Cargando…

The Study of rs693 and rs515135 in APOB in People with Familial Hypercholestrolemia

OBJECTIVE: APOB-related familial hypercholesterolemia (FH) is the most common hereditary hyperchlosterolemia with an autosomal dominant pattern. A number of APOB variants are the most important risk factors for hyperchlosterolemia. APOB is a large glycoprotein that plays an important role in the met...

Descripción completa

Detalles Bibliográficos
Autores principales:	Karami, Fatemeh, Salahshourifar, Iman, Houshmand, Massoud
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Royan Institute 2019
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275425/ https://www.ncbi.nlm.nih.gov/pubmed/30507093 http://dx.doi.org/10.22074/cellj.2019.5692

Ejemplares similares

Associations of the APOB rs693 and rs17240441 polymorphisms with plasma APOB and lipid levels: a meta-analysis
por: Niu, Caiqin, et al.
Publicado: (2017)

The APOB rs693 polymorphism impacts the lipid profile of Brazilian older adults
por: Alves, E.S., et al.
Publicado: (2020)

Distribution of polymorphism rs693 of ApoB gene in a sample of Colombian Caribbeans.
por: Mendoza-Torres, Evelyn, et al.
Publicado: (2019)

Prevalence of ApoB100 rs693 gene polymorphism in metabolic syndrome among female students at King Abdulaziz University
por: Alghamdi, Rana A., et al.
Publicado: (2021)

Familial hypercholestrolemia: clinical examination holds the key!
por: Dewan, Pooja, et al.
Publicado: (2021)

Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian Population
por: Razavian, Takavar, et al.
Publicado: (2020)

Genotype Variations of rs13381800 in TCF4 Gene and rs17039988 in NRXN1 Gene among a Sample of Iranian Patients with Schizophrenia
por: Agahi, Mohadeseh, et al.
Publicado: (2019)

Evaluation of FTO rs9939609 and MC4R rs17782313 Polymorphisms as Prognostic Biomarkers of Obesity: A Population-based Cross-sectional Study
por: Mozafarizadeh, Mina, et al.
Publicado: (2019)

Increased Risk of the APOB rs11279109 Polymorphism for CHD among the Kuwaiti Population
por: Al-Bustan, Suzanne A., et al.
Publicado: (2017)

Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR
por: KHATAMI, Mehri, et al.
Publicado: (2017)

Analysis of the APOB Gene and Apolipoprotein B Serum Levels in a Mexican Population with Acute Coronary Syndrome: Association with the Single Nucleotide Variants rs1469513, rs673548, rs676210, and rs1042034
por: Aceves-Ramírez, Maricela, et al.
Publicado: (2022)

PB2330: CORONARY ARTERY DISEASE (CAD) AND XBAI GENE POLYMORPHISM (RS693) IN EGYPTIAN PATIENTS
por: Almenshawy, A., et al.
Publicado: (2022)

The APOB insertion/deletion polymorphism (rs17240441) influences postprandial lipaemia in healthy adults
por: Vimaleswaran, Karani Santhanakrishnan, et al.
Publicado: (2015)

Correlation Between the APOB rs1042034 SNP and Blood Lipid Characteristics of 2 Ethnic Groups in China
por: Zhang, Fen-Han, et al.
Publicado: (2019)

The effect of CHRNA3 rs1051730 C>T and ABCB1 rs3842 A>G polymorphisms on non-small cell lung cancer and nicotine dependence in Iranian population
por: Veiskarami, Parisa, et al.
Publicado: (2021)

Association of apolipoprotein B XbaI (rs693) polymorphism and gallstone disease risk based on a comprehensive analysis
por: Zhu, Haifeng, et al.
Publicado: (2021)

Comparisons among Machine Learning Models for the Prediction of Hypercholestrolemia Associated with Exposure to Lead, Mercury, and Cadmium
por: Park, Hyejin, et al.
Publicado: (2019)

Investigating Association of rs5918 Human Platelets Antigen 1 and rs1800790 Fibrinogen β Chain as Critical Players with Recurrent Pregnancy Loss
por: Karami, Fatemeh, et al.
Publicado: (2018)

rs12480307 and rs6050307 Polymorphisms of VSX1 Gene in Patient with Keratoconusin Southwest Iran Using PCR-RFLP
por: KARAMI ESHKAFTAKI, Raziyeh, et al.
Publicado: (2018)

Evaluating the Possible Association between PD-1 (Rs11568821, Rs2227981, Rs2227982) and PD-L1 (Rs4143815, Rs2890658) Polymorphisms and Susceptibility to Breast Cancer in a Sample of Southeast Iranian Women
por: Karami, Shima, et al.
Publicado: (2020)

Prevalence of the rs7903146C>T polymorphism in TCF7L2 gene for prediction of type 2 diabetes risk among Iranians of different ethnicities
por: Allahdini, Mojgan, et al.
Publicado: (2015)

Effect of APOB polymorphism rs562338 (G/A) on serum proteome of coronary artery disease patients: a “proteogenomic” approach
por: Zafar, Muneeza, et al.
Publicado: (2021)

A Meta-Analysis for Association of XRCC3 rs861539, MTHFR rs1801133, IL-6 rs1800795, IL-12B rs3212227, TNF-α rs1800629, and TLR9 rs352140 Polymorphisms with Susceptibility to Cervical Carcinoma
por: Parsaeian, Seyedeh Fatemeh, et al.
Publicado: (2021)

Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia
por: Bănescu, Claudia, et al.
Publicado: (2019)

ApoB gene polymorphism (rs676210) and its pharmacogenetics impact on atorvastatin response among Iraqi population with coronary artery disease
por: Abdulfattah, Shaimaa Y., et al.
Publicado: (2021)

Association between interleukin 6 polymorphisms (rs1800796, rs1800795, rs2069837, rs17147230, and rs1800797) and hepatocellular carcinoma susceptibility: a meta-analysis
por: Aleagha, Omid Emami, et al.
Publicado: (2020)

Vitamin D Receptor rs2228570 and rs731236 Polymorphisms are Susceptible Factors for Systemic Lupus Erythematosus
por: Salimi, Saeedeh, et al.
Publicado: (2019)

Association of Different Combinations of ALDH2 rs671, APOE rs429358, rs7412 Polymorphisms with Hypertension in Middle-Aged and Elderly People: A Case–Control Study
por: Lan, Xinping, et al.
Publicado: (2023)

M. & B. 693 in Pneumonia
por: Mody, W. J.
Publicado: (1939)

The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family
por: Khatami, Fatemeh, et al.
Publicado: (2014)

Association of RB1 rs9568036 and CDKN1A rs1801270 Polymorphisms with Retinoblastoma Susceptibility
por: Azimi, Fatemeh, et al.
Publicado: (2022)

Treatment of Lobar Pneumonia with M. & B. 693
por: Jekyll, N. D.
Publicado: (1939)

M. & B. 693 in Indian Strains of Malaria
por: Chopra, R. N., et al.
Publicado: (1939)

Treatment of Lobar Pneumonia with M. & B. 693
por: Caplan, Anthony
Publicado: (1939)

Chemotherapy of Pneumonia by M. & B. 693 in Practice
por: Macrae, James
Publicado: (1939)

Association of ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with Coronary Artery Disease (CAD)
por: Raina, Jyotdeep Kour, et al.
Publicado: (2020)

Risk association, linkage disequilibrium and haplotype analyses of FASN rs4246445, rs2229425, rs2228305 and rs2229422 polymorphisms in overweight and obesity
por: Chong, Eric Tzyy Jiann, et al.
Publicado: (2018)

Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children
por: Buda, Piotr, et al.
Publicado: (2021)

TIRAP Rs8177376, Rs611953, Rs3802814, and Rs8177374 Polymorphisms and Their Association with Cervical Cancer Phenotype and Prognosis
por: Bekampytė, Justina, et al.
Publicado: (2022)

PSMA6 (rs2277460, rs1048990), PSMC6 (rs2295826, rs2295827) and PSMA3 (rs2348071) genetic diversity in Latvians, Lithuanians and Taiwanese
por: Sjakste, Tatjana, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_km67qkcmh4k8vuvtg3td0um4in