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  • 検索条件 : 絞込み (MeSH = Phosphatidylserines / metabolism*)
生物種 リソース名 タイトル
ヒト・動物細胞 UPS-1(RCB4451) ATP11C mutation is responsible for the defect in phosphatidylserine uptake in UPS-1 cells.
遺伝子材料 pMXs-puro-mXkr1(XK)-FLAG (RDB18766) , pMXs-puro-mXkr2 (Xkrx)-FLAG (RDB18767) , pMXs-puro-mXkr4-FLAG (RDB18768) , pMXs-puro-mXkr5-FLAG (RDB18769) , pMXs-puro-mXkr6-FLAG (RDB18770) , pMXs-puro-mXkr7-FLAG (RDB18771) , pMXs-puro-mXkr8-FLAG (RDB18772) , pMXs-puro-mXkr9-FLAG (RDB18773) , pMXs-puro-mXkr4/1DA-FLAG (RDB18774) , pMXs-puro-mXkr8/2DA-FLAG (RDB18775) , ... Xk-related protein 8 and CED-8 promote phosphatidylserine exposure in apoptotic cells.
遺伝子材料 pMXs-puro-mXkr1(XK)-FLAG (RDB18766) , pMXs-puro-mXkr2 (Xkrx)-FLAG (RDB18767) , pMXs-puro-mXkr4-FLAG (RDB18768) , pMXs-puro-mXkr5-FLAG (RDB18769) , pMXs-puro-mXkr6-FLAG (RDB18770) , pMXs-puro-mXkr7-FLAG (RDB18771) , pMXs-puro-mXkr8-FLAG (RDB18772) , pMXs-puro-mXkr9-FLAG (RDB18773) , pMXs-puro-mXkr4/1DA-FLAG (RDB18774) , pMXs-puro-mXkr8/2DA-FLAG (RDB18775) , ... Exposure of phosphatidylserine by Xk-related protein family members during apoptosis.
遺伝子材料 pMXs-puro-mTMEM16A (RDB18742) , pMXs-puro-mTMEM16B (RDB18743) , pMXs-puro-mTMEM16C (RDB18744) , pMXs-puro-mTMEM16D (RDB18745) , pMXs-puro-mTMEM16E (RDB18746) , pMXs-puro-mTMEM16F (RDB18747) , pMXs-puro-mTMEM16G (RDB18748) , pMXs-puro-mTMEM16H (RDB18749) , pMXs-puro-mTMEM16J (RDB18750) , pMXs-puro-mTMEM16F-long (RDB18751) , ... Constitutive exposure of phosphatidylserine on viable cells.
遺伝子材料 human ATP8A1 (RDB18725) , human ATP8A2 (RDB18726) , human ATP8B1 (RDB18727) , human ATP8B2 (RDB18728) , human ATP8B3 (RDB18729) , human ATP8B4 (RDB18730) , human ATP9A (RDB18731) , human ATP9B (RDB18732) , human ATP10A (RDB18733) , human ATP10B (RDB18734) , ... Caspase-mediated cleavage of phospholipid flippase for apoptotic phosphatidylserine exposure.
遺伝子材料 pCX4-mBSG-c-HA (273) (RDB18961) , pCX4-mBSG-c-HA (389) (RDB18962) , pCX4-mNPTN-c-HA (281) (RDB18963) , pCX4-mNPTN-c-HA (397) (RDB18964) , pCX4-mEMB-c-HA (330) (RDB18965) , pCX4-hBSG-c-HA (269) (RDB18966) , pCX4-hBSG-c-HA (385) (RDB18967) , pCX4-hNPTN-c-HA (282) (RDB18968) , pCX4-hNPTN-c-HA (398) (RDB18969) Xkr8 phospholipid scrambling complex in apoptotic phosphatidylserine exposure.
ヒト・動物細胞 B16/BL6(RCB2638) Role of Phosphatidylserine-Derived Negative Surface Charges in the Recognition and Uptake of Intravenously Injected B16BL6-Derived Exosomes by Macrophages.
線虫 tm4762 Calcium ions trigger the exposure of phosphatidylserine on the surface of necrotic cells.
線虫 tm3489 , tm5755 , tm2423 , tm847 , tm2253 Autophagy mediates phosphatidylserine exposure and phagosome degradation during apoptosis through specific functions of GABARAP/LGG-1 and LC3/LGG-2.
ショウジョウバエ 4825R-3 , 4825R-1 Phosphatidylserine synthase regulates cellular homeostasis through distinct metabolic mechanisms.
ショウジョウバエ ER Lipid Defects in Neuropeptidergic Neurons Impair Sleep Patterns in Parkinson's Disease.
ヒト・動物細胞 RAW 264(RCB0535) Phosphatidylserine-stimulated production of N-acyl-phosphatidylethanolamines by Ca2+-dependent N-acyltransferase.
線虫 tm6877 Phosphatidylserine exposure mediated by ABC transporter activates the integrin signaling pathway promoting axon regeneration.
ヒト・動物細胞 293(RCB1637) Cell surface flip-flop of phosphatidylserine is critical for PIEZO1-mediated myotube formation.
ヒト・動物細胞 HL60 , U937 Cell-based evaluation of changes in coagulation activity induced by antineoplastic drugs for the treatment of acute myeloid leukemia.
線虫 tm2078 C. elegans secreted lipid-binding protein NRF-5 mediates PS appearance on phagocytes for cell corpse engulfment.
線虫 tm2087 , tm3117 , tm2078 CED-1, CED-7, and TTR-52 regulate surface phosphatidylserine expression on apoptotic and phagocytic cells.
線虫 tm2078 , tm3117 Caspase-mediated activation of Caenorhabditis elegans CED-8 promotes apoptosis and phosphatidylserine externalization.
線虫 tm4762 Necrotic Cells Actively Attract Phagocytes through the Collaborative Action of Two Distinct PS-Exposure Mechanisms.
ヒト・動物細胞 The linoleic acid derivative DCP-LA selectively activates PKC-epsilon, possibly binding to the phosphatidylserine binding site.