Cargando…

Association between 19-bp Insertion/Deletion Polymorphism of Dopamine β-Hydroxylase and Autism Spectrum Disorder in Thai Patients

Background and Objectives: Autism spectrum disorder (ASD) is a neurodevelopmental disorder the cause of which is not fully known. Genetic factors are believed to play a major role in the etiology of ASD. However, genetic factors have been identified in only some cases, and other causes remain to be...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wongpaiboonwattana, Wikrom, Hnoonual, Areerat, Limprasert, Pornprot
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9504840/ https://www.ncbi.nlm.nih.gov/pubmed/36143905 http://dx.doi.org/10.3390/medicina58091228

Ejemplares similares

Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorder
por: Wongpaiboonwattana, Wikrom, et al.
Publicado: (2020)

Screening for FMR1 CGG Repeat Expansion in Thai Patients with Autism Spectrum Disorder
por: Hnoonual, Areerat, et al.
Publicado: (2021)

Case Report: An Atypical Angelman Syndrome Case With Obesity and Fulfilled Autism Spectrum Disorder Identified by Microarray
por: Hnoonual, Areerat, et al.
Publicado: (2021)

Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder
por: Thongnak, Chuphong, et al.
Publicado: (2018)

Novel Compound Heterozygous Mutations in the TRAPPC9 Gene in Two Siblings With Autism and Intellectual Disability
por: Hnoonual, Areerat, et al.
Publicado: (2019)

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

Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder
por: Hnoonual, Areerat, et al.
Publicado: (2017)

Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literature
por: Charalsawadi, Chariyawan, et al.
Publicado: (2022)

Significant Changes in Plasma Alpha-Synuclein and Beta-Synuclein Levels in Male Children with Autism Spectrum Disorder
por: Sriwimol, Wilaiwan, et al.
Publicado: (2018)

Screening for Subtelomeric Rearrangements in Thai Patients with Intellectual Disabilities Using FISH and Review of Literature on Subtelomeric FISH in 15,591 Cases with Intellectual Disabilities
por: Charalsawadi, Chariyawan, et al.
Publicado: (2016)

Common Clinical Characteristics and Rare Medical Problems of Fragile X Syndrome in Thai Patients and Review of the Literature
por: Charalsawadi, Chariyawan, et al.
Publicado: (2017)

Dopamine-beta hydroxylase polymorphism and cocaine addiction
por: Guindalini, Camila, et al.
Publicado: (2008)

Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population
por: Thongnak, Chuphong, et al.
Publicado: (2016)

A 45-bp insertion/deletion polymorphism of UCP2 gene is associated with metabolic syndrome
por: Hashemi, Mohammad, et al.
Publicado: (2014)

Association of ABO Blood Group Phenotype and Allele Frequency with Chikungunya Fever
por: Rujirojindakul, Pairaya, et al.
Publicado: (2015)

Susceptibility to preeclampsia is associated with a 50-bp insertion/deletion polymorphism at the promoter region of the SOD1 gene
por: Namdari, Somayeh, et al.
Publicado: (2021)

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

Dopamine beta-hydroxylase deficiency
por: Senard, Jean-Michel, et al.
Publicado: (2006)

Role of 14-bp deletion/insertion polymorphism in exon 8 of the HLA-G gene in recurrent spontaneous abortion patients
por: Shankarkumar, U, et al.
Publicado: (2011)

Association of the maternal 14-bp insertion/deletion polymorphism in the histocompatibility leukocyte antigen G gene with recurrent implantation failure
por: Enghelabifar, Mahbubeh, et al.
Publicado: (2014)

A comparison of automated urine analyzers cobas 6500, UN 3000-111b and iRICELL 3000 with manual microscopic urinalysis
por: Tantisaranon, Piraya, et al.
Publicado: (2021)

Comparison of a New In-House and Three Published HLA-B*15:02 Screening Methods for Prevention of Carbamazepine-Induced Severe Drug Reactions
por: Jaruthamsophon, Kanoot, et al.
Publicado: (2016)

Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP Haplotype
por: Limprasert, Pornprot, et al.
Publicado: (2016)

Maternal Age-Specific Rates for Trisomy 21 and Common Autosomal Trisomies in Fetuses from a Single Diagnostic Center in Thailand
por: Jaruthamsophon, Kanoot, et al.
Publicado: (2016)

The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project
por: Combarros, Onofre, et al.
Publicado: (2010)

Association of Angiotensin I Converting Enzyme Insertion/287 bp Deletion Polymorphisms and Proliferative Prostatic Diseases among Lebanese Men
por: El Ezzi, Asmahan A., et al.
Publicado: (2020)

HLA-G 14-bp insertion/deletion polymorphism and risk of coronavirus disease 2019 (COVID-19) among Iraqi patients
por: Ad'hiah, Ali H., et al.
Publicado: (2022)

Plasma dopamine-beta-hydroxylase in neuroblastoma.
por: Schöni, M., et al.
Publicado: (1984)

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

The Relationship between Pre-miR-3131 3-bp Insertion/Deletion Polymorphism and Susceptibility and Clinicopathological Characteristics of Patients with Breast Cancer
por: Azizi, Mahsa, et al.
Publicado: (2020)

A 20-bp insertion/deletion (indel) polymorphism within the CDC25A gene and its associations with growth traits in goat
por: Cui, Wenbo, et al.
Publicado: (2019)

Hyperprolactinemia in Thai children and adolescents with autism spectrum disorder treated with risperidone
por: Hongkaew, Yaowaluck, et al.
Publicado: (2015)

Dopamine and the Development of Executive Dysfunction in Autism Spectrum Disorders
por: Kriete, Trenton, et al.
Publicado: (2015)

HLA-B*15:21 and carbamazepine-induced Stevens-Johnson syndrome: pooled-data and in silico analysis
por: Jaruthamsophon, Kanoot, et al.
Publicado: (2017)

Serum dopamine beta hydroxylase in children with neuroblastoma.
por: Eldeeb, B. B., et al.
Publicado: (1983)

Meta-analysis of HLA-G 14bp insertion/deletion polymorphism and soluble HLA-G revealed an association with digestive cancers initiation and prognosis
por: Dhouioui, Sabrine, et al.
Publicado: (2022)

Development and psychometric evaluation of a Thai Diagnostic Autism Scale for the early diagnosis of Autism Spectrum Disorder
por: Tangviriyapaiboon, Duangkamol, et al.
Publicado: (2021)

Insertions/Deletions-Associated Nucleotide Polymorphism in Arabidopsis thaliana
por: Guo, Changjiang, et al.
Publicado: (2016)

HLA-G 14 bp insertion/deletion polymorphism is not associated to proviral load levels and presence of HAM/TSP in Peruvian HTLV-1 infected individuals
por: Morales, Sandra, et al.
Publicado: (2011)

A 40-bp Insertion/Deletion Polymorphism of Murine Double Minute2 (MDM2) Increased the Risk of Breast Cancer in Zahedan, Southeast Iran
por: Hashemi, Mohammad, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_8avjqa0ogv8biqgl51k4n1m43r