Lista de obras - Antonio Cao - Dominio Público Uruguay

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

Alpha-thalassemia

artículo científico publicado en 2011

COL4A1 is associated with arterial stiffness by genome-wide association scan

artículo científico publicado en 2009

Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulation

artículo científico publicado en 2002

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

artículo científico publicado en 2010

Common variants in the GDF5-UQCC region are associated with variation in human height

artículo científico publicado en 2008

Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia

artículo científico publicado en 2009

Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1

artículo científico publicado en 2007

DAXX is a new AIRE-interacting protein

artículo científico publicado en 2010

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences

artículo científico publicado en 2004

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

scientific journal article

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

artículo científico publicado en 2008

IRAK-M is involved in the pathogenesis of early-onset persistent asthma

artículo científico publicado en 2007

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

artículo científico publicado en 2008

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function

artículo científico publicado en 2008

The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts

artículo científico publicado en 2007

The central arterial burden of the metabolic syndrome is similar in men and women: the SardiNIA Study

artículo científico publicado en 2009

The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity

artículo científico publicado en 2010

Variants in MTNR1B influence fasting glucose levels

artículo científico publicado en 2008

Lista de obras de Antonio Cao

A genome-wide association search for type 2 diabetes genes in African Americans

Alpha-thalassemia

COL4A1 is associated with arterial stiffness by genome-wide association scan

Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulation

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

Common variants in the GDF5-UQCC region are associated with variation in human height

Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia

Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1

DAXX is a new AIRE-interacting protein

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

IRAK-M is involved in the pathogenesis of early-onset persistent asthma

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function

The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts

The central arterial burden of the metabolic syndrome is similar in men and women: the SardiNIA Study

The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity

Variants in MTNR1B influence fasting glucose levels