X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1156) 1156
Book Review (199) 199
Publication (131) 131
Book Chapter (9) 9
Conference Proceeding (5) 5
Data Set (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1009) 1009
humans (768) 768
animals (507) 507
male (435) 435
female (360) 360
sarcoglycans - genetics (332) 332
mice (305) 305
sarcoglycans (295) 295
clinical neurology (287) 287
muscular dystrophies - genetics (274) 274
mutation (266) 266
muscular dystrophy (262) 262
beta-sarcoglycan (250) 250
cytoskeletal proteins - genetics (236) 236
skeletal-muscle (230) 230
membrane glycoproteins - genetics (226) 226
adult (221) 221
neurosciences (220) 220
mutations (201) 201
genetics & heredity (200) 200
glycoprotein complex (199) 199
biochemistry & molecular biology (197) 197
gene (197) 197
dystrophin (195) 195
child (194) 194
sarcoglycan (188) 188
muscle, skeletal - metabolism (181) 181
phenotype (175) 175
adolescent (173) 173
muscle, skeletal - pathology (168) 168
cell biology (156) 156
dystrophin - genetics (147) 147
gamma-sarcoglycan (147) 147
sarcoglycans - metabolism (140) 140
dystrophin - metabolism (136) 136
girdle muscular-dystrophy (134) 134
proteins (130) 130
disease models, animal (124) 124
expression (123) 123
dystroglycans (122) 122
middle aged (122) 122
muscular dystrophies - metabolism (120) 120
delta-sarcoglycan (119) 119
mice, knockout (116) 116
complex (114) 114
immunohistochemistry (114) 114
muscular dystrophies - pathology (113) 113
cytoskeletal proteins - metabolism (112) 112
muscle (106) 106
epsilon-sarcoglycan (105) 105
pedigree (105) 105
child, preschool (103) 103
genetic aspects (103) 103
membrane glycoproteins - metabolism (103) 103
molecular sequence data (103) 103
muscular-dystrophy (102) 102
cardiomyopathy (98) 98
duchenne muscular-dystrophy (97) 97
deficiency (96) 96
alpha-sarcoglycan (95) 95
abridged index medicus (93) 93
membrane glycoproteins - deficiency (93) 93
cytoskeletal proteins - deficiency (91) 91
mice, inbred c57bl (89) 89
research (89) 89
dna mutational analysis (85) 85
dilated cardiomyopathy (84) 84
utrophin (84) 84
cricetinae (80) 80
gene expression (80) 80
dystonic disorders - genetics (79) 79
genetics (79) 79
medicine, research & experimental (79) 79
limb-girdle muscular dystrophy (77) 77
protein (75) 75
analysis (72) 72
article (72) 72
dystrophin-glycoprotein complex (72) 72
sarcoglycan complex (72) 72
sarcoglycans - deficiency (72) 72
muscular dystrophies, limb-girdle - genetics (71) 71
mdx mice (68) 68
mutation - genetics (68) 68
dystroglycan (67) 67
mice, inbred mdx (67) 67
myoclonus - genetics (67) 67
genotype (66) 66
amino acid sequence (65) 65
base sequence (65) 65
genes (64) 64
skeletal muscle (64) 64
dystonia (63) 63
myocardium - metabolism (63) 63
neurology (61) 61
pathology (61) 61
cardiac & cardiovascular systems (60) 60
muscle proteins - genetics (60) 60
biopsy (58) 58
linkage (58) 58
musculoskeletal system (58) 58
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1115) 1115
Spanish (14) 14
Japanese (12) 12
French (6) 6
German (6) 6
Russian (3) 3
Polish (2) 2
Portuguese (2) 2
Chinese (1) 1
Finnish (1) 1
Serbian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


International Journal of Obesity, ISSN 0307-0565, 07/2013, Volume 37, Issue 7, pp. 907 - 913
Journal Article
International Journal of Obesity, ISSN 0307-0565, 04/2015, Volume 39, Issue 4, pp. 650 - 657
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2015, Volume 96, Issue 6, pp. 938 - 947
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2015, Volume 10, Issue 12, pp. e0145602 - e0145602
Journal Article
Cell and Tissue Research, ISSN 0302-766X, 5/2014, Volume 356, Issue 2, pp. 427 - 443
The Sgcb-null mouse, with knocked-down β-sarcoglycan, develops severe muscular dystrophy as in type 2E human limb girdle muscular dystrophy. The mdx mouse,... 
Human Genetics | mdx | Decorin | Collagens | Macrophages | Muscle inflammation | Biomedicine | β-sarcoglycan | Proteomics | Muscle fibrosis | Extracellular matrix | TGF-β | Molecular Medicine | DYSTROPHIN-GLYCOPROTEIN COMPLEX | MESSENGER-RNA EXPRESSION | III COLLAGEN | GIRDLE MUSCULAR-DYSTROPHY | beta-sarcoglycan | CELL BIOLOGY | SKELETAL-MUSCLE | TGF-beta | GROWTH-FACTOR-BETA | GENE-EXPRESSION | MICE | Osteopontin - genetics | Diaphragm - pathology | Transforming Growth Factor beta1 - metabolism | Collagen Type III - metabolism | Collagen Type VI - metabolism | Muscular Dystrophy, Animal - pathology | Collagen Type VI - genetics | RNA, Messenger - biosynthesis | Collagen Type I - genetics | Muscular Dystrophies, Limb-Girdle - genetics | Mice, Inbred mdx | Diaphragm - metabolism | Quadriceps Muscle - pathology | Decorin - genetics | Extracellular Matrix Proteins - metabolism | Macrophages - immunology | Fibrosis - genetics | Collagen Type I - metabolism | Extracellular Matrix Proteins - genetics | Mice, Inbred C57BL | Inflammation - immunology | Transforming Growth Factor beta1 - genetics | Collagen Type III - genetics | Mice, Knockout | Animals | Sarcoglycans - genetics | Dystrophin - genetics | Inflammation - genetics | Mice | Quadriceps Muscle - metabolism | Extracellular Matrix - pathology | Decorin - metabolism | Usage | Collagen | Analysis | Fibrosis | Bone morphogenetic proteins | Inflammation | Transforming growth factors | Dystrophin | Muscular system | Gene expression | Rodents | Muscular dystrophy | Immune system | Index Medicus
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 11/2015, Volume 125, Issue 11, pp. 4186 - 4195
Exon skipping uses antisense oligonucleotides as a treatment for genetic diseases. The antisense oligonucleotides used for exon skipping are designed to bypass... 
HEART | MEDICINE, RESEARCH & EXPERIMENTAL | MURINE SKELETAL-MUSCLE | GLYCOPROTEIN COMPLEX | GENE-EXPRESSION | BETA-SARCOGLYCAN | GAMMA-SARCOGLYCAN | MUTATIONS | DELTA-SARCOGLYCAN | SARCOGLYCAN COMPLEX | DROSOPHILA | Genetic Therapy | Muscular Dystrophy, Animal - genetics | Sequence Deletion | Diaphragm - pathology | Dystrophin-Associated Protein Complex - chemistry | Exons | Humans | Muscle, Skeletal - metabolism | Drosophila melanogaster - genetics | Muscular Dystrophy, Animal - pathology | Recombinant Fusion Proteins - metabolism | Muscular Dystrophies, Limb-Girdle - genetics | Myocardium - metabolism | Oligonucleotides, Antisense - therapeutic use | HEK293 Cells | Protein Engineering | Muscular Dystrophy, Animal - therapy | Diaphragm - metabolism | Sarcolemma - metabolism | Sarcoglycans - biosynthesis | Protein Structure, Tertiary | Oligonucleotides, Antisense - pharmacology | Muscular Dystrophies, Limb-Girdle - therapy | RNA, Messenger - genetics | Sarcoglycans - chemistry | Mice, Transgenic | Myocardium - pathology | Sarcoglycans - deficiency | Protein Interaction Mapping | Animals | Sarcoglycans - genetics | Drosophila Proteins - deficiency | Fibrosis | RNA, Messenger - chemistry | Mice | Drosophila Proteins - genetics | Muscle, Skeletal - pathology | Mutation | Codon, Nonsense - genetics | Care and treatment | Gene mutations | Genetic aspects | Genetic engineering | Health aspects | Muscular dystrophy | Methods | Membrane proteins | Genes | Rodents | Index Medicus | Abridged Index Medicus
Journal Article
Journal Article