262 related articles for article (PubMed ID: 16959783)
1. Characterization and classification of ATP-binding cassette transporter ABCA3 mutants in fatal surfactant deficiency.
Matsumura Y; Ban N; Ueda K; Inagaki N
J Biol Chem; 2006 Nov; 281(45):34503-14. PubMed ID: 16959783
[TBL] [Abstract][Full Text] [Related]
2. Some ABCA3 mutations elevate ER stress and initiate apoptosis of lung epithelial cells.
Weichert N; Kaltenborn E; Hector A; Woischnik M; Schams A; Holzinger A; Kern S; Griese M
Respir Res; 2011 Jan; 12(1):4. PubMed ID: 21214890
[TBL] [Abstract][Full Text] [Related]
3. Functional and trafficking defects in ATP binding cassette A3 mutants associated with respiratory distress syndrome.
Cheong N; Madesh M; Gonzales LW; Zhao M; Yu K; Ballard PL; Shuman H
J Biol Chem; 2006 Apr; 281(14):9791-800. PubMed ID: 16415354
[TBL] [Abstract][Full Text] [Related]
4. Aberrant catalytic cycle and impaired lipid transport into intracellular vesicles in ABCA3 mutants associated with nonfatal pediatric interstitial lung disease.
Matsumura Y; Ban N; Inagaki N
Am J Physiol Lung Cell Mol Physiol; 2008 Oct; 295(4):L698-707. PubMed ID: 18676873
[TBL] [Abstract][Full Text] [Related]
5. Identification and characterization of a novel ABCA3 mutation.
Park SK; Amos L; Rao A; Quasney MW; Matsumura Y; Inagaki N; Dahmer MK
Physiol Genomics; 2010 Jan; 40(2):94-9. PubMed ID: 19861431
[TBL] [Abstract][Full Text] [Related]
6. 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.
Nagata K; Yamamoto A; Ban N; Tanaka AR; Matsuo M; Kioka N; Inagaki N; Ueda K
Biochem Biophys Res Commun; 2004 Nov; 324(1):262-8. PubMed ID: 15465012
[TBL] [Abstract][Full Text] [Related]
7. ABCA3-mediated choline-phospholipids uptake into intracellular vesicles in A549 cells.
Matsumura Y; Sakai H; Sasaki M; Ban N; Inagaki N
FEBS Lett; 2007 Jul; 581(17):3139-44. PubMed ID: 17574245
[TBL] [Abstract][Full Text] [Related]
8. ABCA3 gene mutations in newborns with fatal surfactant deficiency.
Shulenin S; Nogee LM; Annilo T; Wert SE; Whitsett JA; Dean M
N Engl J Med; 2004 Mar; 350(13):1296-303. PubMed ID: 15044640
[TBL] [Abstract][Full Text] [Related]
9. Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency.
Brasch F; Schimanski S; Mühlfeld C; Barlage S; Langmann T; Aslanidis C; Boettcher A; Dada A; Schroten H; Mildenberger E; Prueter E; Ballmann M; Ochs M; Johnen G; Griese M; Schmitz G
Am J Respir Crit Care Med; 2006 Sep; 174(5):571-80. PubMed ID: 16728712
[TBL] [Abstract][Full Text] [Related]
10. Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome.
Wambach JA; Yang P; Wegner DJ; Heins HB; Kaliberova LN; Kaliberov SA; Curiel DT; White FV; Hamvas A; Hackett BP; Cole FS
Am J Respir Cell Mol Biol; 2016 Nov; 55(5):716-721. PubMed ID: 27374344
[TBL] [Abstract][Full Text] [Related]
11. Expression of ABCA3, a causative gene for fatal surfactant deficiency, is up-regulated by glucocorticoids in lung alveolar type II cells.
Yoshida I; Ban N; Inagaki N
Biochem Biophys Res Commun; 2004 Oct; 323(2):547-55. PubMed ID: 15369786
[TBL] [Abstract][Full Text] [Related]
12. Ultrastructural and molecular analysis in fatal neonatal interstitial pneumonia caused by a novel ABCA3 mutation.
Bruder E; Hofmeister J; Aslanidis C; Hammer J; Bubendorf L; Schmitz G; Rufle A; Bührer C
Mod Pathol; 2007 Oct; 20(10):1009-18. PubMed ID: 17660803
[TBL] [Abstract][Full Text] [Related]
13. ABCA3, a key player in neonatal respiratory transition and genetic disorders of the surfactant system.
Peca D; Cutrera R; Masotti A; Boldrini R; Danhaive O
Biochem Soc Trans; 2015 Oct; 43(5):913-9. PubMed ID: 26517903
[TBL] [Abstract][Full Text] [Related]
14. Potentiation of ABCA3 lipid transport function by ivacaftor and genistein.
Kinting S; Li Y; Forstner M; Delhommel F; Sattler M; Griese M
J Cell Mol Med; 2019 Aug; 23(8):5225-5234. PubMed ID: 31210424
[TBL] [Abstract][Full Text] [Related]
15. The surfactant lipid transporter ABCA3 is N-terminally cleaved inside LAMP3-positive vesicles.
Engelbrecht S; Kaltenborn E; Griese M; Kern S
FEBS Lett; 2010 Oct; 584(20):4306-12. PubMed ID: 20863830
[TBL] [Abstract][Full Text] [Related]
16. Disruption of N-linked glycosylation promotes proteasomal degradation of the human ATP-binding cassette transporter ABCA3.
Beers MF; Zhao M; Tomer Y; Russo SJ; Zhang P; Gonzales LW; Guttentag SH; Mulugeta S
Am J Physiol Lung Cell Mol Physiol; 2013 Dec; 305(12):L970-80. PubMed ID: 24142515
[TBL] [Abstract][Full Text] [Related]
17. Functional characterization of four ATP-binding cassette transporter A3 gene (ABCA3) variants.
Hu JY; Yang P; Wegner DJ; Heins HB; Luke CJ; Li F; White FV; Silverman GA; Sessions Cole F; Wambach JA
Hum Mutat; 2020 Jul; 41(7):1298-1307. PubMed ID: 32196812
[TBL] [Abstract][Full Text] [Related]
18. Structure-Based Understanding of ABCA3 Variants.
Onnée M; Fanen P; Callebaut I; de Becdelièvre A
Int J Mol Sci; 2021 Sep; 22(19):. PubMed ID: 34638622
[TBL] [Abstract][Full Text] [Related]
19. ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells.
Yamano G; Funahashi H; Kawanami O; Zhao LX; Ban N; Uchida Y; Morohoshi T; Ogawa J; Shioda S; Inagaki N
FEBS Lett; 2001 Nov; 508(2):221-5. PubMed ID: 11718719
[TBL] [Abstract][Full Text] [Related]
20. Quantification of volume and lipid filling of intracellular vesicles carrying the ABCA3 transporter.
Höppner S; Kinting S; Torrano AA; Schindlbeck U; Bräuchle C; Zarbock R; Wittmann T; Griese M
Biochim Biophys Acta Mol Cell Res; 2017 Dec; 1864(12):2330-2335. PubMed ID: 28887056
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
