| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A looming role of mitochondrial calcium in dictating the lung epithelial integrity and pathophysiology of lung diseases
|
Ray, Archita
|
|
|
55 |
C |
p. 111-121
|
artikel
|
| 2 |
Associations of mitochondrial DNA copy number and deletion rate with early pregnancy loss
|
Ye, Mujin
|
|
|
55 |
C |
p. 48-53
|
artikel
|
| 3 |
ATM mediated-p53 signaling pathway forms a novel axis for senescence control
|
Hwang, Su Young
|
|
|
55 |
C |
p. 54-63
|
artikel
|
| 4 |
Complex I deficiency, due to NDUFAF4 mutations, causes severe mitochondrial dysfunction and is associated to early death and dysmorphia
|
Ugarteburu, Olatz
|
|
|
55 |
C |
p. 78-84
|
artikel
|
| 5 |
Detection of mitochondria-pertinent components in exosomes
|
Wang, Xiaowan
|
|
|
55 |
C |
p. 100-110
|
artikel
|
| 6 |
Diagnostic value of circulating cell-free mtDNA in patients with suspected thyroid cancer: ND4/ND1 ratio as a new potential plasma marker
|
Jiang, Zhiying
|
|
|
55 |
C |
p. 145-153
|
artikel
|
| 7 |
Distinguishing mitochondrial DNA and NUMT sequences amplified with the precision ID mtDNA whole genome panel
|
Cihlar, Jennifer Churchill
|
|
|
55 |
C |
p. 122-133
|
artikel
|
| 8 |
Editorial Board
|
|
|
|
55 |
C |
p. ii
|
artikel
|
| 9 |
Homoplasmic deleterious MT-ATP6/8 mutations in adult patients
|
Rucheton, Benoit
|
|
|
55 |
C |
p. 64-77
|
artikel
|
| 10 |
Low mitochondrial DNA copy number is associated with poor prognosis and treatment resistance in glioblastoma
|
Sravya, Palavalasa
|
|
|
55 |
C |
p. 154-163
|
artikel
|
| 11 |
Mental health and health related quality of life in mitochondrial POLG disease
|
Hikmat, Omar
|
|
|
55 |
C |
p. 95-99
|
artikel
|
| 12 |
Mitochondrial abnormalities in neurodegenerative models and possible interventions: Focus on Alzheimer’s disease, Parkinson’s disease, Huntington’s disease
|
Pantiya, Patcharapong
|
|
|
55 |
C |
p. 14-47
|
artikel
|
| 13 |
Placental mitochondrial DNA mutations and copy numbers in intrauterine growth restricted (IUGR) pregnancy
|
Naha, Ritam
|
|
|
55 |
C |
p. 85-94
|
artikel
|
| 14 |
The contribution of uncoupling protein 2 to mitochondrial Ca2+ homeostasis in health and disease – A short revisit
|
Koshenov, Zhanat
|
|
|
55 |
C |
p. 164-173
|
artikel
|
| 15 |
The effect of short-term methionine restriction on hydrogen peroxide metabolism in Fischer-344 rat skeletal muscle mitochondria
|
Tamanna, Nahid
|
|
|
55 |
C |
p. 1-7
|
artikel
|
| 16 |
The mitochondrial DNA variant m.9032T > C in MT-ATP6 encoding p.(Leu169Pro) causes a complex mitochondrial neurological syndrome
|
Knight, Kaz M.
|
|
|
55 |
C |
p. 8-13
|
artikel
|
| 17 |
The use of a MITO-Porter to deliver exogenous therapeutic RNA to a mitochondrial disease’s cell with a A1555G mutation in the mitochondrial 12S rRNA gene results in an increase in mitochondrial respiratory activity
|
Yamada, Yuma
|
|
|
55 |
C |
p. 134-144
|
artikel
|
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