| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adult-onset Leigh syndrome linked to the novel stop codon mutation m.6579G>A in MT-CO1
|
Poole, Olivia V.
|
|
2019
|
47 |
C |
p. 294-297
|
artikel
|
| 2 |
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene
|
Marchet, Silvia
|
|
2019
|
47 |
C |
p. 24-29
|
artikel
|
| 3 |
A novel pathogenic m.4412G>A MT-TM mitochondrial DNA variant associated with childhood-onset seizures, myopathy and bilateral basal ganglia changes
|
Lim, Albert Z.
|
|
2019
|
47 |
C |
p. 18-23
|
artikel
|
| 4 |
A novel variant m.641A>T in the mitochondrial MT-TF gene is associated with epileptic encephalopathy in adolescent
|
Itkis, Yulia
|
|
2019
|
47 |
C |
p. 10-17
|
artikel
|
| 5 |
Assessment of associations between mitochondrial DNA haplogroups and attention deficit and hyperactivity disorder in Korean children
|
Hwang, In Wook
|
|
2019
|
47 |
C |
p. 174-178
|
artikel
|
| 6 |
A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1
|
Eijkenboom, Ivo
|
|
2019
|
47 |
C |
p. 273-281
|
artikel
|
| 7 |
Calcium phosphate buffer formed in the mitochondrial matrix during preconditioning supports ΔpH formation and ischemic ATP production and prolongs cell survival –A hypothesis
|
Dolowy, Krzysztof
|
|
2019
|
47 |
C |
p. 210-217
|
artikel
|
| 8 |
Circulating mitochondria DNA, a non-invasive cancer diagnostic biomarker candidate
|
Afrifa, Justice
|
|
2019
|
47 |
C |
p. 238-243
|
artikel
|
| 9 |
Corrigendum to “Mitochondria in health and disease” [Mitochondrion 43(2018) 25–29]
|
Chakrabarty, Sanjiban
|
|
2019
|
47 |
C |
p. 331
|
artikel
|
| 10 |
Corrigendum to “Topical Coenzyme Q10 demonstrates mitochondrial-mediated neuroprotection in a rodent model of ocular hypertension” [Mitochondrion 36 (2017) 114–123]
|
Davis, B.M.
|
|
2019
|
47 |
C |
p. 330
|
artikel
|
| 11 |
Editorial Board
|
|
|
2019
|
47 |
C |
p. ii
|
artikel
|
| 12 |
Ethnogenetic analysis reveals that Kohistanis of Pakistan were genetically linked to west Eurasians by a probable ancestral genepool from Eurasian steppe in the bronze age
|
Khan, Sawar
|
|
2019
|
47 |
C |
p. 82-93
|
artikel
|
| 13 |
Evidence that thiol group modification and reactive oxygen species are involved in hydrogen sulfide-induced mitochondrial permeability transition pore opening in rat cerebellum
|
de Moura Alvorcem, Leonardo
|
|
2019
|
47 |
C |
p. 141-150
|
artikel
|
| 14 |
Hypoxia-reoxygenation of primary astrocytes results in a redistribution of mitochondrial size and mitophagy
|
Quintana, Dominic D.
|
|
2019
|
47 |
C |
p. 244-255
|
artikel
|
| 15 |
Increased energetic demand supported by mitochondrial electron transfer chain and astrocyte assistance is essential to maintain the compensatory ability of the dopaminergic neurons in an animal model of early Parkinson's disease
|
Kuter, Katarzyna Z.
|
|
2019
|
47 |
C |
p. 227-237
|
artikel
|
| 16 |
Involvement of increased p53 expression in the decrease of mitochondrial DNA copy number and increase of SUVmax of FDG-PET scan in esophageal squamous cell carcinoma
|
Lin, Chen-Sung
|
|
2019
|
47 |
C |
p. 54-63
|
artikel
|
| 17 |
Is mitochondrial DNA profiling predictive for athletic performance?
|
Stefàno, Erika
|
|
2019
|
47 |
C |
p. 125-138
|
artikel
|
| 18 |
Leukocyte mitochondrial DNA copy number as a potential biomarker indicating poor outcome in biliary atresia and its association with oxidative DNA damage and telomere length
|
Udomsinprasert, Wanvisa
|
|
2019
|
47 |
C |
p. 1-9
|
artikel
|
| 19 |
Mitochondrial dynamics, a key executioner in neurodegenerative diseases
|
Panchal, Komal
|
|
2019
|
47 |
C |
p. 151-173
|
artikel
|
| 20 |
Mitochondrial dysfunction and gut microbiota imbalance: An intriguing relationship in chronic kidney disease
|
Mafra, Denise
|
|
2019
|
47 |
C |
p. 206-209
|
artikel
|
| 21 |
Mitochondrial oxidative phosphorylation capacity of cryopreserved cells
|
Lauridsen, Poul Ejner
|
|
2019
|
47 |
C |
p. 47-53
|
artikel
|
| 22 |
Mito-nuclear interactions modify Drosophila exercise performance
|
Sujkowski, Alyson
|
|
2019
|
47 |
C |
p. 188-205
|
artikel
|
| 23 |
Molecular dynamics simulations on apo ADP/ATP carrier shed new lights on the featured motif of the mitochondrial carriers
|
Yi, Qiuzi
|
|
2019
|
47 |
C |
p. 94-102
|
artikel
|
| 24 |
Myasthenia graves-like symptoms associated with rare mitochondrial mutation (m.5728T>C)
|
Tarnopolsky, Mark
|
|
2019
|
47 |
C |
p. 139-140
|
artikel
|
| 25 |
Natural variability of daily physical activity measured by accelerometry in children with a mitochondrial disease
|
de Vries, Pascal R.
|
|
2019
|
47 |
C |
p. 30-37
|
artikel
|
| 26 |
Novel proteomic changes in brain mitochondria provide insights into mitochondrial dysfunction in mouse models of Huntington's disease
|
Agrawal, Sonal
|
|
2019
|
47 |
C |
p. 318-329
|
artikel
|
| 27 |
Overexpression of carbamoyl-phosphate synthase 1 significantly improves ureagenesis of human liver HepaRG cells only when cultured under shaking conditions
|
Adam, Aziza A.A.
|
|
2019
|
47 |
C |
p. 298-308
|
artikel
|
| 28 |
Overview of thioredoxin system and targeted therapies for acute leukemia
|
Xie, Weiling
|
|
2019
|
47 |
C |
p. 38-46
|
artikel
|
| 29 |
PDE2 regulates membrane potential, respiration and permeability transition of rodent subsarcolemmal cardiac mitochondria
|
Liu, Dawei
|
|
2019
|
47 |
C |
p. 64-75
|
artikel
|
| 30 |
Physical exercise positively modulates DOX-induced hepatic oxidative stress, mitochondrial dysfunction and quality control signaling
|
Santos-Alves, Estela
|
|
2019
|
47 |
C |
p. 103-113
|
artikel
|
| 31 |
Prenatal onset of mitochondrial disease is associated with sideroflexin 4 deficiency
|
Sofou, Kalliopi
|
|
2019
|
47 |
C |
p. 76-81
|
artikel
|
| 32 |
Pyridine nucleotide-disulphide oxidoreductase domain 2 (PYROXD2): Role in mitochondrial function
|
Wang, Tao
|
|
2019
|
47 |
C |
p. 114-124
|
artikel
|
| 33 |
Splitting the functions of Rim2, a mitochondrial iron/pyrimidine carrier
|
Knight, Simon A.B.
|
|
2019
|
47 |
C |
p. 256-265
|
artikel
|
| 34 |
Targeted next generation sequencing identifies novel pathogenic variants and provides molecular diagnoses in a cohort of pediatric and adult patients with unexplained mitochondrial dysfunction
|
Nogueira, Célia
|
|
2019
|
47 |
C |
p. 309-317
|
artikel
|
| 35 |
Temporal profile of serum mitochondrial DNA (mtDNA) in patients with aneurysmal subarachnoid hemorrhage (aSAH)
|
Chaudhry, Shafqat Rasul
|
|
2019
|
47 |
C |
p. 218-226
|
artikel
|
| 36 |
The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort
|
Piekutowska-Abramczuk, Dorota
|
|
2019
|
47 |
C |
p. 179-187
|
artikel
|
| 37 |
The relevance of the supramolecular arrangements of the respiratory chain complexes in human diseases and aging
|
Ramírez-Camacho, Ixchel
|
|
2019
|
47 |
C |
p. 266-272
|
artikel
|
| 38 |
Withaferin A-mediated apoptosis in breast cancer cells is associated with alterations in mitochondrial dynamics
|
Sehrawat, Anuradha
|
|
2019
|
47 |
C |
p. 282-293
|
artikel
|
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