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PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, p. e92921
Journal Article
Nature, ISSN 0028-0836, 10/2015, Volume 526, Issue 7573, pp. 397 - 401
Journal Article
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 06/2019, Volume 10, Issue 1, pp. 2884 - 7
Hereditary retinal degenerations (HRDs) are Mendelian diseases characterized by progressive blindness and caused by ultra-rare mutations. In a genomic screen... 
RP1 | ALLELES | PROTEIN | GENE | MULTIDISCIPLINARY SCIENCES | DISEASE | RISK | MUTATIONS | IDENTIFICATION | RETINITIS-PIGMENTOSA | ASSOCIATION | Blindness | Alleles | Retinal degeneration | Insertion | Retina | Heredity | Mutation
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 4692 - 11
Because exosomes have gained attention as a source of biomarkers, we investigated if miRNAs in exosomes (exo-miRs) can report the disease progression of organ... 
FIBROSIS | BIOCONDUCTOR PACKAGE | BIOGENESIS | MULTIDISCIPLINARY SCIENCES | TARGETING ZEB1 | CELL-DERIVED EXOSOMES | MESENCHYMAL TRANSITION | IDENTIFICATION | MIR-200 FAMILY | EXPRESSION | MICRORNA | Urine | Kidneys | Reperfusion | Ischemia | Fibrosis | MiRNA | mRNA | Exosomes
Journal Article
Journal Article
BMC Nephrology, ISSN 1471-2369, 06/2019, Volume 20, Issue 1, pp. 216 - 7
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 11/2016, Volume 25, Issue 22, pp. 5027 - 5034
Journal Article