Whitsett JA - Search Results

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. Saugstad OD, et al. Among authors: whitsett ja. Acta Paediatr. 2007 Feb;96(2):185-90. doi: 10.1111/j.1651-2227.2007.00016.x. Acta Paediatr. 2007. PMID: 17429902

2

ABCA3 gene mutations in newborns with fatal surfactant deficiency.

Shulenin S, Nogee LM, Annilo T, Wert SE, Whitsett JA, Dean M. Shulenin S, et al. Among authors: whitsett ja. N Engl J Med. 2004 Mar 25;350(13):1296-303. doi: 10.1056/NEJMoa032178. N Engl J Med. 2004. PMID: 15044640 Free article.

3

ABCA3 mutations associated with pediatric interstitial lung disease.

Bullard JE, Wert SE, Whitsett JA, Dean M, Nogee LM. Bullard JE, et al. Among authors: whitsett ja. Am J Respir Crit Care Med. 2005 Oct 15;172(8):1026-31. doi: 10.1164/rccm.200503-504OC. Epub 2005 Jun 23. Am J Respir Crit Care Med. 2005. PMID: 15976379 Free PMC article.

4

Genetic disorders of surfactant homeostasis.

Whitsett JA, Wert SE, Xu Y. Whitsett JA, et al. Biol Neonate. 2005;87(4):283-7. doi: 10.1159/000084875. Epub 2005 Jun 1. Biol Neonate. 2005. PMID: 15985750 Review.

5

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. Garmany TH, et al. Among authors: whitsett ja. Pediatr Res. 2006 Jun;59(6):801-5. doi: 10.1203/01.pdr.0000219311.14291.df. Epub 2006 Apr 26. Pediatr Res. 2006. PMID: 16641205

6

Genetic disorders of surfactant dysfunction.

Wert SE, Whitsett JA, Nogee LM. Wert SE, et al. Among authors: whitsett ja. Pediatr Dev Pathol. 2009 Jul-Aug;12(4):253-74. doi: 10.2350/09-01-0586.1. Pediatr Dev Pathol. 2009. PMID: 19220077 Free PMC article. Review.

7

Fatal familial lung disease caused by ABCA3 deficiency without identified ABCA3 mutations.

Gower WA, Wert SE, Ginsberg JS, Golan A, Whitsett JA, Nogee LM. Gower WA, et al. Among authors: whitsett ja. J Pediatr. 2010 Jul;157(1):62-8. doi: 10.1016/j.jpeds.2010.01.010. Epub 2010 Mar 20. J Pediatr. 2010. PMID: 20304423

8

Genetic disorders influencing lung formation and function at birth.

Whitsett JA, Wert SE, Trapnell BC. Whitsett JA, et al. Hum Mol Genet. 2004 Oct 1;13 Spec No 2:R207-15. doi: 10.1093/hmg/ddh252. Hum Mol Genet. 2004. PMID: 15358727 Review.

9

A common mutation in the surfactant protein C gene associated with lung disease.

Cameron HS, Somaschini M, Carrera P, Hamvas A, Whitsett JA, Wert SE, Deutsch G, Nogee LM. Cameron HS, et al. Among authors: whitsett ja. J Pediatr. 2005 Mar;146(3):370-5. doi: 10.1016/j.jpeds.2004.10.028. J Pediatr. 2005. PMID: 15756222

10

Expression of ABCA3 in developing lung and other tissues.

Stahlman MT, Besnard V, Wert SE, Weaver TE, Dingle S, Xu Y, von Zychlin K, Olson SJ, Whitsett JA. Stahlman MT, et al. Among authors: whitsett ja. J Histochem Cytochem. 2007 Jan;55(1):71-83. doi: 10.1369/jhc.6A6962.2006. Epub 2006 Sep 18. J Histochem Cytochem. 2007. PMID: 16982851

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