X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (670) 670
Publication (97) 97
Book Chapter (25) 25
Book Review (8) 8
Book / eBook (5) 5
Dissertation (2) 2
Conference Proceeding (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (393) 393
index medicus (282) 282
female (209) 209
male (206) 206
mutation (191) 191
clinical neurology (172) 172
mitochondrial dna (148) 148
dna, mitochondrial - genetics (146) 146
middle aged (128) 128
neurosciences (125) 125
adult (120) 120
genetics & heredity (112) 112
article (90) 90
aged (88) 88
genetics (87) 87
disease (85) 85
abridged index medicus (74) 74
mitochondria (70) 70
genetic aspects (69) 69
research (67) 67
phenotype (65) 65
mutations (64) 64
mitochondrial diseases - genetics (63) 63
animals (60) 60
mutation - genetics (59) 59
adolescent (55) 55
young adult (52) 52
pedigree (51) 51
child (47) 47
risk factors (47) 47
gene (46) 46
mtdna (46) 46
neurology (44) 44
gene mutations (43) 43
cohort studies (39) 39
deoxyribonucleic acid--dna (38) 38
genomes (38) 38
genotype (38) 38
biochemistry & molecular biology (37) 37
diagnosis (37) 37
genetic predisposition to disease (37) 37
mitochondria - genetics (37) 37
parkinson disease - genetics (37) 37
heteroplasmy (36) 36
point mutation (36) 36
case-control studies (34) 34
dna (34) 34
magnetic resonance imaging (34) 34
hereditary optic neuropathy (33) 33
physiological aspects (33) 33
dna mutational analysis (31) 31
genetic variation (30) 30
health aspects (30) 30
medical research (30) 30
muscle, skeletal - pathology (30) 30
age of onset (29) 29
aged, 80 and over (28) 28
cell biology (28) 28
genes (28) 28
mitochondrial diseases (28) 28
myopathy (28) 28
parkinson's disease (28) 28
analysis (27) 27
progressive external ophthalmoplegia (27) 27
dna, mitochondrial (26) 26
haplotypes (25) 25
mitochondrial disease (25) 25
brain - pathology (24) 24
child, preschool (24) 24
deletions (24) 24
gene frequency (24) 24
genomics (24) 24
gtp phosphohydrolases - genetics (24) 24
ataxia (23) 23
brain (23) 23
population (23) 23
research article (23) 23
eye diseases (22) 22
mice (22) 22
prevalence (22) 22
neurodegeneration (21) 21
ophthalmology (21) 21
association (20) 20
heterozygote (20) 20
melas (20) 20
dementia (19) 19
disorders (19) 19
dna-directed dna polymerase - genetics (19) 19
epidemiology (19) 19
medicine (19) 19
mitochondria - metabolism (19) 19
optic atrophy (19) 19
original (19) 19
protein (19) 19
studies (19) 19
variants (19) 19
alleles (18) 18
dna polymerase gamma (18) 18
dominant optic atrophy (18) 18
medicine, general & internal (18) 18
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Cell research, ISSN 1001-0602, 07/2019, Volume 29, Issue 10, pp. 781 - 782
Journal Article
JAMA Neurology, ISSN 2168-6149, 01/2017, Volume 74, Issue 1, pp. 11 - 13
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 2279 - 9
Although mitochondrial dysfunction plays a key role in the pathophysiology of acute kidney injury (AKI), the influence of mitochondrial genetic variability in... 
MORTALITY | SURVIVAL | DNA HAPLOGROUPS | MODELS | MULTIDISCIPLINARY SCIENCES | DISEASE | SUSCEPTIBILITY | VALIDATION | HEMODIALYSIS | ACUTE-RENAL-FAILURE | DYSFUNCTION | Heart | Mitochondria | Statistical analysis | Kidneys | Diabetes mellitus | Surgery | Phylogenetics | Population studies | Phylogeny
Journal Article
PLoS genetics, ISSN 1553-7404, 05/2018, Volume 14, Issue 5, p. e1007364
[This corrects the article DOI: 10.1371/journal.pgen.1007126.]. 
Journal Article
Neuroscience Letters, ISSN 0304-3940, 09/2019, Volume 710, p. 132932
Mitochondrial dysfunction is associated with neuroinflammation and neurodegenerative disease, but its role as a driver in these processes is uncertain.... 
Harding’s disease | Mitochondria | Multiple sclerosis | Neurodegeneration | Neuroinflammation | Leber’s hereditary optic neuropathy | LHON-MS | Harding's disease | Leber's hereditary optic neuropathy
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 07/2019, Volume 10, Issue 1, pp. 3280 - 14
Somatic mutations in the mitochondrial genome (mtDNA) have been linked to multiple disease conditions and to ageing itself. In Drosophila, knock-in of a... 
POINT MUTATIONS | STRANDED-DNA | STAGE | MULTIDISCIPLINARY SCIENCES | DISEASE | MODEL | MELANOGASTER | DELETIONS | DNA MUTATIONS | GENOME | MOLECULAR-MECHANISMS | Phenotypes | Drosophila | Genomes | Mitochondrial DNA | Polymerase | Mitochondria | Depletion | Insects | Proofreading | Heteroplasmy | Aging | Mutation | Fitness | Cytidine deaminase
Journal Article
Seminars in Cell & Developmental Biology, ISSN 1084-9521, 10/2019
Journal Article
Brain, ISSN 0006-8950, 07/2013, Volume 136, Issue 7, pp. e237 - e237
Yu-Wai-Man and Chinnery respond to Stephanie Leruez et al.'s commentary (same journal issue) on Yu-Wai-Man et al.'s original article Multi-system neurological... 
Journal Article
Journal Article