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Posttranslational regulation of surfactant protein B expression.
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Surfactant protein B in type II pneumocytes and intra-alveolar surfactant forms of human lungs.
Am J Respir Cell Mol Biol. 2004 Apr;30(4):449-58. doi: 10.1165/rcmb.2003-0262OC. Epub 2003 Sep 11.
3
Pulmonary surfactant protein SP-B promotes exocytosis of lamellar bodies in alveolar type II cells.
FASEB J. 2018 Aug;32(8):4600-4611. doi: 10.1096/fj.201701462RR. Epub 2018 Mar 15.
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Role of -glycosylation of surfactant protein SP-B in lipid and SP-B interacting properties. Implications in disease.
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Developmental and genetic regulation of human surfactant protein B in vivo.
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6
Distribution of surfactant protein A in rat lung.
Am J Respir Cell Mol Biol. 1994 Oct;11(4):405-15. doi: 10.1165/ajrcmb.11.4.7917309.
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Cell-specific posttranslational processing of the surfactant-associated protein SP-B.
Am J Physiol. 1993 Mar;264(3 Pt 1):L290-9. doi: 10.1152/ajplung.1993.264.3.L290.
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Processing of surfactant protein B proprotein by a cathepsin D-like protease.
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Posttranslational processing of surfactant protein C in rat type II cells.
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10
SP-A, SP-B, and SP-C in surfactant subtypes around birth: reexamination of alveolar life cycle of surfactant.
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A therapy for suppressing canonical and noncanonical SARS-CoV-2 viral entry and an intrinsic intrapulmonary inflammatory response.
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Molecular Impact of Conventional and Electronic Cigarettes on Pulmonary Surfactant.
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Gene Therapy Potential for Genetic Disorders of Surfactant Dysfunction.
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Physiology and pathophysiology of human airway mucus.
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GM130 regulates pulmonary surfactant protein secretion in alveolar type II cells.
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The biology of the ABCA3 lipid transporter in lung health and disease.
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Effect of cigarette smoke extract on insulin transport in alveolar epithelial cell line A549.
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Genetic disorders of surfactant dysfunction.
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本文引用的文献

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Pepsinogen C proteolytic processing of surfactant protein B.
J Biol Chem. 2008 Apr 18;283(16):10330-8. doi: 10.1074/jbc.M707516200. Epub 2008 Feb 5.
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Partial SP-B deficiency perturbs lung function and causes air space abnormalities.
Am J Physiol Lung Cell Mol Physiol. 2005 Jun;288(6):L1154-61. doi: 10.1152/ajplung.00392.2004. Epub 2005 Feb 18.
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Mapping and analysis of the lytic and fusogenic domains of surfactant protein B.
Biochemistry. 2005 Jan 25;44(3):861-72. doi: 10.1021/bi0485575.
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Processing of pulmonary surfactant protein B by napsin and cathepsin H.
J Biol Chem. 2004 Apr 16;279(16):16178-84. doi: 10.1074/jbc.M312029200. Epub 2004 Feb 6.
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Pepsinogen C: a type 2 cell-specific protease.
Am J Physiol Lung Cell Mol Physiol. 2004 Feb;286(2):L382-7. doi: 10.1152/ajplung.00310.2003. Epub 2003 Oct 24.
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Involvement of napsin A in the C- and N-terminal processing of surfactant protein B in type-II pneumocytes of the human lung.
J Biol Chem. 2003 Dec 5;278(49):49006-14. doi: 10.1074/jbc.M306844200. Epub 2003 Sep 16.
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Surfactant protein A and B genetic variants in respiratory distress syndrome in singletons and twins.
Am J Respir Crit Care Med. 2003 Nov 15;168(10):1216-22. doi: 10.1164/rccm.200304-524OC. Epub 2003 Aug 28.
8
In vitro surfactant protein B deficiency inhibits lamellar body formation.
Am J Respir Cell Mol Biol. 2003 Aug;29(2):259-66. doi: 10.1165/rcmb.2002-0149OC. Epub 2003 Mar 20.
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Cysteine protease activity is required for surfactant protein B processing and lamellar body genesis.
Am J Respir Cell Mol Biol. 2003 Jan;28(1):69-79. doi: 10.1165/rcmb.2002-0111OC.

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