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Database ID
RNA ID
RNA Type
Disease Type
Disease Category
Sample Source
GEO ID
Detail
exR0079741
PSPN
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079742
PSRC1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079743
PSTK
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079744
PSTPIP1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079745
PSTPIP2
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079746
PTAFR
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079747
PTAR1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079748
PTBP1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079749
PTBP2
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079750
PTBP3
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079751
PTCD1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079752
PTCD2
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079753
PTCD3
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079754
PTCH1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0079755
PTCH2
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail

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