Lista de obras - Cristian A Carvajal - Dominio Público Uruguay

11beta-hydroxysteroid dehydrogenase type 1 is overexpressed in subcutaneous adipose tissue of morbidly obese patients.

artículo científico publicado en 2008

11β-Hydroxysteroid dehydrogenase type-2 and type-1 (11β-HSD2 and 11β-HSD1) and 5β-reductase activities in the pathogenia of essential hypertension.

artículo científico publicado en 2009

11β-hydroxysteroid dehydrogenase type 2 polymorphisms and activity in a Chilean essential hypertensive and normotensive cohort.

artículo científico publicado en 2012

A de novo unequal cross-over mutation between CYP11B1 and CYP11B2 genes causes familial hyperaldosteronism type I

artículo científico publicado en 2010

A new presentation of the chimeric CYP11B1/CYP11B2 gene with low prevalence of primary aldosteronism and atypical gene segregation pattern

artículo científico publicado en 2011

A novel adrenocorticotropin receptor mutation alters its structure and function, causing familial glucocorticoid deficiency.

artículo científico publicado en 2008

A polymorphic GT short tandem repeat affecting beta-ENaC mRNA expression is associated with low renin essential hypertension

artículo científico publicado en 2007

A possible association between primary aldosteronism and a lower beta-cell function

artículo científico publicado en 2007

Age-related changes in 11β-hydroxysteroid dehydrogenase type 2 activity in normotensive subjects.

artículo científico publicado en 2013

Aldosterone Production and Signaling Dysregulation in Obesity.

artículo científico publicado en 2016

Aldosterone promotes autoimmune damage by enhancing Th17-mediated immunity.

artículo científico publicado en 2009

Birth weight is inversely associated with blood pressure and serum aldosterone and cortisol levels in children.

artículo científico publicado en 2012

Citosine-Adenine-Repeat Microsatellite of 11β-hydroxysteroid dehydrogenase 2 Gene in Hypertensive Children.

artículo científico publicado en 2015

Clinical, Biochemical, and Genetic Characteristics of "Nonclassic" Apparent Mineralocorticoid Excess Syndrome

artículo científico publicado en 2019

Congenital lipoid adrenal hyperplasia caused by a novel splicing mutation in the gene for the steroidogenic acute regulatory protein.

artículo científico publicado en 2004

Cortisol/cortisone ratio and matrix metalloproteinase-9 activity are associated with pediatric primary hypertension.

artículo científico publicado en 2016

Detection of a novel severe mutation affecting the CYP21A2 gene in a Chilean male with salt wasting congenital adrenal hyperplasia

artículo científico publicado en 2019

Downregulation of exosomal miR-192-5p and miR-204-5p in subjects with nonclassic apparent mineralocorticoid excess

scientific article published on 27 November 2019

Endothelial cell oxidative stress and signal transduction

artículo científico publicado en 2000

Epigenetics and arterial hypertension: the challenge of emerging evidence.

artículo científico

Frequency of familial hyperaldosteronism type 1 in a hypertensive pediatric population: clinical and biochemical presentation.

artículo científico publicado en 2011

High sodium intake is associated with increased glucocorticoid production, insulin resistance and metabolic syndrome.

artículo científico publicado en 2013

Hypertensive Patients That Respond to Aldosterone Antagonists May Have a Nonclassical 11β-HSD2 Deficiency

artículo científico publicado en 2017

Identification of novel 11β-HSD1 inhibitors by combined ligand- and structure-based virtual screening.

artículo científico publicado en 2014

Increased levels of oxidative stress, subclinical inflammation, and myocardial fibrosis markers in primary aldosteronism patients

artículo científico publicado en 2010

Increased urinary glucocorticoid metabolites are associated with metabolic syndrome, hypoadiponectinemia, insulin resistance and β cell dysfunction

scientific article published on 05 October 2011

LC-MS/MS Method for the Simultaneous Determination of Free Urinary Steroids

artículo científico

Metabolic syndrome and its components are strongly associated with an inflammatory state and insulin resistance in the pediatric population.

artículo científico publicado en 2015

Microribonucleic acid-21 increases aldosterone secretion and proliferation in H295R human adrenocortical cells.

artículo científico publicado en 2008

New splicing mutation of MEN1 gene affecting the translocation of menin to the nucleus.

artículo científico publicado en 2006

Overexpression of 11β-hydroxysteroid dehydrogenase type 1 in visceral adipose tissue and portal hypercortisolism in non-alcoholic fatty liver disease

scientific article published on 04 December 2011

Overexpression of hepatic 5α-reductase and 11β-hydroxysteroid dehydrogenase type 1 in visceral adipose tissue is associated with hyperinsulinemia in morbidly obese patients

artículo científico publicado en 2011

Oxidative stress biomarkers in pediatric sepsis: a prospective observational pilot study.

artículo científico publicado en 2016

Polymorphisms in the RAC1 gene are associated with hypertension risk factors in a Chilean pediatric population.

artículo científico publicado en 2014

Positive association between aldosterone-renin ratio and carotid intima-media thickness in hypertensive children.

artículo científico publicado en 2013

Pregnancy normalized familial hyperaldosteronism type I: a novel role for progesterone?

scientific article published on 19 June 2014

Primary aldosteronism and its impact on the generation of arterial hypertension, endothelial injury and oxidative stress.

scientific article published on April 2010

Primary aldosteronism can alter peripheral levels of transforming growth factor beta and tumor necrosis factor alpha.

artículo científico publicado en 2009

Refractory depression in a patient with peripheral resistance to thyroid hormone (RTH) and the effect of triiodothyronine treatment.

artículo científico publicado en 2007

Serum Cortisol and Cortisone as Potential Biomarkers of Partial 11β-Hydroxysteroid Dehydrogenase Type 2 Deficiency

artículo científico publicado en 2018

Sodium Intake Is associated With Endothelial Damage Biomarkers and Metabolic Dysregulation

artículo científico publicado en 2018

The Aldosterone/Renin Ratio Predicts Cardiometabolic Disorders in Subjects Without Classic Primary Aldosteronism

scientific article published on 01 April 2019

The Expression of RAC1 and Mineralocorticoid Pathway-Dependent Genes are Associated With Different Responses to Salt Intake

artículo científico publicado en 2014

Two homozygous mutations in the 11 beta-hydroxysteroid dehydrogenase type 2 gene in a case of apparent mineralocorticoid excess.

artículo científico publicado en 2003

Urinary Exosomes and Their Cargo: Potential Biomarkers for Mineralocorticoid Arterial Hypertension?

artículo científico publicado en 2017

Usefulness and Pitfalls in Sodium Intake Estimation: Comparison of Dietary Assessment and Urinary Excretion in Chilean Children and Adults.

artículo científico publicado en 2016

[Hepatic steatosis as diabetes type 2 predictor]

artículo científico publicado en 2014

Lista de obras de Cristian A Carvajal

11beta-hydroxysteroid dehydrogenase type 1 is overexpressed in subcutaneous adipose tissue of morbidly obese patients.

11β-Hydroxysteroid dehydrogenase type-2 and type-1 (11β-HSD2 and 11β-HSD1) and 5β-reductase activities in the pathogenia of essential hypertension.

11β-hydroxysteroid dehydrogenase type 2 polymorphisms and activity in a Chilean essential hypertensive and normotensive cohort.

A de novo unequal cross-over mutation between CYP11B1 and CYP11B2 genes causes familial hyperaldosteronism type I

A new presentation of the chimeric CYP11B1/CYP11B2 gene with low prevalence of primary aldosteronism and atypical gene segregation pattern

A novel adrenocorticotropin receptor mutation alters its structure and function, causing familial glucocorticoid deficiency.

A polymorphic GT short tandem repeat affecting beta-ENaC mRNA expression is associated with low renin essential hypertension

A possible association between primary aldosteronism and a lower beta-cell function

Age-related changes in 11β-hydroxysteroid dehydrogenase type 2 activity in normotensive subjects.

Aldosterone Production and Signaling Dysregulation in Obesity.

Aldosterone promotes autoimmune damage by enhancing Th17-mediated immunity.

Birth weight is inversely associated with blood pressure and serum aldosterone and cortisol levels in children.

Citosine-Adenine-Repeat Microsatellite of 11β-hydroxysteroid dehydrogenase 2 Gene in Hypertensive Children.

Clinical, Biochemical, and Genetic Characteristics of "Nonclassic" Apparent Mineralocorticoid Excess Syndrome

Congenital lipoid adrenal hyperplasia caused by a novel splicing mutation in the gene for the steroidogenic acute regulatory protein.

Cortisol/cortisone ratio and matrix metalloproteinase-9 activity are associated with pediatric primary hypertension.

Detection of a novel severe mutation affecting the CYP21A2 gene in a Chilean male with salt wasting congenital adrenal hyperplasia

Downregulation of exosomal miR-192-5p and miR-204-5p in subjects with nonclassic apparent mineralocorticoid excess

Endothelial cell oxidative stress and signal transduction

Epigenetics and arterial hypertension: the challenge of emerging evidence.

Frequency of familial hyperaldosteronism type 1 in a hypertensive pediatric population: clinical and biochemical presentation.

High sodium intake is associated with increased glucocorticoid production, insulin resistance and metabolic syndrome.

Hypertensive Patients That Respond to Aldosterone Antagonists May Have a Nonclassical 11β-HSD2 Deficiency

Identification of novel 11β-HSD1 inhibitors by combined ligand- and structure-based virtual screening.

Increased levels of oxidative stress, subclinical inflammation, and myocardial fibrosis markers in primary aldosteronism patients

Increased urinary glucocorticoid metabolites are associated with metabolic syndrome, hypoadiponectinemia, insulin resistance and β cell dysfunction

LC-MS/MS Method for the Simultaneous Determination of Free Urinary Steroids

Metabolic syndrome and its components are strongly associated with an inflammatory state and insulin resistance in the pediatric population.

Microribonucleic acid-21 increases aldosterone secretion and proliferation in H295R human adrenocortical cells.

New splicing mutation of MEN1 gene affecting the translocation of menin to the nucleus.

Overexpression of 11β-hydroxysteroid dehydrogenase type 1 in visceral adipose tissue and portal hypercortisolism in non-alcoholic fatty liver disease

Overexpression of hepatic 5α-reductase and 11β-hydroxysteroid dehydrogenase type 1 in visceral adipose tissue is associated with hyperinsulinemia in morbidly obese patients

Oxidative stress biomarkers in pediatric sepsis: a prospective observational pilot study.

Polymorphisms in the RAC1 gene are associated with hypertension risk factors in a Chilean pediatric population.

Positive association between aldosterone-renin ratio and carotid intima-media thickness in hypertensive children.

Pregnancy normalized familial hyperaldosteronism type I: a novel role for progesterone?

Primary aldosteronism and its impact on the generation of arterial hypertension, endothelial injury and oxidative stress.

Primary aldosteronism can alter peripheral levels of transforming growth factor beta and tumor necrosis factor alpha.

Refractory depression in a patient with peripheral resistance to thyroid hormone (RTH) and the effect of triiodothyronine treatment.

Serum Cortisol and Cortisone as Potential Biomarkers of Partial 11β-Hydroxysteroid Dehydrogenase Type 2 Deficiency

Sodium Intake Is associated With Endothelial Damage Biomarkers and Metabolic Dysregulation

The Aldosterone/Renin Ratio Predicts Cardiometabolic Disorders in Subjects Without Classic Primary Aldosteronism

The Expression of RAC1 and Mineralocorticoid Pathway-Dependent Genes are Associated With Different Responses to Salt Intake

Two homozygous mutations in the 11 beta-hydroxysteroid dehydrogenase type 2 gene in a case of apparent mineralocorticoid excess.

Urinary Exosomes and Their Cargo: Potential Biomarkers for Mineralocorticoid Arterial Hypertension?

Usefulness and Pitfalls in Sodium Intake Estimation: Comparison of Dietary Assessment and Urinary Excretion in Chilean Children and Adults.

[Hepatic steatosis as diabetes type 2 predictor]