The porcine lung as a potential model for cystic fibrosis - Wikidata - awgldk - TriplyDB

The porcine lung as a potential model for cystic fibrosis

The porcine lung as a potential model for cystic fibrosis

http://www.wikidata.org/entity/Q36846439

about

Asparaginase treatment side-effects may be due to genes with homopolymeric Asn codons (Review-Hypothesis)Microscale imaging of cilia-driven fluid flow Origins of cystic fibrosis lung disease Computed Tomography and Magnetic Resonance Imaging for Longitudinal Characterization of Lung Structure Changes in a Yucatan Miniature Pig Silicosis Model CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium Integrative analysis of differentially expressed microRNAs of pulmonary alveolar macrophages from piglets during H1N1 swine influenza A virus infection Swine influenza H1N1 virus induces acute inflammatory immune responses in pig lungs: a potential animal model for human H1N1 influenza virus.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 Progress and prospects: techniques for site-directed mutagenesis in animal models.Tissue and cellular expression patterns of porcine CFTR: similarities to and differences from human CFTR Airway mucus function and dysfunction.Cellular distribution and function of ion channels involved in transport processes in rat tracheal epithelium.Gel-forming mucins form distinct morphologic structures in airways Porcine nasal epithelial cultures for studies of cystic fibrosis sinusitis Ion channels, phosphorylation and mammalian sperm capacitation.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.Calcium channels in the development, maturation, and function of spermatozoa.Development of an ex vivo porcine lung model for studying growth, virulence, and signaling of Pseudomonas aeruginosa.Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs.Epithelial cells derived from swine bone marrow express stem cell markers and support influenza virus replication in vitro Pseudomonas aeruginosa triggers CFTR-mediated airway surface liquid secretion in swine trachea.Completion of the swine genome will simplify the production of swine as a large animal biomedical model.Biodegradable nanoparticle-entrapped vaccine induces cross-protective immune response against a virulent heterologous respiratory viral infection in pigs Novel small molecule epithelial sodium channel inhibitors as potential therapeutics in cystic fibrosis - a patent evaluation.Efficient intratracheal delivery of airway epithelial cells in mice and pigs New imaging approaches for understanding lung cancer response to treatment.Ferret and pig models of cystic fibrosis: prospects and promise for gene therapy.Hybrid nonviral/viral vector systems for improved piggyBac DNA transposon in vivo delivery Enhancement of respiratory mucosal antiviral defenses by the oxidation of iodide Swine as a model for influenza A virus infection and immunity.Endogenous surface expression of ΔF508-CFTR mediates cAMP-stimulated Cl(-) current in CFTR(ΔF508/ΔF508) pig thyroid epithelial cells Functional invariant NKT cells in pig lungs regulate the airway hyperreactivity: a potential animal model The obesity epidemic: from the environment to epigenetics - not simply a response to dietary manipulation in a thermoneutral environment The porcine chloride channel calcium-activated family member pCLCA4a mirrors lung expression of the human hCLCA4.Production of transgenic cloned pigs expressing the far-red fluorescent protein monomeric Plum.Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets Advances in cell and gene-based therapies for cystic fibrosis lung disease Transparent antifouling material for improved operative field visibility in endoscopy.

P2860

Q26801165-103BE93A-0799-4699-BD6D-581157B9AB9B Q26826635-A1364EF6-A9E5-47A7-BEDA-AFF5F60CBD49 Q28080451-9539B83A-C2AC-4B1D-B346-DE849E448339 Q28390430-71941786-9643-403C-8DA9-CE93D0D9B468 Q28941756-5217F41B-96AB-4007-8CC8-52634303A4F2 Q30371291-C6D69B33-7514-4409-BE8A-4CB8499304D6 Q30392760-13D64CBF-06B1-4358-B962-3179816E01FC Q30487263-A9005FB3-B133-4C9D-AC14-D45EB9C7E003 Q30572016-6856312C-9833-45FE-B7A4-FCA4B37A8E58 Q33559271-8762F7E0-D7B5-4D32-9AD1-FAAF076AC7B5 Q33586056-1849FBC5-29F9-4DC5-BFA6-E115C676F7A2 Q33723578-852E4455-F76F-4844-A016-E6F511199F4A Q33856635-8C6EDD97-3404-4F4D-A795-B62CB8CDF501 Q33865632-E20CF946-7AE5-4C34-AB64-7C3D12E33966 Q33870016-3E1150B3-847A-42EE-91B8-7DB10A9A276E Q33888953-DBB2F27A-21E6-4940-B5A2-1903FFB78A4F Q33994621-67CCCA54-0A8E-455F-80E0-652031F07112 Q34025925-E2D3E52B-1762-4EA7-8E60-12FF6D909A71 Q34052215-CFA4F8DB-FB9D-427A-8096-A54579574ADE Q34059034-18DB11AC-2E4E-4EFF-AB54-21080954FC81 Q34090231-26125C4C-961F-4E79-8481-47692891C584 Q34117733-D15E1268-79E4-483A-A448-951CD5D070FF Q34144306-50575AC5-F691-4565-85A4-3964F9A5916A Q34476881-0297239B-ABF8-4361-B9FA-3F145BDF63CA Q34512592-D935E27A-CF75-413E-8F39-767435B44E18 Q34955473-B10A37E9-ED7F-42C3-BFA2-8C61A0C64664 Q35115851-9A106946-7C7F-4075-B193-DB9D4BC081D9 Q35200105-C67B138F-2A3E-4258-BE83-7567CD99091F Q35200182-A775EA24-EEE6-4EA6-A418-70CD280BAD73 Q35399152-D5EACB4B-D45C-4313-9F5E-0DF0B3732BBF Q35528052-059899B8-BC16-435F-9032-321A5748AEEB Q35635820-A7E1542D-5010-49D7-B71E-1EA02535F471 Q35659018-4F45B08B-3169-455B-BD01-8183F21AAA0D Q35670019-3DA0C384-B279-4673-BEA5-BB08E230D1F2 Q35711118-34C4861C-E082-4AB5-B032-F84ED9F8FCC7 Q35768133-AE6CE3D4-D0DB-43AB-A99F-D927F772183A Q35838047-23AF205B-8144-4D9A-B81D-015A451FBC1A Q35850895-56DE70AA-958D-4FE3-A029-57C111496B07 Q36014033-26FD29EE-BC37-4E3A-8A30-861E13947343 Q36149499-FE45B24E-81A1-415B-B09F-63AB222A83A4

P2860

The porcine lung as a potential model for cystic fibrosis

http://www.wikidata.org/entity/Q36846439

description

2008 nî lūn-bûn

@nan

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

2008年论文

@zh

2008年论文

@zh-cn

name

The porcine lung as a potential model for cystic fibrosis

@en

type

label

The porcine lung as a potential model for cystic fibrosis

@en

prefLabel

The porcine lung as a potential model for cystic fibrosis

@en

P1433

Q36846439-20C5A308-E0A4-4DCE-A162-5148F050B6B7

P1476

Q36846439-2C54D1A5-AECE-4EC3-8903-EE87A539C1B1

P2093

Q36846439-06A7033C-B528-4B61-A67A-CA4828FC9307

Q36846439-32DBFF3B-7799-496A-A82E-572323287E7B

Q36846439-4EC97B38-F712-4CF6-8096-C9216DE220BF

Q36846439-749942CC-177A-4C68-8EFD-AD9138AE405E

Q36846439-A2D59744-CCAC-40DA-9022-5B0B13DB52F2

Q36846439-A72462BC-893C-4FC5-B6DF-00737606F621

Q36846439-CE3CBA89-AE4E-4E47-B536-C48689C766C3

Q36846439-E0FA424A-C711-4C61-895E-1C521B762797

P2860

Q36846439-00909E80-0ACA-4CA9-993D-8D9E98017C62

Q36846439-01C9F265-986C-4005-BA4A-3B6F17DB8BDA

Q36846439-020FDAFE-C265-417E-956D-7C92DF986518

Q36846439-0357C225-0101-456D-8BAF-F3AC04F77552

Q36846439-037FC423-163B-4D32-8B08-C2C86EBD4FB8

Q36846439-03C78C3C-7C62-4122-807A-DE98BBBB97B3

Q36846439-04EA0388-D1CC-40FF-B3DE-603666635BE6

Q36846439-0525DC3D-3D1C-4D38-9AFF-8B8C71C6EC3F

Q36846439-054E7633-95B1-4682-81FC-AD6CE4181C97

Q36846439-05EF7554-63C1-4C6B-80A4-FF16C2D18DAF

P304

Q36846439-EA2689E5-4347-4FAA-BC88-F2DEE364B6CD

P31

Q36846439-924194CD-1616-4374-A34F-98E388622495

P356

Q36846439-E3C5BA18-4D98-482C-8337-32561390AEFA

P433

Q36846439-EADADAFF-A491-4B4F-90A8-B5C67D0242D1

P478

Q36846439-1E512F5A-FE6A-43CC-B868-BA79670F2743

P50

Q36846439-37705957-1046-4CB6-8A4F-F314E00576BB

Q36846439-38F71E3B-F21D-40D6-87D2-EFAF7785256D

Q36846439-459A25D7-ADB1-4697-8A6C-B659D28D8D84

Q36846439-74E80C30-A963-4863-B691-B9D15F2C231B

Q36846439-B1F6C070-F975-4127-BA66-8D31C2AE2018

Q36846439-B77F07AA-924B-495D-9D3C-320E91564013

Q36846439-F97AE232-9E19-4B28-B234-317F84F06B27

P577

Q36846439-6F2B2F53-48C7-494F-A9E2-0E3F2FD2A274

P5875

Q36846439-336F52DE-28AE-418E-A697-736843F5ABED

P698

Q36846439-C08A94FB-AA8C-4CA9-85F7-2C771C37798E

P921

Q36846439-7A3E1602-2B14-46EC-9E67-8F53C7B6945F

P932

Q36846439-F7265534-DF13-46D9-BD05-3D3F642D2354

P356

AJPLUNG.90203.2008

P1433

American Journal of Physiology - Lung Cellular and Molecular Physiology

P1476

The porcine lung as a potential model for cystic fibrosis

@en

P2093

Christopher S Rogers

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

Eman Namati

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

Geoffrey McLennan

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

John T Fisher

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

Juan R Sabater

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

Kim A Brogden

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

Michael J Welsh

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

William M Abraham

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

P2860

Purification of a novel flavoprotein involved in the thyroid NADPH oxidase. Cloning of the porcine and human cdnas

Cystic Fibrosis: Lessons from the Sweat Gland

Lactoperoxidase and human airway host defense

Human beta-defensin 2 is a salt-sensitive peptide antibiotic expressed in human lung

A novel host defense system of airways is defective in cystic fibrosis

Cloned ferrets produced by somatic cell nuclear transfer

The peptide antibiotic LL-37/hCAP-18 is expressed in epithelia of the human lung where it has broad antimicrobial activity at the airway surface

The lactoperoxidase system links anion transport to host defense in cystic fibrosis

Progress toward generating a ferret model of cystic fibrosis by somatic cell nuclear transfer

Predominant constitutive CFTR conductance in small airways

P304

L240-63

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

P31

scholarly article

P356

10.1152/AJPLUNG.90203.2008

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

P433

2

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

P478

295

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

P50

David Meyerholz

Randall S. Prather

John F Engelhardt

Lynda S Ostedgaard

P577

2008-05-16T00:00:00Z

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

P5875

5363857

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

P698

18487356

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

P921

cystic fibrosis

P932

2519845

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