X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (58) 58
animals (44) 44
humans (35) 35
mice (29) 29
genetics & heredity (22) 22
biochemistry & molecular biology (19) 19
genes (17) 17
research (17) 17
cell biology (15) 15
molecular sequence data (15) 15
genetic aspects (14) 14
base sequence (12) 12
cell differentiation (12) 12
expression (12) 12
homeodomain proteins - genetics (12) 12
gene expression (11) 11
muscle, skeletal - metabolism (11) 11
proteins (11) 11
cell line (10) 10
female (10) 10
molecular biology (10) 10
muscular dystrophy, facioscapulohumeral - genetics (10) 10
mutation (10) 10
article (9) 9
cells (9) 9
cells, cultured (9) 9
gene expression regulation (9) 9
gene expression regulation, developmental (9) 9
male (9) 9
activation (8) 8
amino acid sequence (8) 8
gene (8) 8
muscles - cytology (8) 8
myod (8) 8
transfection (8) 8
adult (7) 7
cell lines (7) 7
chromosomes (7) 7
congenital, hereditary, and neonatal diseases and abnormalities (7) 7
developmental biology (7) 7
family (7) 7
fibroblasts (7) 7
gene-expression (7) 7
genetics (7) 7
homeodomain proteins - metabolism (7) 7
mice, transgenic (7) 7
multidisciplinary sciences (7) 7
musculoskeletal diseases (7) 7
myotonic dystrophy - genetics (7) 7
oligonucleotide array sequence analysis (7) 7
rna (7) 7
ctg repeat (6) 6
dna (6) 6
dna-binding proteins - metabolism (6) 6
facioscapulohumeral muscular-dystrophy (6) 6
messenger-rna (6) 6
muscle (6) 6
musculoskeletal system (6) 6
nuclear proteins - genetics (6) 6
physiological aspects (6) 6
skeletal-muscle (6) 6
transcription factors - genetics (6) 6
basic helix-loop-helix transcription factors (5) 5
brain - metabolism (5) 5
chick embryo (5) 5
chromatin (5) 5
chromosome mapping (5) 5
dna methylation (5) 5
dna rearrangements (5) 5
dux4 (5) 5
health aspects (5) 5
methylation (5) 5
middle aged (5) 5
muscle development (5) 5
muscle, skeletal - cytology (5) 5
myoblasts (5) 5
myod protein (5) 5
myogenesis (5) 5
myotonic dystrophy (5) 5
myotonin-protein kinase (5) 5
neurology (5) 5
phenotype (5) 5
protein (5) 5
protein-serine-threonine kinases - genetics (5) 5
rna, messenger - metabolism (5) 5
transcription factors (5) 5
aged (4) 4
binding (4) 4
binding sites (4) 4
cell cycle (4) 4
cell differentiation - genetics (4) 4
cellular differentiation (4) 4
chromosomal proteins, non-histone - genetics (4) 4
cultured cells (4) 4
d4z4 (4) 4
differentiation (4) 4
dna-binding (4) 4
dna-binding proteins - genetics (4) 4
fshd (4) 4
genetic vectors (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5999, pp. 1650 - 1653
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2013, Volume 24, Issue 1, pp. 79 - 85
Journal Article
Journal Article
PLOS Genetics, ISSN 1553-7390, 2013, Volume 9, Issue 4, pp. e1003415 - e1003415
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2016, Volume 98, Issue 5, pp. 1020 - 1029
Journal Article
Journal Article
Journal Article
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2015, Volume 26, Issue 2, pp. 181 - 186
Highlights • Many national registries now exist facilitating patient access to trials. • New functional and patient reported outcome measure is being... 
Neurology | REPEAT | GENE | D4Z4 | FSHD | MUSCLE | NEUROSCIENCES | CLINICAL NEUROLOGY | Magnetic Resonance Imaging | New York | Outcome Assessment (Health Care) | Education | Muscular Dystrophy, Facioscapulohumeral - diagnosis | Humans | Biomarkers | Clinical Trials as Topic | Electromyography | Clinical trials | Diagnostic imaging | Index Medicus
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 10/2014, Volume 24, Issue 9-10, pp. 793 - 793
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2014, Volume 24, Issue 9, pp. 793 - 793
Fascioscapulohumeral muscular dystrophy (FSHD) is associated with partial chromatin relaxation of the D4Z4 macrosatellite repeat array localized on chromosome... 
Neurology
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2016, Volume 24, Issue 1, pp. 78 - 85
Journal Article
Epigenetics, ISSN 1559-2294, 06/2012, Volume 7, Issue 6, pp. 579 - 584
Journal Article