about
Treatment for mitochondrial disordersTreatment for mitochondrial disordersTreatment for mitochondrial myopathyOverexpression of DNA ligase III in mitochondria protects cells against oxidative stress and improves mitochondrial DNA base excision repairReplication-competent human mitochondrial DNA lacking the heavy-strand promoter regionMitochondrial gene replacement in primate offspring and embryonic stem cells.A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex IAn autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3pMitochondrial DNA mutations in human diseaseMitochondrial geneticsMitochondrial DNA disease-molecular insights and potential routes to a cureHistorical perspective on mitochondrial medicineKearns-Sayre syndrome: a case series of 35 adults and childrenCorrelation of the 4977 bp mitochondrial DNA deletion with human sperm dysfunction.Biomarker Validation for Aging: Lessons from mtDNA Heteroplasmy Analyses in Early Cancer Detection.Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorderInvestigation of muscle disease.The mitochondrial DNA 4,977-bp deletion and its implication in copy number alteration in colorectal cancer.Clinical mitochondrial genetics.The neurodegenerative mitochondriopathies.MELAS syndromeMetabolic cardiomyopathies.Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndromeMitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter.Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortionDNA sequences proximal to human mitochondrial DNA deletion breakpoints prevalent in human disease form G-quadruplexes, a class of DNA structures inefficiently unwound by the mitochondrial replicative Twinkle helicase.Mitochondrial replacement therapy in reproductive medicine.Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia.Neuroimaging of mitochondrial disease.A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expressionMaintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines.Mitochondrial DNA: impacting central and peripheral nervous systems.Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation.Mitochondrial DNA mutations in disease and aging
P2860
Q24200432-D0821B24-69E9-405C-9184-C4ABB01B158BQ24244543-D9BFFB0C-5AD5-4B9C-B2A6-10BCCFBF3FD0Q24247852-88C529C7-EE54-4170-A223-10C761A1A338Q24293107-20A4FE9C-B272-4178-BDF8-102C0931F245Q24607395-123FE921-BA51-4D9A-BB51-AE708D38F9C9Q24643001-E23049DC-465C-4E60-BD18-A45E88B39262Q24669970-7829E719-AAE4-4FBD-805D-EFC46444CA74Q24676151-7A55FB95-C6E5-440D-B03D-6524C9F326A7Q24676881-C4B9B599-BA02-4708-ADBC-F09025FE818CQ26849285-25F07367-72BD-43E1-98E1-95F365ADF196Q27005350-B1A88D41-F698-4293-A4EA-126CB80C1398Q28661465-62F9ED04-1D56-45DA-A27A-047A80391D88Q33164555-AFB118F0-4A98-4EDE-B59B-0F2205511E15Q33405486-8A3DDCDD-80CE-41A1-B7A5-03DAA797D7D2Q33520448-AB8ADBA9-5E51-427F-AF2C-0C4038FB8F10Q33593412-81D1D8E9-9277-4061-90CE-4D82952CAF01Q33596549-25173A4D-D7B7-47F1-9A9D-46835B80FE9FQ33672801-181961AA-C19E-4537-AA45-875456441DF2Q33735060-5F663D5A-4258-4B68-B71B-892ECAA72529Q33792617-DC0D9254-8911-4FC0-B7F5-48BD390B7031Q33955376-9003DF9E-CE25-4CA1-A10D-16442B98E623Q33957065-7C6F26BF-0EEB-4BAD-B710-F51639578BAEQ34182102-D3240F7C-C92D-40E3-A1B1-D10E20E0E308Q34216280-D3294F09-B5E4-4739-B21A-43312D3FE384Q34263470-F6926D46-CD5D-43D7-BD33-AEFD7A5C6C68Q34312609-B88685A4-2F5B-4B92-9548-725B94E40028Q34313597-2CB0EC89-E367-4DC4-B7DF-4868B8EBB35FQ34323823-905E2091-7E4C-416E-968D-572D75085142Q34386670-260B0735-3393-4AB5-8B29-C1045F43E937Q34390891-A0D795C3-2770-4574-BA6D-80B22A24DF28Q34396940-218E7819-5648-4ED7-A9D0-9A59EC74A8ADQ34457409-7A54E899-DCE1-47C1-BE38-0CF551525554Q34555959-E7E26B6E-90B6-4512-9F2D-C609AA682936Q34593678-234B0A9A-B7CA-4A03-AC84-D0D1C99063CAQ34627393-934787AC-C80C-4DB5-948A-E5F241D4723CQ34707671-E245A5E9-3CEF-49D7-A64F-ACF9292D0851Q34733032-A4EA3F45-1401-47C4-AAE1-A8A3F92CD08FQ34737643-75AB828A-CFAB-472E-8675-2E1AEC2CA755Q34788426-4B7BE08E-8822-413E-B232-EA2ADE75AA23Q35018267-9F315B15-1C36-4B4F-957A-9D1CCA8F4302
P2860
description
1988 nî lūn-bûn
@nan
1988 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@ast
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@en
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@nl
type
label
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@ast
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@en
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@nl
prefLabel
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@ast
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@en
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@nl
P2093
P356
P1433
P1476
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
@en
P2093
C T Moraes
L P Rowland
P304
P356
10.1212/WNL.38.9.1339
P407
P577
1988-09-01T00:00:00Z