Genotype-specific alterations in vascular smooth muscle cell function in cystic fibrosis piglets. - Wikidata - wikimedia - TriplyDB

Genotype-specific alterations in vascular smooth muscle cell function in cystic fibrosis piglets.

Genotype-specific alterations in vascular smooth muscle cell function in cystic fibrosis piglets.

http://www.wikidata.org/entity/Q37678474

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Reduced blood pressure of CFTR-F508del carriers correlates with diminished arterial reactivity rather than circulating blood volume in mice CFTR and sphingolipids mediate hypoxic pulmonary vasoconstriction Cellular chloride and bicarbonate retention alters intracellular pH regulation in Cftr KO crypt epithelium.Lessons learned from the cystic fibrosis pig.Regulation of vascular tone and arterial blood pressure: role of chloride transport in vascular smooth muscle.Genome editing revolutionize the creation of genetically modified pigs for modeling human diseases.Negative News: Cl- and HCO3- in the Vascular Wall.Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study.

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Genotype-specific alterations in vascular smooth muscle cell function in cystic fibrosis piglets.

http://www.wikidata.org/entity/Q37678474

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 31 October 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Genotype-specific alterations ...... on in cystic fibrosis piglets.

@en

Genotype-specific alterations ...... on in cystic fibrosis piglets.

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type

label

Genotype-specific alterations ...... on in cystic fibrosis piglets.

@en

Genotype-specific alterations ...... on in cystic fibrosis piglets.

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prefLabel

Genotype-specific alterations ...... on in cystic fibrosis piglets.

@en

Genotype-specific alterations ...... on in cystic fibrosis piglets.

@nl

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J.JCF.2013.10.009

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Journal of Cystic Fibrosis

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Genotype-specific alterations ...... on in cystic fibrosis piglets.

@en

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Jinny J Guo

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Kenneth A Volk

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Robert D Roghair

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Vivian Zhu

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P2860

A new generation of Ca2+ indicators with greatly improved fluorescence properties

Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening

Expression and function of cystic fibrosis transmembrane conductance regulator in rat intrapulmonary arteries

Lack of CFTR in skeletal muscle predisposes to muscle wasting and diaphragm muscle pump failure in cystic fibrosis mice

Pigs and humans with cystic fibrosis have reduced insulin-like growth factor 1 (IGF1) levels at birth.

Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children.

High-sweat Na+ in cystic fibrosis and healthy individuals does not diminish thirst during exercise in the heat.

Enhanced Ca2+ entry due to Orai1 plasma membrane insertion increases IL-8 secretion by cystic fibrosis airways

Impact of maternal dexamethasone on coronary PGE(2) production and prostaglandin-dependent coronary reactivity.

Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.

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251-259

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scholarly article

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10.1016/J.JCF.2013.10.009

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3

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13

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Jeffrey L Segar

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2013-10-31T00:00:00Z

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24183914

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cystic fibrosis

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3972271

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