WNT Signaling and Lymphocyte Development

Wnt signaling and cancer

Polakis, P. (2000) · Genes & Development · doi:10.1101/gad.14.15.1837 · Cited by 3,183 · see citing works

Functional interaction of β-catenin with the transcription factor LEF-1

Behrens, J., von Kries, J. P., Kühl, M., Bruhn, L., Wedlich, D., Grosschedl, R., & Birchmeier, W. (1996) · Nature · doi:10.1038/382638a0 · Cited by 2,912 · see citing works

RAG-1-deficient mice have no mature B and T lymphocytes

Mombaerts, P., Iacomini, J., Johnson, R. S., Herrup, K., Tonegawa, S., & Papaioannou, V. E. (1992) · Cell · doi:10.1016/0092-8674(92)90030-g · Cited by 2,898 · see citing works

β‐catenin is a target for the ubiquitin–proteasome pathway

Aberle, H., Bauer, A., Stappert, J., Kispert, A., & Kemler, R. (1997) · The EMBO Journal · doi:10.1093/emboj/16.13.3797 · Cited by 2,533 · see citing works

XTcf-3 Transcription Factor Mediates β-Catenin-Induced Axis Formation in Xenopus Embryos

Molenaar, M., van de Wetering, M., Oosterwegel, M., Peterson-Maduro, J., Godsave, S., Korinek, V., Roose, J., Destrée, O., & Clevers, H. (1996) · Cell · doi:10.1016/s0092-8674(00)80112-9 · Cited by 1,824 · see citing works

Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4

Kořínek, V., Barker, N., Moerer, P., van Donselaar, E. G., Huls, G. A., Peters, P. J., & Clevers, H. C. (1998) · Nature Genetics · doi:10.1038/1270 · Cited by 1,580 · see citing works

Linking Colorectal Cancer to Wnt Signaling

Bienz, M., & Clevers, H. C. (2000) · Cell · doi:10.1016/s0092-8674(00)00122-7 · Cited by 1,516 · see citing works

A new member of the frizzled family from Drosophila functions as a Wingless receptor

Bhanot, P., van den Brink, M. R. M., Samos, C. H., Hsieh, J.-C., Wang, Y., Macke, J. P., Andrew, D. J., Nathans, J., & Nusse, R. (1996) · Nature · doi:10.1038/382225a0 · Cited by 1,504 · see citing works

Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF.

Wetering, M. L. V. D., Cavallo, R. A., Dooijes, D., van Beest, M., van Es, J. V., Loureiro, J., Ypma, A., Hursh, D., Jones, T. L., Bejsovec, A., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)81925-x · Cited by 1,347 · see citing works

LDL-receptor-related proteins in Wnt signal transduction

Tamai, K., Semënov, M. V., Kato, Y., Spokony, R. F., Liu, C., Katsuyama, Y., Hess, F. J., Saint‐Jeannet, J., & He, X. (2000) · Nature · doi:10.1038/35035117 · Cited by 1,334 · see citing works

Functional Interaction of an Axin Homolog, Conductin, with β-Catenin, APC, and GSK3β

Behrens, J., Jerchow, B., Würtele, M., Grimm, J., Asbrand, C., Wirtz, R. M., Kühl, M., Wedlich, D., & Birchmeier, W. (1998) · Science · doi:10.1126/science.280.5363.596 · Cited by 1,255 · see citing works

Axin, a negative regulator of the Wnt signaling pathway, forms a complex with GSK‐3β and β‐catenin and promotes GSK‐3β‐dependent phosphorylation of β‐catenin

Ikeda, S., Kishida, S., Yamamoto, H., Murai, H., Koyama, S., & Kikuchi, A. (1998) · The EMBO Journal · doi:10.1093/emboj/17.5.1371 · Cited by 1,248 · see citing works

Intestinal polyposis in mice with a dominant stable mutation of the β‐catenin gene

Harada, N., Tamai, Y., Ishikawa, T., Sauer, B., Takaku, K., Oshima, M., & Taketo, M. M. (1999) · The EMBO Journal · doi:10.1093/emboj/18.21.5931 · Cited by 1,198 · see citing works

Mutations in T-cell antigen receptor genes α and β block thymocyte development at different stages

Mombaerts, P., Clarke, A. R., Rudnicki, M. A., Iacomini, J., Itohara, S., Lafaille, J. J., Wang, L., Ichikawa, Y., Jaenisch, R., Hooper, M., et al. (1992) · Nature · doi:10.1038/360225a0 · Cited by 1,114 · see citing works

An LDL-receptor-related protein mediates Wnt signalling in mice

Pinson, K. I., Brennan, J., Monkley, S. J., Avery, B. J., & Skarnes, W. C. (2000) · Nature · doi:10.1038/35035124 · Cited by 1,086 · see citing works

Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice.Preprint

van Genderen, C., Okamura, R., Fariñas, I., Quo, R. G., Parslow, T., Bruhn, L., & Grosschedl, R. (1994) · Genes & Development · doi:10.1101/gad.8.22.2691 · Cited by 1,031 · see citing works

Profound block in thymocyte development in mice lacking p56lck

Molina, T. J., Kishihara, K., Siderovski, D. P., van Ewijk, W., Narendran, A., Timms, E. M., Wakeham, A. C., Paige, C. J., Hartmann, K.-U., Veillette, A., et al. (1992) · Nature · doi:10.1038/357161a0 · Cited by 970 · see citing works

arrow encodes an LDL-receptor-related protein essential for Wingless signalling

Wehrli, M., Dougan, S. T., Caldwell, K. A., O’Keefe, L. V., Schwartz, S. L., Vaizel-Ohayon, D., Schejter, E. D., Tomlinson, A., & DiNardo, S. (2000) · Nature · doi:10.1038/35035110 · Cited by 871 · see citing works

Nuclear localization of β-catenin by interaction with transcription factor LEF-1

Huber, O., Korn, R., McLaughlin, J., Ohsugi, M., Herrmann, B. G., & Kemler, R. (1996) · Mechanisms of Development · doi:10.1016/0925-4773(96)00597-7 · Cited by 855 · see citing works

Drosophila Tcf and Groucho interact to repress Wingless signalling activity

Cavallo, R. A., Cox, R. T., Moline, M. M., Roose, J., Polevoy, G. A., Clevers, H., Peifer, M., & Bejsovec, A. (1998) · Nature · doi:10.1038/26982 · Cited by 730 · see citing works

The HMG domain of lymphoid enhancer factor 1 bends DNA and facilitates assembly of functional nucleoprotein structures

Giese, K., Cox, J. S., & Grosschedl, R. (1992) · Cell · doi:10.1016/0092-8674(92)90129-z · Cited by 685 · see citing works

The Xenopus Wnt effector XTcf-3 interacts with Groucho-related transcriptional repressors

Roose, J. P., Molenaar, M., Peterson, J., Hurenkamp, J., Brantjes, H., Moerer, P., van de Wetering, M., Destrée, O., & Clevers, H. C. (1998) · Nature · doi:10.1038/26989 · Cited by 674 · see citing works

LEF-1, a gene encoding a lymphoid-specific protein with an HMG domain, regulates T-cell receptor alpha enhancer function [corrected]Preprint

Travis, A., Amsterdam, A., Bélanger, C., & Grosschedl, R. (1991) · Genes & Development · doi:10.1101/gad.5.5.880 · Cited by 614 · see citing works

An HMG-box-containing T-cell factor required for thymocyte differentiation

Verbeek, S., Izon, D., Hofhuis, F., Robanus-Maandag, E., Riele, H. T., van de Watering, M., Oosterwegel, M., Wilson, A., Macdonald, H., & Clevers, H. (1995) · Nature · doi:10.1038/374070a0 · Cited by 585 · see citing works

Identification and cloning of TCF‐1, a T lymphocyte‐specific transcription factor containing a sequence‐specific HMG box.

Wetering, M., Oosterwegel, M., Dooijes, D., & Clevers, H. (1991) · EMBO Journal · doi:10.1002/j.1460-2075.1991.tb07928.x · Cited by 546 · see citing works

Axin, a Negative Regulator of the Wnt Signaling Pathway, Directly Interacts with Adenomatous Polyposis Coli and Regulates the Stabilization of β-Catenin

Kishida, S., Yamamoto, H., Ikeda, S., Kishida, M., Sakamoto, I., Koyama, S., & Kikuchi, A. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.18.10823 · Cited by 491 · see citing works

Wnt3a-/--like phenotype and limb deficiency in Lef1-/-Tcf1-/- micePreprint

Galcerán, J., Fariñas, I., Depew, M. J., Clevers, H. C., & Grosschedl, R. (1999) · Genes & Development · doi:10.1101/gad.13.6.709 · Cited by 462 · see citing works

β-catenin–sensitive isoforms of lymphoid enhancer factor-1 are selectively expressed in colon cancer

Hovanes, K., Li, T. W. H., Munguia, J. E., Truong, T., Milovanović, T., Marsh, J., Holcombe, R. F., & Waterman, M. L. (2001) · Nature Genetics · doi:10.1038/ng0501-53 · Cited by 458 · see citing works

Wnt Signaling Regulates B Lymphocyte Proliferation through a LEF-1 Dependent Mechanism

Reya, T., O'Riordan, M., Okamura, R., Devaney, E., Willert, K., Nusse, R., & Grosschedl, R. (2000) · Immunity · doi:10.1016/s1074-7613(00)00004-2 · Cited by 450 · see citing works

Crystal Structure of a β-Catenin/Tcf Complex

Graham, T. A., Weaver, C. I., Mao, F., Kimelman, D., & Xu, W. (2000) · Cell · doi:10.1016/s0092-8674(00)00192-6 · Cited by 406 · see citing works

Altered T cell development in mice with a targeted mutation of the CD3‐epsilon gene.

Malissen, M., Gillet, A., Ardouin, L., Bouvier, G., Trucy, J., Ferrier, P., Vivier, É., & MALISSEN, B. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00146.x · Cited by 405 · see citing works

DIX Domains of Dvl and Axin Are Necessary for Protein Interactions and Their Ability To Regulate β-Catenin Stability

Kishida, S., Yamamoto, H., Hino, S.-I., Ikeda, S., Kishida, M., & Kikuchi, A. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.6.4414 · Cited by 400 · see citing works

Hippocampus development and generation of dentate gyrus granule cells is regulated by LEF1

Galcerán, J., Miyashita-Lin, E. M., Devaney, E. J., Rubenstein, J. L. R., & Grosschedl, R. (2000) · Development · doi:10.1242/dev.127.3.469 · Cited by 399 · see citing works

Wingless inactivates glycogen synthase kinase‐3 via an intracellular signalling pathway which involves a protein kinase C.

Cook, D., Fry, M., Hughes, K., Sumathipala, R., Woodgett, J. R., & Dale, T. C. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00830.x · Cited by 388 · see citing works

dishevelled and armadillo act in the Wingless signalling pathway in Drosophila

Noordermeer, J. N., Klingensmith, J., Perrimon, N., & Nusse, R. (1994) · Nature · doi:10.1038/367080a0 · Cited by 378 · see citing works

A thymus-specific member of the HMG protein family regulates the human T cell receptor C alpha enhancer.Preprint

Waterman, M. L., Fischer, W. H., & Jones, K. A. (1991) · Genes & Development · doi:10.1101/gad.5.4.656 · Cited by 359 · see citing works

Ancestry and diversity of the HMG box superfamily

Laudet, V., Stéhelin, D., & Clevers, H. C. (1993) · Nucleic Acids Research · doi:10.1093/nar/21.10.2493 · Cited by 334 · see citing works

Redundant Regulation of T Cell Differentiation and TCRα Gene Expression by the Transcription Factors LEF-1 and TCF-1

Okamura, R. M., Sigvardsson, M., Galcerán, J., Verbeek, S. J., Clevers, H. C., & Grosschedl, R. (1998) · Immunity · doi:10.1016/s1074-7613(00)80454-9 · Cited by 333 · see citing works

Two Members of the Tcf Family Implicated in Wnt/β-Catenin Signaling during Embryogenesis in the Mouse

Kořínek, V., Barker, N., Willert, K., Molenaar, M., Roose, J. P., Wagenaar, G. T. M., Markman, M. W. M., Lamers, W., Destrée, O., & Clevers, H. C. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.3.1248 · Cited by 326 · see citing works

The Yin-Yang of TCF/β-Catenin Signaling

Barker, N., Morin, P. J., & Clevers, H. C. (1999) · Advances in cancer research · doi:10.1016/s0065-230x(08)60783-6 · Cited by 292 · see citing works

ALY, a context-dependent coactivator of LEF-1 and AML-1, is required for TCRalpha enhancer function.Preprint

Bruhn, L., Munnerlyn, A., & Grosschedl, R. (1997) · Genes & Development · doi:10.1101/gad.11.5.640 · Cited by 281 · see citing works

DNA-binding properties of the HMG domain of the lymphoid-specific transcriptional regulator LEF-1.Preprint

Giese, K., Amsterdam, A., & Grosschedl, R. (1991) · Genes & Development · doi:10.1101/gad.5.12b.2567 · Cited by 263 · see citing works

XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development

Brannon, M. K., Brown, J. D., Bates, R. L., Kimelman, D., & Moon, R. T. (1999) · Development · doi:10.1242/dev.126.14.3159 · Cited by 247 · see citing works

Interaction of Axin and Dvl‐2 proteins regulates Dvl‐2‐stimulated TCF‐dependent transcription

Smalley, M. J., Sara, E., Paterson, H., Naylor, S., Cook, D., Jayatilake, H., Fryer, L. G. D., Hutchinson, L., Fry, M., & Dale, T. C. (1999) · The EMBO Journal · doi:10.1093/emboj/18.10.2823 · Cited by 247 · see citing works

The β-catenin–TCF-1 pathway ensures CD4+CD8+ thymocyte survival

Ioannidis, V., Beermann, F., Clevers, H. C., & Held, W. (2001) · Nature Immunology · doi:10.1038/90623 · Cited by 246 · see citing works

Differential expression of the HMG box factors TCF-1 and LEF-1 during murine embryogenesis

Oosterwegel, M. A., van de Wetering, M., Timmerman, J. J., Kruisbeek, A. M., Destrée, O., Meijlink, F. C. P. W., & Clevers, H. C. (1993) · Development · doi:10.1242/dev.118.2.439 · Cited by 246 · see citing works

Critical Involvement of Tcf-1 in Expansion of Thymocytes

Schilham, M. W., Wilson, A., Moerer, P., Benaissa-Trouw, B. J., Cumano, A., & Clevers, H. C. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.161.8.3984 · Cited by 237 · see citing works

Tcf4 can specifically recognize beta-catenin using alternative conformations.

Graham, T. A., Ferkey, D. M., Mao, F., Kimelman, D., & Xu, W. (2001) · Nature Structural Biology · doi:10.1038/nsb718 · Cited by 216 · see citing works

Structure of a human Tcf4-beta-catenin complex.

Poy, F., Lepourcelet, M., Shivdasani, R. A., & Eck, M. J. (2001) · Nature Structural Biology · doi:10.1038/nsb720 · Cited by 200 · see citing works

Wnt signaling is required for thymocyte development and activates Tcf-1 mediated transcription

Staal, F. J. T., Meeldijk, J., Moerer, P., Jay, P., van de Weerdt, B. C. M., Vainio, S. J., Nolan, G. P., & Clevers, H. C. (2001) · European Journal of Immunology · doi:10.1002/1521-4141(200101)31:1 · Cited by 200 · see citing works

Extensive Alternative Splicing and Dual Promoter Usage Generate Tcf-1 Protein Isoforms with Differential Transcription Control Properties

van de Wetering, M., Castrop, J., Kořínek, V., & Clevers, H. C. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.3.745 · Cited by 191 · see citing works

Somatic activation of β-catenin bypasses pre-TCR signaling and TCR selection in thymocyte development

Gounari, F., Aifantis, I., Khazaie, K., Hoeflinger, S., Harada, N., Taketo, M. M., & von Boehmer, H. (2001) · Nature Immunology · doi:10.1038/ni0901-863 · Cited by 167 · see citing works

Activation of the HIV-1 enhancer by the LEF-1 HMG protein on nucleosome-assembled DNA in vitro.Preprint

Sheridan, P. L., Sheline, C. T., Cannon, K. S., Voz, M. L., Pazin, M. J., Kadonaga, J. T., & Jones, K. A. (1995) · Genes & Development · doi:10.1101/gad.9.17.2090 · Cited by 159 · see citing works

LEF‐1 contains an activation domain that stimulates transcription only in a specific context of factor‐binding sites.

Giese, K., & Grosschedl, R. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb06155.x · Cited by 159 · see citing works

The hLEF/TCF-1 alpha HMG protein contains a context-dependent transcriptional activation domain that induces the TCR alpha enhancer in T cells.Preprint

Carlsson, P., Waterman, M. L., & Jones, K. A. (1993) · Genes & Development · doi:10.1101/gad.7.12a.2418 · Cited by 154 · see citing works

Cloning of murine TCF-1, a T cell-specific transcription factor interacting with functional motifs in the CD3-epsilon and T cell receptor alpha enhancers.

Oosterwegel, M. A., van de Wetering, M., Dooijes, D., Klomp, L. W. J., Winoto, A., Georgopoulos, K., Meijlink, F. C. P. W., & Clevers, H. C. (1991) · The Journal of Experimental Medicine · doi:10.1084/jem.173.5.1133 · Cited by 142 · see citing works

Involvement of transcription factors TCF-1 and GATA-3 in the initiation of the earliest step of T cell development in the thymus.

Hattori, N., Kawamoto, H., Fujimoto, S., Kuno, K., & Katsura, Y. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.184.3.1137 · Cited by 142 · see citing works

Distinct roles for P-CREB and LEF-1 in TCR alpha enhancer assembly and activation on chromatin templates in vitro.

Mayall, T. P., Sheridan, P. L., Montminy, M. R., & Jones, K. A. (1997) · Genes & Development · doi:10.1101/gad.11.7.887 · Cited by 118 · see citing works

Sequence-specific HMG box factors recognize 10-12 base pair minor groove motifs

van Beest, M. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m004102200 · Cited by 112 · see citing works

Sequence-specific High Mobility Group Box Factors Recognize 10–12-Base Pair Minor Groove Motifs

van Beest, M., Dooijes, D., van de Wetering, M., Kjærulff, S., Bonvin, A. M. J. J., Nielsen, O., & Clevers, H. C. (2000) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)61506-1 · Cited by 101 · see citing works

The human LEF-1 gene contains a promoter preferentially active in lymphocytes and encodes multiple isoforms derived from alternative splicing

Hovanes, K., Li, T. W. H., & Waterman, M. L. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.9.1994 · Cited by 101 · see citing works

Interaction of Dishevelled and Xenopus Axin-Related Protein Is Required for Wnt Signal Transduction

Itoh, K., Antipova, A. A., Ratcliffe, M., & Sokol, S. Y. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.6.2228-2238.2000 · Cited by 95 · see citing works

Nuclear Localization and Formation of β-Catenin–Lymphoid Enhancer Factor 1 Complexes Are Not Sufficient for Activation of Gene Expression

Prieve, M. G., & Waterman, M. L. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.6.4503 · Cited by 90 · see citing works

Clonal Acquisition of the Ly49A NK Cell Receptor Is Dependent on the trans-Acting Factor TCF-1

Held, W., Kunz, B., Lowin, B., van de Wetering, M., & Clevers, H. C. (1999) · Immunity · doi:10.1016/s1074-7613(00)80118-1 · Cited by 84 · see citing works

The human T cell transcription factor-1 gene. Structure, localization, and promoter characterization.

van de Wetering, M., Oosterwegel, M. A., Holstege, F. C. P., Dooyes, D., Suijkerbuijk, R. F., van Kessel, A. G., & Clevers, H. C. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)42476-3 · Cited by 43 · see citing works

The Schizosaccharomyces pombe mating-type gene mat-Mc encodes a sequence-specific DNA-binding high mobility group box protein.

Dooijes, D., van de Wetering, M., Knippels, L. M. J., & Clevers, H. C. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)74537-2 · Cited by 36 · see citing works

Wnt signalling in stem cells and cancer

Reya, T., & Clevers, H. (2005) · Nature · doi:10.1038/nature03319 · Cited by 3,666 · see citing works

Untitled work

Wyss-Coray (2006) · doi:10.1038/nm1484 · Cited by 1,284 · see citing works

Endothelial cell–cell junctions: happy together

Dejana, E. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1357 · Cited by 1,184 · see citing works

The circadian clock: pacemaker and tumour suppressor

Fu, L., & Lee, C. C. (2003) · Nature reviews. Cancer · doi:10.1038/nrc1072 · Cited by 678 · see citing works

The Wnt signaling pathway and its role in tumor development

Lustig, B., & Behrens, J. (2003) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-003-0431-0 · Cited by 521 · see citing works

Contact inhibition of VEGF-induced proliferation requires vascular endothelial cadherin, β-catenin, and the phosphatase DEP-1/CD148

Lampugnani, M. G., Zanetti, A., Corada, M., Takahashi, T., Balconi, G., Breviario, F., Orsenigo, F., Cattelino, A., Kemler, R., Daniel, T. O., et al. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200209019 · Cited by 410 · see citing works

Bcl11b is required for differentiation and survival of αβ T lymphocytes

Wakabayashi, Y., Watanabe, H., Inoue, J., Takeda, N., Sakata, J., Mishima, Y., Hitomi, J., Yamamoto, T., Utsuyama, M., Niwa, O., et al. (2003) · Nature Immunology · doi:10.1038/ni927 · Cited by 356 · see citing works

β-Catenin Is Dispensable for Hematopoiesis and Lymphopoiesis

Cobas, M., Wilson, A., Ernst, B., Mancini, S., Macdonald, H., Kemler, R., & Radtke, F. (2004) · Journal of Experimental Medicine · doi:10.1084/jem.20031615 · Cited by 401 · see citing works

Myeloma cells suppress bone formation by secreting a soluble Wnt inhibitor, sFRP-2

Oshima, T., Abe, M., Asano, J., Hara, T., Kitazoe, K.-I., Sekimoto, E., Tanaka, Y., Shibata, H., Hashimoto, T., Ozaki, S., et al. (2005) · Blood · doi:10.1182/blood-2004-12-4940 · Cited by 344 · see citing works

An autocrine mechanism for constitutive Wnt pathway activation in human cancer cells

Bafico, A., Liu, G., Goldin, L., Harris, V., & Aaronson, S. A. (2004) · Cancer Cell · doi:10.1016/j.ccr.2004.09.032 · Cited by 321 · see citing works

Wnt5a: its signalling, functions and implication in diseases

Kikuchi, A., Yamamoto, H., Sato, A., & Matsumoto, S. (2011) · Acta Physiologica · doi:10.1111/j.1748-1716.2011.02294.x · Cited by 317 · see citing works

Illegitimate WNT signaling promotes proliferation of multiple myeloma cells

Derksen, P. W. B., Tjin, E. P. M., Meijer, H. P., Klok, M. D., MacGillavry, H. D., van Oers, M. H. J., Lokhorst, H. M., Bloem, A. C., Clevers, H. C., Nusse, R., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0305855101 · Cited by 306 · see citing works

Ubiquitin Ligases and the Immune Response

Liu, Y. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104813 · Cited by 283 · see citing works

Wnt glycoproteins regulate the expression of FoxN1, the gene defective in nude mice

Balc̆iūnaite, G., Keller, M. P., Balciunaite, E., Piali, L., Žuklys, S., Mathieu, Y., Gill, J. W., Boyd, R. L., Sussman, D. J., & Holländer, G. A. (2002) · Nature Immunology · doi:10.1038/ni850 · Cited by 261 · see citing works

The circadian clock in cancer development and therapy

Fu, L., & Kettner, N. M. (2013) · Progress in Molecular Biology and Translational Science · doi:10.1016/b978-0-12-396971-2.00009-9 · Cited by 251 · see citing works

Lymphoid cell growth and transformation are suppressed by a key regulatory element of the gene encoding PU.1

Rosenbauer, F., Owens, B. M., Yu, L., Tumang, J. R., Steidl, U., Kutok, J. L., Clayton, L. K., Wagner, K., Scheller, M., Iwasaki, H., et al. (2006) · Nature Genetics · doi:10.1038/ng1679 · Cited by 237 · see citing works

Notch and the Immune System

Maillard, I. P., Adler, S. H., & Pear, W. S. (2003) · Immunity · doi:10.1016/s1074-7613(03)00325-x · Cited by 219 · see citing works

Human Naive CD8 T Cells Down-Regulate Expression of the WNT Pathway Transcription Factors Lymphoid Enhancer Binding Factor 1 and Transcription Factor 7 (T Cell Factor-1) following Antigen Encounter In Vitro and In Vivo

Willinger, T., Freeman, T. C., Herbert, M., Hasegawa, H., McMichael, A. J., & Callan, M. F. C. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.3.1439 · Cited by 197 · see citing works

Global Regulator SATB1 Recruits β-Catenin and Regulates TH2 Differentiation in Wnt-Dependent Manner

Notani, D., Gottimukkala, K. P., Jayani, R. S., Limaye, A. S., Damle, M., Mehta, S. S., Purbey, P. K., Joseph, J., & Galande, S. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000296 · Cited by 198 · see citing works

Testing the Circadian Gene Hypothesis in Prostate Cancer: A Population-Based Case-Control Study

Zhu, Y. L., Stevens, R. G., Hoffman, A. E., FitzGerald, L. M., Kwon, E. M., Ostrander, E. A., Davis, S., Zheng, T., & Stanford, J. L. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-0648 · Cited by 169 · see citing works

Attenuated Wnt Signaling Perturbs Pancreatic Growth but Not Pancreatic Function

Papadopoulou, S., & Edlund, H. (2005) · Diabetes · doi:10.2337/diabetes.54.10.2844 · Cited by 159 · see citing works

Curcumin inhibits breast cancer stem cell migration by amplifying the E-cadherin/β-catenin negative feedback loop

Mukherjee, S., Mazumdar, M., Chakraborty, S., Manna, A., Saha, S., Khan, P., Bhattacharjee, P., Guha, D., Adhikary, A., Mukherjee, S., et al. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt506 · Cited by 151 · see citing works

The canonical Wnt signaling pathway plays an important role in lymphopoiesis and hematopoiesis

Staal, F. J. T., & Sen, J. M. (2008) · European Journal of Immunology · doi:10.1002/eji.200738118 · Cited by 134 · see citing works

Identification of a global gene expression signature of B-chronic lymphocytic leukemia.

Jelinek, D. F., Tschumper, R. C., Stolovitzky, G. A., Iturria, S. J., Tu, Y., Lepre, J., Shah, N. H., & Kay, N. E. (2003) · PubMed · Cited by 131 · see citing works

Down-regulation of RAB6KIFL/KIF20A, a Kinesin Involved with Membrane Trafficking of Discs Large Homologue 5, Can Attenuate Growth of Pancreatic Cancer Cell

Taniuchi, K., Nakagawa, H., Nakamura, T., Eguchi, H., Ohigashi, H., Ishikawa, O., Katagiri, T., & Nakamura, Y. (2005) · Cancer Research · doi:10.1158/0008-5472.105.65.1 · Cited by 129 · see citing works

The Wnt Receptor, Lrp5, Is Expressed by Mouse Mammary Stem Cells and Is Required to Maintain the Basal Lineage

Badders, N. M., Goel, S., Clark, R. J., Klos, K. S., Kim, S. Y., Bafico, A., Lindvall, C. J., Williams, B. O., & Alexander, C. M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006594 · Cited by 127 · see citing works

Identification of Target Genes of the p16INK4A-pRB-E2F Pathway

Vernell, R., Helin, K., & Müller, H. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304930200 · Cited by 121 · see citing works

β-Catenin stabilization stalls the transition from double-positive to single-positive stage and predisposes thymocytes to malignant transformation

Guo, Z., Dose, M., Kovalovsky, D., Chang, R., O’Neil, J., Look, A. T., von Boehmer, H., Khazaie, K., & Gounari, F. (2007) · Blood · doi:10.1182/blood-2006-11-059071 · Cited by 121 · see citing works

c-Myc mediates pre-TCR-induced proliferation but not developmental progression

Dose, M., Khan, I., Guo, Z., Kovalovsky, D., Krueger, A., von Boehmer, H., Khazaie, K., & Gounari, F. (2006) · Blood · doi:10.1182/blood-2006-02-005900 · Cited by 120 · see citing works

Frizzled 9 knock-out mice have abnormal B-cell development

Ranheim, E. A., Kwan, H. C. K., Reya, T., Wang, Y.-K., Weissman, I. L., & Francke, U. (2004) · Blood · doi:10.1182/blood-2004-06-2334 · Cited by 117 · see citing works

Loss of adenomatous polyposis coli gene function disrupts thymic development

Gounari, F., Chang, R., Cowan, J. M., Guo, Z., Dose, M., Gounaris, E. G., & Khazaie, K. (2005) · Nature Immunology · doi:10.1038/ni1228 · Cited by 108 · see citing works

CGPS: A machine learning-based approach integrating multiple gene set analysis tools for better prioritization of biologically relevant pathways

Chen, A., & Kong, L. (2018) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2018.08.002 · Cited by 106 · see citing works

Wnt signaling in the stem cell niche

Rattis, F. M., Voermans, C., & Reya, T. (2004) · Current Opinion in Hematology · doi:10.1097/01.moh.0000133649.61121.ec · Cited by 106 · see citing works

Dysregulation of TNFα-induced necroptotic signaling in chronic lymphocytic leukemia: suppression of CYLD gene by LEF1

Liu, P., Xu, B., Shen, W., Zhu, H., Wu, W., Fu, Y., Chen, H., Dong, H., Zhu, Y., Miao, K., et al. (2011) · Leukemia · doi:10.1038/leu.2011.357 · Cited by 104 · see citing works

Gene expression analysis of B‐lymphoma cells resistant and sensitive to bortezomib*

Shringarpure, R., Catley, L. P., Bhole, D., Burger, R., Podar, K., Tai, Y., Kessler, B. M., Galardy, P. J., Ploegh, H. L., Tassone, P., et al. (2006) · British Journal of Haematology · doi:10.1111/j.1365-2141.2006.06132.x · Cited by 98 · see citing works

Gene expression profiling reveals a highly specialized genetic program of plasma cells

Underhill, G. H., George, D., Bremer, E. G., & Kansas, G. S. (2003) · Blood · doi:10.1182/blood-2002-08-2673 · Cited by 93 · see citing works

Alternative Splicing of SLC39A14 in Colorectal Cancer is Regulated by the Wnt Pathway

Thorsen, K., Mansilla, F., Schepeler, T., Øster, B., Rasmussen, M. H., Dyrskjøt, L., Karni, R., Akerman, M., Krainer, A. R., Laurberg, S., et al. (2010) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m110.002998 · Cited by 90 · see citing works

Wnt signaling in the thymus

Staal, F. J. T., & Clevers, H. C. (2003) · Current Opinion in Immunology · doi:10.1016/s0952-7915(03)00003-7 · Cited by 86 · see citing works

Epstein-Barr Virus LMP2A Interferes with Global Transcription Factor Regulation When Expressed during B-Lymphocyte Development

Portis, T., & Longnecker, R. (2002) · Journal of Virology · doi:10.1128/jvi.77.1.105-114.2003 · Cited by 81 · see citing works

Activated Thyroid Hormone Promotes Differentiation and Chemotherapeutic Sensitization of Colorectal Cancer Stem Cells by Regulating Wnt and BMP4 Signaling

Catalano, V., Dentice, M., Ambrosio, R., Luongo, C., Carollo, R., Benfante, A., Todaro, M., Stassi, G., & Salvatore, D. (2015) · Cancer Research · doi:10.1158/0008-5472.can-15-1542 · Cited by 79 · see citing works

Secreted Frizzled-Related Protein-1 Improves Postinfarction Scar Formation Through a Modulation of Inflammatory Response

Barandon, L., Casassus, F., Leroux, L., Moreau, C., Allières, C., Lamazière, J. D., Dufourcq, P., Couffinhal, T., & Duplàa, C. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.232280 · Cited by 74 · see citing works

T-Cell Factor 4N (TCF-4N), a Novel Isoform of Mouse TCF-4, Synergizes with β-Catenin To Coactivate C/EBPα and Steroidogenic Factor 1 Transcription Factors

Kennell, J. A., O’Leary, E. E., Gummow, B. M., Hammer, G. D., & MacDougald, O. A. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.15.5366-5375.2003 · Cited by 73 · see citing works

B-cell commitment: deciding on the players

Hardy, R. R. (2003) · Current Opinion in Immunology · doi:10.1016/s0952-7915(03)00012-8 · Cited by 72 · see citing works

Age‐related alterations of gene expression patterns in human CD8⁺ T cells

Cao, J., Gollapudi, S., Sharman, E. H., Jia, Z., & Gupta, S. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2009.00534.x · Cited by 71 · see citing works

Gas1 is induced by VE-cadherin and vascular endothelial growth factor and inhibits endothelial cell apoptosis

Spagnuolo, R. (2003) · Blood · doi:10.1182/blood-2003-07-2459 · Cited by 71 · see citing works

Insect galectins: Roles in immunity and development

Pace, K. E., & Baum, L. G. (2002) · Glycoconjugate Journal · doi:10.1023/b:glyc.0000014092.86763.2f · Cited by 67 · see citing works

DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration

Osada, M., Jardine, L., Misir, R., Andl, T., Millar, S. E., & Pezzano, M. T. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009062 · Cited by 61 · see citing works

Subversion of T lineage commitment by PU.1 in a clonal cell line system

Dionne, C. J., Tse, K. Y., Weiss, A. H., Franco, C. B., Wiest, D. L., Anderson, M. K., & Rothenberg, E. V. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.01.027 · Cited by 54 · see citing works

miR-17-92/p38α Dysregulation Enhances Wnt Signaling and Selects Lgr6+ Cancer Stem-like Cells during Lung Adenocarcinoma Progression

Guinot, A., Oeztuerk-Winder, F., & Ventura, J. (2016) · Cancer Research · doi:10.1158/0008-5472.can-15-3302 · Cited by 53 · see citing works

Circadian clock circuitry in colorectal cancer

Mazzoccoli, G. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i15.4197 · Cited by 47 · see citing works

Loss of Expression of the WNT/β-Catenin-Signaling Pathway Transcription Factors Lymphoid Enhancer Factor-1 (LEF-1) and T Cell Factor-1 (TCF-1) in a Subset of Peripheral T Cell Lymphomas

Dorfman, D. M., Greisman, H. A., & Shahsafaei, A. (2003) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64287-3 · Cited by 48 · see citing works

Response of canonical Wnt/β-catenin signaling pathway in the intestine to microgravity stress in Caenorhabditis elegans

Rui, Q., Dong, S., Jiang, W., & Wang, D. (2019) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2019.109782 · Cited by 47 · see citing works

Role of WNT signaling in normal and malignant hematopoiesis.

Khan, N. I., & Bendall, L. J. (2006) · PubMed · doi:10.14670/hh-21.761 · Cited by 47 · see citing works

Long-range, nonautonomous effects of activated Notch1 on tissue homeostasis in the nail☆

Lin, M., & Kopan, R. (2003) · Developmental Biology · doi:10.1016/j.ydbio.2003.07.007 · Cited by 45 · see citing works

Lack of Bcl11b tumor suppressor results in vulnerability to DNA replication stress and damages

Kamimura, K., Mishima, Y., Obata, M., Endo, T., Aoyagi, Y., & Kominami, R. (2007) · Oncogene · doi:10.1038/sj.onc.1210388 · Cited by 44 · see citing works

Transcriptional Regulation of CD4 Gene Expression by T Cell Factor-1/β-Catenin Pathway

Huang, Z., Xie, H., Ioannidis, V., Held, W., Clevers, H. C., Sadim, M. S., & Sun, Z. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.8.4880 · Cited by 44 · see citing works

Axin expression in thymic stromal cells contributes to an age-related increase in thymic adiposity and is associated with reduced thymopoiesis independently of ghrelin signaling

Yang, H., Youm, Y., Sun, Y., Rim, J., Galbán, C. J., Vandanmagsar, B., & Dixit, V. D. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.1008621 · Cited by 44 · see citing works

Thymus neuroendocrine tumors with CTNNB1 gene mutations, disarrayed ß-catenin expression, and dual intra-tumor Ki-67 labeling index compartmentalization challenge the concept of secondary high-grade neuroendocrine tumor: a paradigm shift

Fabbri, A., Cossa, M., Sonzogni, A., Bidoli, P., Canova, S., Cortinovis, D. L., Abbate, M. I., Calabrese, F., Nannini, N., Lunardi, F., et al. (2017) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/s00428-017-2130-2 · Cited by 42 · see citing works

VE-Cadherin Expression and Clustering Maintain Low Levels of Survivin in Endothelial Cells

Iurlaro, M., Demontis, F., Corada, M., Zanetta, L., Drake, C., Gariboldi, M., Peiró, S., Cano, A., Navarro, P., Cattelino, A., et al. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63287-7 · Cited by 42 · see citing works

Maintenance of HSC by Wnt5a secreting AGM-derived stromal cell line

Buckley, S. M., Ulloa‐Montoya, F., Abts, D., Oostendorp, R. A. J., Dzierzak, E. A., Ekker, S. C., & Verfaillie, C. M. (2010) · Experimental Hematology · doi:10.1016/j.exphem.2010.09.010 · Cited by 40 · see citing works

Plakoglobin Is O-Glycosylated Close to the N-terminal Destruction Box

Hatsell, S. J., Medina, L., Merola, J., Haltiwanger, R. S., & Cowin, P. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301346200 · Cited by 40 · see citing works

HEB in the Spotlight: Transcriptional Regulation of T-Cell Specification, Commitment, and Developmental Plasticity

Braunstein, M., & Anderson, M. K. (2012) · Clinical and Developmental Immunology · doi:10.1155/2012/678705 · Cited by 39 · see citing works

Regulation of human B lymphopoiesis by the transforming growth factor-β superfamily in a newly established coculture system using human mesenchymal stem cells as a supportive microenvironment

Ichii, M., Oritani, K., Yokota, T., Nishida, M., Takahashi, I., Shirogane, T., Ezoe, S., Saitoh, N., Tanigawa, R., Kincade, P. W., et al. (2008) · Experimental Hematology · doi:10.1016/j.exphem.2007.12.013 · Cited by 39 · see citing works

Lymphoid Enhancer Factor-1 Links Two Hereditary Leukemia Syndromes through Core-binding Factor α Regulation of ELA2

Li, F., Person, R., Takemaru, K., Williams, K., Meade-White, K. D., Ozsahin, A. H., Güngör, T., Moon, R. T., & Horwitz, M. S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m310759200 · Cited by 39 · see citing works

Cross-talk between pRb/E2F and Wnt/?-catenin pathways: E2F1 induces axin2 leading to repression of Wnt signalling and to increased cell death

Hughes, T. A., & Brady, H. J. M. (2005) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.09.014 · Cited by 38 · see citing works

Regulation of T-cell receptor Dβ1 promoter by KLF5 through reiterated GC-rich motifs

Yang, X. O., Doty, R. T., Hicks, J., & Willerford, D. M. (2003) · Blood · doi:10.1182/blood-2002-08-2579 · Cited by 38 · see citing works

Wnt-10b promotes differentiation of skin epithelial cells in vitro

Ouji, Y., Yoshikawa, M., Shiroi, A., & Ishizaka, S. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.01.104 · Cited by 37 · see citing works

Dietary Transforming Growth Factor-Beta 2 (TGF-β2) Supplementation Reduces Methotrexate-Induced Intestinal Mucosal Injury in a Rat

Ben-Lulu, S., Pollak, Y., Mogilner, J. G., Bejar, J., Coran, A. G., & Sukhotnik, I. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045221 · Cited by 37 · see citing works

Prevention of epithelial to mesenchymal transition in colorectal carcinoma by regulation of the E-cadherin-β-catenin-vinculin axis

Pal, I., Rajesh, Y., Banik, P., Dey, G., Dey, K. K., Bharti, R., Naskar, D., Chakraborty, S., Ghosh, S. K., Das, S. K., et al. (2019) · Cancer Letters · doi:10.1016/j.canlet.2019.03.008 · Cited by 36 · see citing works

Neural stem cells in the adult ciliary epithelium express GFAP and are regulated by Wnt signaling

Das, A. V., Zhao, X., James, J., Kim, M., Cowan, K. H., & Ahmad, I. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.11.064 · Cited by 36 · see citing works

Gene Expression Profiling of Embryonic Human Neural Stem Cells and Dopaminergic Neurons from Adult Human Substantia Nigra

Marei, H. E. S., Althani, A., Afifi, N. M., Michetti, F., Pescatori, M., D, R. P. M., Casalbore, P., Cenciarelli, C., Schwartz, P. H., & Ahmed, A.-E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028420 · Cited by 34 · see citing works

Pygopus is required for embryonic brain patterning in Xenopus

Lake, B. B., & Kao, K. R. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00305-1 · Cited by 33 · see citing works

Clinical significance of lymphoid enhancer-binding factor 1 expression in acute myeloid leukemia

Fu, Y., Zhu, H., Wu, W., Xu, J., Chen, T., Xu, B., Qian, S., Li, J., & Liu, P. (2013) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.3109/10428194.2013.805759 · Cited by 32 · see citing works

The C. elegans RUNX transcription factor RNT-1/MAB-2 is required for asymmetrical cell division of the T blast cell

Kagoshima, H., Sawa, H., Mitani, S., Bürglin, T. R., Shigesada, K., & Kohara, Y. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.08.034 · Cited by 31 · see citing works

Role of the Wnt/β-catenin network in regulating hematopoiesis

Wilusz, M., & Majka, M. (2008) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-008-0029-y · Cited by 30 · see citing works

Wnt-10b secreted from lymphocytes promotes differentiation of skin epithelial cells

Ouji, Y., Yoshikawa, M., Shiroi, A., & Ishizaka, S. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.02.028 · Cited by 29 · see citing works

Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/β-catenin signaling

Swain, R. K., Katoh, M., Medina, A., & Steinbeißer, H. (2005) · Cell Communication and Signaling · doi:10.1186/1478-811x-3-12 · Cited by 29 · see citing works

Notch and lymphopoiesis: a view from the microenvironment

Parreira, L., Neves, H., & Simões, S. D. M. (2003) · Seminars in Immunology · doi:10.1016/s1044-5323(03)00004-6 · Cited by 27 · see citing works

Over-Expression of hNGF in Adult Human Olfactory Bulb Neural Stem Cells Promotes Cell Growth and Oligodendrocytic Differentiation

Marei, H. E. S., Althani, A., Afifi, N. M., Abdelmaksoud, A., Bernardini, C., Michetti, F., Barba, M., Pescatori, M., Maira, G., Paldino, E., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082206 · Cited by 27 · see citing works

Epstein–Barr virus LMP2A: regulating cellular ubiquitination processes for maintenance of viral latency?

Portis, T., Ikeda, M., & Longnecker, R. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.05.009 · Cited by 27 · see citing works

LEF1 Drives a Central Memory Program and Supports Antitumor Activity of Natural Killer T Cells

Ngai, H., Barragán, G. A., Tian, G., Balzeau, J. C., Zhang, C., Courtney, A. N., Guo, L., Xu, X. Y., Wood, M. S., Drabek, J. M., et al. (2022) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-22-0333 · Cited by 26 · see citing works

Frequent β-catenin overexpression without exon 3 mutation in cutaneous lymphomas

Bellei, B., Pacchiarotti, A., Perez, M., & Faraggiana, T. (2004) · Modern Pathology · doi:10.1038/modpathol.3800181 · Cited by 25 · see citing works

Variation of LEF-1 mRNA expression in low-grade B-cell non-Hodgkin's lymphoma

Howe, D. J., & Bromidge, T. J. (2005) · Leukemia Research · doi:10.1016/j.leukres.2005.06.004 · Cited by 24 · see citing works

Recognizing Paradigm Instability in Theories of Carcinogenesis

Baker, S. G. (2014) · Journal of Advances in Medicine and Medical Research · doi:10.9734/bjmmr/2014/6855 · Cited by 23 · see citing works

Gene expression profiling and analysis of signaling pathways involved in priming and differentiation of human neural stem cells

Cai, Y., Wu, P., Özen, M., Yu, Y., Wang, J., Ittmann, M., & Liu, M. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.11.041 · Cited by 22 · see citing works

Nemo-Like Kinase in Development and Diseases: Insights from Mouse Studies

Daams, R., & Massoumi, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21239203 · Cited by 21 · see citing works

Membrane properties of retinal stem cells/progenitors

Das, A. V., Edakkot, S., Thoreson, W. B., James, J., Bhattacharya, S., & Ahmad, I. (2005) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2005.04.003 · Cited by 21 · see citing works

The human blood DNA methylome identifies crucial role of β-catenin in the pathogenesis of Kawasaki disease

Chen, K., Huang, Y., Guo, M. M., Lin, T., Weng, W.-T., Yang, H.-J., Yang, K. D., & Kuo, H. (2018) · Oncotarget · doi:10.18632/oncotarget.25305 · Cited by 20 · see citing works

Analysis of chronic lymphotic leukemia transcriptomic profile: differences between molecular subgroups

Lewintre, E. J., Martín, C. R., Montaner, D. A., Marín, M., Terol, M. J., Farrás, R., Benet, I., Calvete, J. J., Dopazo, J., & García-Conde, J. (2009) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428190802541807 · Cited by 19 · see citing works

Circadian rhythm in prostate cancer: time to take notice of the clock

Zhu, W., He, Q., Feng, D., Wei, Q., & Yang, L. (2022) · Asian Journal of Andrology · doi:10.4103/aja202255 · Cited by 18 · see citing works

Altered Mucosal Immune-Microbiota Interactions in Familial Adenomatous Polyposis

Noble, A., Durant, L. R., Dilke, S. M., Man, R., Martín, I. R., Patel, R., Hoyles, L., Pring, E. T., Latchford, A. R., Clark, S. K., et al. (2022) · Clinical and Translational Gastroenterology · doi:10.14309/ctg.0000000000000428 · Cited by 16 · see citing works

Stephanthraniline A inhibits the proliferation and activation of T cells in vitro and in vivo

Chen, F., Yang, N., Ye, Y., Sun, H., Li, X., & Xu, S. (2012) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2012.04.012 · Cited by 15 · see citing works

ATP-dependent chromatin remodeling in T cells1This article is part of Special Issue entitled Asilomar Chromatin and has undergone the Journal’s usual peer review process.

Wurster, A. L., & Pazin, M. J. (2012) · Biochemistry and Cell Biology · doi:10.1139/o11-042 · Cited by 15 · see citing works

Initiation and Limitation of Ly-49A NK Cell Receptor Acquisition by T Cell Factor-1

Ioannidis, V., Kunz, B., Tanamachi, D. M., Scarpellino, L., & Held, W. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.2.769 · Cited by 15 · see citing works

Recombinant R-spondin2 and Wnt3a Up- and Down-Regulate Novel Target Genes in C57MG Mouse Mammary Epithelial Cells

Baljinnyam, B., Klauzińska, M., Saffo, S., Callahan, R., & Rubin, J. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029455 · Cited by 13 · see citing works

Glycogen synthase kinase 3 drives thymocyte egress by suppressing β-catenin activation of Akt

Liu, C., Ma, L., Wang, Y., Zhao, J., Chen, P., Chen, X., Wang, Y., Hu, Y., Liu, Y., Jia, X., et al. (2021) · Science Advances · doi:10.1126/sciadv.abg6262 · Cited by 12 · see citing works

Age-dependent transcriptomic profiles of leukocytes in pediatric population

Koutsogiannaki, S., Kim, S., & Yuki, K. (2023) · Clinical Immunology · doi:10.1016/j.clim.2023.109728 · Cited by 10 · see citing works

Tracing the path of cancer initiation: the AA protein-based model for cancer genesis

Adjiri, A. (2018) · BMC Cancer · doi:10.1186/s12885-018-4739-1 · Cited by 10 · see citing works

Harmless effects of argon plasma on caudal fin regeneration and embryogenesis of zebrafish: novel biological approaches for safe medical applications of bioplasma

Nam, M., Kim, G.-Y., Yun, S.-E., Jang, J.-Y., Kim, Y.-H., Choi, E. H., Kang, S., & Rhim, H. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2017.95 · Cited by 10 · see citing works

Wnt signaling in B and T lymphocytes

Qiang, Y. (2004) · Frontiers in bioscience · doi:10.2741/1309 · Cited by 24 · see citing works

Deciphering the role of Notch signaling in lymphopoiesis

Izon, D. J., Punt, J. A., & Pear, W. S. (2002) · Current Opinion in Immunology · doi:10.1016/s0952-7915(02)00321-7 · Cited by 60 · see citing works

An Invitation to T and More

Allman, D., Punt, J. A., Izon, D. J., Aster, J. C., & Pear, W. S. (2002) · Cell · doi:10.1016/s0092-8674(02)00689-x · Cited by 143 · see citing works

Lymphocyte development cell selections events and signals during immune ontogeny

Pillai, S. S. (2000)

Notch signaling in lymphopoiesis

Pear, W. S., & Radtke, F. (2003) · Seminars in Immunology · doi:10.1016/s1044-5323(03)00003-4 · Cited by 96 · see citing works