Cargando…

The Association of CEP135 rs4865047 and NPY2R rs1902491 Single Nucleotide Polymorphisms (SNPs) with Rapid Progression of Proliferative Diabetic Retinopathy in Patients with Type 1 Diabetes Mellitus

BACKGROUND: Diabetic retinopathy has a varied prevalence, severity, and rate of progression. The aim of this study was to determine whether the single nucleotide polymorphisms (SNPs) of the gene encoding a 135-kD centrosomal protein CEP135 rs4865047 and the gene encoding the type 2 NPY protein NPY2R...

Descripción completa

Detalles Bibliográficos
Autores principales:	Derkac, Irmante, Januleviciene, Ingrida, Sepetiene, Ramune, Valiauga, Rasa, Velickiene, Dzilda
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	International Scientific Literature, Inc. 2018
Materias:	Clinical Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295137/ https://www.ncbi.nlm.nih.gov/pubmed/30531682 http://dx.doi.org/10.12659/MSM.909803

Ejemplares similares

Effects of preservative-free tafluprost on tear film osmolarity, tolerability, and intraocular pressure in previously treated patients with open-angle glaucoma
por: Janulevičienė, Ingrida, et al.
Publicado: (2012)

Relation between Exogenous Insulin and Cognitive Function in Type 2 Diabetes Mellitus
por: Šimonienė, Diana, et al.
Publicado: (2021)

Microbiome Changes after Type 2 Diabetes Treatment: A Systematic Review
por: Merkevičius, Kajus, et al.
Publicado: (2021)

Clinical Role of Serum miR107 in Type 2 Diabetes and Related Risk Factors
por: Šimonienė, Diana, et al.
Publicado: (2022)

Microvascular Complications, Peripheral Artery Disease and Mortality in Patients with Type 2 Diabetes Mellitus, in Two Counties of Southern Lithuania over 13 Years: Analysis Using a Cohort Database of the National Health Insurance
por: Piliponienė, Laima, et al.
Publicado: (2021)

Associations between CYP2C8 rs10509681 and rs11572080 gene polymorphisms and age-related macular degeneration
por: Liutkevičienė, Rasa, et al.
Publicado: (2017)

Insulin Resistance in Type 1 Diabetes Mellitus and Its Association with Patient’s Micro- and Macrovascular Complications, Sex Hormones, and Other Clinical Data
por: Šimonienė, Diana, et al.
Publicado: (2019)

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

The Relationship between Body Mass Index (BMI) and Depression According to the rs16139NPY Gene
por: Dolatian, Atieh, et al.
Publicado: (2017)

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)

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)

Methimazole-induced liver injury overshadowed by methylprednisolone pulse therapy: Case report
por: Abramavicius, Silvijus, et al.
Publicado: (2017)

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)

Abnormal centrosomal structure and duplication in Cep135-deficient vertebrate cells
por: Inanç, Burcu, et al.
Publicado: (2013)

IL-10 Gene Rs1800871, Rs1800872, and Rs1800896 Polymorphisms and IL-10 Serum Levels Association with Pituitary Adenoma
por: Palivonaite, Migle, et al.
Publicado: (2022)

Determination of SIRT1 rs12778366, FGFR2 rs2981582, STAT3 rs744166, and RAGE rs1800625 Single Gene Polymorphisms in Patients with Laryngeal Squamous Cell Carcinoma
por: Uloza, Virgilijus, et al.
Publicado: (2019)

The Investigation of Associations between TP53 rs1042522, BBC3 rs2032809, CCND1 rs9344, EGFR rs2227983 Polymorphisms and Breast Cancer Phenotype and Prognosis
por: Bekampytė, Justina, et al.
Publicado: (2021)

The survival rate of laryngeal squamous cell carcinoma: impact of IL1RAP rs4624606, IL1RL1 rs1041973, IL-6 rs1800795, BLK rs13277113, and TIMP3 rs9621532 single nucleotide polymorphisms
por: Pasvenskaite, Agne, et al.
Publicado: (2023)

Association of FGFR2 rs2981582, SIRT1 rs12778366, STAT3 rs744166 gene polymorphisms with pituitary adenoma
por: Glebauskiene, Brigita, et al.
Publicado: (2017)

Association of a Single-Nucleotide Variant rs11100494 of the NPY5R Gene with Antipsychotic-Induced Metabolic Disorders
por: Dobrodeeva, Vera S., et al.
Publicado: (2022)

Association between ACE (rs4646994), FABP2 (rs1799883), MTHFR (rs1801133), FTO (rs9939609) Genes Polymorphism and Type 2 Diabetes with Dyslipidemia
por: Raza, Syed Tasleem, et al.
Publicado: (2017)

Retrospective analysis of age-adjusted body mass index among pre-pregnant women in the Lithuanian urban area during three decades
por: Francaite-Daugeliene, Migle, et al.
Publicado: (2016)

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)

The two-component system CepRS regulates the cephamycin C biosynthesis in Streptomyces clavuligerus F613-1
por: Fu, Jiafang, et al.
Publicado: (2019)

Correlation among decreased regional cerebral oxygen saturation, blood levels of brain injury biomarkers, and cognitive disorder
por: Kumpaitiene, Birute, et al.
Publicado: (2018)

CEP135 isoform dysregulation promotes centrosome amplification in breast cancer cells
por: Ganapathi Sankaran, Divya, et al.
Publicado: (2019)

The SNPs rs429358 and rs7412 of APOE gene are association with cerebral infarction but not SNPs rs2306283 and rs4149056 of SLCO1B1 gene in southern Chinese Hakka population
por: Wu, Heming, et al.
Publicado: (2020)

Two polymorphisms (rs699947, rs2010963) in the VEGFA gene and diabetic retinopathy: an updated meta-analysis
por: Lu, Yan, et al.
Publicado: (2013)

SIRT1 rs10823108 and FOXO1 rs17446614 responsible for genetic susceptibility to diabetic nephropathy
por: Zhao, Yanyan, et al.
Publicado: (2017)

Bld10/Cep135 stabilizes basal bodies to resist cilia-generated forces
por: Bayless, Brian A., et al.
Publicado: (2012)

Functional Analysis of DNMT1 SNPs (rs2228611 and rs2114724) Associated with Schizophrenia
por: Saxena, Sonal, et al.
Publicado: (2021)

Association between ABC family variants rs1800977, rs4149313, and rs1128503 and susceptibility to type 2 diabetes in a Chinese Han population
por: Yan, Ruicheng, et al.
Publicado: (2020)

Adipocyte “Fatty Acid Binding Protein” Gene Polymorphisms (rs1054135, rs16909196 and rs16909187) in Jordanians with Obesity and Type 2 Diabetes Mellitus
por: El-Ryalat, S.W., et al.
Publicado: (2023)

Frequency Distribution of COMT Polymorphisms in Greek Patients with Schizophrenia and Controls: A Study of SNPs rs737865, rs4680, and rs165599
por: Maria, Kotrotsou, et al.
Publicado: (2012)

Metabolic impact of the VDR rs1544410 in diabetic retinopathy
por: de Assis, Caroline Severo, et al.
Publicado: (2022)

Impact of KCNJ11 rs5219, UCP2 rs659366, and MTHFR rs1801133 Polymorphisms on Type 2 Diabetes: A Cross-Sectional Study
por: Lapik, Irina Alexandrovna, et al.
Publicado: (2021)

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 Renalase SNPs rs2296545 and rs2576178 with the Risk of Hypertension: A Meta-Analysis
por: Lv, Yong-Bo, et al.
Publicado: (2016)

Association Between rs3833912/rs16944 SNPs and Risk for Cerebral Palsy in Mexican Children
por: Torres-Merino, Sofia, et al.
Publicado: (2018)

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)

Cannot write session to /tmp/vufind_sessions/sess_95u2vt0iisaddike9emj5ns7hv