| Homo sapiens |
SRX22829583 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
| Homo sapiens |
SRX22829582 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
| Homo sapiens |
SRX22829581 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
| Homo sapiens |
SRX22829580 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599929 |
SRP131195 |
10090 |
HDL |
tissue: HDL |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599928 |
SRP131195 |
10090 |
HDL |
tissue: HDL |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599927 |
SRP131195 |
10090 |
HDL |
tissue: HDL |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599926 |
SRP131195 |
10090 |
HDL |
tissue: HDL |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599925 |
SRP131195 |
10090 |
HDL |
tissue: HDL |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599924 |
SRP131195 |
10090 |
Bile |
tissue: Bile |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599934 |
SRP131195 |
10090 |
APOB |
tissue: APOB |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599933 |
SRP131195 |
10090 |
APOB |
tissue: APOB |
Illumina |
NA |
NA |
| Mus musculus |
SRX3599932 |
SRP131195 |
10090 |
APOB |
tissue: APOB |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599931 |
SRP131195 |
10090 |
APOB |
tissue: APOB |
Bioo |
NA |
NA |
| Mus musculus |
SRX3599930 |
SRP131195 |
10090 |
APOB |
tissue: APOB |
Bioo |
NA |
NA |
| Homo sapiens |
SRX22829589 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
| Mus musculus |
SRX18197101 |
SRP406682 |
10090 |
Spleen |
cell compartment: Whole cell |
other |
NA |
NA |
| Homo sapiens |
SRX22829599 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
| Homo sapiens |
SRX4957483 |
SRP167242 |
9606 |
Urine |
condition: Nephrotic Syndrome |
Illumina_2 |
NA |
NA |
| Mus musculus |
SRX18197100 |
SRP406682 |
10090 |
Bone |
cell compartment: Whole cell |
other |
NA |
NA |
| Homo sapiens |
SRX22829598 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
| Homo sapiens |
SRX4957482 |
SRP167242 |
9606 |
Urine |
condition: Nephrotic Syndrome |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX22829597 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
| Homo sapiens |
SRX4957481 |
SRP167242 |
9606 |
Urine |
condition: Nephrotic Syndrome |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX22829596 |
SRP476635 |
9606 |
embryo |
tissue: embryo |
Bioo |
NA |
NA |
