Lista de obras - Cesar Martin - Dominio Público Uruguay

<i>BIRC6</i> Is Associated with Vulnerability of Carotid Atherosclerotic Plaque

artículo científico publicado en 2020

Activity-associated effect of LDL receptor missense variants located in the cysteine-rich repeats.

artículo científico publicado en 2014

Adenylate Cyclase Toxin promotes bacterial internalisation into non phagocytic cells.

artículo científico publicado en 2015

Adenylate cyclase toxin promotes internalisation of integrins and raft components and decreases macrophage adhesion capacity

artículo científico publicado en 2011

Advantages and versatility of fluorescence-based methodology to characterize the functionality of LDLR and class mutation assignment

artículo científico publicado en 2014

An atlas of O-linked glycosylation on peptide hormones reveals diverse biological roles

artículo científico publicado en 2020

Bordetella adenylate cyclase toxin promotes calcium entry into both CD11b+ and CD11b- cells through cAMP-dependent L-type-like calcium channels.

artículo científico publicado en 2009

Ca2+ influx and tyrosine kinases trigger Bordetella adenylate cyclase toxin (ACT) endocytosis. Cell physiology and expression of the CD11b/CD18 integrin major determinants of the entry route

artículo científico publicado en 2013

Calpain-Mediated Processing of Adenylate Cyclase Toxin Generates a Cytosolic Soluble Catalytically Active N-Terminal Domain.

artículo científico publicado en 2013

Characterization of the First PCSK9 Gain of Function Homozygote

artículo científico publicado en 2015

Cholesterol Efflux Efficiency of Reconstituted HDL Is Affected by Nanoparticle Lipid Composition

scientific article published on 23 September 2020

Double-tailed lipid modification as a promising candidate for oligonucleotide delivery in mammalian cells.

artículo científico publicado en 2013

Functional characterization and classification of frequent low-density lipoprotein receptor variants.

artículo científico publicado en 2014

Functional characterization of splicing and ligand-binding domain variants in the LDL receptor ⬇️

artículo científico publicado el 3 de noviembre de 2011

Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus

article

Human LDL structural diversity studied by IR spectroscopy

artículo científico publicado en 2014

Lipid-modified oligonucleotide conjugates: Insights into gene silencing, interaction with model membranes and cellular uptake mechanisms.

artículo científico publicado en 2016

Membrane restructuring by Bordetella pertussis adenylate cyclase toxin, a member of the RTX toxin family

artículo científico publicado en 2004

Mutation type classification and pathogenicity assignment of sixteen missense variants located in the EGF-precursor homology domain of the LDLR

artículo científico publicado en 2020

Novel functional APOB mutations outside LDL-binding region causing familial hypercholesterolaemia

artículo científico publicado en 2013

PCSK9 and lipoprotein (a) levels are two predictors of coronary artery calcification in asymptomatic patients with familial hypercholesterolemia.

artículo científico publicado en 2016

Pathophysiology of Type 2 Diabetes Mellitus

artículo científico publicado en 2020

Predicted pathogenic mutations in STAP1 are not associated with clinically defined familial hypercholesterolemia

artículo científico publicado en 2019

Replacement of cysteine at position 46 in the first cysteine-rich repeat of the LDL receptor impairs apolipoprotein recognition

artículo científico publicado en 2018

Statin Treatment-Induced Development of Type 2 Diabetes: From Clinical Evidence to Mechanistic Insights ⬇️

artículo científico publicado en 2020

Structural analysis of APOB variants, p.(Arg3527Gln), p.(Arg1164Thr) and p.(Gln4494del), causing Familial Hypercholesterolaemia provides novel insights into variant pathogenicity

artículo científico publicado en 2015

Structural changes induced by acidic pH in human apolipoprotein B-100.

artículo científico publicado en 2016

The importance of an integrated analysis of clinical, molecular, and functional data for the genetic diagnosis of familial hypercholesterolemia.

artículo científico publicado en 2015

The p.Leu167del Mutation in APOE Gene Causes Autosomal Dominant Hypercholesterolemia by Down-regulation of LDL Receptor Expression in Hepatocytes

artículo científico publicado en 2016

The use of targeted exome sequencing in genetic diagnosis of young patients with severe hypercholesterolemia

artículo científico publicado en 2016

miR-27b Modulates Insulin Signaling in Hepatocytes by Regulating Insulin Receptor Expression

artículo científico publicado en 2020

Lista de obras de Cesar Martin

<i>BIRC6</i> Is Associated with Vulnerability of Carotid Atherosclerotic Plaque

Activity-associated effect of LDL receptor missense variants located in the cysteine-rich repeats.

Adenylate Cyclase Toxin promotes bacterial internalisation into non phagocytic cells.

Adenylate cyclase toxin promotes internalisation of integrins and raft components and decreases macrophage adhesion capacity

Advantages and versatility of fluorescence-based methodology to characterize the functionality of LDLR and class mutation assignment

An atlas of O-linked glycosylation on peptide hormones reveals diverse biological roles

Bordetella adenylate cyclase toxin promotes calcium entry into both CD11b+ and CD11b- cells through cAMP-dependent L-type-like calcium channels.

Ca2+ influx and tyrosine kinases trigger Bordetella adenylate cyclase toxin (ACT) endocytosis. Cell physiology and expression of the CD11b/CD18 integrin major determinants of the entry route

Calpain-Mediated Processing of Adenylate Cyclase Toxin Generates a Cytosolic Soluble Catalytically Active N-Terminal Domain.

Characterization of the First PCSK9 Gain of Function Homozygote

Cholesterol Efflux Efficiency of Reconstituted HDL Is Affected by Nanoparticle Lipid Composition

Double-tailed lipid modification as a promising candidate for oligonucleotide delivery in mammalian cells.

Functional characterization and classification of frequent low-density lipoprotein receptor variants.

Functional characterization of splicing and ligand-binding domain variants in the LDL receptor ⬇️

Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus

Human LDL structural diversity studied by IR spectroscopy

Lipid-modified oligonucleotide conjugates: Insights into gene silencing, interaction with model membranes and cellular uptake mechanisms.

Membrane restructuring by Bordetella pertussis adenylate cyclase toxin, a member of the RTX toxin family

Mutation type classification and pathogenicity assignment of sixteen missense variants located in the EGF-precursor homology domain of the LDLR

Novel functional APOB mutations outside LDL-binding region causing familial hypercholesterolaemia

PCSK9 and lipoprotein (a) levels are two predictors of coronary artery calcification in asymptomatic patients with familial hypercholesterolemia.

Pathophysiology of Type 2 Diabetes Mellitus

Predicted pathogenic mutations in STAP1 are not associated with clinically defined familial hypercholesterolemia

Replacement of cysteine at position 46 in the first cysteine-rich repeat of the LDL receptor impairs apolipoprotein recognition

Statin Treatment-Induced Development of Type 2 Diabetes: From Clinical Evidence to Mechanistic Insights ⬇️

Structural analysis of APOB variants, p.(Arg3527Gln), p.(Arg1164Thr) and p.(Gln4494del), causing Familial Hypercholesterolaemia provides novel insights into variant pathogenicity

Structural changes induced by acidic pH in human apolipoprotein B-100.

The importance of an integrated analysis of clinical, molecular, and functional data for the genetic diagnosis of familial hypercholesterolemia.

The p.Leu167del Mutation in APOE Gene Causes Autosomal Dominant Hypercholesterolemia by Down-regulation of LDL Receptor Expression in Hepatocytes

The use of targeted exome sequencing in genetic diagnosis of young patients with severe hypercholesterolemia

miR-27b Modulates Insulin Signaling in Hepatocytes by Regulating Insulin Receptor Expression