322 results on '"Kesimer, Mehmet"'
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52. Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties via hydration
53. Is bipolar hemiarthroplasty an appropriate type of hip articulation following proximal femoral or total femoral resections for musculoskeletal malignancies?
54. Effect of the pandemic on surgical procedures in a tertiary care hospital: A retrospective review.
55. Muskuloskeletal maligniteye bağlı proksimal femur ya da total femur rezeksiyonu yapılan hastalarda bipolar hemiartroplasti yeterli midir?
56. Another Warning Sign: High Nicotine Content in Electronic Cigarettes Disrupts Mucociliary Clearance, the Essential Defense Mechanism of the Lung
57. Membrane-Tethered Mucin 1 is Stimulated by Interferon in Multiple Cell Types and Antagonizes Influenza A Virus Infection in Human Airway Epithelium
58. POST-SECRETORY MATURATION OF MUC5B: DEFECTIVE IN CYSTIC FIBROSIS: S16.4
59. Studying Mucin Secretion from Human Bronchial Epithelial Cell Primary Cultures
60. Mass Spectrometric Analysis of Mucin Core Proteins
61. Impact of COVID-19 pandemic on hand injuries.
62. Innate Immunity and Mucus Structure and Function
63. THE ROLE OF MUCIN-INTERACTOME IN THE INNATE DEFENSE OF THE LUNG: S12.4
64. Vesicular and Extravesicular Protein Signatures From the Airspaces of Ozone-Exposed Mice Reflect Muco-Inflammatory Disturbances.
65. Cigarillos Compromise the Mucosal Barrier and Protein Expression in Airway Epithelia
66. Membrane-bound mucins of the airway mucosal surfaces are densely decorated with keratan sulfate: revisiting their role in the Lung’s innate defense
67. Human Fallopian Tube Epithelial Cell Culture Model To Study Host Responses to Chlamydia trachomatis Infection
68. Current Smoking With or Without Chronic Bronchitis is Independently Associated With Goblet Cell Hyperplasia in Healthy Smokers and COPD Subjects: an Analysis of the SPIROMICS Cohort
69. Airway Mucus Hyperconcentration in Non–Cystic Fibrosis Bronchiectasis
70. The Cystic Fibrosis Transmembrane Conductance Regulator Is Regulated by a Direct Interaction with the Protein Phosphatase 2A
71. MUC5B-CILIA INTERACTIONS, THE BASIS OF AN INNATE IMMUNE PROTECTION MECHANISM: S10.4
72. Urate oxidation during percutaneous transluminal coronary angioplasty and thrombolysis in patients with coronary artery disease
73. Effect of rotational deformities after pediatric femoral fracture on clinical outcome.
74. THE INTERACTION OF MUCINS WITH CILIA, ITS POTENTIAL IMPORTANCE FOR MUCUS CLEARANCE IN THE LARGE AIRWAYS AND HOW IT MIGHT PLAY A ROLE IN MUCUS ADHESION IN CF: S17.4
75. Analyzing the functions of large glycoconjugates through the dissipative properties of their absorbed layers using the gel-forming mucin MUC5B as an example
76. Chronic Exposure to Beta-Blockers Attenuates Inflammation and Mucin Content in a Murine Asthma Model
77. THE STRUCTURAL BASIS OF MUCOSAL PROTECTION IN THE LARGE AIRWAY: S16.4
78. Hereditary Mucin Deficiency Caused by Biallelic Loss-of-Function of MUC5B Defines a Novel Category of Lung Disease
79. Transient nonketotic hyperglycinemia: two case reports and literature review
80. Endotracheal tube mucus as a source of airway mucus for rheological study
81. Mucus accumulation in the lungs precedes structural changes and infection in children with cystic fibrosis
82. Localization of Secretory Mucins MUC5AC and MUC5B in Normal/Healthy Human Airways
83. Identification of salivary mucin MUC7 binding proteins from Streptococcus gordonii
84. Membrane-bound mucins of the airway mucosal surfaces are densely decorated with keratan sulfate: revisiting their role in the Lung's innate defense.
85. Intercellular Communication between Airway Epithelial Cells Is Mediated by Exosome-Like Vesicles
86. Mucin Concentrations and Peripheral Airway Obstruction in Chronic Obstructive Pulmonary Disease
87. Mucus Hydration in Subjects with Stable Chronic Bronchitis: A Comparison of Spontaneous and Induced Sputum
88. Airways mucus pathogenesis in patients with non-cystic fibrosis bronchiectasis
89. SPLUNC1 degradation by the cystic fibrosis mucosal environment drives airway surface liquid dehydration
90. At the Root: Defining and Halting Progression of Early Chronic Obstructive Pulmonary Disease
91. Cigarette smoke modifies and inactivates SPLUNC1, leading to airway dehydration
92. Mucus Hypersecretion, Hyperconcentration and Chronic Bronchitis
93. Evaluation of a SPLUNC1-derived peptide for the treatment of cystic fibrosis lung disease
94. Automated segmentation and quantification of airway mucus with endobronchial optical coherence tomography
95. Little Cigars are More Toxic than Cigarettes and Uniquely Change the Airway Gene and Protein Expression
96. Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airways
97. Airway Epithelial Derived Exosomes on Protecting and Remodeling of the Lung
98. Measuring Airway Mucin 2 in Patients with Severe Chronic Obstructive Pulmonary Disease with Bacterial Colonization
99. Allergic asthma is distinguished by sensitivity of allergen-specific CD4+T cells and airway structural cells to type 2 inflammation
100. Identification of SPLUNC1's ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airways
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