1. ホームページ
  2. 资源与支持
  3. 历年文献

历年文献

历年文献

Distinct contribution of PD-L1 suppression by spatial expression of PD-L1 on tumor and non-tumor cells

Model Organisms：マウス Product & Service：hPD-L1 Research field：tumor and non-tumor cells

Published date：2018-03-22 | References：Cellular & Molecular Immunology

Peli1 negatively regulates noncanonical NF-κB signaling to restrain systemic lupus erythematosus

Model Organisms：マウス Product & Service：Rag1-KO Research field：systemic lupus erythematosus

Published date：2018-03-19 | References：Nature Communications

Tfap2b mutation in mouse results in patent ductus arteriosus and renal malformation

Model Organisms：Mouse Product & Service：Tfap2b Research field：kidney

Published date：2018-03-19 | References：J Surg Res

Anti-osteoporosis activity of a novel Achyranthes bidentata polysaccharide via stimulating bone formation.

Model Organisms：Zebrafish Product & Service：- Research field：Skeleton

Published date：2018-03-01 | References：

Gpr97 Exacerbates AKI by Mediating Sema3A Signaling

Model Organisms：Mouse Product & Service：Adgrg3 Research field：kidney

Published date：2018-02-15 | References：JASN

SNX10 mediates alcohol-induced liver injury and steatosis by regulating the activation of chaperone-mediated autophagy

Model Organisms：Mouse Product & Service：Snx10 Research field：Liver

Published date：2018-02-13 | References：J HEPATOL

Transgenic Expression of A Venous Malformation Related Mutation, TIE2-R849W, Significantly Induces Multiple Malformations of Zebrafish

Model Organisms：Zebrafish Product & Service：TIE2 Research field：Blood vessel

Published date：2018-02-12 | References：Int J Med Sci.

IL-6/STAT3 pathway induced deficiency of RFX1 contributes to Th17-dependent autoimmune diseases via epigenetic regulation

Model Organisms：Mouse Product & Service：Rfx1 Research field：Epigenetic

Published date：2018-02-08 | References：NAT COMMUN

Transcriptional Regulation of the Warburg Effect in Cancer by SIX1.

Model Organisms：マウス Product & Service：SIX1 Research field：Cancer

Published date：2018-02-08 | References：Cancer Cell

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss.

Model Organisms：Zebrafish Product & Service：ifnlr1 Research field：Hearing cell development defects

Published date：2018-02-01 | References：journal of medical genetics

トップに戻る