Cargando…

Insights on the Functional Impact of MicroRNAs Present in Autism-Associated Copy Number Variants

Autism spectrum disorder is a complex neurodevelopmental disorder that appears during the first three years of infancy and lasts throughout a person’s life. Recently a large category of genomic structural variants, denoted as copy number variants (CNVs), were established to be a major contributor of...

Descripción completa

Detalles Bibliográficos
Autores principales:	Vaishnavi, Varadarajan, Manikandan, Mayakannan, Tiwary, Basant K., Munirajan, Arasambattu Kannan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581547/ https://www.ncbi.nlm.nih.gov/pubmed/23451085 http://dx.doi.org/10.1371/journal.pone.0056781

Ejemplares similares

Mining the 3′UTR of Autism-implicated Genes for SNPs Perturbing MicroRNA Regulation
por: Vaishnavi, Varadharajan, et al.
Publicado: (2014)

Haploinsufficiency of Tumor Suppressor Genes is Driven by the Cumulative Effect of microRNAs, microRNA Binding Site Polymorphisms and microRNA Polymorphisms: An In silico Approach
por: Manikandan, Mayakannan, et al.
Publicado: (2012)

Analyzing the expression of candidate microRNAs in primary tumors of oral squamous cell carcinoma
por: Manikandan, Mayakannan, et al.
Publicado: (2014)

Oral squamous cell carcinoma: microRNA expression profiling and integrative analyses for elucidation of tumourigenesis mechanism
por: Manikandan, Mayakannan, et al.
Publicado: (2016)

MicroRNAs - Biology and clinical applications
por: Ranganathan, Kannan, et al.
Publicado: (2014)

Comprehensive analysis of aberrantly expressed lncRNAs and construction of ceRNA network in gastric cancer
por: Arun, Kanagaraj, et al.
Publicado: (2018)

Identification and Characterization of MicroRNAs Associated with Somatic Copy Number Alterations in Cancer
por: Soh, Jihee, et al.
Publicado: (2018)

APOBEC: A molecular driver in cervical cancer pathogenesis
por: Revathidevi, Sundaramoorthy, et al.
Publicado: (2021)

Novel copy number variants in children with autism and additional developmental anomalies
por: Davis, L. K., et al.
Publicado: (2009)

Association testing of copy number variants in schizophrenia and autism spectrum disorders
por: Crespi, Bernard J, et al.
Publicado: (2012)

Differentially expressed microRNAs in lung adenocarcinoma invert effects of copy number aberrations of prognostic genes
por: Tokar, Tomas, et al.
Publicado: (2018)

Dysregulation of post-transcriptional modification by copy number variable microRNAs in schizophrenia with enhanced glycation stress
por: Yoshikawa, Akane, et al.
Publicado: (2021)

Copy number variation of microRNA genes in the human genome
por: Marcinkowska, Malgorzata, et al.
Publicado: (2011)

Decoding microRNAs in autism spectrum disorder
por: Li, Jinyu, et al.
Publicado: (2022)

Genetic variant rs10251977 (G>A) in EGFR-AS1 modulates the expression of EGFR isoforms A and D
por: Dhamodharan, Shankar, et al.
Publicado: (2021)

Regulation of Large Number of Weak Targets—New Insights from Twin-microRNAs
por: Zhao, Yixin, et al.
Publicado: (2018)

Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk
por: Salyakina, Daria, et al.
Publicado: (2011)

New insights into tomato microRNAs
por: Cardoso, Thaís Cunha de Sousa, et al.
Publicado: (2018)

NAT2 genetic variations among South Indian populations
por: Lakkakula, Saikrishna, et al.
Publicado: (2014)

Identification of Species-Specific MicroRNAs Provides Insights into Dynamic Evolution of MicroRNAs in Plants
por: Guo, Zhonglong, et al.
Publicado: (2022)

Assessing the Impact of Copy Number Variants on miRNA Genes in Autism by Monte Carlo Simulation
por: Marrale, Maurizio, et al.
Publicado: (2014)

The Emerging Role of microRNAs in Schizophrenia and Autism Spectrum Disorders
por: Mellios, Nikolaos, et al.
Publicado: (2012)

Recent Progress on Relevant microRNAs in Autism Spectrum Disorders
por: Wu, Xingwang, et al.
Publicado: (2020)

Identification of copy number variants in horses
por: Doan, Ryan, et al.
Publicado: (2012)

Copy Number Variants in Alzheimer’s Disease
por: Cuccaro, Denis, et al.
Publicado: (2016)

Copy number variants in Ebstein anomaly
por: Giannakou, Andreas, et al.
Publicado: (2017)

Psychopathology in adults with copy number variants
por: Adams, Rachael L., et al.
Publicado: (2023)

Novel Candidate Key Drivers in the Integrative Network of Genes, MicroRNAs, Methylations, and Copy Number Variations in Squamous Cell Lung Carcinoma
por: Huang, Tao, et al.
Publicado: (2015)

Insights on the functional interactions between miRNAs and copy number variations in the aging brain
por: Persengiev, Stephan, et al.
Publicado: (2013)

An Insight into the Roles of MicroRNAs and Exosomes in Sarcoma
por: Kohama, Isaku, et al.
Publicado: (2019)

MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders
por: Wong, Anthony, et al.
Publicado: (2022)

LncRNA OIP5-AS1 is overexpressed in undifferentiated oral tumors and integrated analysis identifies as a downstream effector of stemness-associated transcription factors
por: Arunkumar, Ganesan, et al.
Publicado: (2018)

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts
por: Moreno-De-Luca, D, et al.
Publicado: (2013)

High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan
por: Chen, Chia-Hsiang, et al.
Publicado: (2017)

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder
por: Gudmundsson, Olafur O., et al.
Publicado: (2019)

Copy number variations independently induce autism spectrum disorder
por: Yingjun, Xie, et al.
Publicado: (2017)

Genomic Copy Number Variations in the Autism Clinic—Work in Progress
por: Velinov, Milen
Publicado: (2019)

Large mosaic copy number variations confer autism risk
por: Sherman, Maxwell A., et al.
Publicado: (2021)

Copy number variations in Japanese children with autism spectrum disorder
por: Sakamoto, Yui, et al.
Publicado: (2021)

Beyond KRAS mutation status: influence of KRAS copy number status and microRNAs on clinical outcome to cetuximab in metastatic colorectal cancer patients
por: Mekenkamp, Leonie JM, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_u14gfqcub79mqon9vpnlt9nqka