1.
Identification of a hybrid myocardial zone in the mammalian heart ..
[1816]
|
2.
Author Correction: Coronary vessels contribute to de novo endocard..
[1357]
|
3.
Bipotent transitional liver progenitor cells contribute to liver r..
[1320]
|
4.
GATA4 regulates Fgf16 to promote heart repair after injury
[1303]
|
5.
Endocardium Contributes to Cardiac Fat
[1255]
|
6.
Endocardium Minimally Contributes to Coronary Endothelium in the E..
[1223]
|
7.
Mfsd2a(+) hepatocytes repopulate the liver during injury and regen..
[1191]
|
8.
Genetic lineage tracing identifies in situ Kit-expressing cardiomy..
[1177]
|
9.
Use of a dual genetic system to decipher exocrine cell fate conver..
[1173]
|
10.
Genetic targeting of Purkinje fibres by Sema3a-CreERT2
[1159]
|
11.
Genetic lineage tracing discloses arteriogenesis as the main mecha..
[1086]
|
12.
Genetic fate-mapping reveals surface accumulation but not deep org..
[1073]
|
13.
Cell proliferation fate mapping reveals regional cardiomyocyte cel..
[998]
|
14.
Dual genetic approaches for deciphering cell fate plasticity in vi..
[984]
|
15.
Smooth muscle origin of postnatal 2nd CVP is pre-determined in ear..
[954]
|
16.
Embryonic senescent cells re-enter cell cycle and contribute to ti..
[918]
|
17.
CCN1-Induced Cellular Senescence Promotes Heart Regeneration
[836]
|
18.
Genetic Fate Mapping Defines the Vascular Potential of Endocardial..
[771]
|
19.
Vascular Development and Regeneration in the Mammalian Heart
[770]
|
20.
Dual lineage tracing identifies intermediate mesenchymal stage for..
[743]
|
21.
Enhancing the precision of genetic lineage tracing using dual reco..
[702]
|
22.
Genetic lineage tracing with multiple DNA recombinases: A user&rsq..
[700]
|
23.
VGLL4 plays a critical role in heart valve development and homeost..
[694]
|
24.
Lung regeneration by multipotent stem cells residing at the bronch..
[676]
|
25.
Fibroblasts in an endocardial fibroelastosis disease model mainly ..
[622]
|
26.
Genetic Tracing Identifies Early Segregation of the Cardiomyocyte ..
[606]
|
27.
Generation of Piezo1-CreER transgenic mice for visualization and l..
[605]
|
28.
Genetic lineage tracing identifies cardiac mesenchymal-to-adipose ..
[600]
|
29.
Genetic Targeting of Organ-Specific Blood Vessels
[571]
|
30.
In Vivo AAV-CRISPR/Cas9-Mediated Gene Editing Ameliorates Atherosc..
[556]
|
31.
Endocardial Cell Plasticity in Cardiac Development, Diseases and R..
[549]
|
32.
Genetic tracing of hepatocytes in liver homeostasis, injury, and r..
[543]
|
33.
Genetic Lineage Tracing of Nonmyocyte Population by Dual Recombina..
[539]
|
34.
Sca1 marks a reserve endothelial progenitor population that prefer..
[537]
|
35.
Fate Mapping of Sca1(+) Cardiac Progenitor Cells in the Adult Mous..
[530]
|
36.
Functional ProTracer identifies patterns of cell proliferation in ..
[525]
|
37.
Overexpression of Kdr in adult endocardium induces endocardial neo..
[522]
|
38.
Genetic lineage tracing of resident stem cells by DeaLT
[513]
|
39.
Reassessing endothelial-to-mesenchymal transition in cardiovascula..
[512]
|
40.
Apj(+) Vessels Drive Tumor Growth and Represent a Tractable Therap..
[510]
|
41.
Genetic Fate Mapping of Transient Cell Fate Reveals N-Cadherin Act..
[509]
|
42.
Lineage Tracing Reveals the Bipotency of SOX9(+) Hepatocytes durin..
[494]
|
43.
PDGFRb+ mesenchymal cells, but not NG2+ mural cells, contribute to..
[492]
|
44.
Lineage tracing clarifies the cellular origin of tissue-resident m..
[487]
|
45.
Genetic lineage tracing identifies endocardial origin of liver vas..
[482]
|
46.
A dual genetic tracing system identifies diverse and dynamic origi..
[477]
|
47.
Reassessment of c-Kit(+) Cells for Cardiomyocyte Contribution in A..
[469]
|
48.
The Development and Regeneration of Coronary Arteries
[461]
|
49.
Preexisting endothelial cells mediate cardiac neovascularization a..
[459]
|
50.
Hepatocyte generation in liver homeostasis, repair, and regenerati..
[457]
|
51.
The robust, high-throughput, and temporally regulated roxCre and l..
[431]
|
52.
Correction to: Hepatocyte generation in liver homeostasis, repair,..
[419]
|
53.
Genetic Lineage Tracing of Pericardial Cavity Macrophages in the I..
[419]
|
54.
Cardiomyocyte proliferation: remove brakes and push accelerators
[406]
|
55.
Genetic tracing uncovers the importance of epithelial-to-mesenchym..
[404]
|
56.
c-kit(+) cells adopt vascular endothelial but not epithelial cell ..
[402]
|
57.
Generation of a self-cleaved inducible Cre recombinase for efficie..
[391]
|
58.
Arterial Sca1(+) Vascular Stem Cells Generate De Novo Smooth Muscl..
[385]
|
59.
A genetic system for tissue-specific inhibition of cell proliferat..
[375]
|
60.
Proliferation tracing reveals regional hepatocyte generation in li..
[372]
|
61.
Airway secretory cell-derived p63+ progenitors contribute to alveo..
[366]
|
62.
Triple-cell lineage tracing by a dual reporter on a single allele
[360]
|
63.
Seamless Genetic Recording of Transiently Activated Mesenchymal Ge..
[347]
|
64.
Dual genetic tracing reveals a unique fibroblast subpopulation mod..
[341]
|
65.
Bi-directional differentiation of single bronchioalveolar stem cel..
[330]
|
66.
The Formation of Coronary Vessels in Cardiac Development and Disea..
[330]
|
67.
Extension of Endocardium-Derived Vessels Generate Coronary Arterie..
[327]
|
68.
Generation of Plvap-CreER and Car4-CreER for genetic targeting of ..
[307]
|
69.
Dynamics of Endothelial Cell Generation and Turnover in Arteries D..
[306]
|
70.
Tracing the origin of alveolar stem cells in lung repair and regen..
[306]
|
71.
Sca1(+) Cells Minimally Contribute to Smooth Muscle Cells in Ather..
[305]
|
72.
Dual Genetic Lineage Tracing Reveals Capillary to Artery Formation..
[302]
|
73.
Genetic Proliferation Tracing Reveals a Rapid Cell Cycle Withdrawa..
[302]
|
74.
Smooth muscle-derived macrophage-like cells contribute to multiple..
[289]
|
75.
Pre-existing beta cells but not progenitors contribute to new beta..
[286]
|
76.
Application of New Lineage Tracing Techniques in Cardiovascular De..
[285]
|
77.
Intercellular genetic tracing of cardiac endothelium in the develo..
[280]
|
78.
Continuous genetic monitoring of transient mesenchymal gene activi..
[276]
|
79.
Interleaved intersectional strategy enables genetic lineage tracin..
[274]
|
80.
Resident endothelial cells generate hepatocytes through cell fusio..
[271]
|
81.
Monitoring of cell-cell communication and contact history in mamma..
[271]
|
82.
Intermediate basal cell population in prostate homeostasis and can..
[265]
|
83.
Sox17 and Coronary Arteriogenesis in Development
[260]
|
84.
Intercellular genetic tracing by alternative synthetic Notch signa..
[252]
|
85.
Strategies for site-specific recombination with high efficiency an..
[250]
|
86.
Heart Regeneration by Endogenous Stem Cells and Cardiomyocyte Prol..
[249]
|
87.
Genetic dissection of intercellular interactions in vivo by membra..
[248]
|
88.
Alveolar regeneration by airway secretory-cell-derived p63+progeni..
[248]
|
89.
A suite of new Dre recombinase drivers markedly expands the abilit..
[247]
|
90.
胰岛beta细胞再生研究进展
[243]
|
91.
Perfect duet: Dual recombinases improve genetic resolution
[232]
|
92.
JAK/STAT signaling maintains an intermediate cell population durin..
[229]
|
93.
Pancreatic beta cell neogenesis: Debates and updates
[228]
|
94.
Coronary vessel formation in development and regeneration: origins..
[227]
|
95.
Dual Cre and Dre recombinases mediate synchronized lineage tracing..
[224]
|
96.
Dual recombinases-based genetic lineage tracing for stem cell rese..
[217]
|
97.
Simultaneous quantitative assessment of two distinct cell lineages..
[205]
|
98.
Role of Cardiac Fibroblasts in Cardiac Injury and Repair
[202]
|
99.
Synchronized lineage tracing of cell membranes and nuclei by dual ..
[202]
|
100.
Genetic recording of transient endothelial activation in distinct ..
[197]
|