Cargando…

Hsp70-2 gene polymorphism: susceptibility implication in Tunisian patients with coronary artery disease

ABSTRACT: Coronary artery disease (CAD) is a multifactorial disease where genetic and environmental factors interact in complex ways to cause the disease. Heat shock protein genes are involved in the progress of CAD. This implies that genetic variants of Hsp70–2 genes might contribute to the develop...

Descripción completa

Detalles Bibliográficos
Autores principales:	Hrira, Mohamed Yahia, Chkioua, Latifa, Slimani, Afef, Chahed, Henda, Mosbah, Habib, Khaldoun, Hamda Ben, Ferchichi, Salima, Addad, Faouzi, Miled, Abdelhedi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558340/ https://www.ncbi.nlm.nih.gov/pubmed/22834788 http://dx.doi.org/10.1186/1746-1596-7-88

Ejemplares similares

Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population
por: Chkioua, Latifa, et al.
Publicado: (2011)

Molecular analysis of iduronate -2- sulfatase gene in Tunisian patients with mucopolysaccharidosis type II
por: Chkioua, Latifa, et al.
Publicado: (2011)

Correlation of Oxidative Stress Parameters and Inflammatory Markers in Tunisian Coronary Artery Disease Patients
por: Dandana, Azza, et al.
Publicado: (2011)

Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: Implication in Morquio A disease
por: Khedhiri, Souhir, et al.
Publicado: (2011)

Mucopolysaccharidosis type I: molecular characteristics of two novel alpha-L-iduronidase mutations in Tunisian patients
por: Chkioua, Latifa, et al.
Publicado: (2011)

Low erythrocyte catalase enzyme activity is correlated with high serum total homocysteine levels in tunisian patients with acute myocardial infarction
por: Noichri, Yosri, et al.
Publicado: (2013)

Clinical Utility of Serum Cystatin C in Predicting Coronary Artery Disease in Patients Without Chronic Kidney Disease
por: Dandana, Azza, et al.
Publicado: (2014)

Genetic basis of cystinosis in Tunisian patients: Identification of novel mutation in CTNS gene
por: Chkioua, Latifa, et al.
Publicado: (2015)

Brain MRI and biological diagnosis in five Tunisians MLD patients
por: Barboura, Ilhem, et al.
Publicado: (2012)

Pathological interactions between the endothelin-1 and the angiotensin- converting enzyme among Tunisian coronary patients
por: Chalghoum, Abdelkader, et al.
Publicado: (2016)

Relationship of activin A levels with clinical presentation, extent, and severity of coronary artery disease
por: Bouzidi, Nadia, et al.
Publicado: (2017)

Biochemical parameters and oxidative stress markers in Tunisian patients with periodontal disease
por: Gharbi, Ahmed, et al.
Publicado: (2019)

Biochemical Responses to Level-1 Yo-Yo Intermittent Recovery Test in Young Tunisian Football Players
por: Hammouda, Omar, et al.
Publicado: (2012)

Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms
por: Chkioua, Latifa, et al.
Publicado: (2011)

Metabolic interactions between hyperhomocysteinemia and endothelin-1 among Tunisian patients with acute coronary diseases
por: Chalghoum, Abdelkader, et al.
Publicado: (2015)

Molecular analysis in a GALNS study cohort of 15 Tunisian patients: description of a novel mutation
por: Chkioua, Latifa, et al.
Publicado: (2016)

Hepatic Proteins and Inflammatory Markers in Rheumatoid Arthritis Patients
por: BEN-HADJ-MOHAMED, Manel, et al.
Publicado: (2017)

Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP gene
por: Najah, Mohamed, et al.
Publicado: (2013)

Concomitant Effects of Ramadan Fasting and Time-Of-Day on Apolipoprotein AI, B, Lp-a and Homocysteine Responses during Aerobic Exercise in Tunisian Soccer Players
por: Hammouda, Omar, et al.
Publicado: (2013)

Relationship between the A(8002)G intronic polymorphism of pre-pro-endothelin-1 gene and the endothelin-1 concentration among Tunisian coronary patients
por: Chalghoum, Abdelkader, et al.
Publicado: (2015)

Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis
por: Chkioua, Latifa, et al.
Publicado: (2022)

Evaluation of physiological risk factors, oxidant-antioxidant imbalance, proteolytic and genetic variations of matrix metalloproteinase-9 in patients with pressure ulcer
por: Latifa, Khlifi, et al.
Publicado: (2016)

Left atrial appendage closure with Watchman device: Insights from the first-ever Tunisian experience and six-year follow-up
por: Chamtouri, Ikram, et al.
Publicado: (2021)

Long-term predictors of death among Tunisian patients presenting fornon ST-elevation acute coronary syndrome
por: Jomaa, Walid, et al.
Publicado: (2021)

The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patients
por: Chkioua, L, et al.
Publicado: (2020)

Prevalence and prognostic significance of anemia in patients presenting for ST-elevation myocardial infarction in a Tunisian center
por: Jomaa, Walid, et al.
Publicado: (2017)

Risk profile and in-hospital prognosis in elderly patients presenting for acute ST-elevation myocardial infarction in the Tunisian context
por: Jomaa, Walid, et al.
Publicado: (2016)

Risk factors in autism spectrum disorder: A Tunisian case-control study
por: Slama, Senda, et al.
Publicado: (2022)

Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome
por: Chkioua, Latifa, et al.
Publicado: (2018)

Autosomal Dominant Hypercholesterolemia: Needs for Early Diagnosis and Cascade Screening in the Tunisian Population
por: Jelassi, Awatef, et al.
Publicado: (2013)

Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme
por: Chkioua, Latifa, et al.
Publicado: (2021)

Apolipoprotein gene polymorphisms and plasma levels in healthy Tunisians and patients with coronary artery disease
por: Bahri, Raoudha, et al.
Publicado: (2008)

Relationship between high sensitivity C-reactive protein and angiographic severity of coronary artery disease
por: Bouzidi, Nadia, et al.
Publicado: (2020)

Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme
por: Chkioua, Latifa, et al.
Publicado: (2021)

Interaction Effects of the Leu162Val PPARα and Pro12Ala PPARγ2 Gene Variants with Renal Function in Metabolic Syndrome Population
por: Mohamed Youssef, Sarraj, et al.
Publicado: (2013)

Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b
por: Chkioua, Latifa, et al.
Publicado: (2023)

Lower p66Shc promoter methylation in subjects with chronic renal failure
por: Hamdi, Radhia, et al.
Publicado: (2021)

Stenosis and Aneurysm of Coronary Arteries in A Patient with Behcet’s Disease
por: Sonia, Hammami, et al.
Publicado: (2008)

Effect of Short-Term Maximal Exercise on Biochemical Markers of Muscle Damage, Total Antioxidant Status, and Homocysteine Levels in Football Players
por: Hammouda, Omar, et al.
Publicado: (2012)

Association of the methylene-tetrahydrofolate reductase gene rs1801133 C677T variant with serum homocysteine levels, and the severity of coronary artery disease
por: Bouzidi, Nadia, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_dnn9qro9op91ekkk60u82hi193