パスウェイパネル
Reactomeの生物学的パスウェイごとにqRT-PCRプライマーを探せます。
1862 件のパネル
- Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1 3 遺伝子
- Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2 3 遺伝子
- Defective SERPING1 causes hereditary angioedema 3 遺伝子
- Defective VWF binding to collagen type I 3 遺伝子
- Defective cleavage of FV variant at R334 3 遺伝子
- Defective cleavage of FV variant at a.a.534 3 遺伝子
- Defective cofactor function of FVIIIa variant 3 遺伝子
- Defective factor IX causes thrombophilia 3 遺伝子
- Defective factor XII causes hereditary angioedema 3 遺伝子
- Defective visual phototransduction due to STRA6 loss of function 3 遺伝子
- Early Phase of HIV Life Cycle 3 遺伝子
- Electron transport from NADPH to Ferredoxin 3 遺伝子
- Enzymatic degradation of dopamine by COMT 3 遺伝子
- Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 3 遺伝子
- Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 3 遺伝子
- FGFR1c and Klotho ligand binding and activation 3 遺伝子
- FMO oxidises nucleophiles 3 遺伝子
- GLI proteins bind promoters of Hh responsive genes to promote transcription 3 遺伝子
- Glycogen storage disease type IV (GBE1) 3 遺伝子
- Heme assimilation 3 遺伝子
- Hydroxycarboxylic acid-binding receptors 3 遺伝子
- IKBKB deficiency causes SCID 3 遺伝子
- IKBKG deficiency causes anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) (via TLR) 3 遺伝子
- IRE1alpha activates chaperones 3 遺伝子
- Inhibition of nitric oxide production 3 遺伝子
- Inositol transporters 3 遺伝子
- Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA 3 遺伝子
- Integration of viral DNA into host genomic DNA 3 遺伝子
- Interconversion of 2-oxoglutarate and 2-hydroxyglutarate 3 遺伝子
- Interconversion of polyamines 3 遺伝子
- Interleukin-33 signaling 3 遺伝子
- Intestinal hexose absorption 3 遺伝子
- Intracellular metabolism of fatty acids regulates insulin secretion 3 遺伝子
- Intracellular oxygen transport 3 遺伝子
- Lactose synthesis 3 遺伝子
- Loss of MECP2 binding ability to 5mC-DNA 3 遺伝子
- Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD 3 遺伝子
- MECP2 regulates transcription of genes involved in GABA signaling 3 遺伝子
- MET activates STAT3 3 遺伝子
- MTF1 activates gene expression 3 遺伝子
パスウェイデータの出典：Reactome（CC0）。