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

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

4 ic continuum of ILCs that can develop from a common progenitor.

5 e specification of these two lineages from a common progenitor.

6 EMP and lymphoid lineages may develop from a common progenitor.

7 reg cell populations, potentially denoting a common progenitor.

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

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

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

11 ifferent specialized cell types arise from a common progenitor.

12 ric segregation of regulatory factors from a common progenitor.

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

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

15 contain different alleles that share recent common progenitors.

16 connectivity patterns that are produced from common progenitors.

17 s and glia typically arise sequentially from common progenitors.

18 unknown whether these two populations share common progenitors.

19 uence the production of various neurons from common progenitors.

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

21 t of other epithelial cells originating from common progenitors.

22 entally specified sets of cells derived from common progenitors.

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

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

25 L), three of which (L2/L3/L4) emerged from a common progenitor after the loss of the MmpS6/MmpL6-enco

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

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

28 tions shared between different cells imply a common progenitor and are thus naturally occurring marke

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

30 spiny neurons (D1- and D2-MSNs) arise from a common progenitor and that lineage commitment is establi

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

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

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

34 Distinct cell identities derived from a common progenitor are frequently perpetuated by shared T

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

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

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

38 Natural killer (NK) cells develop from common progenitors but diverge into distinct subsets, wh

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

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

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

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

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

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

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

46 ly related, and both tumors developed from a common progenitor cell (CPC) with MYD88 and TBL1XR1 muta

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

48 (2020) show that generating a common progenitor cell for posterior spinal cord and mus

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

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

51 The identification of a common progenitor cell state in vastly distinct processe

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

53 primary and relapse LBCL-IP originate from a common progenitor cell with a small set of genetic alter

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

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

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

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

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

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

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

61 effector, complement component C3, to prime common progenitor cells toward adipogenesis rather than

62 and IgA-producing B cells were derived from common progenitor cells.

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

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

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

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

67 ysis indicates that neurons originating from common progenitors diverge in their gene expression duri

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

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

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

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

72 riginates in the adrenogonadal primordium, a common progenitor for both the adrenocortical and gonada

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

74 ptidase 4(+) mesenchymal cells function as a common progenitor for IPFP adipocytes and synovial linin

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

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

77 5(+)CD133(+)CD38(+) cell fraction contains a common progenitor for the hematopoietic and vascular lin

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

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

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

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

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

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

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

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

86 A common progenitor haplotype spanned across APC I1307K fr

87 Clones of excitatory neurons derived from a common progenitor have been proposed to serve as element

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

89 Cs and perivascular reticular cells from the common progenitor highlighted the close developmental re

90 x (MTBC) are thought to have expanded from a common progenitor in Africa.

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

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

93 o-development of T cells and ILC2 cells from common progenitors in the thymus.

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

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

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

97 sue while biasing lineage selection of their common progenitors - mesenchymal stem cells.

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

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

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

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

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

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

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

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

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

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

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

109 In the developing ChP, we predict a common progenitor pool for epithelial and neuronal cells

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

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

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

113 proportions at overlapping timepoints from a common progenitor pool.

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

115 th pleiotropic effects preferentially act in common progenitor populations to direct the production o

116 larly, how diverse TEC lineages arise from a common progenitor remains poorly understood.

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

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

119 age-restricted transcriptional programs from common progenitor states.

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

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

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

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

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

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

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

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

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

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

130 ough all cardiomyocytes (CMs) originate from common progenitors, the CCS is composed of biologically

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

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

133 92, and gamma-Asp190 may have derived from a common progenitor, these aspartates of the three subunit

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

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

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

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

138 The mechanisms enabling common progenitors to differentiate into alternative cel

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

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

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

142 er, these cells are not derived from the ILC common progenitor, which generates other ILC subsets and

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

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

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

146 s have revealed that pacemaker cells share a common progenitor with the (pro)epicardium, and that the

147 phores in the fin of D. albolineatus share a common progenitor with xanthophores and maintain plastic

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

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

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