356 related articles for article (PubMed ID: 16316951)
1. Ultrastructure of lamellar bodies in congenital surfactant deficiency.
Edwards V; Cutz E; Viero S; Moore AM; Nogee L
Ultrastruct Pathol; 2005; 29(6):503-9. PubMed ID: 16316951
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and review.
Citti A; Peca D; Petrini S; Cutrera R; Biban P; Haass C; Boldrini R; Danhaive O
Ultrastruct Pathol; 2013 Oct; 37(5):356-65. PubMed ID: 24047351
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Deficiency of lamellar bodies in alveolar type II cells associated with fatal respiratory disease in a full-term infant.
Cutz E; Wert SE; Nogee LM; Moore AM
Am J Respir Crit Care Med; 2000 Feb; 161(2 Pt 1):608-14. PubMed ID: 10673207
[TBL] [Abstract][Full Text] [Related]
7. ABCA3 is critical for lamellar body biogenesis in vivo.
Cheong N; Zhang H; Madesh M; Zhao M; Yu K; Dodia C; Fisher AB; Savani RC; Shuman H
J Biol Chem; 2007 Aug; 282(33):23811-7. PubMed ID: 17540762
[TBL] [Abstract][Full Text] [Related]
8. Genetic disorders of surfactant dysfunction.
Wert SE; Whitsett JA; Nogee LM
Pediatr Dev Pathol; 2009; 12(4):253-74. PubMed ID: 19220077
[TBL] [Abstract][Full Text] [Related]
9. Conditional deletion of Abca3 in alveolar type II cells alters surfactant homeostasis in newborn and adult mice.
Besnard V; Matsuzaki Y; Clark J; Xu Y; Wert SE; Ikegami M; Stahlman MT; Weaver TE; Hunt AN; Postle AD; Whitsett JA
Am J Physiol Lung Cell Mol Physiol; 2010 May; 298(5):L646-59. PubMed ID: 20190032
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Absence of lamellar bodies with accumulation of dense bodies characterizes a novel form of congenital surfactant defect.
Tryka AF; Wert SE; Mazursky JE; Arrington RW; Nogee LM
Pediatr Dev Pathol; 2000; 3(4):335-45. PubMed ID: 10890249
[TBL] [Abstract][Full Text] [Related]
12. 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]
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. 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]
15. Inherited disorders of neonatal lung diseases.
Yurdakök M
Turk J Pediatr; 2004; 46(2):105-14. PubMed ID: 15214737
[TBL] [Abstract][Full Text] [Related]
16. Genetic disorders of surfactant homeostasis.
Whitsett JA
Paediatr Respir Rev; 2006; 7 Suppl 1():S240-2. PubMed ID: 16798578
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Surfactant composition and function in patients with ABCA3 mutations.
Garmany TH; Moxley MA; White FV; Dean M; Hull WM; Whitsett JA; Nogee LM; Hamvas A
Pediatr Res; 2006 Jun; 59(6):801-5. PubMed ID: 16641205
[TBL] [Abstract][Full Text] [Related]
19. Clinical, radiological and pathological features of ABCA3 mutations in children.
Doan ML; Guillerman RP; Dishop MK; Nogee LM; Langston C; Mallory GB; Sockrider MM; Fan LL
Thorax; 2008 Apr; 63(4):366-73. PubMed ID: 18024538
[TBL] [Abstract][Full Text] [Related]
20. Genetic disorders of surfactant homeostasis.
Whitsett JA; Wert SE; Xu Y
Biol Neonate; 2005; 87(4):283-7. PubMed ID: 15985750
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
