Lista de obras - Brian C Mansfield - Dominio Público Uruguay

A glucose-6-phosphate hydrolase, widely expressed outside the liver, can explain age-dependent resolution of hypoglycemia in glycogen storage disease type Ia.

artículo científico publicado en 2003

A method for assessing and maintaining the reproducibility of mass spectrometric analyses of complex samples

artículo científico publicado en 2009

A method for monitoring and controlling reproducibility of intensity data in complex electrospray mass spectra: a thermometer ion-based strategy

artículo científico publicado en 2008

A motif in PSG11s mediates binding to a receptor on the surface of the promonocyte cell line THP-1.

artículo científico publicado en 1995

A potential new role for muscle in blood glucose homeostasis

scientific journal article

An evolutionary approach to optimizing glucose-6-phosphatase-α enzymatic activity for gene therapy of glycogen storage disease type Ia

artículo científico publicado en 2019

Angiotensin mediates renal fibrosis in the nephropathy of glycogen storage disease type Ia

artículo científico publicado en 2007

Brain contains a functional glucose-6-phosphatase complex capable of endogenous glucose production

artículo científico publicado en 2005

Characterization of the PSG11 gene.

artículo científico publicado en 1994

Complete normalization of hepatic G6PC deficiency in murine glycogen storage disease type Ia using gene therapy

artículo científico publicado en 2010

Comprehensive serum profiling for the discovery of epithelial ovarian cancer biomarkers

artículo científico publicado en 2011

Construction of a genomic DNA library of Mycobacterium paratuberculosis

artículo científico publicado en 1987

Development and preliminary evaluation of a multivariate index assay for ovarian cancer

artículo científico publicado en 2009

Downregulation of SIRT1 signaling underlies hepatic autophagy impairment in glycogen storage disease type Ia.

artículo científico publicado en 2017

Downregulation of pathways implicated in liver inflammation and tumorigenesis of glycogen storage disease type Ia mice receiving gene therapy.

artículo científico publicado en 2017

Evolutionary analysis of the multigene pregnancy-specific beta 1-glycoprotein family: separation of historical and nonhistorical signals

scientific article published on 01 February 1996

Expression of CEA-related genes in the first trimester human placenta.

artículo científico publicado en 1989

Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-β deficiency

artículo científico publicado en 2015

G-CSF improves murine G6PC3-deficient neutrophil function by modulating apoptosis and energy homeostasis

artículo científico publicado en 2011

Gene therapy for type I glycogen storage diseases

artículo científico publicado en 2007

Gene therapy prevents hepatic tumor initiation in murine glycogen storage disease type Ia at the tumor-developing stage

scientific article published on 06 March 2019

Glucose-6-phosphatase dependent substrate transport in the glycogen storage disease type-1a mouse

artículo científico publicado en 1996

Glucose-6-phosphatase-β, implicated in a congenital neutropenia syndrome, is essential for macrophage energy homeostasis and functionality.

artículo científico publicado en 2012

Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy ⬇️

artículo científico publicado el 26 de octubre de 2010

Glycogen storage disease type Ia mice with less than 2% of normal hepatic glucose-6-phosphatase-α activity restored are at risk of developing hepatic tumors

artículo científico publicado en 2017

Hepatic glucose-6-phosphatase-α deficiency leads to metabolic reprogramming in glycogen storage disease type Ia.

artículo científico publicado en 2018

Inhibition of emergence, hatching, and protein biosynthesis in embryonic Artemia salina

artículo científico publicado en 1980

Isolation of intact larval haemoglobin from the brine shrimp Artemia salina. Prevention of degradation in vitro by proteases induced during larval development

artículo científico publicado en 1980

Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome

artículo científico publicado en 2010

Liver-directed gene therapy for murine glycogen storage disease type Ib.

artículo científico publicado en 2017

Long-term correction of murine glycogen storage disease type Ia by recombinant adeno-associated virus-1-mediated gene transfer

artículo científico publicado en 2006

Mice expressing reduced levels of hepatic glucose-6-phosphatase-α activity do not develop age-related insulin resistance or obesity

artículo científico publicado en 2015

Minimal hepatic glucose-6-phosphatase-α activity required to sustain survival and prevent hepatocellular adenoma formation in murine glycogen storage disease type Ia.

artículo científico publicado en 2015

Molecular biology and gene therapy for glycogen storage disease type Ib.

artículo científico publicado en 2018

Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type Ib.

artículo científico publicado en 2014

Multianalyte profiling of serum antigens and autoimmune and infectious disease molecules to identify biomarkers dysregulated in epithelial ovarian cancer

artículo científico publicado en 2008

My Retina Tracker™: An On-line International Registry for People Affected with Inherited Orphan Retinal Degenerative Diseases and their Genetic Relatives - A New Resource

artículo científico

Necrotic foci, elevated chemokines and infiltrating neutrophils in the liver of glycogen storage disease type Ia.

artículo científico publicado en 2007

Neutrophil stress and apoptosis underlie myeloid dysfunction in glycogen storage disease type Ib

artículo científico publicado en 2008

Normoglycemia alone is insufficient to prevent long-term complications of hepatocellular adenoma in glycogen storage disease type Ib mice

artículo científico publicado en 2009

Novel technology for rapid species-specific detection of Bacillus spores

artículo científico publicado en 2006

Oxidative stress mediates nephropathy in type Ia glycogen storage disease.

artículo científico publicado en 2010

Pregnancy-specific glycoprotein gene expression in recurrent aborters: a potential correlation to interleukin-10 expression

artículo científico publicado en 1999

Prevention of hepatocellular adenoma and correction of metabolic abnormalities in murine glycogen storage disease type Ia by gene therapy ⬇️

artículo científico publicado el 27 de agosto de 2012

Proceedings of the First International Optogenetic Therapies for Vision Symposium

artículo científico publicado en 2013

SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters

artículo científico publicado en 2011

Sequence of a novel pregnancy-specific beta 1-glycoprotein C-terminal domain

artículo científico publicado en 1994

Sirtuin signaling controls mitochondrial function in glycogen storage disease type Ia

scientific article published on 08 May 2018

Species-specific bacteria identification using differential mobility spectrometry and bioinformatics pattern recognition

artículo científico publicado en 2005

Sustained hepatic and renal glucose-6-phosphatase expression corrects glycogen storage disease type Ia in mice

artículo científico publicado en 2002

TIP, a T-cell factor identified using high-throughput screening increases survival in a graft-versus-host disease model

artículo científico publicado en 2003

The SLC37 family of phosphate-linked sugar phosphate antiporters

artículo científico publicado en 2013

The SLC37 family of sugar-phosphate/phosphate exchangers

artículo científico publicado en 2014

The carboxyl-terminal domain of the human pregnancy-specific glycoprotein specifies intracellular retention and stability.

artículo científico publicado en 1993

The gene for glycogen-storage disease type 1b maps to chromosome 11q23.

artículo científico publicado en 1998

The islet-specific glucose-6-phosphatase-related protein, implicated in diabetes, is a glycoprotein embedded in the endoplasmic reticulum membrane.

artículo científico publicado en 2004

The signature motif in human glucose-6-phosphate transporter is essential for microsomal transport of glucose-6-phosphate

artículo científico publicado en 2003

The upstream enhancer elements of the G6PC promoter are critical for optimal G6PC expression in murine glycogen storage disease type Ia.

artículo científico publicado en 2013

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex

artículo científico publicado en 2002

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase/glucose-6-phosphate transporter complexes

artículo científico publicado en 2014

cDNA sequence of the pregnancy-specific beta 1-glycoprotein-11s (PSG-11s).

artículo científico publicado en 1992

Lista de obras de Brian C Mansfield

A glucose-6-phosphate hydrolase, widely expressed outside the liver, can explain age-dependent resolution of hypoglycemia in glycogen storage disease type Ia.

A method for assessing and maintaining the reproducibility of mass spectrometric analyses of complex samples

A method for monitoring and controlling reproducibility of intensity data in complex electrospray mass spectra: a thermometer ion-based strategy

A motif in PSG11s mediates binding to a receptor on the surface of the promonocyte cell line THP-1.

A potential new role for muscle in blood glucose homeostasis

An evolutionary approach to optimizing glucose-6-phosphatase-α enzymatic activity for gene therapy of glycogen storage disease type Ia

Angiotensin mediates renal fibrosis in the nephropathy of glycogen storage disease type Ia

Brain contains a functional glucose-6-phosphatase complex capable of endogenous glucose production

Characterization of the PSG11 gene.

Complete normalization of hepatic G6PC deficiency in murine glycogen storage disease type Ia using gene therapy

Comprehensive serum profiling for the discovery of epithelial ovarian cancer biomarkers

Construction of a genomic DNA library of Mycobacterium paratuberculosis

Development and preliminary evaluation of a multivariate index assay for ovarian cancer

Downregulation of SIRT1 signaling underlies hepatic autophagy impairment in glycogen storage disease type Ia.

Downregulation of pathways implicated in liver inflammation and tumorigenesis of glycogen storage disease type Ia mice receiving gene therapy.

Evolutionary analysis of the multigene pregnancy-specific beta 1-glycoprotein family: separation of historical and nonhistorical signals

Expression of CEA-related genes in the first trimester human placenta.

Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-β deficiency

G-CSF improves murine G6PC3-deficient neutrophil function by modulating apoptosis and energy homeostasis

Gene therapy for type I glycogen storage diseases

Gene therapy prevents hepatic tumor initiation in murine glycogen storage disease type Ia at the tumor-developing stage

Glucose-6-phosphatase dependent substrate transport in the glycogen storage disease type-1a mouse

Glucose-6-phosphatase-β, implicated in a congenital neutropenia syndrome, is essential for macrophage energy homeostasis and functionality.

Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy ⬇️

Glycogen storage disease type Ia mice with less than 2% of normal hepatic glucose-6-phosphatase-α activity restored are at risk of developing hepatic tumors

Hepatic glucose-6-phosphatase-α deficiency leads to metabolic reprogramming in glycogen storage disease type Ia.

Inhibition of emergence, hatching, and protein biosynthesis in embryonic Artemia salina

Isolation of intact larval haemoglobin from the brine shrimp Artemia salina. Prevention of degradation in vitro by proteases induced during larval development

Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome

Liver-directed gene therapy for murine glycogen storage disease type Ib.

Long-term correction of murine glycogen storage disease type Ia by recombinant adeno-associated virus-1-mediated gene transfer

Mice expressing reduced levels of hepatic glucose-6-phosphatase-α activity do not develop age-related insulin resistance or obesity

Minimal hepatic glucose-6-phosphatase-α activity required to sustain survival and prevent hepatocellular adenoma formation in murine glycogen storage disease type Ia.

Molecular biology and gene therapy for glycogen storage disease type Ib.

Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type Ib.

Multianalyte profiling of serum antigens and autoimmune and infectious disease molecules to identify biomarkers dysregulated in epithelial ovarian cancer

My Retina Tracker™: An On-line International Registry for People Affected with Inherited Orphan Retinal Degenerative Diseases and their Genetic Relatives - A New Resource

Necrotic foci, elevated chemokines and infiltrating neutrophils in the liver of glycogen storage disease type Ia.

Neutrophil stress and apoptosis underlie myeloid dysfunction in glycogen storage disease type Ib

Normoglycemia alone is insufficient to prevent long-term complications of hepatocellular adenoma in glycogen storage disease type Ib mice

Novel technology for rapid species-specific detection of Bacillus spores

Oxidative stress mediates nephropathy in type Ia glycogen storage disease.

Pregnancy-specific glycoprotein gene expression in recurrent aborters: a potential correlation to interleukin-10 expression

Prevention of hepatocellular adenoma and correction of metabolic abnormalities in murine glycogen storage disease type Ia by gene therapy ⬇️

Proceedings of the First International Optogenetic Therapies for Vision Symposium

SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters

Sequence of a novel pregnancy-specific beta 1-glycoprotein C-terminal domain

Sirtuin signaling controls mitochondrial function in glycogen storage disease type Ia

Species-specific bacteria identification using differential mobility spectrometry and bioinformatics pattern recognition

Sustained hepatic and renal glucose-6-phosphatase expression corrects glycogen storage disease type Ia in mice

TIP, a T-cell factor identified using high-throughput screening increases survival in a graft-versus-host disease model

The SLC37 family of phosphate-linked sugar phosphate antiporters

The SLC37 family of sugar-phosphate/phosphate exchangers

The carboxyl-terminal domain of the human pregnancy-specific glycoprotein specifies intracellular retention and stability.

The gene for glycogen-storage disease type 1b maps to chromosome 11q23.

The islet-specific glucose-6-phosphatase-related protein, implicated in diabetes, is a glycoprotein embedded in the endoplasmic reticulum membrane.

The signature motif in human glucose-6-phosphate transporter is essential for microsomal transport of glucose-6-phosphate

The upstream enhancer elements of the G6PC promoter are critical for optimal G6PC expression in murine glycogen storage disease type Ia.

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase/glucose-6-phosphate transporter complexes

cDNA sequence of the pregnancy-specific beta 1-glycoprotein-11s (PSG-11s).