Association of C-reactive protein gene polymorphisms with the risk of ischemic stroke: A systematic review and meta-analysis.
Sign Up to like & getrecommendations! Published in 2023 at "Brain and behavior"
DOI: 10.1002/brb3.2976
Abstract: BACKGROUND AND PURPOSE The heterogeneous, complex condition known as ischemic stroke (IS) is brought on by the interaction of a number of risk factors and genetic variables. The association between C-reactive protein (CRP) gene polymorphisms… read more here.
Keywords: gene polymorphisms; association; gene; ischemic stroke ... See more keywords
HOTAIR gene polymorphisms contribute to increased neuroblastoma susceptibility in Chinese children
Sign Up to like & getrecommendations! Published in 2018 at "Cancer"
DOI: 10.1002/cncr.31353
Abstract: Neuroblastoma is the most frequently diagnosed extracranial solid tumor in children. Previous studies have shown that single‐nucleotide polymorphisms in some genes are associated with the risk of multiple cancers, including neuroblastoma. Although Hox transcript antisense… read more here.
Keywords: chinese children; gene polymorphisms; neuroblastoma susceptibility; hotair gene ... See more keywords
Relationship of Serum 25‐Hydroxyvitamin D Concentrations, Diabetes, Vitamin D Receptor Gene Polymorphisms and Incident Venous Thromboembolism
Sign Up to like & getrecommendations! Published in 2024 at "Diabetes/Metabolism Research and Reviews"
DOI: 10.1002/dmrr.70014
Abstract: The association between vitamin D and the risk of venous thromboembolism (VTE) remains inconclusive. We aimed to explore the association of serum 25‐hydroxyvitamin D (25OHD) with incident VTE among participants with and without diabetes, and… read more here.
Keywords: vitamin receptor; venous thromboembolism; serum hydroxyvitamin; gene polymorphisms ... See more keywords
Genetic variations in NER pathway gene polymorphisms and Wilms tumor risk: A six‐center case–control study in East China
Sign Up to like & getrecommendations! Published in 2024 at "IUBMB Life"
DOI: 10.1002/iub.2919
Abstract: The nucleotide excision repair (NER) system is one of the main ways to protect organisms from DNA damage caused by endogenous and exogenous carcinogens. NER deficiency increases genome mutations, chromosomal aberrations, and cancer viability. However,… read more here.
Keywords: gene polymorphisms; wilms tumor; ner pathway; risk ... See more keywords
ALKBH5 gene polymorphisms and Wilms tumor risk in Chinese children: A five‐center case‐control study
Sign Up to like & getrecommendations! Published in 2020 at "Journal of Clinical Laboratory Analysis"
DOI: 10.1002/jcla.23251
Abstract: Wilms tumor is a frequently diagnosed renal cancer among children with unclear genetic causes. N6‐methyladenosine (m6A) modification genes play critical roles in tumorigenesis. However, whether genetic variations of m6A modification genes predispose to Wilms tumor… read more here.
Keywords: m6a modification; gene polymorphisms; alkbh5 gene; wilms tumor ... See more keywords
Analysis of the association between MICA gene polymorphisms and schizophrenia
Sign Up to like & getrecommendations! Published in 2022 at "Journal of Clinical Laboratory Analysis"
DOI: 10.1002/jcla.24721
Abstract: The major histocompatibility complex (MHC) has been implicated in schizophrenia. This study aimed to explore the correlation between the major histocompatibility complex class I polypeptide‐related sequence A (MICA) polymorphisms and schizophrenia. read more here.
Keywords: mica gene; gene polymorphisms; analysis association; analysis ... See more keywords
Association between IL1RL1 gene polymorphisms and allergic rhinitis risk in the Chinese Han population
Sign Up to like & getrecommendations! Published in 2022 at "Journal of Clinical Laboratory Analysis"
DOI: 10.1002/jcla.24747
Abstract: Although it has been confirmed that IL1RL1 is involved in the occurrence of allergic rhinitis (AR), the role of IL1RL1 gene single nucleotide polymorphisms (SNPs) in AR is still unclear. read more here.
Keywords: gene polymorphisms; il1rl1 gene; association il1rl1; allergic rhinitis ... See more keywords
CETP and LCAT Gene Polymorphisms Are Associated with High-Density Lipoprotein Subclasses and Acute Coronary Syndrome.
Sign Up to like & getrecommendations! Published in 2018 at "Lipids"
DOI: 10.1002/lipd.12017
Abstract: We evaluated whether CETP and LCAT gene polymorphisms are statistically associated with the high-density lipoprotein (HDL) size distribution, the cholesterol level of HDL subclasses, and the acute coronary syndrome (ACS) susceptibility. Two CETP gene polymorphisms… read more here.
Keywords: high density; gene polymorphisms; density lipoprotein; hdl ... See more keywords
Association of ECE1 gene polymorphisms and essential hypertension risk in the Northern Han Chinese: A case‒control study
Sign Up to like & getrecommendations! Published in 2020 at "Molecular Genetics & Genomic Medicine"
DOI: 10.1002/mgg3.1188
Abstract: The ECE1 gene polymorphisms have been studied as a candidate gene in essential hypertension, but no consensus has been reached. To systematically explore their possible association, a case‒control study was conducted. read more here.
Keywords: control study; ece1 gene; gene polymorphisms; case control ... See more keywords
Quantitative assessment of TLR4 gene polymorphisms and T2DM risk: A meta‐analysis
Sign Up to like & getrecommendations! Published in 2020 at "Molecular Genetics & Genomic Medicine"
DOI: 10.1002/mgg3.1466
Abstract: Numerous studies have evaluated the association between TLR4 gene polymorphisms and T2DM risk. However, the findings were inconsistent and controversial. read more here.
Keywords: gene polymorphisms; t2dm risk; tlr4 gene; polymorphisms t2dm ... See more keywords
Maternal MTHFR 677C>T, 1298A>C gene polymorphisms and risk of offspring aneuploidy
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DOI: 10.1002/pd.6214
Abstract: The objective was to investigate the association between maternal methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms, crucial for DNA methylation, and risk of offspring aneuploidy. read more here.
Keywords: risk offspring; gene polymorphisms; offspring aneuploidy; maternal mthfr ... See more keywords