201 related articles for article (PubMed ID: 17429902)
1. Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease.
Saugstad OD; Hansen TW; Rønnestad A; Nakstad B; Tølløfsrud PA; Reinholt F; Hamvas A; Coles FS; Dean M; Wert SE; Whitsett JA; Nogee LM
Acta Paediatr; 2007 Feb; 96(2):185-90. PubMed ID: 17429902
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Novel ABCA3 mutations as a cause of respiratory distress in a term newborn.
Gonçalves JP; Pinheiro L; Costa M; Silva A; Gonçalves A; Pereira A
Gene; 2014 Jan; 534(2):417-20. PubMed ID: 24269975
[TBL] [Abstract][Full Text] [Related]
7. [Pulmonary surfactant protein adenosine triphosphate-binding-cassette-A3 gene composite mutations in infant congenital interstitial lung disease: report of a case and review of literature].
Xie N; Chen DH; Lin YN; Wu SZ; Gu YY; Zeng QS; Zhai YY; Yang LY; Xu JX
Zhonghua Er Ke Za Zhi; 2016 Oct; 54(10):761-766. PubMed ID: 27784479
[TBL] [Abstract][Full Text] [Related]
8. ABCA3 deficiency: neonatal respiratory failure and interstitial lung disease.
Bullard JE; Wert SE; Nogee LM
Semin Perinatol; 2006 Dec; 30(6):327-34. PubMed ID: 17142158
[TBL] [Abstract][Full Text] [Related]
9. [Clinical analysis of heterozygous ABCA3 mutations in children].
Xu X; Liu E; Luo Z; Luo J; Fu Z
Zhonghua Er Ke Za Zhi; 2014 Apr; 52(4):244-7. PubMed ID: 24915907
[TBL] [Abstract][Full Text] [Related]
10. Neonatal respiratory insufficiency caused by an (homozygous) ABCA3-stop mutation: a systematic evaluation of therapeutic options.
Winter J; Essmann S; Kidszun A; Aslanidis C; Griese M; Poplawska K; Bartsch M; Schmitz G; Mildenberger E
Klin Padiatr; 2014 Apr; 226(2):53-8. PubMed ID: 24633979
[TBL] [Abstract][Full Text] [Related]
11. Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation.
Bullard JE; Nogee LM
Pediatr Res; 2007 Aug; 62(2):176-9. PubMed ID: 17597647
[TBL] [Abstract][Full Text] [Related]
12. Genotype-phenotype correlations for infants and children with ABCA3 deficiency.
Wambach JA; Casey AM; Fishman MP; Wegner DJ; Wert SE; Cole FS; Hamvas A; Nogee LM
Am J Respir Crit Care Med; 2014 Jun; 189(12):1538-43. PubMed ID: 24871971
[TBL] [Abstract][Full Text] [Related]
13. Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes.
Hamvas A; Nogee LM; Wegner DJ; Depass K; Christodoulou J; Bennetts B; McQuade LR; Gray PH; Deterding RR; Carroll TR; Kammesheidt A; Kasch LM; Kulkarni S; Cole FS
J Pediatr; 2009 Dec; 155(6):854-859.e1. PubMed ID: 19647838
[TBL] [Abstract][Full Text] [Related]
14. ATP-binding cassette member A3 (E292V) gene mutation and pulmonary morbidity in very-low-birth-weight infants.
Härtel C; Felderhoff-Müser U; Gebauer C; Hoehn T; Kribs A; Laux R; Möller J; Segerer H; Teig N; von der Wense A; Wieg C; Stichtenoth G; Herting E; Göpel W;
Acta Paediatr; 2012 Apr; 101(4):380-3. PubMed ID: 22145626
[TBL] [Abstract][Full Text] [Related]
15. [Detection of genetic defect within ABCA3 from newborns with respiratory distress syndrome].
Zhou XH; Hui ZY; Li Y; Song HX; Zhang W; Xiao M; Wang FH; Liu L
Zhonghua Er Ke Za Zhi; 2012 Feb; 50(2):111-6. PubMed ID: 22455634
[TBL] [Abstract][Full Text] [Related]
16. A New
Mitsiakos G; Tsakalidis C; Karagianni P; Gialamprinou D; Chatziioannidis I; Papoulidis I; Tsanakas I; Soubasi V
Medicina (Kaunas); 2019 Jul; 55(7):. PubMed ID: 31331098
[TBL] [Abstract][Full Text] [Related]
17. Null ABCA3 in humans: large homozygous ABCA3 deletion, correlation to clinical-pathological findings.
Carrera P; Ferrari M; Presi S; Ventura L; Vergani B; Lucchini V; Cogo PE; Carnielli VP; Somaschini M; Tagliabue P
Pediatr Pulmonol; 2014 Mar; 49(3):E116-20. PubMed ID: 24420869
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Respiratory failure in a term infant with cis and trans mutations in ABCA3.
Jackson T; Wegner DJ; White FV; Hamvas A; Cole FS; Wambach JA
J Perinatol; 2015 Mar; 35(3):231-2. PubMed ID: 25712598
[TBL] [Abstract][Full Text] [Related]
20. Fatal familial lung disease caused by ABCA3 deficiency without identified ABCA3 mutations.
Gower WA; Wert SE; Ginsberg JS; Golan A; Whitsett JA; Nogee LM
J Pediatr; 2010 Jul; 157(1):62-8. PubMed ID: 20304423
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
