Lista de obras - Nihan Erginel-Unaltuna - Dominio Público Uruguay

A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness

scientific article published on 01 January 2004

A new F-box protein 7 gene mutation causing typical Parkinson's disease

artículo científico publicado en 2015

A novel protein involved in heart development in Ambystoma mexicanum is localized in endoplasmic reticulum

artículo científico publicado en 2008

ADAM-9, ADAM-15, and ADAM-17 are upregulated in macrophages in advanced human atherosclerotic plaques in aorta and carotid and femoral arteries--Tampere vascular study

artículo científico publicado en 2009

APOC3 -482C>T polymorphism, circulating apolipoprotein C-III and smoking: interrelation and roles in predicting type-2 diabetes and coronary disease

artículo científico publicado en 2010

Apolipoprotein A-I positively associated with diabetes in women independently of apolipoprotein E genotype and apolipoprotein B levels.

artículo científico publicado en 2010

Association between non-coding polymorphisms of HOPX gene and syncope in hypertrophic cardiomyopathy.

artículo científico publicado en 2014

Association between selected cholesterol-related gene polymorphisms and Alzheimer's disease in a Turkish cohort

scientific article published on 25 January 2019

Association of C-reactive protein (CRP) gene allelic variants with serum CRP levels and hypertension in Turkish adults.

artículo científico publicado en 2009

Association of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patients

article

CYP19A1, MIF and ABCA1 genes are targets of the RORα in monocyte and endothelial cells.

artículo científico publicado en 2016

Clinical variability in ataxia-telangiectasia

artículo científico publicado en 2015

DNA testing for Huntington disease in the Turkish population

artículo científico publicado en 2003

Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease

artículo científico publicado en 2001

Endothelial dysfunction in patients with asthma: the role of polymorphisms of ACE and endothelial NOS genes

artículo científico publicado en 2004

Endothelial function and endothelial nitric oxide synthase intron 4a/b polymorphism in primary hyperparathyroidism

artículo científico publicado en 2009

Gender specific association of ABCA1 gene R219K variant in coronary disease risk through interactions with serum triglyceride elevation in Turkish adults.

artículo científico publicado en 2013

Gender- and obesity-specific effect of apolipoprotein C3 gene (APOC3) -482C>T polymorphism on triglyceride concentration in Turkish adults

artículo científico publicado en 2011

Gender-modulated impact of apolipoprotein A5 gene (APOA5) -1131T>C and c.56C>G polymorphisms on lipids, dyslipidemia and metabolic syndrome in Turkish adults

artículo científico publicado en 2008

Gender-specific associations of the APOA1 -75G>A polymorphism with several metabolic syndrome components in Turkish adults.

artículo científico publicado en 2014

Gene polymorphisms of endothelial nitric oxide synthase enzyme associated with pulmonary hypertension in patients with COPD.

artículo científico publicado en 2003

Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population

artículo científico publicado en 2012

Genomic organization and expression of KCNJ8/Kir6.1, a gene encoding a subunit of an ATP-sensitive potassium channel

artículo científico publicado en 1998

HLA-DQ alleles in patients with celiac disease in Turkey

artículo científico publicado en 2001

High serum apolipoprotein E determines hypertriglyceridemic dyslipidemias, coronary disease and apoA-I dysfunctionality.

artículo científico publicado en 2012

Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

artículo científico publicado en 2012

Identification of potential target genes of ROR-alpha in THP1 and HUVEC cell lines

artículo científico publicado en 2017

Immunofluorescent studies on titin and myosin in developing hearts of normal and cardiac mutant axolotls

artículo científico publicado en 1994

Improved method for molecular diagnosis of myotonic dystrophy type 1 (DM1).

artículo científico publicado en 2004

Isolation and analysis of genes mainly expressed in adult mouse heart using subtractive hybridization cDNA library.

artículo científico publicado en 2012

LRRK2 mutations are uncommon in Turkey.

artículo científico publicado en 2011

Lipoprotein(a) level and MIF gene variant predict incident metabolic syndrome and mortality

artículo científico publicado en 2016

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

scientific journal article

Low "quotient" Lp(a) concentration mediates autoimmune activation and independently predicts cardiometabolic risk

artículo científico publicado en 2014

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients

artículo científico publicado en 2016

Negative results in screening for possible new sequence variations on ATP-binding cassette transporter A1 gene in Turkish adults with metabolic syndrome.

artículo científico

Niemann-Pick type C fibroblasts have a distinct microRNA profile related to lipid metabolism and certain cellular components

artículo científico publicado en 2010

Oxidative stress-mediated (sex-specific) loss of protection against type-2 diabetes by macrophage migration inhibitory factor (MIF)-173G/C polymorphism

artículo científico publicado en 2014

Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease's patients

artículo científico publicado en 2020

Pretreatment with octreotide modulates iNOS gene expression, mimics surgical delay, and improves flap survival

artículo científico publicado en 2010

Prevalence of Prader–Willi Syndrome among Infants with Hypotonia

artículo científico publicado en 2014

Risk of obesity and metabolic syndrome associated with FTO gene variants discloses clinically relevant gender difference among Turks

artículo científico publicado en 2016

Role of simvastatin and RORα activity in the macrophage apoptotic pathway

artículo científico publicado en 2017

Sequence variations of NKX2-5 and HAND1 genes in patients with atrial isomerism.

artículo científico publicado en 2011

Sex- and Obesity-specific Association of Aromatase (CYP19A1) Gene Variant with Apolipoprotein B and Hypertension

artículo científico publicado en 2015

The APOE -219G/T and +113G/C polymorphisms affect insulin resistance among Turks

artículo científico publicado en 2010

The S447X variant of lipoprotein lipase gene is associated with metabolic syndrome and lipid levels among Turks

artículo científico publicado en 2007

The effect of angiotensin converting enzyme gene polymorphism on chronic allograft dysfunction in living donor renal transplant recipients

article

The variations of BOP gene in hypertrophic cardiomyopathy.

artículo científico publicado en 2010

Ventricular pre-excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation

artículo científico publicado en 2006

Lista de obras de Nihan Erginel-Unaltuna

A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness

A new F-box protein 7 gene mutation causing typical Parkinson's disease

A novel protein involved in heart development in Ambystoma mexicanum is localized in endoplasmic reticulum

ADAM-9, ADAM-15, and ADAM-17 are upregulated in macrophages in advanced human atherosclerotic plaques in aorta and carotid and femoral arteries--Tampere vascular study

APOC3 -482C>T polymorphism, circulating apolipoprotein C-III and smoking: interrelation and roles in predicting type-2 diabetes and coronary disease

Apolipoprotein A-I positively associated with diabetes in women independently of apolipoprotein E genotype and apolipoprotein B levels.

Association between non-coding polymorphisms of HOPX gene and syncope in hypertrophic cardiomyopathy.

Association between selected cholesterol-related gene polymorphisms and Alzheimer's disease in a Turkish cohort

Association of C-reactive protein (CRP) gene allelic variants with serum CRP levels and hypertension in Turkish adults.

Association of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patients

CYP19A1, MIF and ABCA1 genes are targets of the RORα in monocyte and endothelial cells.

Clinical variability in ataxia-telangiectasia

DNA testing for Huntington disease in the Turkish population

Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease

Endothelial dysfunction in patients with asthma: the role of polymorphisms of ACE and endothelial NOS genes

Endothelial function and endothelial nitric oxide synthase intron 4a/b polymorphism in primary hyperparathyroidism

Gender specific association of ABCA1 gene R219K variant in coronary disease risk through interactions with serum triglyceride elevation in Turkish adults.

Gender- and obesity-specific effect of apolipoprotein C3 gene (APOC3) -482C>T polymorphism on triglyceride concentration in Turkish adults

Gender-modulated impact of apolipoprotein A5 gene (APOA5) -1131T>C and c.56C>G polymorphisms on lipids, dyslipidemia and metabolic syndrome in Turkish adults

Gender-specific associations of the APOA1 -75G>A polymorphism with several metabolic syndrome components in Turkish adults.

Gene polymorphisms of endothelial nitric oxide synthase enzyme associated with pulmonary hypertension in patients with COPD.

Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population

Genomic organization and expression of KCNJ8/Kir6.1, a gene encoding a subunit of an ATP-sensitive potassium channel

HLA-DQ alleles in patients with celiac disease in Turkey

High serum apolipoprotein E determines hypertriglyceridemic dyslipidemias, coronary disease and apoA-I dysfunctionality.

Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

Identification of potential target genes of ROR-alpha in THP1 and HUVEC cell lines

Immunofluorescent studies on titin and myosin in developing hearts of normal and cardiac mutant axolotls

Improved method for molecular diagnosis of myotonic dystrophy type 1 (DM1).

Isolation and analysis of genes mainly expressed in adult mouse heart using subtractive hybridization cDNA library.

LRRK2 mutations are uncommon in Turkey.

Lipoprotein(a) level and MIF gene variant predict incident metabolic syndrome and mortality

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Low "quotient" Lp(a) concentration mediates autoimmune activation and independently predicts cardiometabolic risk

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients

Negative results in screening for possible new sequence variations on ATP-binding cassette transporter A1 gene in Turkish adults with metabolic syndrome.

Niemann-Pick type C fibroblasts have a distinct microRNA profile related to lipid metabolism and certain cellular components

Oxidative stress-mediated (sex-specific) loss of protection against type-2 diabetes by macrophage migration inhibitory factor (MIF)-173G/C polymorphism

Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease's patients

Pretreatment with octreotide modulates iNOS gene expression, mimics surgical delay, and improves flap survival

Prevalence of Prader–Willi Syndrome among Infants with Hypotonia

Risk of obesity and metabolic syndrome associated with FTO gene variants discloses clinically relevant gender difference among Turks

Role of simvastatin and RORα activity in the macrophage apoptotic pathway

Sequence variations of NKX2-5 and HAND1 genes in patients with atrial isomerism.

Sex- and Obesity-specific Association of Aromatase (CYP19A1) Gene Variant with Apolipoprotein B and Hypertension

The APOE -219G/T and +113G/C polymorphisms affect insulin resistance among Turks

The S447X variant of lipoprotein lipase gene is associated with metabolic syndrome and lipid levels among Turks

The effect of angiotensin converting enzyme gene polymorphism on chronic allograft dysfunction in living donor renal transplant recipients

The variations of BOP gene in hypertrophic cardiomyopathy.

Ventricular pre-excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation