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Surfactant protein C
Surfactant Protein-C in the Maintenance of Lung Integrity and Function Stephan W
Single-Cell Transcriptomics Identifies Dysregulated Metabolic Programs of Aging Alveolar Progenitor Cells in Lung Fibrosis
Idiopathic Pulmonary Fibrosis: Pathogenesis and Management
Lung Stem Cells
Systematic Review of Drug Effects in Humans and Models with Surfactant-Processing Disease
M(2-9), a Cecropin-Melittin Hybrid Peptide
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Isolating the Role of Corticosterone in the Hypothalamic-Pituitary-Gonadal Genomic Stress Response
Human IL-32 Expression Protects Mice Against a Hypervirulent Strain of Mycobacterium Tuberculosis
Lipid–Protein and Protein–Protein Interactions in the Pulmonary Surfactant System and Their Role in Lung Homeostasis
Simple, Helical Peptoid Analogs of Lung Surfactant Protein B
I WO 2015/019381 Al Fig. 2
Supplemental Table S1. Primers for Sybrgreen Quantitative RT-PCR Assays
The Pulmonary Surfactant System: Biochemical and Clinical Aspects L
Supplemental Figure 1 Characterization of Lung Tumors In
Straightforward Method for the Preparation of Lysine-Based Double-Chained Anionic Surfactants
Structure, Function and Deficiency Diseases of Lung
122602 Hydrophobic Surfactant Proteins in Lung Function
Top View
Transcriptome Profiling Reveals the Complexity of Pirfenidone Effects in IPF
Expression of Surfactant Protein-C, S100A8, S100A9, and B Cell Markers in Renal Allografts: Investigation of the Prognostic Value
Personalised Medicine in Interstitial Lung Diseases
Molecular Mechanisms of Early Lung Specification and Branching
A Novel Surfactant Protein C L55F Mutation Associated with Interstitial Lung Disease Alters Subcellular Localization of Prosp-C in A549 Cells
Pulmonary Puzzle Thorax: First Published As 10.1136/Thx.2007.092650A on 19 November 2008
The Genetic Basis of Idiopathic Pulmonary Fibrosis
Review of the British Thoracic Society Winter Meeting 2017, 6–8
Ultrastructural Support in Paediatric Pathology
Pulmonary Alveolar Proteinosis
Genetic Mutations in Surfactant Protein C Are a Rare Cause of Sporadic
The Role of Megalin (LRP-2/Gp330) During Development ⁎ Carolyn E
Successful Treatment of Neonatal Respiratory Failure Caused by a Novel Surfactant Protein C P.Cys121gly Mutation with Hydroxychloroquine
(12) Patent Application Publication (10) Pub. No.: US 2011/0023143 A1 Weinstein Et Al
Mechanical Ventilation Effect on Surfactant Content, Function, and Lung Compliance in the Newborn Rat
Rituximab Therapy in Pulmonary Alveolar Proteinosis Improves
Application of Molecular Dynamics Simulations to Pulmonary Lung Surfactant
Thesis for Word XP
Surfactant Protein C-Associated Interstitial Lung Disease; Three
Lessons from a Rare Familial Dementia: Amyloid and Beyond
Understanding Idiopathic Interstitial Pneumonia: a Gene-Based Review of Stressed Lungs
Surfactant Replacement Therapy
Wnt Signaling Regulates Trans-Differentiation of Stem Cell Like
(12) Patent Application Publication (10) Pub. No.: US 2011/0030072 A1 Weinstein Et Al
WO 2017/136652 Al 10 August 2017 (10.08.2017) P O P C T
E3 Ubiquitin Ligase RFWD2 Controls Lung Branching Through Protein-Level Regulation of ETV Transcription Factors
SFTPC Mutations Cause SP-C Degradation and Aggregate Formation Without Increasing ER Stress
Noninfectious Lung Injury After Hematopoietic Stem Cell Transplantation: Idiopathic Pneumonia Syndrome
The Surfactant Protein C Mutation A116D Alters Cellular Processing
別表1 調査対象遺伝子リスト Genesymbol 遺伝子名 Gene ID
Rhoa and ERK Signalling Regulate the Expression of the Transcription
Role of Unfolded Proteins in Lung Disease Thorax: First Published As 10.1136/Thoraxjnl-2019-213738 on 19 October 2020
Fibrotic Idiopathic Interstitial Lung Disease: the Molecular and Cellular Key Players
Conditional Depletion of Airway Progenitor Cells Induces Peribronchiolar Fibrosis
Activin a Contributes to the Development of Hyperoxia-Induced
Integration of Transcriptomic and Proteomic Pro Les Identi Es Potential Biomarkers in Idiopathic Pulmonary Fibrosis
A Novel Surfactant Protein C Mutation Resulting in Aberrant Protein Processing and Altered Subcellular Localization Causes Infantile Interstitial Lung Disease
Curriculum Vitae Page 2
Contributions of Alveolar Epithelial Cell Quality Control to Pulmonary Fibrosis
Transgenic Mice Expressing the Sh Ble Bleomycin Resistance Gene Are Protected Against Bleomycin-Induced Pulmonary Fibrosis1
Neonatal Respiratory Failure Associated with Mutation in the Surfactant Protein C Gene
ᵪ ᵪ Patient / Legal Guardian (Signature) Doctor (Date, Signature)
Development of Novel Synthetic Lung Surfactants for Treatment of Respiratory Distress Syndrome
VIEW Open Access the Potential of Antisense Oligonucleotide Therapies for Inherited Childhood Lung Diseases Kelly M
Alapati-2019.Pdf