Cargando…

Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes

Detalles Bibliográficos
Autores principales:	Sadikovic, Bekim, Wang, Jing, El-Hattab, Ayman W., Landsverk, Megan, Douglas, Ganka, Brundage, Ellen K., Craigen, William J., Schmitt, Eric S., Wong, Lee-Jun C.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2017
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695760/ https://www.ncbi.nlm.nih.gov/pubmed/29155871 http://dx.doi.org/10.1371/journal.pone.0188610

Ejemplares similares

Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
por: Sadikovic, Bekim, et al.
Publicado: (2010)

Correction: Complex Breakpoints and Template Switching Associated with Non-canonical Termination of Homologous Recombination in Mammalian Cells
por: Hartlerode, Andrea J., et al.
Publicado: (2016)

Thermodynamic analysis of DNA hybridization signatures near mitochondrial DNA deletion breakpoints
por: Lakshmanan, Lakshmi Narayanan, et al.
Publicado: (2021)

Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3′ Breakpoints
por: Hjelm, Brooke E., et al.
Publicado: (2023)

Fast detection of deletion breakpoints using quantitative PCR
por: Abildinova, Gulshara, et al.
Publicado: (2016)

Breakpoint junction features of seven DMD deletion mutations
por: Keegan, Niall P., et al.
Publicado: (2019)

Correction: Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing
Publicado: (2017)

Deletion of VDAC1 Hinders Recovery of Mitochondrial and Renal Functions After Acute Kidney Injury
por: Nowak, Grazyna, et al.
Publicado: (2020)

Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients
por: Rendtorff, Nanna Dahl, et al.
Publicado: (2022)

Mitochondrial Cardiomyopathies
por: El-Hattab, Ayman W., et al.
Publicado: (2016)

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

DNA Methylation Episignatures in Neurodevelopmental Disorders Associated with Large Structural Copy Number Variants: Clinical Implications
por: Rooney, Kathleen, et al.
Publicado: (2022)

The effect of citrulline and arginine supplementation on lactic acidemia in MELAS syndrome()
por: El-Hattab, Ayman W., et al.
Publicado: (2013)

Correction: SoftSearch: Integration of Multiple Sequence Features to Identify Breakpoints of Structural Variations
Publicado: (2014)

Mitochondrial Membranes and Mitochondrial Genome: Interactions and Clinical Syndromes
por: Almannai, Mohammed, et al.
Publicado: (2022)

A Case of SF3B1-Positive Myelodysplastic/Myeloproliferative Neoplasm with Ring Sideroblasts and Thrombocytosis
por: Lazo-Langner, Alejandro, et al.
Publicado: (2019)

Small Deletion Variants Have Stable Breakpoints Commonly Associated with Alu Elements
por: de Smith, Adam J., et al.
Publicado: (2008)

Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints
por: Dong, Dawei W, et al.
Publicado: (2014)

Prenatal cytogenomic identification and molecular refinement of compound heterozygous STRC deletion breakpoints
por: Shi, Lisong, et al.
Publicado: (2019)

Splice-Break: exploiting an RNA-seq splice junction algorithm to discover mitochondrial DNA deletion breakpoints and analyses of psychiatric disorders
por: Hjelm, Brooke E, et al.
Publicado: (2019)

Nitric Oxide Deficiency in Mitochondrial Disorders: The Utility of Arginine and Citrulline
por: Almannai, Mohammed, et al.
Publicado: (2021)

Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication
por: Linden, Stefanie C., et al.
Publicado: (2021)

Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms
por: Abyzov, Alexej, et al.
Publicado: (2015)

Complex Breakpoints and Template Switching Associated with Non-canonical Termination of Homologous Recombination in Mammalian Cells
por: Hartlerode, Andrea J., et al.
Publicado: (2016)

Evolution of gene regulation in ruminants differs between evolutionary breakpoint regions and homologous synteny blocks
por: Farré, Marta, et al.
Publicado: (2019)

Complexity in Genetic Epilepsies: A Comprehensive Review
por: Rastin, Cassandra, et al.
Publicado: (2023)

Correction: Population Biology of Schistosoma Mating, Aggregation, and Transmission Breakpoints: More Reliable Model Analysis for the End-Game in Communities at Risk
Publicado: (2015)

Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations
por: Elfferich, Peter, et al.
Publicado: (2011)

Correlations between long inverted repeat (LIR) features, deletion size and distance from breakpoint in human gross gene deletions
por: Aygun, Nevim
Publicado: (2015)

Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 Multiple Osteochondromas families
por: Jennes, Ivy, et al.
Publicado: (2011)

Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequences
por: Bacolla, Albino, et al.
Publicado: (2016)

Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms
por: Malhotra, Ankit, et al.
Publicado: (2013)

Mitochondrial Fission and Fusion: Molecular Mechanisms, Biological Functions, and Related Disorders
por: Al Ojaimi, Mode, et al.
Publicado: (2022)

Correction: DNA breakpoint assay reveals a majority of gross duplications occur in tandem reducing VUS classifications in breast cancer predisposition genes
por: Richardson, Marcy E., et al.
Publicado: (2018)

Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation
por: Koczkowska, Magdalena, et al.
Publicado: (2018)

Correction: TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants
por: Dines, Jennifer N., et al.
Publicado: (2018)

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint
por: Sha, Yan-Wei, et al.
Publicado: (2018)

IKZF1 Deletions with COBL Breakpoints Are Not Driven by RAG-Mediated Recombination Events in Acute Lymphoblastic Leukemia
por: Lopes, Bruno A., et al.
Publicado: (2019)

Mapping of deletion breakpoints at the CDKN2A locus in melanoma: detection of MTAP-ANRIL fusion transcripts
por: Xie, Huaping, et al.
Publicado: (2016)

Diagnostic Utility of Genome-Wide DNA Methylation Analysis in Mendelian Neurodevelopmental Disorders
por: Haghshenas, Sadegheh, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_sdf91f53qb1uardrif246e2bvv