X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
chemistry (20) 20
metallurgy (20) 20
humans (19) 19
organic chemistry (17) 17
derivatives thereof (14) 14
index medicus (14) 14
nucleic acids (14) 14
nucleosides (14) 14
nucleotides (14) 14
sugars (14) 14
male (13) 13
animals (12) 12
female (11) 11
mice (9) 9
cardiac & cardiovascular systems (7) 7
dogs (7) 7
middle aged (7) 7
peripheral vascular disease (7) 7
acyclic, carbocyclic or heterocyclic compounds containingelements other than carbon, hydrogen, halogen, oxygen, nitrogen,sulfur, selenium or tellurium (6) 6
aged (6) 6
analysis (6) 6
beer (6) 6
biochemistry (6) 6
disease models, animal (6) 6
enzymology (6) 6
fermentation or enzyme-using processes to synthesise a desiredchemical compound or composition or to separate optical isomersfrom a racemic mixture (6) 6
genetic aspects (6) 6
microbiology (6) 6
mutation or genetic engineering (6) 6
spirits (6) 6
vinegar (6) 6
wine (6) 6
gene (5) 5
oxidative stress (5) 5
adult (4) 4
atherosclerosis (4) 4
base sequence (4) 4
biochemistry & molecular biology (4) 4
disease (4) 4
dog diseases - genetics (4) 4
genetic research (4) 4
genetics (4) 4
genetics & heredity (4) 4
hematology (4) 4
heterocyclic compounds (4) 4
human necessities (4) 4
hygiene (4) 4
medical colleges (4) 4
medical or veterinary science (4) 4
motor neurons - metabolism (4) 4
muscular atrophy, spinal - genetics (4) 4
neurons (4) 4
preparations for medical, dental, or toilet purposes (4) 4
cells (3) 3
coronary angiography (3) 3
coronary heart disease (3) 3
culture media (3) 3
expression (3) 3
homozygote (3) 3
identification (3) 3
immunohistochemistry (3) 3
in-vivo (3) 3
lysosomal storage (3) 3
medicine & public health (3) 3
medicine, research & experimental (3) 3
mice, transgenic (3) 3
motor neurons - pathology (3) 3
mouse (3) 3
mouse model (3) 3
multidisciplinary sciences (3) 3
mutant mice (3) 3
mutation (3) 3
mutation, missense (3) 3
nervous system (3) 3
neurodegeneration (3) 3
neurology (3) 3
neuronal ceroid-lipofuscinoses - genetics (3) 3
neurosciences (3) 3
pedigree (3) 3
reactive oxygen species - metabolism (3) 3
research (3) 3
risk factors (3) 3
severity of illness index (3) 3
smn protein (3) 3
specific therapeutic activity of chemical compounds ormedicinal preparations (3) 3
survival of motor neuron 1 protein - genetics (3) 3
survival of motor neuron 2 protein - genetics (3) 3
toll-like receptor-4 (3) 3
activation (2) 2
amyotrophic lateral sclerosis (2) 2
animal models (2) 2
animals, newborn (2) 2
anthocyanin (2) 2
apolipoprotein-e (2) 2
article (2) 2
biomedicine (2) 2
biophysics (2) 2
canine (2) 2
cardiology (2) 2
cell survival (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2009, Volume 106, Issue 8, pp. 2794 - 2799
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, p. e46353
Journal Article
Nature Communications, ISSN 2041-1723, 01/2017, Volume 8, Issue 1, p. 14152
Haploinsufficiency of the SLC2A1 gene and paucity of its translated product, the glucose transporter-1 (Glut1) protein, disrupt brain function and cause the... 
SPINAL MUSCULAR-ATROPHY | PERMEABILITY | MULTIDISCIPLINARY SCIENCES | IN-VIVO | BARRIER | MOUSE | CENTRAL-NERVOUS-SYSTEM | MICE | GLUCOSE TRANSPORTERS | ADENOASSOCIATED VIRUSES | HAPLOINSUFFICIENCY
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 09/2010, Volume 30, Issue 36, pp. 12005 - 12019
Spinal muscular atrophy (SMA) is a common (similar to 1: 6400) autosomal recessive neuromuscular disorder caused by a paucity of the survival of motor neuron... 
LOCALIZATION | TERMINALS | PRODUCT | MOUSE MODEL | IN-VIVO | LEADS | RELEASE | IDENTIFICATION | NEUROSCIENCES | NEUROMUSCULAR-JUNCTIONS | SINGLE NUCLEOTIDE | Membrane Potentials - genetics | Age Factors | Synaptic Transmission - genetics | Humans | Gene Expression Regulation, Developmental - genetics | Nerve Degeneration - genetics | Synapses - pathology | Stem Cells - metabolism | Survival of Motor Neuron 2 Protein - metabolism | Choline O-Acetyltransferase - metabolism | Motor Neurons - pathology | Behavior, Animal | Muscular Atrophy, Spinal - genetics | Basic Helix-Loop-Helix Transcription Factors - metabolism | Survival of Motor Neuron 2 Protein - genetics | Isometric Contraction - physiology | Miniature Postsynaptic Potentials - genetics | Neuromuscular Junction - pathology | Disease Models, Animal | Animals, Newborn | Muscular Atrophy, Spinal - mortality | Muscular Atrophy, Spinal - metabolism | Receptors, Cholinergic - metabolism | Synapses - physiology | Kaplan-Meier Estimate | Mice, Transgenic | Oligodendrocyte Transcription Factor 2 | Mutation - genetics | Muscular Atrophy, Spinal - pathology | Motor Neurons - metabolism | Nerve Tissue Proteins - metabolism | Motor Activity - genetics | Patch-Clamp Techniques | Animals | Cell Count - methods | Analysis of Variance | Muscle, Skeletal - physiopathology | Luminescent Proteins - genetics | Mice | Muscle, Skeletal - pathology | Electromyography - methods
Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 2006, Volume 89, Issue 3, pp. 254 - 260
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 02/2009, Volume 106, Issue 8, pp. 2794 - 2799
Journal Article
ISSN 2041-1723, 2017
Haploinsufficiency of the SLC2A1 gene and paucity of its translated product, the glucose transporter-1 (Glut1) protein, disrupt brain function and cause the... 
Neurology | Microcirculation disorders | Brain--Abnormalities | Neurobiology | Glucose
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 09/2010, Volume 30, Issue 36, pp. 12005 - 12019
Spinal muscular atrophy (SMA) is a common (61:6400) autosomal recessive neuromuscular disorder caused by a paucity of the survival of motor neuron (SMN)... 
Journal Article