Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 29

Cited In for PubMed (Select 10712351)

1.

Diseases of pulmonary surfactant homeostasis.

Whitsett JA, Wert SE, Weaver TE.

Annu Rev Pathol. 2015;10:371-93. doi: 10.1146/annurev-pathol-012513-104644.

2.

The molecular era of surfactant biology.

Whitsett JA.

Neonatology. 2014;105(4):337-43. doi: 10.1159/000360649. Epub 2014 May 30. Review.

PMID:
24931326
3.

Genetic risk factors associated with respiratory distress syndrome.

Jo HS.

Korean J Pediatr. 2014 Apr;57(4):157-63. doi: 10.3345/kjp.2014.57.4.157. Epub 2014 Apr 30. Review.

4.

Interstitial lung disease: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases.

Rosas IO, Dellaripa PF, Lederer DJ, Khanna D, Young LR, Martinez FJ.

Ann Am Thorac Soc. 2014 Apr;11 Suppl 3:S169-77. doi: 10.1513/AnnalsATS.201312-429LD. Review.

5.

An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy.

Kurland G, Deterding RR, Hagood JS, Young LR, Brody AS, Castile RG, Dell S, Fan LL, Hamvas A, Hilman BC, Langston C, Nogee LM, Redding GJ; American Thoracic Society Committee on Childhood Interstitial Lung Disease (chILD) and the chILD Research Network.

Am J Respir Crit Care Med. 2013 Aug 1;188(3):376-94. doi: 10.1164/rccm.201305-0923ST. Review.

6.

Diffuse lung disease in children: summary of a scientific conference.

Hamvas A, Deterding R, Balch WE, Schwartz DA, Albertine KH, Whitsett JA, Cardoso WV, Kotton DN, Kourembanas S, Hagood JS.

Pediatr Pulmonol. 2014 Apr;49(4):400-9. doi: 10.1002/ppul.22805. Epub 2013 Jun 24.

7.

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Wambach JA, Wegner DJ, Depass K, Heins H, Druley TE, Mitra RD, An P, Zhang Q, Nogee LM, Cole FS, Hamvas A.

Pediatrics. 2012 Dec;130(6):e1575-82. doi: 10.1542/peds.2012-0918. Epub 2012 Nov 19.

8.

An intronic ABCA3 mutation that is responsible for respiratory disease.

Agrawal A, Hamvas A, Cole FS, Wambach JA, Wegner D, Coghill C, Harrison K, Nogee LM.

Pediatr Res. 2012 Jun;71(6):633-7. doi: 10.1038/pr.2012.21. Epub 2012 Feb 15.

9.

Genetic Basis of Children's Interstitial Lung Disease.

Nogee LM.

Pediatr Allergy Immunol Pulmonol. 2010 Mar;23(1):15-24.

10.

Surfactant dysfunction.

Gower WA, Nogee LM.

Paediatr Respir Rev. 2011 Dec;12(4):223-9. doi: 10.1016/j.prrv.2011.01.005. Epub 2011 Mar 5. Review.

11.

Altered surfactant homeostasis and recurrent respiratory failure secondary to TTF-1 nuclear targeting defect.

Peca D, Petrini S, Tzialla C, Boldrini R, Morini F, Stronati M, Carnielli VP, Cogo PE, Danhaive O.

Respir Res. 2011 Aug 25;12:115. doi: 10.1186/1465-9921-12-115.

12.

Cultured human airway epithelial cells (calu-3): a model of human respiratory function, structure, and inflammatory responses.

Zhu Y, Chidekel A, Shaffer TH.

Crit Care Res Pract. 2010;2010. pii: 394578. doi: 10.1155/2010/394578. Epub 2010 Jun 27.

13.

Surfactant protein-C promoter variants associated with neonatal respiratory distress syndrome reduce transcription.

Wambach JA, Yang P, Wegner DJ, An P, Hackett BP, Cole FS, Hamvas A.

Pediatr Res. 2010 Sep;68(3):216-20. doi: 10.1203/00006450-201011001-00421.

14.

Transcriptional regulation of SP-B gene expression by nitric oxide in H441 lung epithelial cells.

Boggaram V, Chandru H, Gottipati KR, Thakur V, Das A, Berhane K.

Am J Physiol Lung Cell Mol Physiol. 2010 Aug;299(2):L252-62. doi: 10.1152/ajplung.00062.2010. Epub 2010 Apr 23.

15.

Patient-derived granulocyte/macrophage colony-stimulating factor autoantibodies reproduce pulmonary alveolar proteinosis in nonhuman primates.

Sakagami T, Beck D, Uchida K, Suzuki T, Carey BC, Nakata K, Keller G, Wood RE, Wert SE, Ikegami M, Whitsett JA, Luisetti M, Davies S, Krischer JP, Brody A, Ryckman F, Trapnell BC.

Am J Respir Crit Care Med. 2010 Jul 1;182(1):49-61. doi: 10.1164/rccm.201001-0008OC. Epub 2010 Mar 11.

16.

Alveolar surfactant homeostasis and the pathogenesis of pulmonary disease.

Whitsett JA, Wert SE, Weaver TE.

Annu Rev Med. 2010;61:105-19. doi: 10.1146/annurev.med.60.041807.123500. Review.

17.

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. doi: 10.1016/j.jpeds.2009.06.006. Epub 2009 Aug 3.

18.

Genetic disorders of surfactant dysfunction.

Wert SE, Whitsett JA, Nogee LM.

Pediatr Dev Pathol. 2009 Jul-Aug;12(4):253-74. doi: 10.2350/09-01-0586.1. Review.

19.

Pulmonary surfactant surface tension influences alveolar capillary shape and oxygenation.

Ikegami M, Weaver TE, Grant SN, Whitsett JA.

Am J Respir Cell Mol Biol. 2009 Oct;41(4):433-9. doi: 10.1165/rcmb.2008-0359OC. Epub 2009 Feb 6.

20.

Genetic predisposition to respiratory diseases: infiltrative lung diseases.

Steele MP, Brown KK.

Respiration. 2007;74(6):601-8. Review.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk