Cargando…

Candidate Modifier Genes for the Penetrance of Leber’s Hereditary Optic Neuropathy

Leber’s hereditary optic neuropathy (LHON) is a maternally transmitted disease caused by mitochondria DNA (mtDNA) mutation. It is characterized by acute and subacute visual loss predominantly affecting young men. The mtDNA mutation is transmitted to all maternal lineages. However, only approximately...

Descripción completa

Detalles Bibliográficos
Autores principales:	Cheng, Hui-Chen, Chi, Sheng-Chu, Liang, Chiao-Ying, Yu, Jenn-Yah, Wang, An-Guor
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569928/ https://www.ncbi.nlm.nih.gov/pubmed/36233195 http://dx.doi.org/10.3390/ijms231911891

Ejemplares similares

Leber Hereditary Optic Neuropathy: Molecular Pathophysiology and Updates on Gene Therapy
por: Chi, Sheng-Chu, et al.
Publicado: (2022)

Low disease risk and penetrance in Leber hereditary optic neuropathy
por: Watson, Eloise C., et al.
Publicado: (2023)

Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?
por: Mackey, David A., et al.
Publicado: (2023)

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy
por: Giordano, Carla, et al.
Publicado: (2014)

Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy
por: Hudson, Gavin, et al.
Publicado: (2010)

A Female Patient with Down Syndrome and Low-Penetrance Leber's Hereditary Optic Neuropathy
por: Frousiakis, Starleen E., et al.
Publicado: (2014)

Leber hereditary optic neuropathy: current perspectives
por: Meyerson, Cherise, et al.
Publicado: (2015)

Leber’s hereditary optic neuropathy - Case report
por: Iorga, Raluca Eugenia, et al.
Publicado: (2018)

Leber’s Hereditary Optic Neuropathy – Case Discussion
por: Culea, Cristina, et al.
Publicado: (2019)

Arterial sheathing in Leber hereditary optic neuropathy
por: Zhou, Henry W., et al.
Publicado: (2022)

Clinical Overview of Leber Hereditary Optic Neuropathy
por: Stramkauskaitė, Almina, et al.
Publicado: (2022)

Leber’s Hereditary Optic Neuropathy and Hypertrophic Cardiomyopathy
por: Hey, Thomas Morris, et al.
Publicado: (2022)

Developments in the Treatment of Leber Hereditary Optic Neuropathy
por: Chen, Benson S., et al.
Publicado: (2022)

Leber’s Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
por: Abu-Amero, Khaled K.
Publicado: (2011)

Gene–environment interactions in Leber hereditary optic neuropathy
por: Kirkman, Matthew Anthony, et al.
Publicado: (2009)

Leber’s hereditary optic neuropathy is multiorgan not mono-organ
por: Finsterer, Josef, et al.
Publicado: (2016)

The Progress of Gene Therapy for Leber's Optic Hereditary Neuropathy
por: Zhang, Yong, et al.
Publicado: (2018)

Leber hereditary optic neuropathy: bridging the translational gap
por: Jurkute, Neringa, et al.
Publicado: (2017)

Leber’s Hereditary Optic Neuropathy – Reply Letter to the Editor
por: Manole, Cristina, et al.
Publicado: (2020)

Gene Therapies for the Treatment of Leber Hereditary Optic Neuropathy
por: Sahel, José-Alain, et al.
Publicado: (2021)

Leber Hereditary Optic Neuropathy: Review of Treatment and Management
por: Hage, Rabih, et al.
Publicado: (2021)

Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy
por: Amaral-Fernandes, Marcela Scabello, et al.
Publicado: (2011)

Clinical application of multicolor imaging in Leber hereditary optic neuropathy
por: Cheng, Yufang, et al.
Publicado: (2022)

Leber’s hereditary optic neuropathy companied with multiple-related diseases
por: Sun, Ming-ming, et al.
Publicado: (2022)

Identification of novel mitochondrial mutations in Leber’s hereditary optic neuropathy
por: Kumar, Manoj, et al.
Publicado: (2010)

Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation.
por: Hwang, Jeong-Min, et al.
Publicado: (2002)

Persistence of the treatment effect of idebenone in Leber’s hereditary optic neuropathy
por: Klopstock, T., et al.
Publicado: (2013)

Secondary Post-Geniculate Involvement in Leber’s Hereditary Optic Neuropathy
por: Rizzo, Giovanni, et al.
Publicado: (2012)

MRI in Leber's hereditary optic neuropathy: the relationship to multiple sclerosis
por: Matthews, Lucy, et al.
Publicado: (2015)

Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes
por: Shimada, Yoshiaki, et al.
Publicado: (2016)

Mitochondrial genetics and therapeutic overview of Leber's hereditary optic neuropathy
por: Manickam, Agaath Hedina, et al.
Publicado: (2017)

Renal artery aneurysm associated with Leber hereditary optic neuropathy
por: Jones, Ruth Ellen, et al.
Publicado: (2017)

Leber's hereditary optic neuropathy: Shifting our attention to the macula
por: Asanad, Samuel, et al.
Publicado: (2018)

Nationwide epidemiological survey of Leber hereditary optic neuropathy in Japan
por: Ueda, Kaori, et al.
Publicado: (2017)

Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy
por: Coussa, Razek Georges, et al.
Publicado: (2019)

Leber Hereditary Optic Neuropathy: Case Report and Literature Review
por: Filatov, Asia, et al.
Publicado: (2020)

Increased Protein S-Glutathionylation in Leber’s Hereditary Optic Neuropathy (LHON)
por: Zhou, Lei, et al.
Publicado: (2020)

Childhood-Onset Leber Hereditary Optic Neuropathy: Particular Features
por: Cunha, Ana Maria, et al.
Publicado: (2021)

Establishing risk of vision loss in Leber hereditary optic neuropathy
por: Lopez Sanchez, M. Isabel G., et al.
Publicado: (2021)

The epidemiology and mutation types of Leber’s hereditary optic neuropathy in Thailand
por: Sathianvichitr, Kanchalika, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_c7vsvqebs1sbijtndn32ucreni