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beta-sarcoglycan (272) 272
humans (197) 197
muscular dystrophies - genetics (112) 112
male (102) 102
mutations (98) 98
female (96) 96
gamma-sarcoglycan (94) 94
sarcoglycans (92) 92
animals (90) 90
gene (89) 89
membrane glycoproteins - genetics (83) 83
cytoskeletal proteins - genetics (82) 82
neurosciences (79) 79
clinical neurology (78) 78
muscular dystrophy (76) 76
skeletal-muscle (75) 75
adult (72) 72
girdle muscular-dystrophy (72) 72
glycoprotein complex (72) 72
genetics & heredity (69) 69
child (63) 63
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adolescent (57) 57
biochemistry & molecular biology (57) 57
mice (57) 57
muscle, skeletal - metabolism (54) 54
delta-sarcoglycan (53) 53
complex (47) 47
alpha-sarcoglycan (46) 46
dystroglycans (45) 45
molecular sequence data (45) 45
index medicus (43) 43
muscle, skeletal - pathology (43) 43
sarcoglycan (43) 43
immunohistochemistry (42) 42
dystrophin (41) 41
membrane glycoproteins - metabolism (40) 40
missense mutations (40) 40
cytoskeletal proteins - metabolism (39) 39
phenotype (39) 39
cell biology (38) 38
muscle (38) 38
sarcoglycans - genetics (38) 38
deficiency (37) 37
dystrophin - metabolism (37) 37
expression (37) 37
linkage (37) 37
pedigree (37) 37
muscular dystrophies - metabolism (36) 36
limb-girdle muscular dystrophy (35) 35
protein (35) 35
dystrophin - genetics (33) 33
muscular dystrophies - pathology (33) 33
sarcoglycan complex (33) 33
cytoskeletal proteins - deficiency (32) 32
membrane glycoproteins - deficiency (32) 32
proteins (31) 31
amino acid sequence (30) 30
dna mutational analysis (30) 30
maps (29) 29
sarcoglycans - metabolism (29) 29
base sequence (28) 28
biopsy (28) 28
chromosome mapping (26) 26
epsilon-sarcoglycan (26) 26
extracellular-matrix (26) 26
glycoprotein (26) 26
middle aged (26) 26
recessive muscular-dystrophy (26) 26
child, preschool (25) 25
genes, recessive (25) 25
muscular dystrophies, limb-girdle - genetics (25) 25
utrophin (22) 22
muscular dystrophies - classification (21) 21
sarcoglycanopathy (21) 21
dystroglycan (20) 20
dystrophin-glycoprotein complex (20) 20
identification (20) 20
mice, knockout (20) 20
musculoskeletal diseases (20) 20
dysferlin (19) 19
genetic aspects (19) 19
limb girdle muscular dystrophy (19) 19
localization (19) 19
muscle proteins - genetics (19) 19
research (19) 19
adhalin deficiency (18) 18
blotting, western (18) 18
calpain - genetics (18) 18
duchenne muscular-dystrophy (18) 18
age of onset (17) 17
genetic linkage (17) 17
genetics (17) 17
genotype (17) 17
muscle, skeletal - chemistry (17) 17
muscular dystrophies - physiopathology (17) 17
deficient mice (16) 16
fluorescent antibody technique (16) 16
glycoprotein-complex (16) 16
linkage analysis (16) 16
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MOVEMENT DISORDERS, ISSN 0885-3185, 11/2016, Volume 31, Issue 11, pp. 1694 - 1703
BackgroundMyoclonus-dystonia is a neurogenic movement disorder caused by mutations in the gene encoding -sarcoglycan. By contrast, mutations in the -, -, -,... 
NERVOUS-SYSTEM | GAMMA-SARCOGLYCAN | PLASMA-MEMBRANE | CLINICAL NEUROLOGY | ALPHA-SARCOGLYCAN | sarcoglycan | ZETA-SARCOGLYCAN | dystonia | GLYCOPROTEIN COMPLEX | DYT11 | MOLECULAR PATHOGENESIS | PSYCHIATRIC-DISORDERS | BETA-SARCOGLYCAN | DELTA-SARCOGLYCAN
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 05/2019, Volume 9, Issue 1, pp. 6915 - 15
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 12/2018, Volume 129, pp. 364 - 371
Journal Article
Neurotherapeutics, ISSN 1933-7213, 10/2018, Volume 15, Issue 4, pp. 849 - 862
Journal Article
BMC Genomics, ISSN 1471-2164, 03/2018, Volume 19, Issue 1, pp. 202 - 14
Background: White striping (WS) is an emerging muscular defect occurring on breast and thigh muscles of broiler chickens. It is characterized by the presence... 
QTL | Chicken | GWAS | EQTL | Meat quality | White striping | FED REPRESENTATIVE 1957 | COMMERCIAL CONDITIONS | CARCASS COMPOSITION | GIRDLE MUSCULAR-DYSTROPHY | eQTL | SKELETAL-MUSCLE | MYOPATHIES | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ULTIMATE PH | GENETICS & HEREDITY | BETA-SARCOGLYCAN | FILLETS | MUTATIONS | Quantitative trait loci | Usage | Quality | Breast | Genetic aspects | Research | Meat
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 13624 - 10
Journal Article
FRONTIERS IN GENETICS, ISSN 1664-8021, 01/2019, Volume 9, p. 727
Background: Limb-girdle muscular dystrophy (LGMD) is an increasingly heterogeneous category of inherited muscle diseases, mainly affecting the muscles of... 
nonsense mutation | SPLICE-SITE VARIANT | homozygous variant | SARCOGLYCAN COMPLEX | limb-girdle muscular dystrophies | LGMD | SGCD | GENE | GENETICS & HEREDITY | BETA-SARCOGLYCAN | LGMD2F | OSTEOGENESIS IMPERFECTA | targeted NGS
Journal Article
Frontiers in Bioscience - Landmark, ISSN 1093-9946, 01/2016, Volume 21, Issue 4, pp. 744 - 756
Journal Article
MBIO, ISSN 2150-7511, 03/2019, Volume 10, Issue 2, p. e02869-18
Recognition of functional receptors by viruses is a key determinant for their host range, tissue tropism, and disease potential. The highly pathogenic Lassa... 
ALPHA-DYSTROGLYCAN | proteomics | tropism | viral entry | MUSCULAR-DYSTROPHY | MICROBIOLOGY | virus receptor | LYMPHOCYTIC CHORIOMENINGITIS VIRUS | SARCOGLYCAN COMPLEX | PROTEIN COMPLEX | arenavirus | OLD-WORLD | STRUCTURAL BASIS | BETA-SARCOGLYCAN | LARGE GLYCANS | DELTA-SARCOGLYCAN
Journal Article
Cell, ISSN 0092-8674, 2004, Volume 117, Issue 7, pp. 953 - 964
Reduced ligand binding activity of α-dystroglycan is associated with muscle and central nervous system pathogenesis in a growing number of muscular... 
PERIPHERAL-NERVE | HUMAN LARGE GENE | ALPHA-DYSTROGLYCAN | CONGENITAL MUSCULAR-DYSTROPHY | LAMININ | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCOPROTEIN COMPLEX | BETA-SARCOGLYCAN | EXTRACELLULAR-MATRIX | SARCOGLYCAN COMPLEX | DEFICIENCY | CELL BIOLOGY | Protein Structure, Tertiary | Receptors, Laminin - metabolism | Rabbits | Recombinant Fusion Proteins - isolation & purification | Membrane Glycoproteins - metabolism | Cytoskeletal Proteins - genetics | Membrane Glycoproteins - chemistry | Cells, Cultured | Muscle, Skeletal - metabolism | Glycosylation | Stem Cells - cytology | Cytoskeletal Proteins - chemistry | Recombinant Fusion Proteins - chemistry | Dystroglycans | Recombinant Fusion Proteins - metabolism | Blotting, Western | Membrane Glycoproteins - genetics | Mice, Knockout | Glycosyltransferases - metabolism | Animals | Adenoviridae - genetics | Cytoskeletal Proteins - metabolism | Mice | Protein Processing, Post-Translational | Laminin | Research | Gene expression | Mucins | Muscle; Skeletal/metabolism | Protein Processing; Post-Translational | Blotting; Western | Research Support; U.S. Gov't; P.H.S | Receptors; Laminin/metabolism | Cells; Cultured | Glycosyltransferases/metabolism | Protein Structure; Tertiary | Mice; Knockout | Membrane Glycoproteins/chemistry/genetics/metabolism | Adenoviridae/genetics | Research Support; Non-U.S. Gov't | Cytoskeletal Proteins/chemistry/genetics/metabolism | Stem Cells/cytology | Recombinant Fusion Proteins/chemistry/isolation & purification/metabolism
Journal Article