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Journal Article
Annals of Neurology, ISSN 0364-5134, 08/2018, Volume 84, Issue 2, pp. 234 - 245
ObjectiveDuchenne muscular dystrophy (DMD) is a severe X-linked recessive disease caused by loss-of-function dystrophin (DMD) mutations in boys, who typically... 
SKELETAL-MUSCLE | CELLS | ACTIVATION | TGF-BETA | VARIANTS | ANGIOGENESIS | THROMBOSPONDIN-1 | PHENOTYPE | ASSOCIATION | NEUROSCIENCES | MDX MICE | CLINICAL NEUROLOGY | Regulators | Chromatin | Transforming growth factor-b | Genomes | Single-nucleotide polymorphism | Gene expression | Patients | Loci | Muscular dystrophy | Proteins | Signaling | Coding | Nitric oxide | Duchenne's muscular dystrophy | Dystrophy | Mutation | Growth factors | Dystrophin | Tags | Thrombospondin
Journal Article
Science Translational Medicine, ISSN 1946-6234, 03/2010, Volume 2, Issue 23, pp. 23ra19 - ra19
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2008, Volume 359, Issue 14, pp. 1456 - 1463
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 08/2008, Volume 118, Issue 8, pp. 2908 - 2916
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2008, Volume 105, Issue 19, pp. 6998 - 7003
Significant morbidity and mortality among patients with diabetes mellitus result largely from a greatly increased incidence of microvascular complications.... 
Diabetic angiopathies | Diabetic retinopathy | Kidneys | Diabetes complications | Diabetic nephropathies | Medical genetics | Type 2 diabetes mellitus | Diabetes | Epics | Type 1 diabetes mellitus | Association | SNP | End stage renal disease | Proliferative diabetic retinopathy | Diabetic microvascular complication | MULTIDISCIPLINARY SCIENCES | association | NEPHROPATHY | end stage renal disease | ALLELIC VARIATION | HUMAN GENOME | BLOOD-GROUPS | DISEASE | RETINOPATHY | UTAH MORMONS | SUSCEPTIBILITY LOCUS | proliferative diabetic retinopathy | EXPRESSION | diabetic microvascular complication | Haplotypes | Retina - metabolism | Luciferases - metabolism | Kidney - pathology | Humans | RNA, Messenger - metabolism | Promoter Regions, Genetic - genetics | Diabetic Retinopathy - complications | Kidney - metabolism | Erythropoietin - metabolism | Genes, Reporter | Cell Line | Genetic Predisposition to Disease | RNA, Messenger - genetics | Gene Expression Regulation | Diabetic Nephropathies - genetics | Diabetic Retinopathy - genetics | Diabetic Nephropathies - complications | Erythropoietin - genetics | Animals | Alleles | Polymorphism, Single Nucleotide - genetics | Mice | Retina - pathology | Cohort Studies | Eye | Medical examination | Erythropoietin | Development and progression | Genetic aspects | Properties | Identification and classification | Genetic polymorphisms | Genotype & phenotype | Kidney diseases | Gene expression | Eyes & eyesight | Polymorphism | Index Medicus | Biological Sciences
Journal Article
International Journal of Endocrinology, ISSN 1687-8337, 2017, Volume 2017, pp. 9601735 - 6
Background. Fine needle aspiration (FNA) remains the first-line diagnostic in management of thyroid nodules and reduces unnecessary surgeries. However, it is... 
HYPERPARATHYROIDISM | METAANALYSIS | MALIGNANCY RISK | ENDOCRINOLOGY & METABOLISM | STATE | CYTOLOGY | LESIONS | Usage | Care and treatment | Biopsy, Needle | Research | Diagnosis | Thyroid diseases
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