X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (106) 106
Book Review (16) 16
Publication (6) 6
Book / eBook (5) 5
Dissertation (4) 4
Magazine Article (2) 2
Newspaper Article (2) 2
Book Chapter (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (66) 66
humans (61) 61
female (36) 36
male (28) 28
oxidative phosphorylation (24) 24
dna, mitochondrial - genetics (23) 23
clinical neurology (21) 21
mutation (21) 21
adult (18) 18
genetics & heredity (18) 18
middle aged (18) 18
child (13) 13
molecular sequence data (13) 13
abridged index medicus (12) 12
base sequence (12) 12
adolescent (11) 11
cytochrome-c-oxidase (11) 11
aged (10) 10
pediatrics (10) 10
hereditary optic neuropathy (9) 9
skeletal-muscle (9) 9
kearns-sayre syndrome (8) 8
lactic-acidosis (8) 8
mutations (8) 8
neurosciences (8) 8
point mutation (8) 8
child, preschool (7) 7
disease (7) 7
dna (7) 7
dna mutational analysis (7) 7
leigh-syndrome (7) 7
mitochondria (7) 7
mitochondrial dna (7) 7
pedigree (7) 7
aged, 80 and over (6) 6
biochemistry & molecular biology (6) 6
infant (6) 6
myopathy (6) 6
phenotype (6) 6
polymerase chain reaction (6) 6
sequence deletion (6) 6
alzheimer disease - genetics (5) 5
animals (5) 5
endocrinology & metabolism (5) 5
gene (5) 5
genetic aspects (5) 5
infant, newborn (5) 5
muscle (5) 5
myoclonic epilepsy (5) 5
parkinsons-disease (5) 5
research (5) 5
risk factors (5) 5
abnormalities (4) 4
biopsy (4) 4
brain - metabolism (4) 4
children (4) 4
complex-i (4) 4
complex-i deficiency (4) 4
dna, mitochondrial (4) 4
health aspects (4) 4
magnetic resonance imaging (4) 4
medical research (4) 4
medicine, research & experimental (4) 4
merrf syndrome - genetics (4) 4
mitochondria - metabolism (4) 4
mitochondrial diseases - diagnosis (4) 4
mitochondrial encephalomyopathies - genetics (4) 4
mitochondrial myopathies - genetics (4) 4
mitochondrial myopathy (4) 4
muscle, skeletal - pathology (4) 4
neurology (4) 4
neuromuscular diseases - genetics (4) 4
nursing (4) 4
parkinson disease - genetics (4) 4
ragged-red fibers (4) 4
saccharomyces-cerevisiae (4) 4
united states (4) 4
young adult (4) 4
age (3) 3
age-associated accumulation (3) 3
alzheimer's disease (3) 3
amino acid sequence (3) 3
blotting, southern (3) 3
brain - pathology (3) 3
cardiomyopathy (3) 3
chromosome deletion (3) 3
cohort studies (3) 3
damage (3) 3
deafness - genetics (3) 3
deficiency (3) 3
deletion (3) 3
deletions (3) 3
diabetes mellitus, type 2 - genetics (3) 3
diabetes mellitus, type 2 - metabolism (3) 3
diagnosis, differential (3) 3
dna - genetics (3) 3
dna damage (3) 3
dna, mitochondrial - metabolism (3) 3
education (3) 3
electron transport complex iv - genetics (3) 3
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


Journal of Inherited Metabolic Disease, ISSN 0141-8955, 2019, Volume 42, Issue 3, pp. 394 - 395
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 4/2010, Volume 25, Issue 4, pp. 529 - 529
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 04/2010, Volume 25, Issue 4, pp. 529 - 529
Journal Article
2005, Oxidative stress and disease series, ISBN 0824754425, xix, 619
Book
Journal of Child Neurology, ISSN 0883-0738, 2008, Volume 23, Issue 9, pp. 1089 - 1090
Journal Article
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 04/1999, Volume 58, Issue 4, pp. 335 - 345
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 09/2008, Volume 23, Issue 9, pp. 1089 - 1090
Journal Article
Genomics, ISSN 0888-7543, 1993, Volume 17, Issue 1, pp. 171 - 184
Journal Article
Cell, ISSN 0092-8674, 1990, Volume 61, Issue 6, pp. 931 - 937
An A to G transition mutation at nucleotide pair 8344 in human mitochondrial DNA (mtDNA) has been identified as the cause of MERRF. The mutation alters the TψC... 
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 1995, Volume 1271, Issue 1, pp. 141 - 151
A wide variety of mitochondrial DNA (mtDNA) mutations have recently been identified in degenerative diseases of the brain, heart, skeletal muscle, kidney and... 
Mitochondrion | Oxidative phosphorylation | mtDNA mutation | HUMAN BRAIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUSCLE | GLUCOKINASE | KEARNS-SAYRE SYNDROME | DIABETES-MELLITUS | MITOCHONDRION | BIOPHYSICS | GENE | COMPLEX-I | INCREASE | OXIDATIVE PHOSPHORYLATION | HEREDITARY OPTIC NEUROPATHY | MTDNA MUTATION | DELETIONS
Journal Article
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.