25 results for author:"Nogee L.M." in Literature citations
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| Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome. Wambach J.A., Wegner D.J., Depass K., Heins H., Druley T.E., Mitra R.D., An P., Zhang Q., Nogee L.M., Cole F.S. et al. Pediatrics 130:e1575-82(2012) · Mapped (4) |
| An intronic ABCA3 mutation that is responsible for respiratory disease. Agrawal A., Hamvas A., Cole F.S., Wambach J.A., Wegner D., Coghill C., Harrison K., Nogee L.M. Pediatr. Res. 71:633-637(2012) · Mapped (4) |
| High-resolution structure of a BRICHOS domain and its implications for anti-amyloid chaperone activity on lung surfactant protein C. Willander H., Askarieh G., Landreh M., Westermark P., Nordling K., Keranen H., Hermansson E., Hamvas A., Nogee L.M., Bergman T. et al. Proc. Natl. Acad. Sci. U.S.A. 109:2325-2329(2012) · UniProtKB (1) |
| Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children. Flamein F., Riffault L., Muselet-Charlier C., Pernelle J., Feldmann D., Jonard L., Durand-Schneider A.M., Coulomb A., Maurice M., Nogee L.M. et al. Hum. Mol. Genet. 21:765-775(2012) · Mapped (4) |
| Fatal familial lung disease caused by ABCA3 deficiency without identified ABCA3 mutations. Gower W.A., Wert S.E., Ginsberg J.S., Golan A., Whitsett J.A., Nogee L.M. J. Pediatr. 157:62-68(2010) · Mapped (4) |
| Genetic disorders of surfactant dysfunction. Wert S.E., Whitsett J.A., Nogee L.M. Pediatr. Dev. Pathol. 12:253-274(2009) · Mapped (12) |
| Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA. Suzuki T., Sakagami T., Rubin B.K., Nogee L.M., Wood R.E., Zimmerman S.L., Smolarek T., Dishop M.K., Wert S.E., Whitsett J.A. et al. J. Exp. Med. 205:2703-2710(2008) · UniProtKB (1) |
| Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene. McBee A.D., Wegner D.J., Carlson C.S., Wambach J.A., Yang P., Heins H.B., Saugstad O.D., Trusgnich M.A., Watkins-Torry J., Nogee L.M. et al. Pediatr. Pulmonol. 43:443-450(2008) · Mapped (3) |
| Population and disease-based prevalence of the common mutations associated with surfactant deficiency. Garmany T.H., Wambach J.A., Heins H.B., Watkins-Torry J.M., Wegner D.J., Bennet K., An P., Land G., Saugstad O.D., Henderson H. et al. Pediatr. Res. 63:645-649(2008) · Mapped (12) |
| Clinical, radiological and pathological features of ABCA3 mutations in children. Doan M.L., Guillerman R.P., Dishop M.K., Nogee L.M., Langston C., Mallory G.B., Sockrider M.M., Fan L.L. Thorax 63:366-373(2008) · Mapped (4) |
| Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation. Bullard J.E., Nogee L.M. Pediatr. Res. 62:176-179(2007) · Mapped (7) |
| Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease. Saugstad O.D., Hansen T.W., Ronnestad A., Nakstad B., Tollofsrud P.A., Reinholt F., Hamvas A., Coles F.S., Dean M., Wert S.E. et al. Acta Paediatr. 96:185-190(2007) · Mapped (4) |
| ABCA3 mutations associated with pediatric interstitial lung disease. Bullard J.E., Wert S.E., Whitsett J.A., Dean M., Nogee L.M. Am. J. Respir. Crit. Care Med. 172:1026-1031(2005) · Mapped (4) |
| A common mutation in the surfactant protein C gene associated with lung disease. Cameron H.S., Somaschini M., Carrera P., Hamvas A., Whitsett J.A., Wert S.E., Deutsch G., Nogee L.M. J. Pediatr. 146:370-375(2005) · Mapped (1) |
| Variable phenotype associated with SP-C gene mutations: fatal case with the I73T mutation. Percopo S., Cameron H.S., Nogee L.M., Pettinato G., Montella S., Santamaria F. Eur. Respir. J. 24:1072-1073(2004) · UniProtKB (1) |
| N-terminally extended surfactant protein (SP) C isolated from SP-B-deficient children has reduced surface activity and inhibited lipopolysaccharide binding. Li J., Ikegami M., Na C.L., Hamvas A., Espinassous Q., Chaby R., Nogee L.M., Weaver T.E., Johansson J. Biochemistry 43:3891-3898(2004) · Mapped (8) |
| ABCA3 gene mutations in newborns with fatal surfactant deficiency. Shulenin S., Nogee L.M., Annilo T., Wert S.E., Whitsett J.A., Dean M. N. Engl. J. Med. 350:1296-1303(2004) · UniProtKB (1) |
| Alterations in SP-B and SP-C expression in neonatal lung disease. Nogee L.M. Annu. Rev. Physiol. 66:601-623(2004) · Mapped (8) |
| Expression of a human surfactant protein C mutation associated with interstitial lung disease disrupts lung development in transgenic mice. Bridges J.P., Wert S.E., Nogee L.M., Weaver T.E. J. Biol. Chem. 278:52739-52746(2003) · Mapped (5) |
| Mutations in the surfactant protein C gene associated with interstitial lung disease. Nogee L.M., Dunbar A.E., Wert S., Askin F., Hamvas A., Whitsett J.A. Chest 121:20S-21S(2002) · Mapped (3) |
| Surfactant protein deficiency in familial interstitial lung disease. Amin R.S., Wert S.E., Baughman R.P., Tomashefski J.F. Jr., Nogee L.M., Brody A.S., Hull W.M., Whitsett J.A. J. Pediatr. 139:85-92(2001) · Mapped (4) |
| A mutation in the surfactant protein C gene associated with familial interstitial lung disease. Nogee L.M., Dunbar A.E., Wert S.E., Askin F., Hamvas A., Whitsett J.A. N. Engl. J. Med. 344:573-579(2001) · Mapped (1) |
| A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds. Nogee L.M., Garnier G., Dietz H.C., Singer L., Murphy A.M., deMello D.E., Colten H.R. J. Clin. Invest. 93:1860-1863(1994) · Mapped (2) |
| Aberrant processing of surfactant protein C in hereditary SP-B deficiency. Vorbroker D.K., Profitt S.A., Nogee L.M., Whitsett J.A. Am. J. Physiol. 268:L647-56(1995) · Mapped (1) |
| Partial deficiency of surfactant protein B in an infant with chronic lung disease. Ballard P.L., Nogee L.M., Beers M.F., Ballard R.A., Planer B.C., Polk L., deMello D.E., Moxley M.A., Longmore W.J. Pediatrics 96:1046-1052(1995) · UniProtKB (1) |