ライフサイエンスコーパス: variant surface glycoprotein

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1 of infective metacyclic forms expressing the variant surface glycoprotein.

2 ling endosomes, of pre-existing cell surface variant surface glycoprotein.

3 expressing normal mature GPI anchors on its variant surface glycoprotein.

4 NA sequences of the eight genes encoding the variant surface glycoprotein 117 (VSG) family.

5 is responsible for this release, transgenic variant surface glycoprotein 117 (VSG117) was expressed

6 nd surface proteomes, being dominated by the variant surface glycoprotein (African) or mucins (Americ

7 ct midgut stage, enabling rapid recycling of variant surface glycoprotein and antibody clearance from

8 its encoding the major cell surface antigens variant surface glycoprotein and procyclin.

9 ne pool is competent for transfer to nascent variant surface glycoprotein and represents 38% of glyco

10 nvariable regions of variable major protein, variant surface glycoprotein, and pilin, which are not a

11 on of VSG genes that encode their protective variant surface glycoprotein coat.

12 expression of VSG genes that encode distinct Variant Surface Glycoprotein coats.

13 osphatidylinositol anchor of the trypanosome variant surface glycoprotein contains myristate as its s

14 T. brucei results in derepression of silent variant surface glycoprotein ESs, as had previously been

15 nfection that is driven primarily by soluble variant surface glycoprotein exposure, and it may be tha

16 his influences the choice of a monocistronic variant surface glycoprotein expression site.

17 Secondly, knockdown of clathrin or the variant surface glycoprotein failed to perturb transcrip

18 of the bacterial aspartate receptor and the variant surface glycoprotein from Trypanosoma brucei.

19 In bloodstream-form trypanosomes, only one variant surface glycoprotein gene (VSG) expression site

20 at, isolated from the upstream region of the variant surface glycoprotein gene of Trypanosoma brucei,

21 n hosts by switching the expression of their variant surface glycoprotein genes (vsg).

22 alternating expression of telomere-proximal variant surface glycoprotein genes (vsgs), which is cont

23 m-specific epigenetic silencing of telomeric variant surface glycoprotein genes involved in antigenic

24 Transcription of telomere proximal variant surface glycoprotein genes is mono-allelic in bl

25 can trypanosome relies upon the silencing of variant surface glycoprotein genes that are found adjace

26 ed transcriptional switching of subtelomeric variant surface glycoprotein genes, continues to operate

27 mmals and involves switches in expression of variant surface glycoprotein genes, which are co-transcr

28 anscribed by a different polymerase than the variant surface glycoprotein genes.

29 lates with epigenetic silencing of telomeric variant surface glycoprotein genes.

30 ages stimulated with the trypanosome soluble variant surface glycoprotein in vitro and in macrophages

31 TbVps34 knockdown inhibits export of variant surface glycoprotein, indicating a function in e

32 interfering with the endocytic transport of variant surface glycoprotein is a highly desirable strat

33 somes, where the ratio of mRNAs for GP63 and variant surface glycoprotein is about 1:150.

34 somes are glycolipid A, the precursor of the variant surface glycoprotein membrane anchor, and glycol

35 lded from their hosts' defenses by a coat of variant surface glycoprotein molecules, each of which is

36 iable major protein of Borrelia hermsii, the variant surface glycoprotein of African trypanosomes, an

37 deposition of newly synthesized GPI-anchored variant surface glycoprotein on the cell surface.

38 n myristoylation of the enormous quantity of variant surface glycoprotein produced.

39 to maintain the cell density of its crucial variant surface glycoprotein protective coat.

40 isotopic sugar composition of the parasites variant surface glycoprotein synthesized in cells incuba

41 s, the parasite loses the 10(7) molecules of variant surface glycoprotein that formed its surface coa

42 e parasite's major cell-surface proteins-the variant surface glycoprotein (VSG) and procyclin.

43 ucei depends upon switches in its protective Variant Surface Glycoprotein (VSG) coat by antigenic var

44 Variable subregions within the variant surface glycoprotein (VSG) coat displayed by Afr

45 ng T-independent B-cell response against the variant surface glycoprotein (VSG) coat expressed by try

46 brucei relies on antigenic variation of its variant surface glycoprotein (VSG) coat for survival.

47 e response by repeatedly replacing its dense variant surface glycoprotein (VSG) coat from its large g

48 eping Sickness, constantly changes its dense variant surface glycoprotein (VSG) coat to avoid elimina

49 st antibodies by periodically changing their variant surface glycoprotein (VSG) coat.

50 host immune system through replacement of a variant surface glycoprotein (VSG) coat.

51 genic variation, a periodic switching of its variant surface glycoprotein (VSG) coat.

52 tigenic variation by periodic changes in its variant surface glycoprotein (VSG) coat.

53 sticated antigenic variation of a protective variant surface glycoprotein (VSG) coat.

54 here it is protected by an essential coat of Variant Surface Glycoprotein (VSG) comprising approximat

55 Changes in variant surface glycoprotein (Vsg) expression allow Tryp

56 has about twenty telomeric bloodstream form Variant Surface Glycoprotein (VSG) expression sites (BES

57 gulation of the RNA polymerase I transcribed variant surface glycoprotein (VSG) expression sites (ESs

58 ranscription is altered at telomere-proximal variant surface glycoprotein (VSG) expression sites (ESs

59 a unique subset of protein-coding genes-the variant surface glycoprotein (VSG) expression sites and

60 mis-regulation of telomere-proximal silenced variant surface glycoprotein (VSG) expression sites and

61 e living in the human bloodstream, expresses variant surface glycoprotein (VSG) from 1 of 15 bloodstr

62 mulated PI-PLC cleavage of the GPI anchor of variant surface glycoprotein (VSG) from Trypanosoma bruc

63 e-I (pol-I) to transcribe just one telomeric variant surface glycoprotein (VSG) gene at a time, produ

64 some consists of a putative bloodstream-form variant surface glycoprotein (VSG) gene expression site

65 d from the metacyclic variant antigen type 4 variant surface glycoprotein (VSG) gene expression site,

66 hese features are reminiscent of a vestigial variant surface glycoprotein (VSG) gene expression site.

67 gulates RNA polymerase I (Pol I)-transcribed variant surface glycoprotein (VSG) gene expression sites

68 ukaryote, Trypanosoma brucei transcribes its variant surface glycoprotein (VSG) gene expression sites

69 also located within the silent subtelomeric variant surface glycoprotein (VSG) gene expression sites

70 he metacyclic variant antigen type 7 (MVAT7) variant surface glycoprotein (VSG) gene in bloodstream T

71 ation through DNA-repair processes involving Variant Surface Glycoprotein (VSG) gene rearrangements a

72 elic expression of one of about 20 telomeric variant surface glycoprotein (VSG) gene-expression sites

73 periodically switching the expression of its variant surface glycoprotein (VSG) genes (vsg) among an

74 chromosomes contain nontranscribed copies of variant surface glycoprotein (VSG) genes and are thought

75 lelic expression and reversible silencing of variant surface glycoprotein (VSG) genes found adjacent

76 Trypanosoma brucei expresses variant surface glycoprotein (VSG) genes in a strictly m

77 aintenance and transcriptional regulation of variant surface glycoprotein (VSG) genes in Trypanosoma

78 ion in Trypanosoma brucei is used for moving variant surface glycoprotein (VSG) genes into expression

79 e, relies upon rearrangement of subtelomeric variant surface glycoprotein (VSG) genes to achieve anti

80 ubtelomeric arrays contain an archive of 806 variant surface glycoprotein (VSG) genes used by the par

81 elically expresses one of approximately 1500 variant surface glycoprotein (VSG) genes while multiplyi

82 African trypanosomes possess hundreds of variant surface glycoprotein (VSG) genes, but only one i

83 the evolution of a massive archive of silent Variant Surface Glycoprotein (VSG) genes, which are acti

84 oallelically expresses one of more than 1000 Variant Surface Glycoprotein (VSG) genes.

85 lencing of a repository of telomere-adjacent variant surface glycoprotein (VSG) genes.

86 nsport and secretion of wild-type and mutant variant surface glycoprotein (VSG) is characterized.

87 sitol (GPI) anchor of the Trypanosoma brucei variant surface glycoprotein (VSG) is unique in having e

88 m of antigenic variation in parasites is the variant surface glycoprotein (VSG) of African trypanosom

89 The variant surface glycoprotein (VSG) of African trypanosom

90 Th1 cell responses to the variant surface glycoprotein (VSG) of African trypanosom

91 The variant surface glycoprotein (VSG) of bloodstream form T

92 The coat consists of ten million copies of variant surface glycoprotein (VSG) that is expressed fro

93 regularly switches its major surface antigen variant surface glycoprotein (VSG) to evade mammalian ho

94 nses and B-cell responses to the trypanosome variant surface glycoprotein (VSG) was measured.

95 e bloodstream stage surface coat composed of variant surface glycoprotein (VSG) with a new coat compo

96 ly synthesized secretory proteins, including variant surface glycoprotein (VSG), confirming its role

97 loodstream, African trypanosomes express the variant surface glycoprotein (VSG), continual switching

98 s evade immune destruction by changing their variant surface glycoprotein (VSG), encoded in a telomer

99 by expressing its major surface antigen, the Variant Surface Glycoprotein (VSG), in a monoallelic man

100 anchor substituents associated with the shed variant surface glycoprotein (VSG), plus the host-activa

101 rucei relies on RNA Pol I for expressing the variant surface glycoprotein (VSG), the key protein in a

102 The role of variant surface glycoprotein (VSG)-specific Th cell resp

103 mune system is a dense coat that comprises a variant surface glycoprotein (VSG).

104 d is densely covered with highly immunogenic Variant Surface Glycoprotein (VSG).

105 a single type of glycoprotein molecule, the variant surface glycoprotein (VSG).

106 ularly changing their antigenic coat made of variant surface glycoprotein (VSG).

107 ted by a densely packed surface monolayer of variant surface glycoprotein (VSG).

108 by switching their dense protective coat of Variant Surface Glycoprotein (VSG).

109 t immune response by frequently changing its variant surface glycoprotein (VSG).

110 panosomes engineered to express GPI-anchored variant surface glycoprotein (VSG).

111 Acylated GPI-PLC was active against variant surface glycoprotein (VSG).

112 y RAD51-directed homologous recombination of Variant Surface Glycoproteins (VSG) genes, most of which

113 prevention due to antigenic variation of the Variant Surface Glycoproteins (VSG) that coat parasites

114 ing by periodically replacing a monolayer of variant surface glycoproteins (VSG) that covers its cell

115 Similarly, defective glycosylation of the variant surface glycoprotein (VSG221) as well as the lys

116 Trypanosoma brucei switches between variant surface glycoproteins (VSGs) allowing immune esc

117 ation, the sequential expression of distinct variant surface glycoproteins (VSGs) at extremely high d

118 sequentially expressing genes for different variant surface glycoproteins (VSGs) from telomere-linke

119 ification of surface-exposed epitopes on the variant surface glycoproteins (VSGs) of African trypanos

120 The GPI anchors of Trypanosoma brucei variant surface glycoproteins (VSGs) undergo rounds of i

121 chieved by periodically expressing different variant surface glycoproteins (VSGs).

122 acity to encode >1000 antigenically distinct variant surface glycoproteins (VSGs).

123 coprotein of bloodstream-form T. brucei, the variant surface glycoprotein, was unaffected in the TbGT

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