ライフサイエンスコーパス: common progenitor

1 that these different cell types arise from a common progenitor ().

2 basophils and mast cells are derived from a common progenitor.

3 ion years since these genera diverged from a common progenitor.

4 o endocrine cells by lineage as they share a common progenitor.

5 ifferent specialized cell types arise from a common progenitor.

6 ric segregation of regulatory factors from a common progenitor.

7 ction(s) of these strains into humans from a common progenitor.

8 nents, DCIS and IDC may have diverged from a common progenitor.

9 oss of Pten, implying that they arose from a common progenitor.

10 f 16 interconnected cells that derive from a common progenitor.

11 entally specified sets of cells derived from common progenitors.

12 unknown whether these two populations share common progenitors.

13 connectivity patterns that are produced from common progenitors.

14 uence the production of various neurons from common progenitors.

15 d that the liver and pancreas originate from common progenitors.

16 t of other epithelial cells originating from common progenitors.

17 contain different alleles that share recent common progenitors.

18 or development of V2a and V2b INs from their common progenitors; (2) it simultaneously activates the

19 gest that these immigrant cells arise from a common progenitor, a dlx-negative basal forebrain stem c

20 H-ras-1 on chromosome 11p, consists of four common progenitor alleles and several dozen rare alleles

21 or gene conversion-type events involving the common progenitor alleles.

22 , describes DCIS and IDC as diverging from a common progenitor and progressing through grades in para

23 opose that insulin and ghrelin cells share a common progenitor and that Nkx2.2 and Pax4 are required

24 ineages, which are believed to derive from a common progenitor, and suggest that it operates in paral

25 tory epithelium supporting cells may share a common progenitor, and that expression of Mash1 may be a

26 Thus, CD133-CD55- common progenitors are the main source of CXCL12 and Kit

27 simple duplication and differentiation of a common progenitor, as might have been anticipated based

28 ontaining enolase superfamily evolved from a common progenitor but catalyze different reactions using

29 hair cells and supporting cells arise from a common progenitor, but how these progenitors are generat

30 They arise from a common progenitor, but little is known about the molecul

31 tor cell per se but differences imposed on a common progenitor by broadened EBV gene expression.

32 d vascular cells are thought to arise from a common progenitor called the haemangioblast.

33 steoblasts and chondrocytes, the CD133-CD55- common progenitors can give rise to marrow reticular str

34 gic trees showed a pattern compatible with a common progenitor cell (CPC) origin in 13 cases.

35 ncies share their ancestry in a less evolved common progenitor cell (CPC) that bears only a subset of

36 Thus, metastatic melanoma recurs from a common progenitor cell and phenotypic changes occur arou

37 date is the fibrocyte, which may represent a common progenitor cell for several mesenchymal lineages.

38 lesions are clonally related, derived from a common progenitor cell or of independent cellular origin

39 cates that these two growth factors act on a common progenitor cell that has, at a minimum, two fates

40 e tissue are linked processes arising from a common progenitor cell, but having an inverse relationsh

41 and endothelial (End) lineages derive from a common progenitor cell, the hemangioblast: specifically,

42 ir origins within a genetically less evolved common progenitor cell.

43 ng the activity of competing regulators in a common progenitor cell.

44 on factor in specifying alternate fates of a common progenitor cell.

45 megakaryocyte (MK) lineages as well as their common progenitor cells (MEPs).

46 mportant determinant of lineage selection by common progenitor cells in the skin.

47 hrough either a 'rich' or 'sparse' ancestral common progenitor clone (CPC).

48 are thought to form in a single burst from a common progenitor cloud of molecular gas.

49 at both types of striated muscle derive from common progenitors comes from clonal analyses that have

50 These cells are produced by common progenitors deriving from the ventricular epithel

51 + single-positive (SP) thymocytes arise from common progenitor double positive (DP) cells that expres

52 erythroid cells are thought to derive from a common progenitor during hematopoietic differentiation.

53 and one SC were observed, suggesting that a common progenitor exists that can remain bipotential up

54 fferentiation and support the existence of a common progenitor for all endocrine cells in the colon.

55 g ES cell differentiation that constitutes a common progenitor for embryonic erythroid and definitive

56 Thus, NEP cells represent a common progenitor for motoneurons and other spinal cord

57 Recent studies support the existence of a common progenitor for the cardiac and endothelial cell l

58 5(+)CD133(+)CD38(+) cell fraction contains a common progenitor for the hematopoietic and vascular lin

59 coustic ganglia, revealing the presence of a common progenitor for the two functional classes of neur

60 these data point towards the existence of a common progenitor for these two lineages, the presence o

61 existence of hemangioblasts, which serve as common progenitors for hematopoietic cells and cardiobla

62 elated protein Sfrp5 in the mouse identifies common progenitors for the outflow tract (OFT), LV, atri

63 d Gna15 arising by tandem duplication from a common progenitor gene in vertebrates.

64 nd plant catalases might have derived from a common progenitor gene sequence.

65 on index classes if and only if they share a common progenitor gene.

66 dial part of the ear harbors a population of common progenitors giving both neurons and hair cells un

67 A common progenitor haplotype spanned across APC I1307K fr

68 arge superfamilies of enzymes derived from a common progenitor have emerged by duplication and diverg

69 an RORgammat(+) developmental pathway from a common progenitor in SLTs.

70 development and diversification of DCs from common progenitors in the bone marrow.

71 he possibility that they have evolved from a common progenitor, it has been difficult to examine this

72 ed on these findings, we hypothesized that a common progenitor may differentiate into the three tumor

73 OBs, suppression of the self-renewal of this common progenitor may represent a key mechanism of the a

74 that, following asymmetric cell division of common progenitors, NK4/NKX2-5 promotes GATAa/GATA4/5/6

75 es and that ETS1 promotes the fitness of the common progenitor of all ILCs.

76 y support the presence of phytochrome in the common progenitor of green algae and land plants.

77 ated embryonic stem (ES) cells represent the common progenitor of hematopoietic and endothelial cells

78 gnized by at least one C2H2-ZF domain in the common progenitor of placental mammals, but that extant

79 one both editing and CSR and show them to be common progenitors of CXP tumors.

80 y expressed in Flk1(+) cells, which serve as common progenitors of endothelial cells, blood cells, an

81 Olig gene expression is proposed to mark the common progenitors of motoneurons and oligodendrocytes.

82 require TBX1 and segregate precociously from common progenitors of the second heart field (SHF) and p

83 ad transcription factor, is expressed in the common progenitors of V2a and V2b INs and is required di

84 ystem to label either neurons derived from a common progenitor or isolated single neurons, in the Dro

85 and cell-tracing experiments indicate that a common progenitor pool in the posterior region of the SH

86 subtypes, are sequentially generated from a common progenitor pool in the vertebrate hindbrain.

87 rough incremental allocation of cells from a common progenitor pool, and that the lineage composition

88 proportions at overlapping timepoints from a common progenitor pool.

89 , multiple motor neuron classes arise from a common progenitor population; however, the mechanisms un

90 Furthermore, adoptive transfer of common progenitors revealed that kidney F4/80(+)CD11c(+)

91 of CXCL12 and Kitl expression in CD133-CD55- common progenitors severely disrupted the BM niche forma

92 These data define a novel B-cell/myeloid common progenitor (termed the BMP) and imply a less rest

93 haematopoietic and endothelial cells share a common progenitor, termed the haemangioblast.

94 Both blood and blood vessels derive from a common progenitor, termed the hemangioblast, but the fac

95 Accumulating studies support the idea that a common progenitor, termed the hemangioblast, generates b

96 eroendocrine, and Paneth cells) arise from a common progenitor that expresses Math1, whereas absorpti

97 major cell types of the retina arise from a common progenitor that expresses Notch1.

98 l ligament fibroblasts) are descended from a common progenitor (the cranial neural crest).

99 Because these cells differentiate from a common progenitor, the composition of their intracellula

100 poietic and endothelial cells develop from a common progenitor, the hemangioblast, or directly from m

101 precursors are hypothesized to arise from a common progenitor, the hemangioblast.

102 tulating cytokine-induced differentiation of common progenitors, the effect of various reported gene

103 throid cells and megakaryocytes arise from a common progenitor, their terminal maturation follows ver

104 92, and gamma-Asp190 may have derived from a common progenitor, these aspartates of the three subunit

105 ough all mouse mast cells are derived from a common progenitor, these effector cells exhibit tissue-s

106 equence of their developmental dependency on common progenitor tissue interactions and signaling path

107 recursor cell (OPC) formation by acting on a common progenitor to determine neuronal versus oligodend

108 EKLF and KLF2 may have coordinate roles in a common progenitor to erythroid and endothelial cells.

109 The mechanisms enabling common progenitors to differentiate into alternative cel

110 Wang et al. point to the existance of a common progenitor tumor stem cell that gives rise to gen

111 ommon pathways, and despite diverging from a common progenitor under different selective pressures fo

112 samples suggests divergent evolution from a common progenitor, whereas modular expression profiling

113 Fitness was measured relative to their common progenitor, which had evolved on glucose at 37 de

114 genetic tags, we found that B1 cells share a common progenitor with embryonic cells of the cortex, st

115 of the mature NPY+ cell population shares a common progenitor with POMC+ cells.

116 ng plasmacytoid dendritic cells (pDCs) share common progenitors with antigen-presenting classical den

117 Evidence suggests that Th17 cells share common progenitors with immunosuppressive CD4(+) inducib

118 Bone marrow macrophages (BMMs) share common progenitors with osteoclasts and are critical com