Cargando…

The Author Reply: Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions

Detalles Bibliográficos
Autor principal:	Lee, Young-Mock
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Yonsei University College of Medicine 2019
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6342714/ https://www.ncbi.nlm.nih.gov/pubmed/30666847 http://dx.doi.org/10.3349/ymj.2019.60.2.232

Ejemplares similares

Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions
por: Finsterer, Josef
Publicado: (2019)

Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions
por: Finsterer, Josef
Publicado: (2020)

Novel and recurrent nuclear gene variations in a cohort of Chinese progressive external ophthalmoplegia patients with multiple mtDNA deletions
por: Hou, Yue, et al.
Publicado: (2022)

Precision modeling of mitochondrial disease in rats via DdCBE-mediated mtDNA editing
por: Qi, Xiaolong, et al.
Publicado: (2021)

MELAS and Kearns–Sayre overlap syndrome due to the mtDNA m. A3243G mutation and large-scale mtDNA deletions
por: Yu, Nian, et al.
Publicado: (2016)

Ophthalmoplegia in Mitochondrial Disease
por: Lee, Sang-Jun, et al.
Publicado: (2018)

Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions
por: Fuke, Satoshi, et al.
Publicado: (2014)

Precision modeling of mitochondrial diseases in zebrafish via DdCBE-mediated mtDNA base editing
por: Guo, Jiayin, et al.
Publicado: (2021)

Biallelic Variants in ENDOG Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions
por: Nasca, Alessia, et al.
Publicado: (2022)

When man got his mtDNA deletions?
por: Popadin, Konstantin, et al.
Publicado: (2014)

Resolving the Enigma of the Clonal Expansion of mtDNA Deletions
por: Kowald, Axel, et al.
Publicado: (2018)

Reply to: Double trouble progressive external ophthalmoplegia and Huntington's disease
por: Filosto, Massimiliano, et al.
Publicado: (2016)

Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion
por: Varga, Noémi Ágnes, et al.
Publicado: (2018)

ALS spinal neurons show varied and reduced mtDNA gene copy numbers and increased mtDNA gene deletions
por: Keeney, Paula M, et al.
Publicado: (2010)

Mitochondrial DNA (mtDNA) haplotypes and dysfunctions in presbyacusis
por: MOSTAFA, H., et al.
Publicado: (2014)

mtDNA Deletion in an Iranian Infant with Pearson Marrow Syndrome
por: Arzanian, Mohammad Taghi, et al.
Publicado: (2010)

Response to: ‘when man got his mtDNA deletions?’
por: Taylor, Sean D, et al.
Publicado: (2014)

De Novo Development of mtDNA Deletion Due to Decreased POLG and SSBP1 Expression in Humans
por: Lee, Yeonmi, et al.
Publicado: (2021)

mtDNA, Metastasis, and the Mitochondrial Unfolded Protein Response (UPR(mt))
por: Kenny, Timothy C., et al.
Publicado: (2017)

Ancient mtDNA Genetic Variants Modulate mtDNA Transcription and Replication
por: Suissa, Sarit, et al.
Publicado: (2009)

In vivo methylation of mtDNA reveals the dynamics of protein–mtDNA interactions
por: Rebelo, Adriana P., et al.
Publicado: (2009)

The Author Reply: Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS
por: Lee, Young-Mock
Publicado: (2019)

Mitochondrial activity in gametes and transmission of viable mtDNA
por: Milani, Liliana, et al.
Publicado: (2015)

Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I
por: Danhelovska, Tereza, et al.
Publicado: (2020)

mtDNA deletions responsible for unsuccessful pregnancy after in- vitro fertilization
Publicado: (2020)

Partial tandem duplication of mtDNA–tRNA(Phe) impairs mtDNA translation in late-onset mitochondrial myopathy
por: Arzuffi, Paola, et al.
Publicado: (2012)

Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria
por: Matic, Stanka, et al.
Publicado: (2018)

Authors' reply — Clozapine for mitochondrial psychosis
por: Demily, Caroline, et al.
Publicado: (2017)

Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling
por: Goffart, Steffi, et al.
Publicado: (2009)

Where mtDNA is made
por: LeBrasseur, Nicole
Publicado: (2003)

Melanesian mtDNA Complexity
por: Friedlaender, Jonathan S., et al.
Publicado: (2007)

Mitochondrial Replication Assay (MIRA) for Efficient in situ Quantification of Nascent mtDNA and Protein Interactions with Nascent mtDNA (mitoSIRF)
por: Lozen, Macy, et al.
Publicado: (2023)

Mitochondrial Network State Scales mtDNA Genetic Dynamics
por: Aryaman, Juvid, et al.
Publicado: (2019)

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects
por: Roels, Frank, et al.
Publicado: (2009)

The mtDNA mutator mouse: Dissecting mitochondrial involvement in aging
por: Edgar, Daniel, et al.
Publicado: (2009)

Mitochondrial Dysfunction Associated with mtDNA in Metabolic Syndrome and Obesity
por: Todosenko, Natalia, et al.
Publicado: (2023)

DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated?
por: Maresca, Alessandra, et al.
Publicado: (2015)

The spectrum of mitochondrial DNA (mtDNA) mutations in pediatric CNS tumors
por: Kaneva, Kristiyana, et al.
Publicado: (2021)

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

Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletions
por: Lehmann, Diana, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_dj2rk17j3rqemv135lnfkiivuh