X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
msto1 (6) 6
ataxia (4) 4
myopathy (4) 4
humans (3) 3
mitochondrial dynamics (3) 3
mutation (3) 3
proteins (3) 3
ataxia - etiology (2) 2
ataxia - genetics (2) 2
brief report (2) 2
brief reports (2) 2
cell cycle proteins - genetics (2) 2
cells (2) 2
cerebellar ataxia (2) 2
child (2) 2
child, preschool (2) 2
cytoskeletal proteins - genetics (2) 2
drosophila (2) 2
female (2) 2
fibroblasts (2) 2
fission (2) 2
fusion (2) 2
genes (2) 2
genetic aspects (2) 2
genetics & heredity (2) 2
index medicus (2) 2
infant (2) 2
infant, newborn (2) 2
medicine, research & experimental (2) 2
mitochondria (2) 2
mitochondrial dna (2) 2
mitochondrial dynamics - genetics (2) 2
mitochondrial dynamics - physiology (2) 2
mitochondrial fusion (2) 2
morphology (2) 2
muscular diseases - etiology (2) 2
muscular diseases - genetics (2) 2
mutation - genetics (2) 2
mutations (2) 2
neurosciences (2) 2
protein (2) 2
recessive mutations (2) 2
rna (2) 2
saccharomyces (2) 2
skeletal abnormalities (2) 2
aggregation (1) 1
als (1) 1
amyotrophic lateral sclerosis (1) 1
amyotrophic-lateral-sclerosis (1) 1
analysis (1) 1
animal genetic engineering (1) 1
animals (1) 1
association (1) 1
cardiovascular diseases - physiopathology (1) 1
cell cycle proteins (1) 1
cerebellar atrophy (1) 1
cerebellum (1) 1
children's hospitals (1) 1
clinical neurology (1) 1
cytoplasm (1) 1
cytoskeletal proteins (1) 1
diabetes mellitus - physiopathology (1) 1
disease (1) 1
disorder (1) 1
division (1) 1
dna-sequencing data (1) 1
dnm1l (1) 1
dominant optic atrophy (1) 1
elméleti orvostudományok (1) 1
encephalopathy (1) 1
endocrinology & metabolism (1) 1
expression (1) 1
family (1) 1
fbxl4 (1) 1
frontotemporal lobar degeneration (1) 1
fusion protein (1) 1
gene (1) 1
genetics, gene therapy & genetic disease (1) 1
lactates (1) 1
lactic acid (1) 1
localization (1) 1
mechanisms (1) 1
medical colleges (1) 1
medical genetics (1) 1
medical research (1) 1
medicine, experimental (1) 1
membrane fusion (1) 1
metabolism (1) 1
mff (1) 1
mfn2 (1) 1
misato (1) 1
mitochondria] fission (1) 1
mitochondrial (1) 1
mitochondrial degradation (1) 1
mitochondrial disease (1) 1
mitochondrial diseases - physiopathology (1) 1
mitochondrial disorder (1) 1
mitochondrial fission (1) 1
mitochondrial proteins - metabolism (1) 1
mitophagy (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


European Journal of Medical Genetics, ISSN 1769-7212, 2019
Human MSTO1 is involved in the regulation of mitochondrial distribution and morphology and its unregulated expression leads to mitochondrial disorder. Despite... 
Mutations | MSTO1 | Whole exome sequencing | Cerebellar ataxia | Mitochondrial disorder
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 06/2019, Volume 29, Issue 6, pp. 448 - 455
Recessive mutations in the gene, encoding for a mitochondrial distribution and morphology regulator, have been recently described in a very limited number of... 
Cerebellar atrophy | Ataxia | MSTO1 | Muscular dystrophy | Progressive cerebellar involvement | PROTEIN | MITOCHONDRIAL | RECESSIVE MUTATIONS | MYOPATHY | NEUROSCIENCES | CLINICAL NEUROLOGY
Journal Article
Frontiers in Molecular Neuroscience, ISSN 1662-5099, 12/2018, Volume 11, pp. 463 - 463
Amyotrophic lateral sclerosis (ALS) is a late-onset progressive neurodegenerative disorder that affects both upper and lower motor neurons, leading to muscle... 
ALS | Amyotrophic lateral sclerosis | Zebrafish | TARDBP | TDP-43 | RECESSIVE MUTATIONS | AMYOTROPHIC-LATERAL-SCLEROSIS | FRONTOTEMPORAL LOBAR DEGENERATION | amyotrophic lateral sclerosis | NEUROSCIENCES | FAMILY | SPINOCEREBELLAR ATAXIA | MSTO1 | zebrafish | EXPRESSION | AGGREGATION | MOTOR DEFICITS | Animal genetic engineering | Nervous system diseases | RNA | Analysis | Protein binding
Journal Article
No results were found for your search.

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