X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
alpha-sarcoglycan (112) 112
humans (80) 80
animals (72) 72
beta-sarcoglycan (49) 49
gamma-sarcoglycan (45) 45
mice (45) 45
sarcoglycans (45) 45
skeletal-muscle (41) 41
glycoprotein complex (39) 39
index medicus (38) 38
epsilon-sarcoglycan (37) 37
muscular dystrophy (37) 37
neurosciences (36) 36
male (35) 35
clinical neurology (34) 34
muscular dystrophies - genetics (34) 34
gene (32) 32
sarcoglycans - genetics (31) 31
girdle muscular-dystrophy (30) 30
cytoskeletal proteins - genetics (29) 29
female (29) 29
dystrophin (28) 28
membrane glycoproteins - genetics (28) 28
mutation (28) 28
biochemistry & molecular biology (27) 27
cell biology (27) 27
sarcoglycan (25) 25
genetics & heredity (24) 24
muscle, skeletal - metabolism (24) 24
mutations (24) 24
cytoskeletal proteins - metabolism (23) 23
delta-sarcoglycan (23) 23
child (21) 21
dystroglycans (21) 21
immunohistochemistry (21) 21
membrane glycoproteins - metabolism (21) 21
muscle (21) 21
muscle, skeletal - pathology (21) 21
missense mutations (20) 20
muscular-dystrophy (19) 19
skeletal muscle (19) 19
smooth-muscle (19) 19
dystrophin - metabolism (18) 18
expression (18) 18
medicine, research & experimental (18) 18
complex (17) 17
molecular sequence data (17) 17
sarcoglycans - metabolism (17) 17
dystrophin-glycoprotein complex (16) 16
adult (15) 15
muscular dystrophies - metabolism (15) 15
cytoskeletal proteins - deficiency (14) 14
disease models, animal (14) 14
duchenne muscular-dystrophy (14) 14
membrane glycoproteins - deficiency (14) 14
membrane proteins - metabolism (14) 14
proteins (14) 14
adolescent (13) 13
amino acid sequence (13) 13
child, preschool (13) 13
mice, inbred c57bl (13) 13
utrophin (13) 13
α-sarcoglycan (13) 13
biotechnology & applied microbiology (12) 12
deficiency (12) 12
dystrophin - genetics (12) 12
limb-girdle muscular dystrophy (12) 12
mice, knockout (12) 12
muscular dystrophies, limb-girdle - genetics (12) 12
phenotype (12) 12
recessive muscular-dystrophy (12) 12
deficient mice (11) 11
glycoprotein (11) 11
biopsy (10) 10
dependovirus - genetics (10) 10
extracellular-matrix (10) 10
gene therapy (10) 10
musculoskeletal system (10) 10
nitric-oxide synthase (10) 10
adhalin (9) 9
alpha-sarcoglycan gene (9) 9
cell membrane - metabolism (9) 9
clinical trials (9) 9
dysferlin (9) 9
gene expression (9) 9
genes, recessive (9) 9
genetic therapy (9) 9
genetic therapy - methods (9) 9
middle aged (9) 9
muscle proteins - genetics (9) 9
muscle proteins - metabolism (9) 9
muscle, skeletal - physiopathology (9) 9
muscular dystrophies - pathology (9) 9
sarcoglycan complex (9) 9
sarcolemma (9) 9
adhalin deficiency (8) 8
dna mutational analysis (8) 8
genetic aspects (8) 8
genetic vectors (8) 8
mdx mice (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


SCIENCE TRANSLATIONAL MEDICINE, ISSN 1946-6234, 06/2012, Volume 4, Issue 140
Mesoangioblasts are stem/progenitor cells derived from a subset of pericytes found in muscle that express alkaline phosphatase. They have been shown to... 
PLURIPOTENT STEM-CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | SKELETAL-MUSCLE | THERAPY | MULTIPOTENT | REGENERATION | MESOANGIOBLASTS | GENERATION | GENE-TRANSFER | PERICYTES | ALPHA-SARCOGLYCAN | CELL BIOLOGY
Journal Article
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
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 01/2007, Volume 104, Issue 1, pp. 264 - 269
Duchenne muscular dystrophy is a relatively common disease that affects skeletal muscle, leading to progressive paralysis and death. There is currently no... 
alpha-sarcoglycan-null mice | MULTIDISCIPLINARY SCIENCES | MOUSE | MESOANGIOBLASTS | HCT 1026 | SKELETAL-MUSCLE | SIGNALING PATHWAY | mdx mice | L-ARGININE | GROWTH-FACTOR | skeletal muscle | EXPRESSION | satellite cells
Journal Article
MOLECULAR THERAPY, ISSN 1525-0016, 04/2017, Volume 25, Issue 4, pp. 855 - 869
Limb-girdle muscular dystrophy type 2E (LGMD2E), resulting from mutations in beta-sarcoglycan (SGCB), is a progressive dystrophy with deteriorating muscle... 
MEDICINE, RESEARCH & EXPERIMENTAL | INVOLVEMENT | GIRDLE MUSCULAR-DYSTROPHY | TRANSDUCTION | LIMB-GIRDLE | ALPHA-SARCOGLYCAN | GENE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | VASCULAR DELIVERY | MOUSE MODEL | GENETICS & HEREDITY | VECTORS | EXPRESSION
Journal Article
Nature, ISSN 0028-0836, 11/2008, Volume 456, Issue 7221, pp. 511 - 515
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2010, Volume 11, Issue 11, pp. 1057 - 1065
Summary Background Bortezomib-induced peripheral neuropathy is a dose-limiting toxicity in patients with multiple myeloma, often requiring adjustment of... 
Hematology, Oncology and Palliative Medicine | APOPTOSIS | DEXAMETHASONE | EFFICACY | ONCOLOGY | REFRACTORY MYELOMA | PHASE-II | INDUCTION | STEM-CELL TRANSPLANTATION | NEUROTOXICITY | CANCER | LINES | Peripheral Nervous System Diseases - chemically induced | Prospective Studies | Humans | Middle Aged | Boronic Acids - adverse effects | Gene Expression Profiling | Young Adult | Multiple Myeloma - drug therapy | Time Factors | Antineoplastic Agents - adverse effects | Adult | Odds Ratio | Peripheral Nervous System Diseases - genetics | Genetic Predisposition to Disease | Bortezomib | Multiple Myeloma - diagnosis | Risk Assessment | Europe | Gene Frequency | Risk Factors | Treatment Outcome | Chi-Square Distribution | Adolescent | Pyrazines - adverse effects | Vincristine - adverse effects | Aged | Polymorphism, Single Nucleotide | Neoplasm Staging | Multiple Myeloma - genetics | Antimitotic agents | Care and treatment | Antineoplastic agents | Analysis | Multiple myeloma | Toxicity | Clinical trials | Nervous system | Superoxide dismutase | Single-nucleotide polymorphism | Myeloma | Peripheral neuropathy | DNA repair | Mitochondria | Coding | Cell cycle | Peripheral blood | Age | Peripheral nervous system | Enzymes | Excretion | Data processing | Inflammation | Gene expression | Metabolism | Vincristine | Quality of life | Queens | Caspase-9 | Plasma cells | Peroxisome proliferator-activated receptors | Apoptosis | Cancer
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 07/2018, Volume 233, Issue 7, pp. 5142 - 5159
Journal Article
Journal Article