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 ed surfaces and secreted the beta-casein and milk fat globules.

3 XOR loss alters the proteome of milk fat globules.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

28 ats and discoidin-like domains 3 (EDIL3) and milk fat globule-EGF factor 8 (MFGE8), two glycoproteins

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

30 In our previous study, milk fat globule-EGF factor 8 protein (MFGE8) was identi

31 din, a 50-amino-acid cleavage product of the milk fat globule-EGF factor 8 protein, is one of the mos

32 poEC was shown to be mediated in part by the milk fat globule-EGF factor 8 protein/integrin a(v) B(5)

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

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

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

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

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

38 ly shown that binding of the integrin ligand milk fat globule epidermal growth factor like 8 (MFGE8)

39 eviously shown that the avB5 integrin ligand milk fat globule epidermal growth factor like 8 (MFGE8)

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

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

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

43 Human milk fat globule epidermal growth factor-factor VIII (MF

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

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

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

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

48 sociated with eat-me signals, such as Mfge8 (milk fat globule-epidermal growth factor factor 8), and

49 Milk fat globule-epidermal growth factor-factor 8 (MFGE8

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

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

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

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

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

55 The human milk fat globule membrane (hMFGM) and Lactobacillus modu

56 of soluble and insoluble fractions for both milk fat globule membrane (MFGM) and skim milk.

57 Human milk (HM) contains large milk fat globule membrane (MFGM) coated lipid droplets,

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

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

60 Bovine milk fat globule membrane (MFGM) has shown many health b

61 Milk fat globule membrane (MFGM) is a biologically funct

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

63 y for working mothers, though its effects on milk fat globule membrane (MFGM) lipids are not fully un

64 Milk fat globule membrane (MFGM) phospholipids have been

65 Milk fat globule membrane (MFGM) proteins are receiving

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

67 whole milk, insoluble protein aggregates at milk fat globule membrane (MFGM) were formed by disulfid

68 The milk fat globule membrane (MFGM), which surrounds and st

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

70 rition, the effects of polar lipids-enriched milk fat globule membrane (MFGM-PL) supplementation to d

71 igate whether maternal polar lipids-enriched milk fat globule membrane (MFGM-PL) supplementation to h

72 ontaining added protein, vitamin D, calcium, milk fat globule membrane (phospholipids and other bioac

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

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

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

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

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

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

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

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

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

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

83 nal proteolysis of lactoferrin and bioactive milk fat globule membrane proteins.

84 Proteosomes (P) based on milk fat globule membrane's phospholipids (MPs), whey pr

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

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

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

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

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

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

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

92 d the removal of the milk fat and associated milk fat globule membranes (MFGM) during production of i

93 f the lipidome and proteome was performed on milk fat globule membranes (MFGM) originating from milk

94 rotein formula (EF) supplemented with bovine milk fat globule membranes (MFGMs) until 6 mo of age had

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

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

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

98 e secreted into the milk collecting ducts as milk fat globule (MFG) where they are exposed to microfl

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

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

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

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

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

104 Bulk RNA sequencing of milk fat globules (MFGs), milk cells, and breast tissue

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

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

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

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

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

110 Loss of XOR delays milk fat globule secretion.

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

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

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

114 f these lipids is linked to the structure of milk fat globules, which are influenced by diet and feed