ライフサイエンスコーパス: FTCD

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1 FTCD appears to be a dynamic component of the Golgi, and

2 FTCD is already dispersed into small punctate structures

3 FTCD is not observed in tubules originating from the Gol

4 FTCD remains associated with Golgi fragments during micr

5 nate process in which vimentin filaments and FTCD integrate into chimeric fibers.

6 d ectopic expression of a liver autoantigen (FTCD) in the thymus leading to reduced numbers of circul

7 se cytoskeletal systems appear unaffected by FTCD expression.

8 protein formiminotransferase cyclodeaminase (FTCD) participates in this interaction.

9 mmalian formiminotransferase cyclodeaminase (FTCD), a 0.5 million Dalton homo-octameric enzyme, plays

10 8K is a formiminotransferase cyclodeaminase (FTCD), a bifunctional enzyme that catalyzes two consecut

11 porcine formiminotransferase cyclodeaminase (FTCD), suggesting that 58K is rat FTCD.

12 antigen formiminotransferase cyclodeaminase (FTCD).

13 cells results in the formation of extensive FTCD-containing fibers originating from the Golgi region

14 Instead, FTCD relocates from the Golgi, but the time course of it

15 y full length cDNA for p60 and porcine liver FTCD.

16 m liver tubulin, were able to bind rat liver FTCD.

17 s with vimentin filaments and the ability of FTCD to specifically interacts with both Golgi membrane

18 cance of the microtubule binding activity of FTCD is thus called into question, but an association of

19 called into question, but an association of FTCD with the Golgi apparatus has now been established.

20 ture of two strong antigenic determinants of FTCD recognized by autoantibodies from patients with aut

21 Expression of FTCD in cultured cells results in the formation of exten

22 to be the richest tissue source, by far, of FTCD.

23 hich was shown to contain very low levels of FTCD, but not to tubulin in liver, which was determined

24 e results show that extraction parameters of FTCD are similar to those of GM130, a tightly associated

25 To define parameters of FTCD association with the Golgi, comparison of its behav

26 gs) leading to an increased proliferation of FTCD-specific autoreactive T and B cells.

27 component of the Golgi, and a proportion of FTCD molecules cycle between the Golgi and earlier compa

28 K was concluded to be a rat liver version of FTCD.

29 Rat FTCD is structurally similar to porcine FTCD, a metabolic enzyme involved in conversion of histi

30 at the peripherally associated Golgi protein FTCD binds directly to vimentin subunits and to polymeri

31 Rat FTCD is structurally similar to porcine FTCD, a metaboli

32 deaminase (FTCD), suggesting that 58K is rat FTCD.

33 for the first time, including CCT6B, SALL3, FTCD and PC.

34 inct from mannosidase II relocation and that FTCD provides a novel marker to study Golgi dynamics.

35 s and promote their association suggest that FTCD might be a candidate protein integrating the Golgi

36 These results suggest that FTCD relocation is temporally and spatially distinct fro

37 The FTCD-mediated regulation of vimentin IF is not a seconda

38 Formation of the FTCD fibers is obligatorily coupled to vimentin assembly

39 Determination of the FTCD structure by X-ray crystallography and electron cry

40 The assembly of the FTCD/vimentin fibers causes a coordinate change in the s

41 he binding of thin vimentin filaments to the FTCD octamer.

42 individual elements that are tethered to the FTCD/vimentin fibers.

43 e presence of a reduced central tolerance to FTCD, a strong regulatory T-cell response was able to in

44 amed liver, restored peripheral tolerance to FTCD, and induced remission of AIH.

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