Homo sapiens |
SRX18107120 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Caenorhabditis elegans |
SRX7067982 |
SRP227316 |
6239 |
L3 stage |
genotype: eri-1(mg366);GFP::NRDE-3 |
NEB |
NA |
NA |
Caenorhabditis elegans |
SRX7067983 |
SRP227316 |
6239 |
L3 stage |
genotype: eri-1(mg366);cde-1(tm936);GFP::NRDE-3 |
NEB |
NA |
NA |
Caenorhabditis elegans |
SRX7067984 |
SRP227316 |
6239 |
young adult stage |
genotype: GFP::HRDE-1 |
NEB |
NA |
NA |
Caenorhabditis elegans |
SRX7067985 |
SRP227316 |
6239 |
young adult stage |
genotype: cde-1(tm936);GFP::HRDE-1 |
NEB |
NA |
NA |
Homo sapiens |
SRX18107125 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
SRX18107126 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
SRX18107127 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
SRX18107128 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
SRX18107121 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
SRX18107122 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
SRX18107123 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
SRX18107124 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
ERX3436010 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
ERX3436011 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
ERX3436012 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
ERX3436013 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
ERX3436014 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
SRX18107129 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |
Homo sapiens |
ERX3436015 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
ERX3436016 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
ERX3436017 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
ERX3436018 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
Autosomal dominant polycystic kidney disease |
NA |
Homo sapiens |
ERX3436019 |
ERP116071 |
9606 |
NA |
cellular component: extracellular vesicular exosome |
Illumina |
normal |
NA |
Homo sapiens |
SRX18107130 |
SRP405648 |
9606 |
NGN2-iNs |
cell line: NGN2-iNs |
Illumina |
NA |
NA |