Cargando…

Correction: MitoLSDB: A Comprehensive Resource to Study Genotype to Phenotype Correlations in Human Mitochondrial DNA Variations

Detalles Bibliográficos
Autores principales:	K, Shamnamole, Jalali, Saakshi, Scaria, Vinod, Bhardwaj, Anshu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2020
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377409/ https://www.ncbi.nlm.nih.gov/pubmed/32702028 http://dx.doi.org/10.1371/journal.pone.0236810

Ejemplares similares

MitoLSDB: A Comprehensive Resource to Study Genotype to Phenotype Correlations in Human Mitochondrial DNA Variations
por: K, Shamnamole, et al.
Publicado: (2013)

Navigating the dynamic landscape of long noncoding RNA and protein-coding gene annotations in GENCODE
por: Jalali, Saakshi, et al.
Publicado: (2016)

Distinct and Modular Organization of Protein Interacting Sites in Long Non-coding RNAs
por: Jalali, Saakshi, et al.
Publicado: (2018)

Integrative transcriptome analysis suggest processing of a subset of long non-coding RNAs to small RNAs
por: Jalali, Saakshi, et al.
Publicado: (2012)

tbvar: a comprehensive genome variation resource for Mycobacterium tuberculosis
por: Joshi, Kandarp Rakeshkumar, et al.
Publicado: (2014)

Genome-wide computational analysis of potential long noncoding RNA mediated DNA:DNA:RNA triplexes in the human genome
por: Jalali, Saakshi, et al.
Publicado: (2017)

Systematic Transcriptome Wide Analysis of lncRNA-miRNA Interactions
por: Jalali, Saakshi, et al.
Publicado: (2013)

MitoTox: a comprehensive mitochondrial toxicity database
por: Lin, Yu-Te, et al.
Publicado: (2021)

lncRNome: a comprehensive knowledgebase of human long noncoding RNAs
por: Bhartiya, Deeksha, et al.
Publicado: (2013)

Circad: a comprehensive manually curated resource of circular RNA associated with diseases
por: Rophina, Mercy, et al.
Publicado: (2020)

MUSTARD—a comprehensive resource of mutation-specific therapies in cancer
por: Mittal, Gauri, et al.
Publicado: (2021)

Resources, challenges and way forward in rare mitochondrial diseases research
por: Rajput, Neeraj Kumar, et al.
Publicado: (2015)

MitoRes: a resource of nuclear-encoded mitochondrial genes and their products in Metazoa
por: Catalano, Domenico, et al.
Publicado: (2006)

Screening Currency Notes for Microbial Pathogens and Antibiotic Resistance Genes Using a Shotgun Metagenomic Approach
por: Jalali, Saakshi, et al.
Publicado: (2015)

zflncRNApedia: A Comprehensive Online Resource for Zebrafish Long Non-Coding RNAs
por: Dhiman, Heena, et al.
Publicado: (2015)

ESC: a comprehensive resource for SARS-CoV-2 immune escape variants
por: Rophina, Mercy, et al.
Publicado: (2021)

Dynamic Expression of Long Non-Coding RNAs (lncRNAs) in Adult Zebrafish
por: Kaushik, Kriti, et al.
Publicado: (2013)

WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson’s Disease
por: Kumar, Mukesh, et al.
Publicado: (2020)

MitoScore, MitoGrade, or MitoSure: what does embryonic mitochondrial deoxyribonucleic acid quantification actually measure and is it useful?
por: Paulson, Richard J.
Publicado: (2022)

HGV&TB: a comprehensive online resource on human genes and genetic variants associated with tuberculosis
por: Sahajpal, Ruchika, et al.
Publicado: (2014)

MitoMiner v4.0: an updated database of mitochondrial localization evidence, phenotypes and diseases
por: Smith, Anthony C, et al.
Publicado: (2019)

MitoBreak: the mitochondrial DNA breakpoints database
por: Damas, Joana, et al.
Publicado: (2014)

MitoFish and MitoAnnotator: A Mitochondrial Genome Database of Fish with an Accurate and Automatic Annotation Pipeline
por: Iwasaki, Wataru, et al.
Publicado: (2013)

Temperature-Specific and Sex-Specific Fitness Effects of Sympatric Mitochondrial and Mito-Nuclear Variation in Drosophila obscura
por: Erić, Pavle, et al.
Publicado: (2022)

MitoTrace: A Computational Framework for Analyzing Mitochondrial Variation in Single-Cell RNA Sequencing Data
por: Wang, Mingqiang, et al.
Publicado: (2023)

MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases
por: Ratnaike, Thiloka E, et al.
Publicado: (2021)

ATP7A Clinical Genetics Resource – A comprehensive clinically annotated database and resource for genetic variants in ATP7A gene
por: Mhaske, Aditi, et al.
Publicado: (2020)

V-MitoSNP: visualization of human mitochondrial SNPs
por: Chuang, Li-Yeh, et al.
Publicado: (2006)

The optic nerve: A “mito-window” on mitochondrial neurodegeneration
por: Maresca, Alessandra, et al.
Publicado: (2013)

mito-QC illuminates mitophagy and mitochondrial architecture in vivo
por: McWilliams, Thomas G., et al.
Publicado: (2016)

Mitochondrial Stress Responses and “Mito-Inflammation” in Cystic Fibrosis
por: Patergnani, Simone, et al.
Publicado: (2020)

Mitochondrial Oxidative Stress and “Mito-Inflammation”: Actors in the Diseases
por: Patergnani, Simone, et al.
Publicado: (2021)

MitoZoa 2.0: a database resource and search tools for comparative and evolutionary analyses of mitochondrial genomes in Metazoa
por: D'Onorio de Meo, Paolo, et al.
Publicado: (2012)

Phenotypic and genotypic variation in Iranian Pistachios
por: Aliakbarkhani, Somayeh Tayefeh, et al.
Publicado: (2015)

DALIA- a comprehensive resource of Disease Alleles in Arab population
por: Vatsyayan, Aastha, et al.
Publicado: (2021)

MitoMiner: a data warehouse for mitochondrial proteomics data
por: Smith, Anthony C., et al.
Publicado: (2012)

MitoVariome: a variome database of human mitochondrial DNA
por: Lee, Yong Seok, et al.
Publicado: (2009)

MitoTimer: A novel tool for monitoring mitochondrial turnover
por: Hernandez, Genaro, et al.
Publicado: (2013)

Mito-FUNCAT-FACS reveals cellular heterogeneity in mitochondrial translation
por: Kimura, Yusuke, et al.
Publicado: (2022)

Identification of unique and shared mitochondrial DNA mutations in neurodegeneration and cancer by single-cell mitochondrial DNA structural variation sequencing (MitoSV-seq)
por: Jaberi, Elham, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_rnbgrhi9otoeotig4l409hottl