Nogee LM - Search Results

1

Expression of a human surfactant protein C mutation associated with interstitial lung disease disrupts lung development in transgenic mice.

Bridges JP, Wert SE, Nogee LM, Weaver TE. Bridges JP, et al. Among authors: nogee lm. J Biol Chem. 2003 Dec 26;278(52):52739-46. doi: 10.1074/jbc.M309599200. Epub 2003 Oct 2. J Biol Chem. 2003. PMID: 14525980 Free article.

2

Increased expression of pulmonary surfactant proteins in oxygen-exposed rats.

Nogee LM, Wispé JR, Clark JC, Weaver TE, Whitsett JA. Nogee LM, et al. Am J Respir Cell Mol Biol. 1991 Feb;4(2):102-7. doi: 10.1165/ajrcmb/4.2.102. Am J Respir Cell Mol Biol. 1991. PMID: 1991071

3

Human surfactant protein B: structure, function, regulation, and genetic disease.

Whitsett JA, Nogee LM, Weaver TE, Horowitz AD. Whitsett JA, et al. Among authors: nogee lm. Physiol Rev. 1995 Oct;75(4):749-57. doi: 10.1152/physrev.1995.75.4.749. Physiol Rev. 1995. PMID: 7480161 Review.

4

Surfactant protein B deficiency: clinical, histological and molecular evaluation.

Williams GD, Christodoulou J, Stack J, Symons P, Wert SE, Murrell MJ, Nogee LM. Williams GD, et al. Among authors: nogee lm. J Paediatr Child Health. 1999 Apr;35(2):214-20. doi: 10.1046/j.1440-1754.1999.00307.x. J Paediatr Child Health. 1999. PMID: 10365365

5

Hereditary surfactant protein B deficiency resulting from a novel mutation.

Somaschini M, Wert S, Mangili G, Colombo A, Nogee L. Somaschini M, et al. Intensive Care Med. 2000 Jan;26(1):97-100. doi: 10.1007/s001340050019. Intensive Care Med. 2000. PMID: 10663288

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. Cutz E, et al. Among authors: nogee lm. Am J Respir Crit Care Med. 2000 Feb;161(2 Pt 1):608-14. doi: 10.1164/ajrccm.161.2.9905062. Am J Respir Crit Care Med. 2000. PMID: 10673207

7

Allelic heterogeneity in hereditary surfactant protein B (SP-B) deficiency.

Nogee LM, Wert SE, Proffit SA, Hull WM, Whitsett JA. Nogee LM, et al. Am J Respir Crit Care Med. 2000 Mar;161(3 Pt 1):973-81. doi: 10.1164/ajrccm.161.3.9903153. Am J Respir Crit Care Med. 2000. PMID: 10712351

8

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. Tryka AF, et al. Among authors: nogee lm. Pediatr Dev Pathol. 2000 Jul-Aug;3(4):335-45. doi: 10.1007/s100249910048. Pediatr Dev Pathol. 2000. PMID: 10890249

9

Prolonged survival in hereditary surfactant protein B (SP-B) deficiency associated with a novel splicing mutation.

Dunbar AE 3rd, Wert SE, Ikegami M, Whitsett JA, Hamvas A, White FV, Piedboeuf B, Jobin C, Guttentag S, Nogee LM. Dunbar AE 3rd, et al. Among authors: nogee lm. Pediatr Res. 2000 Sep;48(3):275-82. doi: 10.1203/00006450-200009000-00003. Pediatr Res. 2000. PMID: 10960490

10

Recurrent familial neonatal deaths: hereditary surfactant protein B deficiency.

Andersen C, Ramsay JA, Nogee LM, Shah J, Wert SE, Paes B, Nowaczyk MJ. Andersen C, et al. Among authors: nogee lm. Am J Perinatol. 2000;17(4):219-24. doi: 10.1055/s-2000-9418. Am J Perinatol. 2000. PMID: 11041444

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