3, a product of a responsible gene for abca3 for fatal surfactant deficiency in newborns, exhibits unique ATP hydrolysis activity and generates intracellular multilamellar vesicles.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17618459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-007-0542-8

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/17618459

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