Cargando…

Association Analyses of SNAP25, HNMT, FCHSD1, and DBH Single-Nucleotide Polymorphisms with Parkinson’s Disease in a Northern Chinese Population

PURPOSE: Sequencing potentially causal and susceptible genes and genome-wide association studies in samples from Parkinson’s disease (PD) patients has revealed several related loci. The genes for synaptosome-associated protein of 25 kDa (SNAP25), histamine-N-methyltransferase (HNMT), FCH and double...

Descripción completa

Detalles Bibliográficos
Autores principales:	Dai, Cuiyun, Zhang, Yichi, Zhan, Xiaoni, Tian, Meihui, Pang, Hao
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove 2021
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166815/ https://www.ncbi.nlm.nih.gov/pubmed/34079266 http://dx.doi.org/10.2147/NDT.S304062

Ejemplares similares

FCHSD1 and FCHSD2 Are Expressed in Hair Cell Stereocilia and Cuticular Plate and Regulate Actin Polymerization In Vitro
por: Cao, Huiren, et al.
Publicado: (2013)

Association of Dopamine Beta-Hydroxylase (DBH) Polymorphisms with Susceptibility to Parkinson’s Disease
por: Shao, Peng, et al.
Publicado: (2016)

Relationships of Cerebrospinal Fluid Alzheimer’s Disease Biomarkers and COMT, DBH, and MAOB Single Nucleotide Polymorphisms
por: Babić Leko, Mirjana, et al.
Publicado: (2020)

Role of Dopamine β Hydroxylase (DBH) in Parkinson's disease patients of Indian population
por: Ghosh, Arunibha, et al.
Publicado: (2014)

Mapping of the binding sites of human histamine N-methyltransferase (HNMT) monoclonal antibodies
por: Schwelberger, Hubert G., et al.
Publicado: (2017)

FCHSD2 controls oncogenic ERK1/2 signaling outcome by regulating endocytic trafficking
por: Xiao, Guan-Yu, et al.
Publicado: (2020)

Deafness-related protein PDZD7 forms complex with the C-terminal tail of FCHSD2
por: Wang, Huang, et al.
Publicado: (2022)

Associations of Polymorphisms in HRH2, HRH3, DAO, and HNMT Genes with Risk of Chronic Heart Failure
por: He, Gong-Hao, et al.
Publicado: (2016)

Female genetic distribution bias in mitochondrial genome observed in Parkinson’s Disease patients in northern China
por: Chu, Qiaohong, et al.
Publicado: (2015)

Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene
por: Verhoeven, Willem M A, et al.
Publicado: (2020)

Thr105Ile (rs11558538) polymorphism in the histamine N-methyltransferase (HNMT) gene and risk for Parkinson disease: A PRISMA-compliant systematic review and meta-analysis
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2016)

SNAP-25 Single Nucleotide Polymorphisms, Brain Morphology and Intelligence in Children With Borderline Intellectual Functioning: A Mediation Analysis
por: Blasi, Valeria, et al.
Publicado: (2021)

Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretion
por: Hu, Ming, et al.
Publicado: (2021)

Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretion
por: Hu, Ming, et al.
Publicado: (2021)

Molecular Identification of Carnosine N-Methyltransferase as Chicken Histamine N-Methyltransferase-Like Protein (HNMT-Like)
por: Drozak, Jakub, et al.
Publicado: (2013)

Sexually Dimorphic Effects of Histamine Degradation by Enteric Glial Histamine N-Methyltransferase (HNMT) on Visceral Hypersensitivity
por: McClain, Jonathon L., et al.
Publicado: (2023)

Polymorphism rs1108580 in DBH gene is associated with the risk of depression in alcohol-dependent patients
por: Nikolishin, A., et al.
Publicado: (2022)

Heritable Influence of DBH on Adrenergic and Renal Function: Twin and Disease Studies
por: Pasha, Dalal N., et al.
Publicado: (2013)

Dataset of permanent plots of trees with dbh >10cm in Mashpi rainforest biodiversity reserve, a remnant of the Chocó forest in Northern Ecuador
por: Toasa, German, et al.
Publicado: (2020)

Analysis of ADORA2A, MTA1, PTGDS, PTGS2, NSF, and HNMT Gene Expression Levels in Peripheral Blood of Patients with Early Stages of Parkinson's Disease
por: Semenova, Ekaterina I., et al.
Publicado: (2023)

Electrostatic anchoring precedes stable membrane attachment of SNAP25/SNAP23 to the plasma membrane
por: Weber, Pascal, et al.
Publicado: (2017)

Correction: Heritable Influence of DBH on Adrenergic and Renal Function: Twin and Disease Studies
Publicado: (2014)

Foxo1 regulates Dbh expression and the activity of the sympathetic nervous system in vivo
por: Kajimura, Daisuke, et al.
Publicado: (2014)

Role of SNAP25 on the occurrence and development of eosinophilic gastritis
por: Zhang, Jie, et al.
Publicado: (2023)

Antiallodynic effect of PhAR‐DBH‐Me involves cannabinoid and TRPV1 receptors
por: Quiñonez‐Bastidas, Geovanna Nallely, et al.
Publicado: (2020)

Dbh(+) catecholaminergic cardiomyocytes contribute to the structure and function of the cardiac conduction system in murine heart
por: Sun, Tianyi, et al.
Publicado: (2023)

The Interaction of Polymorphisms of IL10 and DBH Was Associated with General Symptoms of PANSS with TD in Chinese Han Schizophrenic Patients
por: Sun, Hongqiang, et al.
Publicado: (2013)

Lack of Association Between Dopamine Beta-Hydroxylase (DBH) 19-bp Insertion/Deletion Polymorphism and Risk of Schizophrenia
por: Shakiba, Mansour, et al.
Publicado: (2016)

SNAP23 decreases insulin secretion by competitively inhibiting the interaction between SNAP25 and STX1A
por: Chen, Jun, et al.
Publicado: (2023)

Genetic diversity of tyrosine hydroxylase (TH) and dopamine β-hydroxylase (DBH) genes in cattle breeds
por: Lourenco-Jaramillo, Diana Lelidett, et al.
Publicado: (2012)

Characterization of hypotensive and vasorelaxant effects of PHAR-DBH-Me a new cannabinoid receptor agonist
por: López-Canales, Oscar Alberto, et al.
Publicado: (2022)

Synaptosomal-associated protein 25 (Snap-25) gene Polymorphism frequency in fibromyalgia syndrome and relationship with clinical symptoms
por: Balkarli, Ayse, et al.
Publicado: (2014)

SNAP-25 is expressed in islets of Langerhans and is involved in insulin release
Publicado: (1995)

Sequential exocytosis of insulin granules is associated with redistribution of SNAP25
por: Takahashi, Noriko, et al.
Publicado: (2004)

SNAP25 is a potential prognostic biomarker for prostate cancer
por: Di, Longjiang, et al.
Publicado: (2022)

The Role of SNAP-25 in Autism Spectrum Disorders Onset Patterns
por: Bolognesi, Elisabetta, et al.
Publicado: (2023)

Snapping Hip and Snapping Finger
por: Cotterill, J. M.
Publicado: (1910)

Association Between Polymorphisms of DRD2, COMT, DBH, and MAO-A Genes and Migraine Susceptibility: A Meta-Analysis
por: Chen, Hu, et al.
Publicado: (2015)

Association of Impulsivity and Polymorphic MicroRNA-641 Target Sites in the SNAP-25 Gene
por: Németh, Nóra, et al.
Publicado: (2013)

The Exocytosis Associated SNAP25-Type Protein, SlSNAP33, Increases Salt Stress Tolerance by Modulating Endocytosis in Tomato
por: Salinas-Cornejo, Josselyn, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_01pg82pia4vkpe91ne0cnf195q