Lista de obras - Lynda S Ostedgaard - Dominio Público Uruguay

A 45-kDa protein antigenically related to band 3 is selectively expressed in kidney mitochondria ⬇️

artículo científico publicado el 1 de febrero de 1991

A C-terminal motif found in the β 2 -adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na + /H + exchanger regulatory factor family of PDZ proteins ⬇️

artículo científico publicado el 21 de julio de 1998

A microRNA network regulates expression and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulator

artículo científico publicado en 2012

A shortened adeno-associated virus expression cassette for CFTR gene transfer to cystic fibrosis airway epithelia.

artículo científico publicado en 2005

Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia ⬇️

artículo científico publicado el 1 de agosto de 1992

Acidic pH increases airway surface liquid viscosity in cystic fibrosis

artículo científico publicado en 2016

Airway acidification initiates host defense abnormalities in cystic fibrosis mice.

artículo científico publicado en 2016

Alteration of protein function by a silent polymorphism linked to tRNA abundance

artículo científico publicado en 2017

Association of domains within the cystic fibrosis transmembrane conductance regulator

artículo científico publicado en 1997

Bovine AAV transcytosis inhibition by tannic acid results in functional expression of CFTR in vitro and altered biodistribution in vivo.

artículo científico publicado en 2011

Curcumin stimulates cystic fibrosis transmembrane conductance regulator Cl- channel activity.

artículo científico publicado en 2004

Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility

artículo científico publicado en 2015

Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth

artículo científico publicado en 2010

Cystic fibrosis problem probed by proteolysis

artículo científico publicado en 1998

Cystic fibrosis transmembrane conductance regulator Cl- channels with R domain deletions and translocations show phosphorylation-dependent and -independent activity

artículo científico publicado en 2000

Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice.

artículo científico publicado en 2011

Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation

artículo científico publicado en 1992

Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs

artículo científico publicado en 2008

Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator.

artículo científico publicado en 1996

Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia

artículo científico publicado en 2003

Erythrocyte incorporation of ingested 58-iron by infants

artículo científico publicado en 1988

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

artículo científico publicado en 1990

Gel-forming mucins form distinct morphologic structures in airways

artículo científico publicado en 2017

Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.

artículo científico publicado en 2015

Human–mouse cystic fibrosis transmembrane conductance regulator (CFTR) chimeras identify regions that partially rescue CFTR-ΔF508 processing and alter its gating defect ⬇️

artículo científico publicado el 30 de diciembre de 2011

Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast

artículo científico publicado en 1993

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

artículo científico publicado en 2014

Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs

artículo científico publicado en 2013

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

artículo científico publicado en 1992

Motile cilia of human airway epithelia contain hedgehog signaling components that mediate noncanonical hedgehog signaling

artículo científico publicado en 2018

Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in

artículo científico publicado en 2015

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

artículo científico publicado en 1993

Pancreatic and biliary secretion are both altered in cystic fibrosis pigs.

artículo científico publicado en 2012

Processing and function of CFTR-DeltaF508 are species-dependent

artículo científico publicado en 2007

Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies

artículo científico publicado en 2016

Structural biology. The ABC of a versatile engine.

artículo científico publicado en 1998

The amino-terminal portion of CFTR forms a regulated Cl- channel.

artículo científico publicado en 1994

The porcine lung as a potential model for cystic fibrosis

artículo científico publicado en 2008

The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs

artículo científico publicado en 2011

Understanding how cystic fibrosis mutations cause a loss of Cl- channel function.

artículo científico publicado en 1996

Lista de obras de Lynda S Ostedgaard

A 45-kDa protein antigenically related to band 3 is selectively expressed in kidney mitochondria ⬇️

A C-terminal motif found in the β 2 -adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na + /H + exchanger regulatory factor family of PDZ proteins ⬇️

A microRNA network regulates expression and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulator

A shortened adeno-associated virus expression cassette for CFTR gene transfer to cystic fibrosis airway epithelia.

Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia ⬇️

Acidic pH increases airway surface liquid viscosity in cystic fibrosis

Airway acidification initiates host defense abnormalities in cystic fibrosis mice.

Alteration of protein function by a silent polymorphism linked to tRNA abundance

Association of domains within the cystic fibrosis transmembrane conductance regulator

Bovine AAV transcytosis inhibition by tannic acid results in functional expression of CFTR in vitro and altered biodistribution in vivo.

Curcumin stimulates cystic fibrosis transmembrane conductance regulator Cl- channel activity.

Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility

Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth

Cystic fibrosis problem probed by proteolysis

Cystic fibrosis transmembrane conductance regulator Cl- channels with R domain deletions and translocations show phosphorylation-dependent and -independent activity

Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice.

Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation

Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs

Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator.

Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia

Erythrocyte incorporation of ingested 58-iron by infants

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

Gel-forming mucins form distinct morphologic structures in airways

Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.

Human–mouse cystic fibrosis transmembrane conductance regulator (CFTR) chimeras identify regions that partially rescue CFTR-ΔF508 processing and alter its gating defect ⬇️

Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

Motile cilia of human airway epithelia contain hedgehog signaling components that mediate noncanonical hedgehog signaling

Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

Pancreatic and biliary secretion are both altered in cystic fibrosis pigs.

Processing and function of CFTR-DeltaF508 are species-dependent

Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies

Structural biology. The ABC of a versatile engine.

The amino-terminal portion of CFTR forms a regulated Cl- channel.

The porcine lung as a potential model for cystic fibrosis

The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs

Understanding how cystic fibrosis mutations cause a loss of Cl- channel function.