ライフサイエンスコーパス: Fas protein

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1 h resulted in cell surface expression of the Fas protein.

2 been damaged by gamma-irradiation expressed Fas protein.

3 h response by events such as ligation of the Fas protein.

4 agus demonstrated cell surface expression of Fas protein.

5 t is unknown whether they express functional Fas protein.

6 strates that lpr mice can produce functional Fas protein.

7 s demonstrated abundant, appropriately sized Fas protein.

8 on and is not due to decreased production of Fas protein.

9 ometry and then analyzed for the presence of Fas protein.

10 ed 2-microm vesicles with both GM1 lipid and Fas protein abundance enriched in a subpopulation of the

11 s affecting the intracellular portion of the FAS protein also have an increased risk of B-cell lympho

12 FAP-1 (PTPN13, PTP-BAS) interacts with human Fas protein and prevents its export from the cytoplasm t

13 apoptosis through dimerization of engineered Fas proteins and regulation of transcription through dim

14 This mutation results in defective Fas protein, defective lymphocytic apoptosis, and accele

15 explored FAS transcript levels, cell-surface FAS protein expression and susceptibility to FAS-mediate

16 s T cell and B cell independent and required Fas protein expression by host cells, but not on islets.

17 mmunohistochemistry demonstrated the lack of Fas protein expression on dermal lymphocytes in one case

18 ndent increase in (i) the multimerization of Fas protein, (ii) the protein expression of Fas ligand,

19 abbit hearts demonstrated an upregulation of Fas protein in ischemic cardiomyocytes, and treatment wi

20 n tumor cells, and platinum colocalized with FAS protein in lipid rafts.

21 tion of intact Fas message and low levels of Fas protein in lpr mice has led to the consideration of

22 ury was associated with a marked increase in Fas protein in lung.

23 ly reduced Fas mRNA levels and expression of Fas protein in mouse hepatocytes, and the effects persis

24 The amount of Fas protein in the vesicles containing raft domains mark

25 , human colorectal cancer patients with high Fas protein in their tumor cells had a longer time befor

26 Fas protein is expressed in corneal epithelial, keratocy

27 Instead, considerably more Fas protein is found in the cytoplasm of cells expressin

28 ophageal adenocarcinoma cell line, wild-type Fas protein is retained in the cytoplasm, and this corre

29 Interestingly, the reduced Fas protein level on the cell surface is not accompanied

30 rect correlation among FAS transcript level, FAS protein level, and FAS-mediated apoptotic sensitivit

31 The Fas protein level, before and after wounding, was dramat

32 Fas protein levels and cleaved caspase-8 increased in MN

33 ence analysis of fas cDNAs revealed that the fas protein product has characteristics of an extracellu

34 Blocking of Fas protein reduced the number of apoptotic cells in the

35 nflammatory skin disease, the ability of the Fas protein to trigger apoptosis in the distinct cell su

36 FAP-1 gene expression that finally restricts Fas protein trafficking, thereby, facilitating the survi

37 In contrast, dynamin-2 facilitates Fas protein translocation from the Golgi apparatus via t

38 the Fas mRNA and flow cytometric analysis of Fas protein using a specific mouse monoclonal antibody.

39 Fas protein was detected predominantly in the tubule cel

40 icting for a truncated death domain, whereas Fas protein was expressed by dermal lymphocytes in the o

41 Antiserum directed against Fas protein was found to stain neurons but not glia in t

42 An approximately Mr 48,000 Fas protein was identified by Western blot analysis in t

43 Also, TNF receptor superfamily member 6 (FAS) protein was overexpressed in phosphaplatin-treated

44 FasL and Fas proteins were detected by flow cytometry and Western

45 The retention of wild-type Fas protein within the cytoplasm may represent a mechani

46 CM101 infusion led to elevated levels of Fas protein within the tumors as well as a decrease in t

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