X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (32) 32
biochemistry & molecular biology (13) 13
genetics & heredity (13) 13
animals (11) 11
molecular sequence data (11) 11
muscular dystrophy (11) 11
muscular dystrophy, facioscapulohumeral - genetics (11) 11
base sequence (10) 10
female (10) 10
gene expression (10) 10
index medicus (10) 10
fshd (9) 9
male (9) 9
amino acid sequence (8) 8
chromosomes (8) 8
cell line (7) 7
chromosome mapping (7) 7
chromosomes, human, pair 4 (7) 7
dna rearrangements (7) 7
facioscapulohumeral muscular-dystrophy (7) 7
genetic aspects (7) 7
musculoskeletal diseases (7) 7
research (7) 7
article (6) 6
cells, cultured (6) 6
congenital, hereditary, and neonatal diseases and abnormalities (6) 6
gene (6) 6
mice (6) 6
neurosciences (6) 6
analysis (5) 5
d4z4 (5) 5
gene expression profiling (5) 5
methylation (5) 5
middle aged (5) 5
muscle, skeletal - metabolism (5) 5
muscular dystrophies - genetics (5) 5
myoblasts - metabolism (5) 5
polymerase chain reaction (5) 5
transcription, genetic (5) 5
adult (4) 4
aged (4) 4
biopsy (4) 4
child (4) 4
chromosomes, human, pair 4 - genetics (4) 4
dna (4) 4
dna methylation (4) 4
expression (4) 4
facioscapulohumeral muscular dystrophy (4) 4
genetic variation (4) 4
genetics (4) 4
icf syndrome (4) 4
immunology (4) 4
muscle (4) 4
mutation (4) 4
repeat (4) 4
repetitive sequences, nucleic acid (4) 4
tandem repeat sequences (4) 4
alleles (3) 3
binding sites (3) 3
chromatin (3) 3
clinical neurology (3) 3
cricetinae (3) 3
development and progression (3) 3
dna - genetics (3) 3
drosophila (3) 3
fibroblasts - metabolism (3) 3
gene mutations (3) 3
gene-expression (3) 3
genes (3) 3
health aspects (3) 3
heterochromatin (3) 3
hybridization (3) 3
hypomethylation (3) 3
in situ hybridization, fluorescence (3) 3
influenza vaccines - immunology (3) 3
karyotyping (3) 3
locus (3) 3
medicine, research & experimental (3) 3
microscopy, fluorescence (3) 3
muscles (3) 3
muscular dystrophy, facioscapulohumeral - metabolism (3) 3
muscular-dystrophy (3) 3
myoblasts (3) 3
oxidative stress (3) 3
phenotype (3) 3
proteins (3) 3
repetitive sequences, nucleic acid - genetics (3) 3
research article (3) 3
risk (3) 3
sequence homology, amino acid (3) 3
vaccines (3) 3
young adult (3) 3
4q35 (2) 2
abridged index medicus (2) 2
actinin - metabolism (2) 2
adolescent (2) 2
adults (2) 2
allergy and immunology (2) 2
amino acids (2) 2
antibodies, viral - blood (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
PLoS Genetics, ISSN 1553-7390, 07/2009, Volume 5, Issue 7, p. e1000559
Facioscapulohumeral dystrophy (FSHD) is an autosomal dominant muscular dystrophy in which no mutation of pathogenic gene(s) has been identified. Instead, the... 
MAMMALIAN CHROMATIN | CONTROL REGION | HP1 PROTEINS | FISSION YEAST | NIPPED-B | ICF SYNDROME | GENETICS & HEREDITY | MUSCULAR-DYSTROPHY | DE-LANGE-SYNDROME | SILENT-CHROMATIN | GENE ACTIVATION
Journal Article
Journal Article
Nature Neuroscience, ISSN 1097-6256, 05/2017, Volume 20, Issue 5, pp. 648 - 660
Journal Article
Brain, ISSN 0006-8950, 2006, Volume 129, Issue 4, pp. 996 - 1013
Journal Article
Annals of Neurology, ISSN 0364-5134, 2005, Volume 58, Issue 4, pp. 569 - 576
Facioscapulohumeral muscular dystrophy (FSHD) progressively affects the facial, shoulder, and upper arm muscles and is associated with contractions of the... 
DIAGNOSIS | REPEAT | GENE | 4Q35 | FSHD | PHENOTYPE | HYBRIDIZATION | CHROMOSOMES | DNA REARRANGEMENTS | LOCUS | NEUROSCIENCES | CLINICAL NEUROLOGY | Genetic Variation | Repetitive Sequences, Nucleic Acid - genetics | Age Factors | Humans | Alleles | Linear Models | Muscular Dystrophy, Facioscapulohumeral - genetics | Methylation | Restriction Mapping | Chromosomes, Human, Pair 4
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 04/2010, Volume 18, Issue 4, pp. 448 - 456
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 10/1997, Volume 139, Issue 2, pp. 507 - 515
PDZ motifs are protein-protein interaction domains that often bind to COOH-terminal peptide sequences. The two PDZ proteins characterized in skeletal muscle,... 
Messenger RNA | Complementary DNA | Neurons | Cell lines | Muscles | Amino acids | Muscular dystrophies | Chromosomes | Genetic mutation | Skeletal muscle | FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY | SKELETAL-MUSCLE | GENE | NITRIC-OXIDE SYNTHASE | IN-SITU HYBRIDIZATION | TUMOR-SUPPRESSOR PROTEIN | C-ELEGANS | DNA REARRANGEMENTS | BINDING | DROSOPHILA | CELL BIOLOGY | Muscle proteins | Cytoskeleton | Analysis
Journal Article
Journal Article