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1 ovo mutation detection, linkage analysis and lineage tracing.
2 ney with in situ expression studies and cell lineage tracing.
3 t can be addressed using single cell dynamic lineage tracing.
4 he dorsal aspect of the prostatic urethra by lineage tracing.
5  precision of conventional Cre-loxP-mediated lineage tracing.
6 he Cell Stem Cell tenth anniversary theme of lineage tracing.
7 single-cell readouts now enables large-scale lineage tracing.
8 ese growth regulators as markers for genetic lineage tracing.
9 essential for many pooled screens and clonal lineage tracing.
10  and identify cell type-specific markers for lineage tracing.
11                                              Lineage tracing (a method used to track each cell though
12  glandular fission, and more rapid stem cell lineage tracing, a process that can be suppressed by exo
13 , histology, and RNAscope in an SMC-specific lineage-tracing Ahr knockout mouse model of atherosclero
14                                              Lineage tracing aims to identify all progeny arising fro
15                                              Lineage tracing aims to identify the progeny of a define
16                                              Lineage tracing analysis revealed the conversion of beta
17                                              Lineage tracing analysis with dual-fluorescent reporter
18                                           By lineage tracing analysis, we also found that collagen-ex
19                                 In addition, lineage-tracing analysis indicated that all mTECs have a
20                                     Notably, lineage-tracing analysis revealed Swi/Snf-deficient beta
21                                              Lineage-tracing analysis revealed that descendants of Sf
22  use next generation sequencing for antibody lineage tracing and B cell fate mapping.
23 y of skeletal muscle-resident macrophages by lineage tracing and bone marrow transplant experiments.
24 h the origin(s) of infarct fibroblasts using lineage tracing and bone marrow transplants and a robust
25                                              Lineage tracing and busulfan challenge show that these a
26                                        Using lineage tracing and DNA pulse-chase analyses, we identif
27                                              Lineage tracing and fate mapping, overlapping yet distin
28                                        Using lineage tracing and flow cytometry, approximately 40% of
29                                              Lineage tracing and functional analyses demonstrate that
30                                  We combined lineage tracing and functional analyses in a sequential
31                         Here we show through lineage tracing and genetic ablation that BMI1(+) CSCs m
32                                        Using lineage tracing and genetic label-retention assays, we s
33                                              Lineage tracing and IgH repertoire analyses revealed min
34                                              Lineage tracing and immunohistochemical analyses reveale
35              Data from in vivo imaging, cell-lineage tracing and knockout studies in mice, as well as
36                                        Using lineage tracing and label retention experiments, we show
37       By timing the interval between LGR5(+) lineage tracing and lethal injury, we show that ISC rege
38         We use two complementary approaches, lineage tracing and live fluorescent microscopy, which b
39 including genome-wide screens, gene therapy, lineage tracing and molecular recording.
40                             Here we use cell lineage tracing and multiple in vivo approaches to study
41 l RNA sequencing in combination with in vivo lineage tracing and organoid models to finely map the tr
42                                              Lineage tracing and quantitative clonal analysis reveal
43 pithelial lineage relationships, we combined lineage tracing and recovery from transient in vivo mTEC
44                        A method for combined lineage tracing and scRNA-seq reveals the interplay betw
45                                    Combining lineage tracing and scRNA-seq, we show that Lgr5 marks E
46                     By combining pulse-chase lineage tracing and single-cell RNA sequencing, we obser
47 eterogeneity of these cells as determined by lineage tracing and single-cell sequencing in developmen
48 on to known ectodermal contributions, we use lineage tracing and time-lapse imaging in zebrafish to i
49                                Using in vivo lineage tracing and triple negative breast cancer (TNBC)
50                                              Lineage-tracing and activity-tracing studies in the mous
51                                  Here, using lineage-tracing and molecular genetic studies in the roo
52                       In zebrafish, previous lineage-tracing and mutant analyses suggested that SHF v
53                                Using genetic lineage-tracing and neural crest-deficient mutants in ze
54                                Using genetic lineage-tracing and scanning-block face electron microsc
55 irculating memory (TCIRCM), and TRM pools by lineage-tracing and single-cell transcriptome analysis.
56  origin of melanoma, we combined single-cell lineage-tracing and transcriptomics approaches with time
57                       Using explant studies, lineage tracing, and clonal analysis, we demonstrate tha
58 ation with molecular identification, genetic-lineage tracing, and mutant analyses.
59                     We employ genetics, cell lineage tracing, and single molecule imaging to show tha
60     Recent studies have applied transgenics, lineage-tracing, and transcriptomics to help decipher th
61 s of this study were to evaluate, by using a lineage tracing approach, the contribution of peribiliar
62 is healing, Gli1 expression was examined via lineage tracing approaches and the effect of Smo deletio
63 oadly review the origins of fate mapping and lineage tracing approaches.
64                                Sophisticated lineage-tracing approaches for analyzing embryogenesis h
65    Here we show, using unbiased quantitative lineage-tracing approaches, biophysical modelling and in
66                            Using genetic and lineage-tracing approaches, we describe novel dorsal and
67 me-lapse imaging, protocol optimization, and lineage-tracing approaches.
68 d by analysing clonal data from in vivo cell lineage-tracing assays.
69                                  Independent lineage tracing based on Stmn1 and Ki67 expression confi
70                                              Lineage tracing by using Cdh5cre(ERt2)/Rosa-YFP reporter
71    Here, we describe the CRISPR array repair lineage tracing (CARLIN) mouse line and corresponding an
72 e wide-ranging applications, such as in deep lineage tracing, cellular barcoding, molecular recording
73                                Using genetic lineage tracing, clonal analysis, multiplexed in situ hy
74                                        Using lineage tracing combined with whole brain clearing, we p
75                                      We used lineage tracing, conditional deletion, mosaic analysis a
76                                              Lineage tracing confirmed that germ cells die as clones
77                                              Lineage tracing confirmed that LDB1-depleted, insulin-ne
78                                      Genetic lineage tracing confirms the presence of the Tbx6(+) NMP
79 escent, self-renew, and, as shown by genetic lineage tracing, contribute to all 3 pancreatic lineages
80  an experimental model system using in vitro lineage tracing coupled with exome, transcriptome and in
81 n the intestinal epithelium, and a year-long lineage-tracing course revealed that genetic blockade of
82 y, we generate the most complex experimental lineage tracing dataset to date, 34,557 human cells cont
83                       In the latter, genetic lineage tracing demonstrated the epicardial origin of fi
84 igorous control of Cre-loxP recombination in lineage tracing, effectively circumventing potential unc
85  should broadly enable large-scale mammalian lineage tracing efforts.
86                                              Lineage tracing established that Hey-deficient ECs are u
87  the preparation and validation of cells for lineage tracing, establishment of grafts and label induc
88 rall data size, and accomplish high-fidelity lineage tracing even for increased imaging time interval
89 y regulator, we disclose molecular proof and lineage tracing evidence showing the distinct MSCs contr
90                   This study provides direct lineage tracing evidence that a cardiomyoblast populatio
91                            Recently, genetic lineage tracing experiments have revealed chondrocyte pr
92                                              Lineage tracing experiments in Foxc1 mutant mouse cerebe
93 lytic approach, we show that data from eight lineage tracing experiments is consistent with tissue ma
94                                              Lineage tracing experiments of the gastric corpus in mic
95 ID deletion, single-cell RNA sequencing, and lineage tracing experiments point to selection of relati
96                                              Lineage tracing experiments revealed accumulation of ex-
97                                              Lineage tracing experiments show that Bglap-expressing c
98                                              Lineage tracing experiments show that GATA/CD24hi cells
99                                              Lineage tracing experiments show that MECs contribute to
100                                 We performed lineage tracing experiments to determine the fates of pe
101 ow transplantation and Cre recombinase-based lineage tracing experiments, we rule out cell fusion eve
102 oit a Prdm1.CreERT2-LacZ reporter allele for lineage tracing experiments.
103                                Using genetic-lineage-tracing experiments and an in situ labeling appr
104                            We performed cell lineage-tracing experiments and analyzed the microbiomes
105 fferentiation process was validated by using lineage-tracing experiments based on Sox18Cre(ERt2)/Rosa
106                                     However, lineage-tracing experiments demonstrate that cells from
107                                              Lineage-tracing experiments identified villin-expressing
108                                       Recent lineage-tracing experiments in chick and zebrafish embry
109                                     Here, by lineage-tracing experiments in fetal or postnatal mice,
110                                      In vivo lineage-tracing experiments in molars showed the contrib
111                                              Lineage-tracing experiments indicated that the majority
112 sed Sox9 and Ngn3 mRNA levels in islets, but lineage-tracing experiments revealed that neoformed beta
113                                              Lineage-tracing experiments revealed that PW1(+) cells d
114                                              Lineage-tracing experiments revealed that the cells that
115                                              Lineage-tracing experiments showed that CC10(+), but not
116 terior axis, as demonstrated by foundational lineage-tracing experiments that showed the restricted d
117 troversies, including the failure of initial lineage-tracing experiments to confirm a major role for
118                                     However, lineage-tracing experiments using an inducible Tbx18-Cre
119                           Here, by combining lineage-tracing experiments with a model of severe gland
120                                     Based on lineage-tracing experiments, non-hepatocytes did not con
121                                      Through lineage-tracing experiments, we show that bLECs arise fr
122 vide the first direct evidence using genetic lineage tracing for two basic assumptions in Schwann cel
123  we review major discoveries in neural crest lineage tracing from a historical perspective.
124 reased epidermal proliferation with expanded lineage tracing from epidermal stem cells positive for L
125                                  Here we use lineage-tracing from development, through adult homoeost
126   Parp1 knockout in preadipocytes in a mouse lineage-tracing genetic model increases adipogenesis, le
127                                Retrospective lineage tracing harnesses naturally occurring mutations
128                                 In the lung, lineage tracing has been used to identify distinct epith
129   Single-cell RNA sequencing (scRNA-seq) and lineage tracing identified a TCF-1(+)Ly108(+)PD-1(+) CD8
130                                              Lineage tracing identified intrinsic recruitment of Scx-
131            For example, photoconversion cell-lineage tracing identified migratory and proliferative c
132                            Here, using AXIN2 lineage tracing in BAC-transgenic mice, we confirm the r
133                                        Using lineage tracing in Lgr5-EGFP-CreERT2/Rosa26-Tomato and L
134                                      Genetic lineage tracing in mice indicates that gastrin expressio
135                                           By lineage tracing in mice, we have shown recently that clu
136                                 Furthermore, lineage tracing in postnatal and adult glands provides t
137 ncoding and optimal transport principles for lineage tracing in settings where existing experimental
138 ion of stem cell-derived clones using sparse lineage tracing in the regenerating mouse olfactory epit
139                Here, I have used single-cell lineage tracing in the whole mouse uterus to demonstrate
140 here, using gene expression and fate mapping/lineage tracing in zebrafish, that pineal progenitors or
141                                 Quantitative lineage-tracing in vivo revealed that conditional deleti
142                                      Genetic lineage tracing indicated that stromal cells blocking th
143 s of pancreatic ductal adenocarcinoma, where lineage tracing indicates that Cytokeratin-Synaptophysin
144                                              Lineage tracing involves the identification of all ances
145                                              Lineage tracing is a powerful tool that can be used to u
146 , IPMNs and PDAC expressed the duct-specific lineage tracing marker yellow fluorescent protein.
147    Here we present CRISPR-UMI, a single-cell lineage-tracing methodology for pooled screening to acco
148                       In this study, we used lineage tracing methods to determine the lineage relatio
149      When compared to existing retrospective lineage tracing methods, RETrace achieved higher accurac
150        Parallel advances in sequencing-based lineage-tracing methods now facilitate the mapping of cl
151 anced in vivo imaging techniques, transgenic lineage tracing mice, and clinical interventional studie
152 nd rabies virus approaches in transgenic SVZ-lineage-tracing mice, SVZ-derived neurons synaptically i
153                            We used a genetic lineage tracing model to investigate whether endothelial
154 dressed major concerns with the Tri-PyMT EMT lineage tracing model, which provides us with a powerful
155        Here, we demonstrate that a murine EC lineage-tracing model (Cdh5-Cre(ERT2):ZSGreen(l/s/l) mic
156                In this study, we use genetic lineage-tracing models and adoptive transfer protocols t
157                                 Using murine lineage-tracing models and gene expression profiling, we
158                     Herein we use multicolor lineage-tracing models to confirm that the mature SMC ca
159 vascular-cell-specific and pericyte-specific lineage-tracing models to trace the fate of perivascular
160  post-Aire MHCII(lo) subset as identified by lineage-tracing models.
161   In this study, we combined immunocompetent lineage tracing mouse models of GBM with high-resolution
162  bulk RNA sequencing, and an innovative dual lineage tracing mouse to understand the mechanism by whi
163              We generated a new Abcg2-driven lineage-tracing mouse model with efficient labeling of S
164                                        Using lineage tracing, murine models of heart calcification an
165 utively express either Cre-GFP or Tomato for lineage tracing of a mutant and a reference group of cel
166   We used single-cell sequencing and genetic lineage tracing of c-kit(+) cells to determine whether v
167                   Here, we performed in vivo lineage tracing of cells with an expression history of I
168                                              Lineage tracing of cranial neural crest cells revealed t
169  line (Kim1-GCE) in order to perform genetic lineage tracing of dedifferentiated cells while measurin
170                     In toto live imaging and lineage tracing of drl-based reporters captures the dyna
171                                    Recently, lineage tracing of endothelial cells in mouse models all
172                            Here we show that lineage tracing of Gdf5-expressing joint interzone cells
173  the risk for allergy, temporally controlled lineage tracing of group 2 innate lymphoid cells (ILC2s)
174 of FoxP3 in a fraction of apoB(+) T(regs) in lineage tracing of hyperlipidemic Apoe(-/-) mice.
175                                              Lineage tracing of Luminal-C cells indicated that Dist-L
176                  Tamoxifen-inducible genetic lineage tracing of mature adipocytes and single-cell RNA
177                                              Lineage tracing of peri-injury Axin2(+) hepatocytes show
178         Here, we performed clonal multicolor lineage tracing of skeletal muscle stem cells (MuSCs) to
179 ith specific expression patterns and perform lineage tracing of subpopulations of escort cells and fo
180 ed sustained clonogenic growth in vitro, and lineage-tracing of Prox1(+) cells revealed long-lived cl
181                    METHODS AND Using genetic lineage tracing or bone marrow transplant, we found no e
182  We focus on the most recent developments in lineage tracing, permitted by advances in single-cell ge
183                  By combining in vivo clonal lineage tracing, proliferation kinetics, single-cell tra
184                   Recent advances in genetic lineage tracing provide insight into epithelial lineage
185                                              Lineage tracing provided formal genetic proof that the u
186                                              Lineage tracing provides key insights into the fate of i
187                                   Transgenic lineage tracing revealed strong clonal competition that
188            Trajectory modeling together with lineage tracing revealed that airway and alveolar stem c
189         Consistent with these findings, cell lineage tracing revealed that IH(30) increased the propo
190                                      Genetic lineage tracing revealed that pericentral Lgr5(+) hepato
191                                      In vivo lineage tracing revealed that the gene transfer of SeV-G
192                              Genetic in vivo lineage tracing revealed that the Krt15 promoter marks a
193                                      Genetic lineage tracing revealed that the stemness of a bladder
194                                Here, genetic lineage tracing revealed that, during murine embryonic d
195                             Endothelial cell lineage tracing showed that BNP directly stimulated the
196 ohistochemistry, flow cytometry, and genetic lineage tracing showed that infiltrating CCR2 cells incl
197 CreERT2 marks both AMFs as well as ALFs, and lineage tracing shows that ALFs are retained in adult al
198                                      Genetic lineage tracing shows that specific diencephalic ependym
199                                 Quantitative lineage tracing shows that THRA mutation-containing prog
200                              We used genetic lineage tracing, single-cell RNA sequencing, and organoi
201                 Here, by using live imaging, lineage tracing, single-cell transcriptomics and genetic
202                                  We combined lineage tracing, single-cell transcriptomics, and electr
203  these dedifferentiating cells using several lineage-tracing strains and single-cell mRNA-seq, and we
204                   We use multiple models and lineage tracing strategies to show that this squamous-co
205                                    Intricate lineage-tracing strategies and experimental models of re
206                                    Recently, lineage-tracing strategies have revealed that Gdf5-linea
207                          Using 2 independent lineage-tracing strategies in murine models, we show tha
208                         In contrast to other lineage-tracing strategies, the method described here as
209                            Moreover, using a lineage tracing strategy, we provide evidence that high
210                     Here, we have employed a lineage-tracing strategy that uses a tamoxifen-dependent
211               Employing a p63(CreERT2)-based lineage-tracing strategy, we identified a unipotent fate
212                                      Using a lineage-tracing strategy, we specifically labeled fetal-
213 nd in vivo Matrigel plug assay together with lineage tracing studies and single cell RNA-sequencing t
214                                      Genetic lineage tracing studies demonstrate that the native endo
215                                              Lineage tracing studies demonstrated that Ctsk-Cre could
216                                              Lineage tracing studies demonstrated that the original G
217 ar smooth muscle cells (VSMCs), we performed lineage tracing studies in mice to further clarify this
218                                              Lineage tracing studies in mouse suggest that chondrocyt
219                            Furthermore, cell lineage tracing studies revealed that the Axin2(+)-mesen
220                    Integrating cell-specific lineage tracing studies, spatially specific mRNA transcr
221                                Here, we used lineage tracing studies-labelling cells expressing Cx3cr
222 l types can complicate the interpretation of lineage-tracing studies and has caused controversy in ma
223                                     However, lineage-tracing studies have highlighted flaws in the in
224                                       Recent lineage-tracing studies have shown that mature hepatocyt
225                                           In lineage-tracing studies of mice, we found that Gli1(+) P
226                                              Lineage-tracing studies revealed that these MAC2+ cells
227             In particular, we revisit recent lineage-tracing studies that shed light on this issue an
228 cuss how advancing technologies have refined lineage-tracing studies, and how clonal analysis can be
229       Based on evidence from in vivo genetic lineage-tracing studies, pericytes have been identified
230 ent studies with single cell transplants and lineage tracing suggest that adult HSCs are diverse in t
231 opment and validation of a recombinase-based lineage tracing system for the chicken embryo to further
232               Here we describe a new genetic lineage tracing system that incorporates the Dre-rox rec
233              By using a newly developed dual-lineage tracing system, we show that bipotent alveolar c
234 re, using a newly generated Hoxa11-CreER(T2) lineage-tracing system, we show Hoxa11-lineage marked ce
235    However, recent investigations using cell lineage tracing techniques have demonstrated that many,
236 d for DNA-based information storage and cell lineage tracing technologies.
237                 Recent studies using genetic lineage tracing technology have implicated diverse organ
238 nfluential study based on fluorescence-based lineage tracing technology provided evidence that very f
239                                        Using lineage tracing technology, we demonstrate that after ch
240         Here, we have developed a novel dual lineage-tracing technology, using a combination of two r
241                                        Using lineage tracing, temporal single-cell analyses, and chro
242 including their own, that suggested based on lineage tracing that mural cells are adipogenic, contras
243                      Here we show by genetic lineage tracing that PROM1(+) cells are derived in part
244                 Here, we demonstrate by cell lineage tracing that the gills of a cartilaginous fish,
245                                 In a genetic lineage tracing the WT1(CreERT2+/-)Rosa(tdT+/-) mouse mo
246 reatly enhance biomedical research involving lineage tracing, the evaluation of stem cell therapy, an
247     Here we combine clonal analysis, genetic lineage tracing, tissue transplantation, and mutant char
248 ostembryonic day 5 (P5) gonads and performed lineage tracing to analyze primordial follicles and wave
249                               EMBLEM extends lineage tracing to any eukaryotic organism without genet
250 and robust statistical analyses with in vivo lineage tracing to define a detailed map of the postnata
251 ysis, cell proliferation assays, and genetic lineage tracing to define the lineage relations and rest
252 Beattie et al. (2017) use elegant MADM-based lineage tracing to demonstrate cell-intrinsic and global
253  (2017) and Kohler et al. (2017) use in vivo lineage tracing to demonstrate that these two possibilit
254 CGA), functional approaches, and single-cell lineage tracing to derive a unified model of cellular st
255                   We next employed inducible lineage tracing to fate map, through Cre recombinase-med
256 lls were present, which we showed by genetic lineage tracing to have a non-hematopoietic origin.
257                         Here, we used random lineage tracing to localize and quantify clonal expansio
258                          Here we use genetic lineage tracing to mark the Nppa(+) or Hey2(+) cardiomyo
259 ith smooth muscle cell (SMC) and endothelial lineage tracing to survey all plaque cell types and rigo
260                            Here, we use cell lineage tracing to test the embryonic origin of the phar
261 . report on their employment of a battery of lineage-tracing tools to address the developmental origi
262                                Using genetic lineage tracing, transcriptome, and functional studies,
263                                              Lineage-tracing, transcriptome, and chromatin analyses s
264                      We observed that in the lineage-tracing transgenic mice Cdh5-CreER(T2)::R26R-EYF
265 firm the fidelity and sensitivity of the EMT lineage tracing (Tri-PyMT) model and highlight the diffe
266  of EMT in metastasis, we established an EMT lineage tracing (Tri-PyMT) model, in which tumor cells u
267                                      Genetic lineage tracing unravels cell fate and plasticity in dev
268 ble Hnf1b:CreER(T2) in the lung, we employed lineage tracing using an mTmG (G) reporter allele.
269                                              Lineage tracing using EdU-labeling demonstrates that don
270                                              Lineage tracing using Fsp1-Cre: R26R-EYFP mice revealed
271                                              Lineage tracing using global fluorescence labeling techn
272                                              Lineage tracing using Rosa-td tomato (Col2-Cre-ERT2) mic
273                                              Lineage tracing was induced in Lrig1-CreERT2/+;R26R-YFP/
274                                              Lineage tracing was used to rule out repopulation from n
275                                        Using lineage tracing we demonstrated that MEndoT-derived cell
276           By combining unbiased and targeted lineage tracing, we address the events leading to islet
277                Using single-cell RNA-seq and lineage tracing, we analyzed cellular diversity in medul
278                            Through inducible lineage tracing, we demonstrate that these cells can gen
279                 Using additional prospective lineage tracing, we demonstrate that while SHF ventricul
280                              Through in vivo lineage tracing, we demonstrated the power of this appro
281 ene deletion, small molecule inhibition, and lineage tracing, we elucidated TGFbeta-dependent and TGF
282                                      Through lineage tracing, we extend these observations to all lon
283 pair models, single-cell transcriptomics and lineage tracing, we find that alveolar type-2 epithelial
284 ing single-cell RNA sequencing (RNA-seq) and lineage tracing, we found that transforming growth facto
285                                   Using cell lineage tracing, we further demonstrate that trunk neura
286        Using scRNA-seq profiling and genetic lineage tracing, we show that RUNX1(+) PLCs are unaffect
287                                   Using cell lineage tracing, we show that skate trunk vertebrae aris
288                         Using sonic hedgehog lineage tracing, we show that the third and fourth ventr
289 -seq, trajectory analysis, and combinatorial lineage tracing, we showed here that the Neurog3(+) cell
290                                Using genetic lineage tracing, we systematically investigated the role
291 ing a combination of single-cell RNA-seq and lineage-tracing, we find that progenitor cells are the p
292          Time-lapse imaging and genetic cell-lineage tracing were used to identify a source of GDNF-t
293                               Using temporal lineage tracing, whole-mount confocal imaging, and quant
294            Using single-cell RNA sequencing, lineage tracing, whole-organ explant, and live-cell imag
295                             We have combined lineage tracing with antibody cloning from single B cell
296            By combining Cxcr4-CreER-mediated lineage tracing with Cxcr4 inhibition or conditional Cxc
297 marked by sox10, plp1a, gfap or s100 Rather, lineage tracing with lipophilic dye or inducible Sox10-C
298 pithelial lineages in adult animals, and via lineage tracing with stable barcodes, we found that each
299 assay from explanted heart tubes and genetic lineage tracing with the endocardial specific Nfatc1-Cre
300          Here, we show using Myh11-CreER(T2) lineage-tracing with inducible SMC and pericyte (SMC-P)

 
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