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