Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis. - Wikidata - wikimedia - TriplyDB

Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.

Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.

http://www.wikidata.org/entity/Q35987585

about

Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770 Molecular mechanism of pancreatic and salivary gland fluid and HCO3 secretion Airway Gland Structure and Function Irbit mediates synergy between ca(2+) and cAMP signaling pathways during epithelial transport in mice Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process.Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs Marked increases in mucociliary clearance produced by synergistic secretory agonists or inhibition of the epithelial sodium channel.Functional regulation of cystic fibrosis transmembrane conductance regulator-containing macromolecular complexes: a small-molecule inhibitor approach Compartmentalized cyclic adenosine 3',5'-monophosphate at the plasma membrane clusters PDE3A and cystic fibrosis transmembrane conductance regulator into microdomains.Distribution and size of mucous glands in the ferret tracheobronchial tree.Mucus secretion from individual submucosal glands of the ferret trachea.Defective fluid secretion from submucosal glands of nasal turbinates from CFTR-/- and CFTR (ΔF508/ΔF508) pigs.Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis.Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs.CFTR and calcium-activated chloride channels in primary cultures of human airway gland cells of serous or mucous phenotype Pseudomonas aeruginosa Homoserine lactone activates store-operated cAMP and cystic fibrosis transmembrane regulator-dependent Cl- secretion by human airway epithelia Protease-activated receptor 2 mediates mucus secretion in the airway submucosal gland.Intracellular Cl- as a signaling ion that potently regulates Na+/HCO3- transporters.In vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glands Single nucleotide polymorphisms in the 3'UTR of VPAC-1 cooperate in modulating gene expression and impact differently on the interaction with miR525-5p.Proteomic analysis of pure human airway gland mucus reveals a large component of protective proteins.Chloride secretion by cultures of pig tracheal gland cells.The porcine lung as a potential model for cystic fibrosis Update in cystic fibrosis 2007.Anion secretion by a model epithelium: more lessons from Calu-3.Autonomic neural control of intrathoracic airways.Vasoactive intestinal Peptide inhaled agonists: potential role in respiratory therapeutics Airway and lung remodelling in chronic pulmonary obstructive disease: a role for muscarinic receptor antagonists?The gating of the CFTR channel.Role of tyrosine phosphorylation in the muscarinic activation of the cystic fibrosis transmembrane conductance regulator (CFTR).Basolateral chloride loading by the anion exchanger type 2: role in fluid secretion by the human airway epithelial cell line Calu-3.Acute intratracheal Pseudomonas aeruginosa infection in cystic fibrosis mice is age-independent.Cultures of human tracheal gland cells of mucous or serous phenotype.Introduction to section IV: biophysical methods to approach CFTR structure.CK2 is a key regulator of SLC4A2-mediated Cl-/HCO3- exchange in human airway epithelia.Why mouse airway submucosal gland serous cells do not secrete fluid in response to cAMP stimulation.CFTR Modulator Therapies in Pediatric Cystic Fibrosis: Focus on Ivacaftor.Carbachol-induced colonic mucus formation requires transport via NKCC1, K⁺ channels and CFTR.Transgenic animals may help resolve a sticky situation in cystic fibrosis.cAMP-activated Ca2+ signaling is required for CFTR-mediated serous cell fluid secretion in porcine and human airways.

P2860

Q24644303-67DAD1E6-AB35-483D-98F1-630A421674EE Q26852694-5E6C3D18-0D1A-4D90-8558-B33618A0A2B2 Q28082284-399B63E4-9F08-4DC8-B6FB-64274DF8DE96 Q28594050-031DF872-AB41-454B-B737-FD11FAA9BCFB Q30487263-20668050-03C2-4E1B-AD49-751D594A4E3D Q30572016-2201E1A9-9DD3-407F-AF7A-F0E39DCD56BD Q30828169-BF9B6DAF-9EC1-423B-8203-8A18F1FE0DCB Q30998341-9ECD80A3-2409-438D-BED1-C919B75271FF Q33721181-76B2BD7F-54EB-4619-8B05-E8CC1FB69CF5 Q33894239-AD3A4D4D-DE5E-4756-87C7-7E0C965EDECA Q33994621-EF81EFBC-0866-4A60-9F0B-14FDC16C2FEA Q34025925-F46EE479-6FDA-4FBD-8103-3AA7EB0EF837 Q34090196-DE85E16F-5895-4234-A703-7E86334E49E6 Q34090231-3559E63B-A815-4DE2-B616-41D8E6C90FE0 Q34212692-9AF9B2E6-B96E-440C-AACC-4A2547398DE9 Q34251347-7CC632FC-9C85-4F15-A4E4-D30001ECA47C Q34391395-A15874F9-6AB1-42D3-8652-76AC3D6BE535 Q35031357-704F66A6-04CD-43B5-B66E-52E7859A4CAE Q35035031-7739ACA0-9CB6-4B14-B04C-465540BE2A5E Q35414146-45A2C239-FEC0-4736-9C5A-0164CB15A1ED Q35565801-B025219F-B8CC-497D-8481-F790121C0E09 Q35994809-506DF933-6C8D-4371-9AE5-5F8997CE1EB9 Q36846439-6DE4A1CA-94A7-44FB-A99A-48F689D0DC93 Q37156059-1725F1E3-5554-46C6-8A7A-E84373C4368E Q37830789-17C54DC4-885E-4ABF-AA5A-E9FCB50C9C31 Q38116834-56A36DA6-B51B-45C1-BC59-4966A24CC8E2 Q38128288-4E969DCC-3CCB-4506-BABB-1E036C3FF4F2 Q38270131-9816ADD0-76D4-4D98-B659-B3AF9C514BD5 Q38970505-73B1488F-3194-4D16-9D30-B2EEAA7B50D1 Q39140433-7AEF4F92-9A42-478C-BA93-EB3AF17537F9 Q39313392-45F6BA53-2D88-486A-874E-0BD82455E6BE Q40075329-3E44312E-E0F4-4F9F-B948-78112EAE9BB8 Q40311179-52942241-2512-430B-8BB1-BBE588933503 Q41136041-D20154F5-8325-493F-9E40-5067B561D12D Q41368424-C01BA5E3-7AB1-4569-B235-A4F15B7F91C9 Q41520948-C22E1A51-B1C0-4228-81A2-FA421652FDF6 Q41641680-BEACD451-0192-4946-B445-7A46881E6EAC Q41813130-E352C8B6-DE76-4A45-A7B3-FAAFD2360705 Q41815692-A1153DB5-29A4-4CA6-97A7-CAAE7DD0BE57 Q42008867-58649882-73BC-4961-AA01-B1F8ED4C4287

P2860

Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.

http://www.wikidata.org/entity/Q35987585

description

2007 nî lūn-bûn

@nan

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

2007年论文

@zh

2007年论文

@zh-cn

name

Synergistic airway gland mucus ...... ol is lost in cystic fibrosis.

@ast

Synergistic airway gland mucus ...... ol is lost in cystic fibrosis.

@en

type

label

Synergistic airway gland mucus ...... ol is lost in cystic fibrosis.

@ast

Synergistic airway gland mucus ...... ol is lost in cystic fibrosis.

@en

prefLabel

Synergistic airway gland mucus ...... ol is lost in cystic fibrosis.

@ast

Synergistic airway gland mucus ...... ol is lost in cystic fibrosis.

@en

P1433

Q35987585-8FDDA3F0-35E5-4B8D-BAC0-24D1B122E428

P1476

Q35987585-DCFBFF51-0B18-4FDF-AB51-A808135DCCF3

P2093

Q35987585-151FCBE4-BB56-4EDC-B5DB-B2D831B81104

Q35987585-26B01534-FACD-46F0-ACB6-16AADCB1A726

Q35987585-2EDAD14A-4FA8-45FB-9C75-5BFABFE448CF

Q35987585-4CFC2A28-F965-4292-855D-D3CDD350249E

Q35987585-6A12A3A1-5A01-4849-A5B3-FD419B158F48

Q35987585-9013E34F-0010-44AA-B3F5-E15B4BF33816

Q35987585-A9EE2444-F0D2-4F6B-A7F5-5FCA7A17CF67

P2860

Q35987585-013AD059-CF5E-445F-BEF5-C0CC414A3653

Q35987585-01A66B06-6EE2-4667-9E06-0A1E50C287CF

Q35987585-02F249E4-F7CB-4AD9-BEA5-91B661647AE4

Q35987585-0CD6C24D-1CBA-48A1-8A00-C1E025D59ABE

Q35987585-13FD9897-DD1F-4BCD-BB9E-5C7ACAE0EB88

Q35987585-14BE0237-CAA5-4EBE-AE86-41A3E1EF624C

Q35987585-31DAD016-37B9-4913-B7E8-69E5C3891A89

Q35987585-488443ED-6E17-4EC9-98CE-B296AD1A4B3C

Q35987585-492EF222-A3C7-4079-B3FB-A07B126BB614

Q35987585-4A62A448-F813-43F9-B65B-E4D7BAEBB5B9

P304

Q35987585-10151427-D0A2-4B2A-AD9D-626AA0CEE1D7

P31

Q35987585-899B34A1-99C5-4A5F-B290-E2AEBC406893

P356

Q35987585-011019B8-C301-4032-BEB6-5D71E34E15C1

P407

Q35987585-39A36D1F-0E01-43D0-85D1-AAD3C73C4105

P433

Q35987585-23F3CDB5-0BCD-43A7-810D-98B54B638BF9

P478

Q35987585-6AC3E1AC-E79E-4898-86E7-A932D3BC1260

P50

Q35987585-D68053FF-4A88-40B0-ABD2-341A64B49C98

P577

Q35987585-AC4F56D2-23D9-4910-8ED4-2D2A06C9A93D

P5875

Q35987585-AE623ACD-1B2E-4631-8225-A8ECF9B862C0

P698

Q35987585-471891FD-0E00-4DBB-823B-2E2673AECACF

P921

Q35987585-11726256-A7A3-432D-A3E2-85733DD28381

P932

Q35987585-A10AC2DF-4100-428B-8B11-9D034697A073

P356

P1433

Journal of Clinical Investigation

P1476

Synergistic airway gland mucus ...... hol is lost in cystic fibrosis

@en

P2093

Jeffrey J Wine

http://www.w3.org/2001/XMLSchema#string

Jin V Wu

http://www.w3.org/2001/XMLSchema#string

John W Hanrahan

http://www.w3.org/2001/XMLSchema#string

Juan P Ianowski

http://www.w3.org/2001/XMLSchema#string

Mauri E Krouse

http://www.w3.org/2001/XMLSchema#string

Nam Soo Joo

http://www.w3.org/2001/XMLSchema#string

Robert C Robbins

http://www.w3.org/2001/XMLSchema#string

P2860

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

Deficient vasoactive intestinal peptide innervation in the sweat glands of cystic fibrosis patients

Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

Projections and pathways of VIP- and nNOS-containing airway neurons in ferret trachea.

New models of the tracheal airway define the glandular contribution to airway surface fluid and electrolyte composition.

Measurement of the bronchial mucous gland layer: a diagnostic yardstick in chronic bronchitis.

Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion.

Mucus clearance as a primary innate defense mechanism for mammalian airways.

Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

Submucosal glands and airway defense.

P304

3118-3127

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1172/JCI31992

http://www.w3.org/2001/XMLSchema#string

P407

P433

10

http://www.w3.org/2001/XMLSchema#string

P478

117

http://www.w3.org/2001/XMLSchema#string

P50

P577

2007-10-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

5986561

http://www.w3.org/2001/XMLSchema#string

P698

17853942

http://www.w3.org/2001/XMLSchema#string

P921

cystic fibrosis

P932

1974867

http://www.w3.org/2001/XMLSchema#string