Lista de obras - Ronald C. Rubenstein - Dominio Público Uruguay

A simplified cyclic adenosine monophosphate-mediated sweat rate test for quantitative measure of cystic fibrosis transmembrane regulator (CFTR) function

artículo científico publicado en 2000

Abnormal regulatory interactions of I148T-CFTR and the epithelial Na+ channel in Xenopus oocytes

artículo científico publicado en 2006

Carrier screening, incidence of cystic fibrosis, and difficult decisions

artículo científico publicado en 2009

Cystic fibrosis as a risk factor for recurrent venous thrombosis at a pediatric tertiary care hospital

artículo científico publicado en 2006

Cystic fibrosis transmembrane conductance regulator contributes to reacidification of alkalinized lysosomes in RPE cells ⬇️

artículo científico publicado el 9 de mayo de 2012

Cystic fibrosis transmembrane conductance regulator differentially regulates human and mouse epithelial sodium channels in Xenopus oocytes

artículo científico publicado en 2004

Differential effects of Hsc70 and Hsp70 on the intracellular trafficking and functional expression of epithelial sodium channels

artículo científico publicado en 2006

Differential modulation of a polymorphism in the COOH terminus of the alpha-subunit of the human epithelial sodium channel by protein kinase Cdelta

artículo científico publicado en 2005

ERp29 Regulates ΔF508 and Wild-type Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Trafficking to the Plasma Membrane in Cystic Fibrosis (CF) and Non-CF Epithelial Cells ⬇️

artículo científico publicado el 27 de abril de 2011

ERp29 as a regulator of Insulin biosynthesis

scientific article published on 20 May 2020

ERp29 regulates epithelial sodium channel functional expression by promoting channel cleavage.

artículo científico publicado en 2014

Editorial Focus: CFTR-dependent bicarbonate secretion by Calu-3 cells

artículo científico publicado en 2018

Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation

artículo científico publicado en 2010

Elevation of 1-Hour Plasma Glucose During Oral Glucose Tolerance Testing Is Associated With Worse Pulmonary Function in Cystic Fibrosis ⬇️

artículo científico publicado el 12 de enero de 2011

Elevation of one hour plasma glucose during oral glucose tolerance testing.

artículo científico publicado en 2015

Evidence of CFTR function in cystic fibrosis after systemic administration of 4-phenylbutyrate

artículo científico publicado en 2002

Functional polymorphism in the carboxyl terminus of the alpha-subunit of the human epithelial sodium channel

artículo científico publicado en 2004

Future directions in early cystic fibrosis lung disease research: an NHLBI workshop report

artículo científico publicado en 2012

Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis

artículo científico publicado en 2020

Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytes

artículo científico publicado en 2002

Genistein restores functional interactions between Delta F508-CFTR and ENaC in Xenopus oocytes

artículo científico publicado en 2001

High prevalence of aquagenic wrinkling of the palms in patients with cystic fibrosis and association with measurable increases in transepidermal water loss.

artículo científico publicado en 2012

Hsc70 negatively regulates epithelial sodium channel trafficking at multiple sites in epithelial cells ⬇️

artículo científico publicado el 24 de julio de 2013

Hsp70 promotes epithelial sodium channel functional expression by increasing its association with coat complex II and its exit from endoplasmic reticulum.

artículo científico publicado en 2012

IL-17A induces Pendrin expression and chloride-bicarbonate exchange in human bronchial epithelial cells

artículo científico publicado en 2014

Intracellular trafficking of a polymorphism in the COOH terminus of the alpha-subunit of the human epithelial sodium channel is modulated by casein kinase 1.

artículo científico publicado en 2007

Long-term treatment with oral N-acetylcysteine: affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial

artículo científico publicado en 2014

Molecular Chaperones as Targets to Circumvent the CFTR Defect in Cystic Fibrosis

artículo científico publicado en 2012

Multiple residues in the distal C terminus of the α-subunit have roles in modulating human epithelial sodium channel activity.

artículo científico publicado en 2012

Nocturnal saturation and glucose tolerance in children with cystic fibrosis.

artículo científico publicado en 2011

Patient and parent perceptions of the diagnosis and management of cystic fibrosis-related diabetes.

artículo científico publicado en 2014

Regulation of endogenous ENaC functional expression by CFTR and ΔF508-CFTR in airway epithelial cells.

artículo científico publicado en 2010

Regulatory interactions of N1303K-CFTR and ENaC in Xenopus oocytes: evidence that chloride transport is not necessary for inhibition of ENaC.

artículo científico publicado en 2006

Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation.

artículo científico publicado en 2011

Risk Factors for Death of Patients with Cystic Fibrosis Awaiting Lung Transplantation

artículo científico publicado en 2006

Seeing is believing: imaging early lung disease in cystic fibrosis

artículo científico publicado en 2014

The KDEL receptor has a role in the biogenesis and trafficking of the epithelial sodium channel (ENaC)

scientific article published on 25 October 2019

Use of protein repair therapy in the treatment of cystic fibrosis ⬇️

artículo científico publicado el 1 de junio de 1998

Lista de obras de Ronald C. Rubenstein

A simplified cyclic adenosine monophosphate-mediated sweat rate test for quantitative measure of cystic fibrosis transmembrane regulator (CFTR) function

Abnormal regulatory interactions of I148T-CFTR and the epithelial Na+ channel in Xenopus oocytes

Carrier screening, incidence of cystic fibrosis, and difficult decisions

Cystic fibrosis as a risk factor for recurrent venous thrombosis at a pediatric tertiary care hospital

Cystic fibrosis transmembrane conductance regulator contributes to reacidification of alkalinized lysosomes in RPE cells ⬇️

Cystic fibrosis transmembrane conductance regulator differentially regulates human and mouse epithelial sodium channels in Xenopus oocytes

Differential effects of Hsc70 and Hsp70 on the intracellular trafficking and functional expression of epithelial sodium channels

Differential modulation of a polymorphism in the COOH terminus of the alpha-subunit of the human epithelial sodium channel by protein kinase Cdelta

ERp29 Regulates ΔF508 and Wild-type Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Trafficking to the Plasma Membrane in Cystic Fibrosis (CF) and Non-CF Epithelial Cells ⬇️

ERp29 as a regulator of Insulin biosynthesis

ERp29 regulates epithelial sodium channel functional expression by promoting channel cleavage.

Editorial Focus: CFTR-dependent bicarbonate secretion by Calu-3 cells

Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation

Elevation of 1-Hour Plasma Glucose During Oral Glucose Tolerance Testing Is Associated With Worse Pulmonary Function in Cystic Fibrosis ⬇️

Elevation of one hour plasma glucose during oral glucose tolerance testing.

Evidence of CFTR function in cystic fibrosis after systemic administration of 4-phenylbutyrate

Functional polymorphism in the carboxyl terminus of the alpha-subunit of the human epithelial sodium channel

Future directions in early cystic fibrosis lung disease research: an NHLBI workshop report

Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis

Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytes

Genistein restores functional interactions between Delta F508-CFTR and ENaC in Xenopus oocytes

High prevalence of aquagenic wrinkling of the palms in patients with cystic fibrosis and association with measurable increases in transepidermal water loss.

Hsc70 negatively regulates epithelial sodium channel trafficking at multiple sites in epithelial cells ⬇️

Hsp70 promotes epithelial sodium channel functional expression by increasing its association with coat complex II and its exit from endoplasmic reticulum.

IL-17A induces Pendrin expression and chloride-bicarbonate exchange in human bronchial epithelial cells

Intracellular trafficking of a polymorphism in the COOH terminus of the alpha-subunit of the human epithelial sodium channel is modulated by casein kinase 1.

Long-term treatment with oral N-acetylcysteine: affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial

Molecular Chaperones as Targets to Circumvent the CFTR Defect in Cystic Fibrosis

Multiple residues in the distal C terminus of the α-subunit have roles in modulating human epithelial sodium channel activity.

Nocturnal saturation and glucose tolerance in children with cystic fibrosis.

Patient and parent perceptions of the diagnosis and management of cystic fibrosis-related diabetes.

Regulation of endogenous ENaC functional expression by CFTR and ΔF508-CFTR in airway epithelial cells.

Regulatory interactions of N1303K-CFTR and ENaC in Xenopus oocytes: evidence that chloride transport is not necessary for inhibition of ENaC.

Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation.

Risk Factors for Death of Patients with Cystic Fibrosis Awaiting Lung Transplantation

Seeing is believing: imaging early lung disease in cystic fibrosis

The KDEL receptor has a role in the biogenesis and trafficking of the epithelial sodium channel (ENaC)

Use of protein repair therapy in the treatment of cystic fibrosis ⬇️