1 esults did not predict patterns in the field
transplantation experiment.
2 orter lines for time-lapse imaging and mouse
transplantation experiments.
3 n as shown by cell dissociation, sorting and
transplantation experiments.
4 lso engrafted secondary recipients in serial
transplantation experiments.
5 species, are a valuable tool in preclinical
transplantation experiments.
6 advantage when tested in serial competitive
transplantation experiments.
7 identities have been examined through recent
transplantation experiments.
8 the prototype Fab by chain shuffling and CDR
transplantation experiments.
9 etabolism and restore HSC activity in serial
transplantation experiments.
10 pulate hemoablated recipients in competitive
transplantation experiments.
11 renewal are typically defined through serial
transplantation experiments.
12 eptor (IL-7R) sustained vasculitis in serial
transplantation experiments.
13 Sweden, a prediction we validated in field
transplantation experiments.
14 ty to expand after re-infection in serial re-
transplantation experiments.
15 autonomous manner as revealed by competitive
transplantation experiments.
16 ained hematopoietic reconstitution in serial
transplantation experiments.
17 ution in competitive repopulation and serial
transplantation experiments.
18 cells in competitive repopulation and serial
transplantation experiments.
19 tituted recipient bone marrow in competitive
transplantation experiments.
20 s in BP regulation, we performed cross-renal
transplantation experiments.
21 is required for ISV development we performed
transplantation experiments.
22 erve-derived SC or dermal fibroblast (Fibro)
transplantation (Experiment 2).
23 erves over one year in an in situ reciprocal
transplantation experiment (
20 m vs. 300 m and fjord hea
24 of the gut mycobiome was confirmed in fecal
transplantation experiments:
adult maternally separated
25 que to assign developmental ancestry, somite
transplantation experiments and Cre-lox fate-mapping, we
26 Transplantation experiments and model predictions that m
27 Transplantation experiments and mutant analysis reveal t
28 Lung transcriptomics, bone marrow
transplantation experiments,
and analysis of cellular cy
29 istics of the head organizer, as measured by
transplantation experiments,
and by the expression of ge
30 We performed a reciprocal
transplantation experiment at three elevations, plus a g
31 icant attention in the 1970s when orthotopic
transplantation experiments between quail and chick embr
32 Cell
transplantation experiments confirm that smu function is
33 In this study, mammary gland
transplantation experiments confirm that the increase in
34 Further fecal transplantation and culture
transplantation experiments confirm the involvement of g
35 Tumor
transplantation experiments confirm the stromal role of
36 Renal
transplantation experiments confirmed that extrarenal tr
37 Bone marrow
transplantation experiments confirmed that the hematopoi
38 Transplantation experiments confirmed that these develop
39 In competitive mouse bone marrow (BM)
transplantation experiments,
Cxcr4 haploinsufficiency wa
40 Cell
transplantation experiments demonstrate that Hh acts dir
41 Zebrafish moesin1 knockdown and cell
transplantation experiments demonstrate that Moesin1 is
42 Bone marrow
transplantation experiments demonstrate that NPM promote
43 Importantly,
transplantation experiments demonstrate that the introni
44 Cell
transplantation experiments demonstrate that the proximi
45 Bacterial community
transplantation experiments demonstrated a causal role o
46 Analysis of engraftment in murine
transplantation experiments demonstrated an increase in
47 mia onset was delayed, and limiting dilution
transplantation experiments demonstrated functional loss
48 Bone marrow
transplantation experiments demonstrated that ACAT1 defi
49 in the hematopoietic system and fetal liver
transplantation experiments demonstrated that anemia was
50 Bone marrow
transplantation experiments demonstrated that both const
51 Competitive
transplantation experiments demonstrated that Fzd6(-) (/
52 These
transplantation experiments demonstrated that giaSCs hav
53 BM
transplantation experiments demonstrated that PAR-1 in n
54 Long-term
transplantation experiments demonstrated that the double
55 have lost myeloid differentiation potential,
transplantation experiments described here reveal that a
56 PyV-mT hyperplasias together with classical
transplantation experiments designed to test the growth
57 In short-term
transplantation experiments,
donor EpoR-HM bone marrow c
58 respond to these signals, we performed cell
transplantation experiments during gastrulation.
59 In heterotopic
transplantation experiments,
En protein expression corre
60 Finally, 2-step
transplantation experiments established a differentiatio
61 Large-scale single-cell
transplantation experiments established that T-ALLs can
62 Transplantation experiments established the Pxmp2(-/-) m
63 ells (HSC/Ps) fail to effectively engraft in
transplantation experiments,
exhibiting normal proximal
64 Transplantation experiments failed to demonstrate a role
65 In
transplantation experiments, &
gt;350 backcross 1 progeny we
66 (FasL) genes (lpr and gld, respectively) in
transplantation experiments has resulted in contradictor
67 Transplantation experiments have been performed to deter
68 Transplantation experiments have revealed a developmenta
69 Transplantation experiments have shown that these aberra
70 cy, are observed in in vitro assays and cell
transplantation experiments;
however, the extent to whic
71 Bone marrow
transplantation experiments identify hematopoietic cells
72 Through bone marrow
transplantation experiments in a transgenic mouse model
73 Transplantation experiments in chick embryos indicate th
74 Transplantation experiments in dogs with transduced auto
75 We corroborate this finding with
transplantation experiments in European and North Americ
76 Transplantation experiments in germfree mice indicate th
77 In this study, performing thymus
transplantation experiments in mice, we report that thym
78 Using competitive bone marrow
transplantation experiments in mice, we show that ionizi
79 med oncogenic mechanism of miR-125b, we used
transplantation experiments in mice.
80 Transplantation experiments in MISTRG mice established a
81 Using a series of bone marrow
transplantation experiments in MMP-9(+/+) and MMP-9(-/-)
82 ith self-renewal capacity is based on thymus
transplantation experiments in which host-derived thymoc
83 genitors respond directly to Hh signals, and
transplantation experiments in zebrafish demonstrate tha
84 Sex-mismatched cell
transplantation experiments indicate that multiple cell
85 In vitro organ culture and in vivo
transplantation experiments indicate that signals from t
86 Transplantation experiments indicate that the expression
87 Furthermore, bone marrow
transplantation experiments indicate that the immune sys
88 Transplantation experiments indicate that the R-Ras defi
89 Transplantation experiments indicate they have a high an
90 Bone marrow
transplantation experiments indicated that A(2b)AR bone
91 Transplantation experiments indicated that CD41-KO-assoc
92 BM
transplantation experiments indicated that local p21Cip1
93 Reciprocal
transplantation experiments indicated that TGF-beta2 exp
94 Bone marrow
transplantation experiments indicated that the majority
95 Transplantation experiments indicated that these defects
96 Strikingly,
transplantation experiments indicated that these progeni
97 However, secondary
transplantation experiments indicated that when the bone
98 se results, together with recent quail-chick
transplantation experiments indicating that even very la
99 Pseudovivipary is usually retained in
transplantation experiments,
indicating that the trait i
100 Using bone marrow
transplantation experiments into wild-type recipients, w
101 Recently,
transplantation experiments involving permanently labele
102 Bone marrow
transplantation experiments isolated the attenuation to
103 In serial
transplantation experiments,
My-bi HSCs contributed sign
104 Transplantation experiments of mammary epithelium and of
105 cell activity as judged by limiting dilution
transplantation experiments of primary mammary epithelia
106 Moreover,
transplantation experiments performed across major histo
107 Bone marrow
transplantation experiments performed in lethally irradi
108 Results from thymus
transplantation experiments proved further that depletio
109 Sl17H/Sl17H recipient mice was diminished in
transplantation experiments,
providing evidence for a ro
110 Serial
transplantation experiments reconstitute the tumors, sug
111 The
transplantation experiments reveal a heterogeneous popul
112 Transplantation experiments reveal that dnRok2 cells in
113 Transplantation experiments reveal that EpCAM(+) cells a
114 Our cell
transplantation experiments reveal that in zebrafish, Sm
115 Transplantation experiments reveal that neuron-neuron in
116 Spermatogonial
transplantation experiments revealed a depletion of sper
117 Transplantation experiments revealed that 6 week-old spe
118 Orthotopic
transplantation experiments revealed that CTSB overexpre
119 Bone marrow
transplantation experiments revealed that endothelial Sh
120 in mice with defects in adipogenesis and in
transplantation experiments revealed that intradermal ad
121 Bone marrow
transplantation experiments revealed that MAVS in cells
122 Bone marrow
transplantation experiments revealed that nonhematopoiet
123 Furthermore, bone marrow
transplantation experiments revealed that T cell-derived
124 Results from cell
transplantation experiments revealed that the cultured F
125 Micromere
transplantation experiments revealed that the defects in
126 Bone marrow
transplantation experiments revealed that the effector c
127 Bone marrow
transplantation experiments revealed that the enhancemen
128 Transplantation experiments revealed that the hypertroph
129 Bone marrow
transplantation experiments revealed that TLR4 expressed
130 Bone marrow
transplantation experiments revealed unremarkable influe
131 Eye
transplantation experiments show that astray function is
132 Cell
transplantation experiments show that cells derived from
133 Cell
transplantation experiments show that cloche acts cell-a
134 Finally, cell
transplantation experiments show that dino is required o
135 Transplantation experiments show that loss of vangl2 dis
136 Cell
transplantation experiments show that the cell movement
137 Chimeric and competitive bone marrow
transplantation experiments show that the defect in myel
138 Micromere
transplantation experiments show that the gene is not in
139 Bone marrow
transplantation experiments show that the increased radi
140 Cell
transplantation experiments show that this effect is cel
141 Similarly, adoptive transfer and bone marrow
transplantation experiments showed differential diabetes
142 Accordingly, competitive BM
transplantation experiments showed that ApoE acted cell
143 Transplantation experiments showed that homozygosity for
144 Bone marrow
transplantation experiments showed that most of the extr
145 Transplantation experiments showed that the mammary stro
146 Bone marrow
transplantation experiments showed that the newly formed
147 In serial
transplantation experiments,
STAT5ab(-/-) and c-Mpl(-/-)
148 ; quantitation of droplet histone levels and
transplantation experiments suggest that histones are tr
149 Transplantation experiments suggest that neural crest pr
150 Bone marrow
transplantation experiments suggest that REGgamma's func
151 Transplantation experiments suggest that the effects of
152 BM
transplantation experiments suggested that the AAA pheno
153 Moreover, in utero
transplantation experiments suggested that the rostrocau
154 ell types in clonogenic colony assays and in
transplantation experiments,
suggesting that the lineage
155 ce from single-cell analyses and genetic and
transplantation experiments suggests that satellite cell
156 oocyte counts to genetic lineage tracing and
transplantation experiments support a paradigm shift in
157 this patterning process and the quail-chick
transplantation experiments that have provided the found
158 We present evidence from overexpression and
transplantation experiments that Tbx18 controls fissure
159 lity, despite evidence from embryo and ovary
transplantation experiments that they could gestate and
160 We present direct evidence, based upon cell
transplantation experiments,
that the expression of one
161 In bone marrow
transplantation experiments,
the development of POI requ
162 ven fluorophore transgenics in hematopoietic
transplantation experiments to assess true multilineage
163 We then used blastula stage
transplantation experiments to demonstrate that rods fro
164 colony-forming cell (ECFC) assays and murine
transplantation experiments to examine human vasculogene
165 d high CO2 for 4.5 y, followed by reciprocal
transplantation experiments to test for adaptation.
166 Serial
transplantation experiments to test self-renewal reveale
167 Bone marrow
transplantation experiments using gene-targeted mice, bo
168 In bone-marrow
transplantation experiments using irradiated allogeneic
169 tes non-HSCs away from HSCs, and single-cell
transplantation experiments using the enriched populatio
170 dothelial cells or pericytes, we carried out
transplantation experiments using these mice as donors o
171 Moreover, reciprocal bone marrow
transplantation experiments using TNF receptor-deficient
172 Macrophage depletion and bone marrow
transplantation experiments validated the functional rel
173 A seven month
transplantation experiment was conducted to rebuild the
174 Using cell
transplantation experiments,
we determine that the Tcf7l
175 Using
transplantation experiments,
we find that in mosaic vess
176 Using cross-
transplantation experiments,
we found that deletion of p
177 Using genetic, pharmacological, and
transplantation experiments,
we provide evidence that en
178 Using
transplantation experiments,
we provide evidence that th
179 Finally, using sequential
transplantation experiments,
we show that the node, head
180 he enhanced vascular thrombosis, bone marrow
transplantation experiments were performed between Fv+/+
181 Bone marrow
transplantation experiments were performed to determine
182 sion of a constitutively active receptor and
transplantation experiments were used to confirm that BM
183 arterial ketone body ratio, orthotopic liver
transplantation) experiments were conducted using Brattl
184 ability to produce early leukemia in vivo in
transplantation experiments,
were found only in mice wit
185 fects are experimentally validated in serial
transplantation experiments where Bcl11a (-/-) HSCs are
186 This notion is based on thymus
transplantation experiments where it was shown that thym
187 lia in vitro generation refined for advanced
transplantation experiments,
which provides a combined i
188 Transplantation experiments with either whole bone marro
189 This finding was confirmed in xenograft
transplantation experiments with lentiviral-infected sho
190 This lays the foundation for competitive
transplantation experiments with mutant zebrafish HSCs a
191 troviral transduction and hematopoietic cell
transplantation experiments with p21(WAF1)-deficient cel