Cargando…

Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents

INTRODUCTION: Positive regulatory domain containing 16 (PRDM16) protein represents the key regulator of brown adipose tissue (BAT) development. It induces brown fat phenotype and represses white adipose tissue specific genes through the association with C-terminal binding co-repressor proteins (CtBP...

Descripción completa

Detalles Bibliográficos
Autores principales:	Maksimovic, Nela, Vidovic, Vanja, Damnjanovic, Tatjana, Jekic, Biljana, Majkic Singh, Nada, Simeunovic, Slavko, Bozovic, Dara Savic, Vidovic, Stojko, Novakovic, Ivana
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Termedia Publishing House 2021
Materias:	Clinical Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259392/ https://www.ncbi.nlm.nih.gov/pubmed/37313181 http://dx.doi.org/10.5114/aoms/113174

Ejemplares similares

Association of the Brain-derived Neurotrophic Factor Val66Met Polymorphism with Body Mass Index, Fasting Glucose Levels and Lipid Status in Adolescents
por: Vidović, V, et al.
Publicado: (2020)

GPX3 rs8177412 Polymorphism Modifies Risk of Upper Urothelial Tumors in Patients with Balkan Endemic Nephropathy
por: Radic Savic, Zana, et al.
Publicado: (2023)

Prevalence of Five Pharmacologically Most Important CYP2C9 and CYP2C19 Allelic Variants in the Population from the Republic of Srpska in Bosnia and Herzegovina
por: Vidović, Stojko, et al.
Publicado: (2021)

Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients
por: Perovic, Dijana, et al.
Publicado: (2022)

KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures
por: Dimitrijevic, Sanja, et al.
Publicado: (2022)

Degree of genetic homozygosity and distribution of AB0 blood types among patients with spina bifida occulta and spina bifida aperta
por: Nikolic, Dejan, et al.
Publicado: (2010)

Germline PRDM1 Variant rs2185379 in Long-Term Recurrence-Free Survivors of Advanced Ovarian Cancer
por: Mitamura, Takashi, et al.
Publicado: (2022)

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)

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)

Association of SOD2 (rs4880) and GPX1 (rs1050450) Gene Polymorphisms with Risk of Balkan Endemic Nephropathy and its Related Tumors
por: Dragicevic, Biljana, et al.
Publicado: (2019)

Catechol-O-methyltransferase rs4680 and rs4818 haplotype association with treatment response to olanzapine in patients with schizophrenia
por: Nikolac Perkovic, Matea, et al.
Publicado: (2020)

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)

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)

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

Haplotypic and Genotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Polymorphisms and Treatment Resistance in Schizophrenia
por: Sagud, Marina, et al.
Publicado: (2018)

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

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)

Physical activity evaluation in Yugoslav Study of the Precursors of Atherosclerosis in School Children – YUSAD study
por: Simeunovic, Slavko, et al.
Publicado: (2010)

CTBP1 and CTBP2 mutations underpinning neurological disorders: a systematic review
por: Acosta-Baena, Natalia, et al.
Publicado: (2022)

Genotypic and Haplotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Gene Polymorphisms with Particular Clinical Symptoms in Schizophrenia
por: Sagud, Marina, et al.
Publicado: (2023)

Genetic Variations of DAOA (rs947267 and rs3918342) and COMT Genes (rs165599 and rs4680) in Schizophrenia and Bipolar I Disorder
por: Ahmadi, Leila, et al.
Publicado: (2018)

Functional Analysis of the rs774872314, rs116171003, rs200231898 and rs201107751 Polymorphisms in the Human RORγT Gene Promoter Region
por: Ratajewski, Marcin, et al.
Publicado: (2017)

Associations of rs823128, rs1572931, and rs823156 polymorphisms with reduced Parkinson’s disease risks
por: Bai, Ye, et al.
Publicado: (2017)

The Association between Five Genetic Variants in MicroRNAs (rs2910164, rs11614913, rs3746444, rs11134527, and rs531564) and Cervical Cancer Risk: A Meta-Analysis
por: Liu, Jia, et al.
Publicado: (2021)

The Correlation of Mouse Double Minute 4 (MDM4) Polymorphisms (rs4245739, rs1563828, rs11801299, rs10900598, and rs1380576) with Cancer Susceptibility: A Meta-Analysis
por: Chen, Jian, et al.
Publicado: (2022)

RAD51B (rs8017304 and rs2588809), TRIB1 (rs6987702, rs4351379, and rs4351376), COL8A1 (rs13095226), and COL10A1 (rs1064583) Gene Variants with Predisposition to Age-Related Macular Degeneration
por: Vilkeviciute, Alvita, et al.
Publicado: (2019)

Evaluation of MC4R [RS17782313, RS17700633], AGRP [RS3412352] and POMC [RS1042571] polymorphisms with obesity in Northern India
por: Srivastava, Apurva, et al.
Publicado: (2014)

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)

Haplotypes of HTRA1 rs1120638, TIMP3 rs9621532, VEGFA rs833068, CFI rs10033900, ERCC6 rs3793784, and KCTD10 rs56209061 Gene Polymorphisms in Age-Related Macular Degeneration
por: Liutkeviciene, Rasa, et al.
Publicado: (2019)

Progression of liver fibrosis in HIV/HCV genotype 1 co-infected patients is related to the T allele of the rsI2979860 polymorphism of the IL28B gene
por: Lutz, P, et al.
Publicado: (2011)

Deciphering the Role of the rs2651899, rs10166942, and rs11172113 Polymorphisms in Migraine: A Meta-Analysis
por: Siokas, Vasileios, et al.
Publicado: (2022)

The 5Rs dilemma of radiotherapy for non-malignant diseases: 5Rs to darken OR 5Rs to shine
por: Montero, Angel, et al.
Publicado: (2023)

The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of Neuromyelitis Optica in A Chinese Population
por: Lan, Wenjing, et al.
Publicado: (2015)

Polymorphisms FTO rs9939609, PPARG rs1801282 and ADIPOQ rs4632532 and rs182052 but not lifestyle are associated with obesity related-traits in Mexican children
por: Muñoz-Yáñez, C, et al.
Publicado: (2016)

Gene Polymorphisms in FAS (Rs3740286 and Rs4064) Are Involved in Endometriosis Development in Brazilian Women, but not those in CASP8 (rs13416436 and rs2037815)
por: Pissetti, Cristina Wide, et al.
Publicado: (2018)

RS and composites
por: Panico, Giuliano
Publicado: (2017)

Polymorphisms of Antioxidant Enzymes SOD2 (rs4880) and GPX1 (rs1050450) Are Associated with Bladder Cancer Risk or Its Aggressiveness
por: Nikic, Predrag, et al.
Publicado: (2023)

(5RS,10SR,15RS)-Trimethyltruxene
por: Thomas, Kandace R., et al.
Publicado: (2011)

Association of TFPI polymorphisms rs8176592, rs10931292, and rs10153820 with venous thrombosis: A meta-analysis
por: Zhang, Yunhong, et al.
Publicado: (2019)

ESR2 gene variants (rs1256049, rs4986938, and rs1256030) and their association with breast cancer risk
por: Gallegos-Arreola, Martha Patricia, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_j7ove5806al4h7u0afum67sklo