ライフサイエンスコーパス: milk fat globule

1 bolism proteins associated with the secreted milk fat globule.

2 XOR loss alters the proteome of milk fat globules.

3 e in vivo upper digestive tract digestion of milk fat globules.

4 -binding protein that decorates membranes of milk fat globules.

5 s from a baculovirus vector, and in secreted milk-fat globules.

6 r difference between the native emulsions of milk fat globules and processed submicronic emulsions in

7 caseins are secreted by exocytosis, whereas milk fat globules are released by budding, enwrapped by

8 Human milk fat globules, by enveloping cell contents during th

9 brane-associated proteins (e.g., lactadherin/milk fat globule E8 and spermadhesin alanine-tryptophan-

10 hat GM-CSF is required for the expression of milk fat globule EGF 8 (MFG-E8) in antigen-presenting ce

11 Milk fat globule EGF factor 8 (MFG-E8) binds to apoptoti

12 c cells (IDCs) release exosomes that contain milk fat globule EGF factor VIII (MFGE8), a protein requ

13 requires alphavbeta5 integrin and its ligand milk fat globule EGF factor-8 (MFG-E8) but not the recep

14 Here, we show that milk fat globule EGF-8 (MFG-E8), a secreted protein expr

15 ns, Mer receptor tyrosine kinase (MerTK) and Milk fat globule EGF-like factor 8 (MFG-E8), were transi

16 Milk-fat globule EGF factor-8 (MFG-E8, SED1, lactadherin

17 Milk fat globule- EGF factor 8 (MFG-E8) is a bridge prot

18 Milk fat globule-EGF 8 (MFGE8) plays important, nonredun

19 to the EGF domain of Del-1 and its homologue milk fat globule-EGF 8.

20 We identified downregulation of milk fat globule-EGF factor 8 (MFG-E8) as a contributor

21 Milk fat globule-EGF factor 8 (MFG-E8) maintains the int

22 s up-regulated the collagen-targeting factor milk fat globule-EGF factor 8 (MFG-E8), stimulated colla

23 photoreceptors, or its extracellular ligand milk fat globule-EGF factor 8 (MFG-E8).

24 Milk fat globule-EGF factor 8 (MFG-E8)/lactadherin parti

25 ce lacking the gene that encodes the protein Milk Fat Globule-EGF factor 8 (Mfge8(-/-)) develop exagg

26 phagocytic machinery, including the opsonin milk fat globule-EGF factor 8 (Mfge8) and the downstream

27 ore examined the effect of recombinant human milk fat globule-EGF factor 8 (rhMFG-E8) in mitigating d

28 Milk fat globule-EGF-factor 8 (Mfge8) is a milk glycopro

29 Milk fat globule epidermal growth factor (EGF)-factor VI

30 tive protein tyrosine kinase (Mertk) and the milk fat globule epidermal growth factor (Mfge8), in dir

31 Milk fat globule epidermal growth factor 8 (Mfge8) is a

32 was affected by Cx43 was found to be MFG-E8 (milk fat globule epidermal growth factor 8), which is in

33 sting of PS exposure, the PS-binding protein milk fat globule epidermal growth factor-8, and its micr

34 Milk fat globule epidermal growth factor-factor 8 (MFG-E

35 Milk fat globule epidermal growth factor-factor 8 (MFG-E

36 te alphavbeta3 and adhere to vitronectin and milk-fat globule epidermal growth factor VIII protein.

37 nd that these cardiac myofibroblasts secrete milk fat globule-epidermal growth factor 8 (MFG-E8), whi

38 sis-regulating integrin-beta3 and its ligand milk fat globule-epidermal growth factor 8 protein and e

39 The glycoprotein milk fat globule-epidermal growth factor factor 8 (MFG-E

40 Milk fat globule-epidermal growth factor-factor VIII (MF

41 that functions in the budding and release of milk-fat globules from the apical surface during lactati

42 integrations between green tea catechins and milk fat globules in a cheese matrix were investigated u

43 e the dynamics of the MFGM at the surface of milk fat globules in relation to temperature and time, a

44 tn and ADPH, similar to the situation in the milk fat globule itself.

45 red with other dairy foods, butter is low in milk fat globule membrane (MFGM) content, which encloses

46 The bovine milk fat globule membrane (MFGM) has many associated bio

47 The microstructure of the milk fat globule membrane (MFGM) is still poorly underst

48 otein densities and supplemented with bovine milk fat globule membrane (MFGM) reduces differences in

49 d are secreted into milk associated with the milk fat globule membrane (MFGM).

50 ribution of the endoplasmic reticulum to the milk fat globule membrane and a role for SNAREs in membr

51 f putative chemical interactions between the milk fat globule membrane and green tea catechins provid

52 Bioactive lipids of the milk fat globule membrane become concentrated in two co-

53 ly and physically bound cholesterol from the milk fat globule membrane by enzymatic action.

54 catechins are localised in association with milk fat globule membrane domains as they contain both h

55 Human lactadherin, a milk fat globule membrane glycoprotein, inhibits human r

56 quines, we undertook a proteomic analysis of milk fat globule membrane proteins from donkey milk and

57 Size-exclusion chromatography of solubilized milk fat globule membrane proteins showed that XOR forme

58 idin domain has been identified in mammalian milk fat globule membrane proteins, blood coagulation fa

59 a-lactalbumin, lactoferrin, osteopontin, and milk fat globule membrane proteins.

60 complexes due to interactions between MFGM (milk fat globule membrane) proteins and skim milk protei

61 and the secretory vesicles contribute to the milk fat globule membrane.

62 used to decipher the cellular origins of the milk fat globule membrane.

63 d-dependent complex with Btn and ADPH in the milk fat globule membrane.

64 Lactadherin, a glycoprotein of the milk-fat globule membrane, contains tandem C domains wit

65 ther more minor fragments of lower Mr in the milk-fat-globule membrane.

66 m lactating bovine mammary tissue and in the milk-fat-globule membrane.

67 is a dairy by-product with a high content of milk fat globule membranes (MFGMs), whose protein consti

68 both cytoplasmic lipid droplets and secreted milk fat globule membranes was used to decipher the cell

69 y, suggesting selective association with the milk fat globule membranes.

70 Targeting of exosomes to DCs is mediated via milk fat globule (MFG)-E8/lactadherin, CD11a, CD54, phos

71 odissected mammary epithelial cells (LCMEC), milk fat globules (MFG) and antibody-captured milk mamma

72 and size on the lipid composition of bovine milk fat globules (MFG) and their membranes (MFGM) was i

73 The mechanism underlying the shift in milk-fat-globule (MFG) mean diameter upon changing the c

74 rovided useful information about the role of milk fat globules (MFGs) in high-fat dairy systems, such

75 One novel protein, the milk fat globule protein epidermal growth factor 8 (MFG-

76 -M phase of the cell cycle, and induction of milk fat globule protein, milk fat membrane globule prot

77 y through structural interactions with other milk fat globule proteins including butyrophilin (Btn) a

78 standardized milk emulsion containing native milk fat globules referred to as minimally-processed emu

79 ne secretion mechanism, but does not prevent milk fat globule secretion.

80 Loss of XOR delays milk fat globule secretion.

81 The recovery of different catechins from the milk fat globule suspensions was found to vary, suggesti

82 Owing to the number and large size of milk fat globules, the membrane surface needed for their

83 Secreted milk fat globules were isolated from mouse milk of wild-