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                             49 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications Angural, Arshia
 2019
 46 C p. 209-213
 artikel
2 Adaptation of Mge1 to oxidative stress by local unfolding and altered Interaction with mitochondrial Hsp70 and Mxr2 Karri, Srinivasu
 2019
 46 C p. 140-148
 artikel
3 A deafness-associated mitochondrial DNA mutation altered the tRNASer(UCN) metabolism and mitochondrial function Xue, Ling
 2019
 46 C p. 370-379
 artikel
4 Alloreactivity and allorecognition of syngeneic and allogeneic mitochondria Ramirez-Barbieri, Giovanna
 2019
 46 C p. 103-115
 artikel
5 A mitochondrial DNA D loop insertion detected almost exclusively in non-replicating tissues with maternal inheritance across three generations Sharma, Mehul A.
 2019
 46 C p. 298-301
 artikel
6 Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution Santibanez-Koref, Mauro
 2019
 46 C p. 302-306
 artikel
7 BCPP compounds, PET probes for early therapeutic evaluations, specifically bind to mitochondrial complex I Kazami, Sayaka
 2019
 46 C p. 97-102
 artikel
8 Cardiomyocyte mitochondrial dysfunction in diabetes and its contribution in cardiac arrhythmogenesis El Hadi, Hamza
 2019
 46 C p. 6-14
 artikel
9 Cell-free mitochondrial DNA in progressive multiple sclerosis Lowes, Hannah
 2019
 46 C p. 307-312
 artikel
10 Cerebrospinal fluid neurofilament light is associated with survival in mitochondrial disease patients Sofou, Kalliopi
 2019
 46 C p. 228-235
 artikel
11 Chebulinic acid and Boeravinone B act as anti-aging and anti-apoptosis phyto-molecules during oxidative stress Biradar, Shivtej P.
 2019
 46 C p. 236-246
 artikel
12 Comment on “establishment of human retinal mitoscriptome gene expression signature for diabetic retinopathy using cadaver eyes” Li, Chenyu
 2019
 46 C p. 326
 artikel
13 CPEO – Like mitochondrial myopathy associated with m.8340G>A mutation Tarnopolsky, Mark A.
 2019
 46 C p. 69-72
 artikel
14 Deep sequencing discovery of causal mtDNA mutations in a patient with unspecific neurological disease Spangenberg, Lucía
 2019
 46 C p. 337-344
 artikel
15 Development of a triplex mtDNA qPCR assay to assess quantification, degradation, inhibition, and amplification target copy numbers Kavlick, Mark F.
 2019
 46 C p. 41-50
 artikel
16 Editorial Board 2019
 46 C p. ii
 artikel
17 Effects of air pollution on mitochondrial function, mitochondrial DNA methylation, and mitochondrial peptide expression Breton, Carrie V.
 2019
 46 C p. 22-29
 artikel
18 Effects of mitochondrial disease/dysfunction on pregnancy: A retrospective study Karaa, Amel
 2019
 46 C p. 214-220
 artikel
19 Exercise-induced reductions in mitochondrial ADP sensitivity contribute to the induction of gene expression and mitochondrial biogenesis through enhanced mitochondrial H2O2 emission Miotto, Paula M.
 2019
 46 C p. 116-122
 artikel
20 Frequency and association of mitochondrial genetic variants with neurological disorders Cruz, Ana Carolina P.
 2019
 46 C p. 345-360
 artikel
21 Gene therapy for the mitochondrial genome: Purging mutations, pacifying ailments Aravintha Siva, M.
 2019
 46 C p. 195-208
 artikel
22 Genetic analysis in a cohort of patients with hereditary optic neuropathies in Southwest of China Guo, Hong
 2019
 46 C p. 327-333
 artikel
23 Genomic and transcriptomic characterization of the mitochondrial-rich oncocytic phenotype on a thyroid carcinoma background Cavadas, Bruno
 2019
 46 C p. 123-133
 artikel
24 Identification of a novel mitochondrial complex I assembly factor ACDH-12 in Caenorhabditis elegans Chuaijit, Sirithip
 2019
 46 C p. 91-96
 artikel
25 Intramitochondrial transfer and engineering of mammalian mitochondrial genomes in yeast Yoon, Young Geol
 2019
 46 C p. 15-21
 artikel
26 Is there a mutation gradient along vertebrate mitochondrial genome mediated by genome replication? Xia, Xuhua
 2019
 46 C p. 30-40
 artikel
27 Meta-analysis of genotype-phenotype analysis of OPA1 mutations in autosomal dominant optic atrophy Ham, Michelle
 2019
 46 C p. 262-269
 artikel
28 Metabolic features and regulation of the healing cycle—A new model for chronic disease pathogenesis and treatment Naviaux, Robert K.
 2019
 46 C p. 278-297
 artikel
29 Microglia polarization by mitochondrial metabolism modulation: A therapeutic opportunity in neurodegenerative diseases Di Stadio, Arianna
 2019
 46 C p. 334-336
 artikel
30 Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell lines Li, Dan
 2019
 46 C p. 313-320
 artikel
31 Mitochondrial genomics in the cancer cell line encyclopedia and a scoring method to effectively pair cell lines for cytoplasmic hybridization Grandhi, S.
 2019
 46 C p. 256-261
 artikel
32 Mitochondrial haplotypes are not associated with mice selectively bred for high voluntary wheel running Wone, Bernard W.M.
 2019
 46 C p. 134-139
 artikel
33 Mitochondrial β-oxidation of saturated fatty acids in humans Adeva-Andany, María M.
 2019
 46 C p. 73-90
 artikel
34 Mitochondria-targeted quinones suppress the generation of reactive oxygen species, programmed cell death and senescence in plants Samuilov, Vitaly D.
 2019
 46 C p. 164-171
 artikel
35 Multichromosomal structure of the onion mitochondrial genome and a transcript analysis Tsujimura, Mai
 2019
 46 C p. 179-186
 artikel
36 Muscle contractility of leg muscles in patients with mitochondrial myopathies Poulsen, Nanna Scharff
 2019
 46 C p. 221-227
 artikel
37 Mutation in Cytochrome B gene causes debility and adverse effects on health of sheep Pal, Aruna
 2019
 46 C p. 393-404
 artikel
38 Nuclear-Mitochondrial interactions influence susceptibility to HIV-associated neurocognitive impairment Smieszek, S.
 2019
 46 C p. 247-255
 artikel
39 Optimised detection of mitochondrial DNA strand breaks Hanna, Rebecca
 2019
 46 C p. 172-178
 artikel
40 Organellar transcriptome sequencing reveals mitochondrial localization of nuclear encoded transcripts Sabharwal, Ankit
 2019
 46 C p. 59-68
 artikel
41 Peroxynitrite nitrates adenine nucleotide translocase and voltage-dependent anion channel 1 and alters their interactions and association with hexokinase II in mitochondria Yang, Meiying
 2019
 46 C p. 380-392
 artikel
42 PPARδ modulation rescues mitochondrial fatty acid oxidation defects in the mdx model of muscular dystrophy Bell, Eric L.
 2019
 46 C p. 51-58
 artikel
43 Profiling of genomic alterations of mitochondrial DNA in gingivobuccal oral squamous cell carcinoma: Implications for disease progress Palodhi, Arindam
 2019
 46 C p. 361-369
 artikel
44 The first direct activity assay for the mitochondrial protease OMA1 Tobacyk, Julia
 2019
 46 C p. 1-5
 artikel
45 The m.11778 A > G variant associated with the coexistence of Leber's hereditary optic neuropathy and multiple sclerosis-like illness dysregulates the metabolic interplay between mitochondrial oxidative phosphorylation and glycolysis Uittenbogaard, Martine
 2019
 46 C p. 187-194
 artikel
46 The mitochondrial effects of embelin are independent of its MAP kinase regulation: Role of p53 in conferring selectivity towards cancer cells Avisetti, Deepa R.
 2019
 46 C p. 158-163
 artikel
47 Toxic medications in Leber's hereditary optic neuropathy Kogachi, Kaitlin
 2019
 46 C p. 270-277
 artikel
48 Tracing the maternal origin of the common wall lizard (Podarcis muralis) on the northern range margin in Central Europe Jablonski, Daniel
 2019
 46 C p. 149-157
 artikel
49 Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss Khatami, Somayeh
 2019
 46 C p. 321-325
 artikel
                             49 gevonden resultaten
 
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