X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (174) 174
humans (133) 133
amyotrophic lateral sclerosis (117) 117
neurosciences (115) 115
animals (100) 100
amyotrophic-lateral-sclerosis (97) 97
mutation (65) 65
amyotrophic lateral sclerosis - genetics (64) 64
frontotemporal lobar degeneration (60) 60
mutations (60) 60
als (54) 54
male (54) 54
tdp-43 (54) 54
article (50) 50
female (50) 50
neurology (49) 49
proteins (49) 49
genetic aspects (47) 47
nervous system diseases (46) 46
neurodegeneration (46) 46
neurons (46) 46
protein binding (45) 45
rna-binding protein fus - genetics (45) 45
analysis (43) 43
amyotrophic lateral sclerosis - pathology (40) 40
clinical neurology (40) 40
mice (37) 37
rna-binding protein fus - metabolism (37) 37
pathology (36) 36
rna (36) 36
fus (35) 35
gene (35) 35
cell biology (34) 34
amyotrophic lateral sclerosis - metabolism (33) 33
middle aged (32) 32
biochemistry & molecular biology (30) 30
dementia (30) 30
frontotemporal dementia (30) 30
neurodegenerative diseases (30) 30
sarcoma (30) 30
disease (29) 29
hexanucleotide repeat (28) 28
research article (28) 28
dna-binding proteins - genetics (27) 27
dna-binding proteins - metabolism (27) 27
genes (27) 27
genetics (27) 27
aged (26) 26
binding proteins (26) 26
gene expression (26) 26
adult (25) 25
protein (25) 25
motor neurons - metabolism (23) 23
biology (22) 22
fus protein (22) 22
medicine (22) 22
neuroscience (22) 22
stress granules (21) 21
fus/tls (20) 20
physiological aspects (20) 20
research (20) 20
spinal cord (20) 20
development and progression (19) 19
mutation - genetics (19) 19
disease models, animal (18) 18
nervous system (18) 18
alzheimers-disease (17) 17
molecular biology (17) 17
multidisciplinary sciences (17) 17
science (17) 17
spinal cord - pathology (17) 17
immunohistochemistry (16) 16
medical colleges (16) 16
mental disorders (16) 16
mice, inbred c57bl (16) 16
motor neurons (16) 16
motor-neurons (16) 16
aged, 80 and over (15) 15
brain - pathology (15) 15
c9orf72 (15) 15
cells, cultured (15) 15
degeneration (15) 15
genetics & heredity (15) 15
neurons - metabolism (15) 15
phenotype (15) 15
prion-like domains (15) 15
rna-binding proteins (15) 15
rodents (15) 15
animal models (14) 14
deoxyribonucleic acid--dna (14) 14
medical research (14) 14
messenger-rna (14) 14
mice, transgenic (14) 14
nutritional and metabolic diseases (14) 14
rna-binding protein (14) 14
dna (13) 13
genetic research (13) 13
geriatrics & gerontology (13) 13
internal medicine (13) 13
motor neuron diseases (13) 13
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


Science, ISSN 0036-8075, 2/2009, Volume 323, Issue 5918, pp. 1205 - 1208
Journal Article
Journal Article
Journal Article
Applied Physics Letters, ISSN 0003-6951, 06/2011, Volume 98, Issue 26, pp. 262502 - 262502-3
The ferrohydrodynamic properties of magnetic nanoparticles govern resolution and signal strength in magnetic particle imaging (MPI), a medical imaging modality... 
PHYSICS, APPLIED
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 2009, Volume 390, Issue 3, pp. 947 - 951
Journal Article
Brain Research, ISSN 0006-8993, 2009, Volume 1287, pp. 1 - 19
Abstract To improve delivery of human insulin-like growth factor-1 (hIGF-1) to brain and spinal cord, we generated a soluble IGF-1:tetanus toxin fragment C... 
Neurology | SOD1 G93A transgenic mice | Amyotrophic lateral sclerosis | Drug delivery | IGF-1 | Motor neuron | Fusion protein | Tetanus toxin fragment C | transgenic mice | SOD1 | RETROGRADE AXONAL-TRANSPORT | TETANUS TOXIN | ESCHERICHIA-COLI | AMYOTROPHIC-LATERAL-SCLEROSIS | NEUROSCIENCES | RECEPTOR-BINDING DOMAIN | GANGLIOSIDE BINDING | SOD1(G93A) transgenic mice | MOUSE MODEL | CENTRAL-NERVOUS-SYSTEM | MOTOR-NEURON DEATH | GROWTH-FACTOR-I | Spinal Cord - metabolism | Genetic Vectors - administration & dosage | Humans | Recombinant Fusion Proteins - therapeutic use | Baculoviridae - genetics | Male | Insulin-Like Growth Factor I - genetics | Genetic Vectors - therapeutic use | Amyotrophic Lateral Sclerosis - drug therapy | Motor Neurons - pathology | Tetanus Toxin - genetics | Spinal Cord - pathology | Insulin-Like Growth Factor I - administration & dosage | Female | Insulin-Like Growth Factor I - therapeutic use | Peptide Fragments - genetics | Recombinant Fusion Proteins - administration & dosage | Injections, Spinal | Mice, Inbred C57BL | Peptide Fragments - administration & dosage | Cells, Cultured | Mice, Transgenic | Injections, Intramuscular | Tetanus Toxin - therapeutic use | Disease Progression | Genetic Vectors - genetics | Amyotrophic Lateral Sclerosis - mortality | Motor Neurons - metabolism | Amyotrophic Lateral Sclerosis - pathology | Animals | Tetanus Toxin - administration & dosage | Recombinant Fusion Proteins - genetics | Mice | Peptide Fragments - therapeutic use | Drug Delivery Systems - methods | Spodoptera - genetics | Drugs | Drug delivery systems | Neurons | Analysis | Tetanus | Peptide hormones | Gangliosides | Vehicles
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 07/2009, Volume 385, Issue 3, pp. 380 - 384
Journal Article
JBJS Reviews, ISSN 2329-9185, 04/2016, Volume 4, Issue 4, p. 1
Journal Article
JBJS reviews, 04/2016, Volume 4, Issue 4, p. e51
Segmental motion is a fundamental characteristic of the thoracic spine; however, studies of segmental ranges of motion have not been summarized or analyzed.... 
Humans | Middle Aged | Range of Motion, Articular - physiology | Aged, 80 and over | Adult | Aged | Thoracic Vertebrae - physiology | Thoracic Vertebrae - anatomy & histology
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 07/2019, Volume 402, pp. 62 - 68
to determine the occurrence of homozygous rare, damaging variants in a genetically relatively homogenous group of amyotrophic lateral sclerosis (ALS) patients.... 
ALS | Homozygosity | Whole-exome-sequencing | PROTEIN | FORM | RISK | NEUROSCIENCES | CLINICAL NEUROLOGY | INHIBITION | GENES | JEWISH | COHORT | MUTATIONS | Jews | Amyotrophic lateral sclerosis | Nervous system diseases
Journal Article
Journal Article