ライフサイエンスコーパス: autophagy-related protein

1 ides) are PtdIns3P and PtdIns(3,5)P2 binding autophagy related proteins.

2 s and enhances autophagic flux by modulating autophagy-related proteins.

3 phore assembly site and interacted with Atg (autophagy related) proteins.

4 ptor-interacting protein kinase 2 (RIP2) and autophagy-related protein 16-1 (ATG16L1).

5 t is a locus on chromosome 10 containing the autophagy-related protein 18 (ATG18) associated with dec

6 phagy receptors, such as the Pichia pastoris autophagy-related protein 30 (Atg30), which controls the

7 unoblot and in GFP-LC3 transgenic mice), and autophagy-related protein 5 protein expression.

8 n expression of autophagy markers LC3 II and autophagy-related protein 5.

9 eracting serine-threonine kinase-2 (RIPK-2), autophagy-related protein-5 (ATG5), ATG7 and ATG16L1 but

10 Using autophagy-related protein 7 (Atg7) as an autophagic mark

11 autophagy-related protein beclin 1 (BCN1) or autophagy-related protein 7 (ATG7) in immortalized human

12 Atg7(Deltapan) mice that lack the essential autophagy-related protein 7 (ATG7) in pancreatic epithel

13 patocytes, autophagy was inhibited by 3MA or autophagy-related protein 7 (Atg7) small interfering RNA

14 Expression of autophagy-related protein 7 (Atg7), Beclin-1, and Atg12,

15 es, vacuolar protein sorting 34 (VPS34), and autophagy-related protein 7 (ATG7), could rescue the PA-

16 Similarly, knock down of autophagy-related protein 7 and TLR7 by use of siRNA sig

17 ethyladenine (3-MA) or were transfected with autophagy-related protein 7 or TLR7 small interfering RN

18 autophagy as defined by the requirement for autophagy-related protein 7.

19 may utilize autophagy for replication as the autophagy-related protein-7 (ATG-7), microtubule-associa

20 Here we describe a novel interaction between autophagy-related protein 8 (Atg8) and fatty acid syntha

21 evisiae, the integral membrane protein Atg9 (autophagy-related protein 9) cycles between mitochondria

22 lyses of the functions and dynamics of known autophagy-related proteins and for screening new genes.

23 However, autophagy-related proteins are also essential for the ea

24 These data indicate that multiple autophagy-related proteins are important for one or more

25 found that ER content is expanded in mature autophagy-related protein (Atg) 7-deficient T lymphocyte

26 ential components of the autophagic pathway, autophagy-related protein (Atg)5, Beclin1, and Ulk1, wer

27 We analyzed changes in autophagy-related proteins (Atg).

28 ovide cardioprotection in mice that lack the autophagy-related protein Atg5 in cardiomyocytes.

29 ed the previously described functions of the autophagy-related proteins Atg5-Atg12, but NLRX1 did not

30 gested that high expression of the essential autophagy-related protein, Atg7, was associated with sho

31 The identification of conserved autophagy-related proteins (ATGs) that mediate bulk degr

32 In this study, we found that knockdown of autophagy-related protein beclin 1 (BCN1) or autophagy-r

33 smodium vivax depends only on the downstream autophagy-related proteins Beclin 1, PI3K, and ATG5, but

34 We report that a recently discovered autophagy-related protein, Beclin 2, interacts with KSHV

35 ing compartment by a mechanism that involved autophagy-related proteins, but not the conventional aut

36 tion or knockdown of presenilins alters many autophagy-related proteins demonstrating a buildup of au

37 and by measuring LC3B protein lipidation and autophagy-related protein expressions.

38 Western blot analysis indicated that several autophagy-related proteins fluctuated during the procedu

39 Early and sustained expression of autophagy-related proteins in this genetically precise m

40 ubiquitin-binding protein SQSTM1/p62 and the autophagy-related protein LC3, silencing of p62 and LC3

41 he proximal tubules and reduced ratio of the autophagy-related protein LC3-II/I in the kidney post-UU

42 We found that the autophagy-related proteins LC3 and p62 localized to wild

43 ar calcium overload that is dependent on the autophagy-related proteins LC3 and p62 upon hyperactivat

44 ganese superoxide dismutase-2 (SOD2) and the autophagy-related proteins LC3II and Gabarapl1 also are

45 during Plasmodium infection and the roles of autophagy-related proteins may provide an urgently neede

46 of autophagic vacuoles and conversion of an autophagy-related protein, microtubule-associated protei

47 is paralleled by increased expression of the autophagy-related protein, p62.

48 The recruitment of autophagy-related proteins plays a key role in multiple

49 embryonic fibroblasts deficient in Atg5, an autophagy-related protein required for autophagosome for

50 es autophagy by acting directly on essential autophagy-related proteins strategically located in the

51 genous and induced clusters co-localize with autophagy-related proteins such as Atg16L1, LC3B and Rab

52 Autophagy-related proteins such as Beclin-1 are involved

53 rotein synthesis, including that of specific autophagy-related proteins that are up-regulated in resp

54 ytoplasmic accumulation of active Lyn and of autophagy-related proteins Ulk1 and Atg7.

55 or with small interfering RNAs specific for autophagy-related proteins, which are essential for auto