Dermal β-catenin activity in response to epidermal Wnt ligands is required for fibroblast proliferation and hair follicle initiation

Generalized lacZ expression with the ROSA26 Cre reporter strain

Soriano, P. (1999) · Nature Genetics · doi:10.1038/5007 · Cited by 5,237 · see citing works

Wnt/β-Catenin/Tcf Signaling Induces the Transcription of Axin2, a Negative Regulator of the Signaling Pathway

Jho, E., Zhang, T., Domon–Dell, C., Joo, C., Freund, J., & Costantini, F. D. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.4.1172-1183.2002 · Cited by 1,683 · see citing works

The Biology of Hair Follicles

Paus, R., & Cotsarelis, G. (1999) · New England Journal of Medicine · doi:10.1056/nejm199908123410706 · Cited by 1,438 · see citing works

β-Catenin Controls Hair Follicle Morphogenesis and Stem Cell Differentiation in the Skin

Huelsken, J., Vogel, R., Erdmann, B., Cotsarelis, G., & Birchmeier, W. (2001) · Cell · doi:10.1016/s0092-8674(01)00336-1 · Cited by 1,352 · 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

Towards an integrated view of Wnt signaling in development

van Amerongen, R., & Nusse, R. (2009) · Development · doi:10.1242/dev.033910 · Cited by 1,168 · see citing works

Inactivation of the β-catenin gene by Wnt1-Cre -mediated deletion results in dramatic brain malformation and failure of craniofacial development

Brault, V., Moore, R., Kutsch, S., Ishibashi, M., Rowitch, D. H., McMahon, A. P., Sommer, L., Boussadia, O., & Kemler, R. (2001) · Development · doi:10.1242/dev.128.8.1253 · Cited by 1,089 · see citing works

WNT Signals Are Required for the Initiation of Hair Follicle Development

Andl, T., Reddy, S. T., Gaddapara, T., & Millar, S. E. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00167-3 · Cited by 1,088 · see citing works

Multiple roles for activated LEF/TCF transcription complexes during hair follicle development and differentiation

DasGupta, R., & Fuchs, E. V. (1999) · Development · doi:10.1242/dev.126.20.4557 · Cited by 995 · see citing works

Molecular Mechanisms Regulating Hair Follicle Development

Millar, S. E. (2002) · Journal of Investigative Dermatology · doi:10.1046/j.0022-202x.2001.01670.x · Cited by 967 · see citing works

The secret life of the hair follicle

Hardy, M. H. (1992) · Trends in Genetics · doi:10.1016/0168-9525(92)90350-d · Cited by 931 · see citing works

Sonic hedgehog regulates growth and morphogenesis of the tooth

Dassule, H. R., Lewis, P. M., Bei, M., Maas, R. L., & McMahon, A. P. (2000) · Development · doi:10.1242/dev.127.22.4775 · Cited by 806 · see citing works

Sonic hedgehog signaling is essential for hair development

St‐Jacques, B., Dassule, H. R., Karavanova, I. D., Botchkarev, V. A., Li, J., Danielian, P. S., McMahon, J. A., Lewis, P. M., Paus, R., & McMahon, A. P. (1998) · Current Biology · doi:10.1016/s0960-9822(98)70443-9 · Cited by 764 · see citing works

Wntless, a Conserved Membrane Protein Dedicated to the Secretion of Wnt Proteins from Signaling Cells

Bänziger, C., Soldini, D., Schütt, C., Zipperlen, P., Hausmann, G., & Basler, K. (2006) · Cell · doi:10.1016/j.cell.2006.02.049 · Cited by 764 · see citing works

Induction of hair growth by implantation of cultured dermal papilla cells

Jahoda, C. A. B., Horne, K. A., & OLIVER, R. F. (1984) · Nature · doi:10.1038/311560a0 · Cited by 646 · see citing works

Secretion of Wnt Ligands Requires Evi, a Conserved Transmembrane Protein

Bartscherer, K., Pelte, N., Ingelfinger, D., & Boutros, M. (2006) · Cell · doi:10.1016/j.cell.2006.04.009 · Cited by 580 · see citing works

Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of β-catenin in micePreprint

Grigoryan, T., Wend, P., Klaus‐Bergmann, A., & Birchmeier, W. (2008) · Genes & Development · doi:10.1101/gad.1686208 · Cited by 558 · see citing works

A comprehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis

van der Veen, C., Handjiski, B., Paus, R., Müller-Röver, S., Maurer, M., Eichmüller, S., Ling, G., Hofmann, U., Foitzik, K., & Mecklenburg, L. (1999) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.1999.00740.x · Cited by 553 · see citing works

Molecular principles of hair follicle induction and morphogenesis

Schmidt‐Ullrich, R., & Paus, R. (2005) · BioEssays · doi:10.1002/bies.20184 · Cited by 549 · see citing works

Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis

Reddy, S., Andl, T., Bagasra, A., Lu, M. M., Epstein, D. J., Morrisey, E. E., & Millar, S. E. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00452-x · Cited by 489 · see citing works

Sox9 Is Essential for Outer Root Sheath Differentiation and the Formation of the Hair Stem Cell Compartment

Vidal, V., Chaboissier, M., Lützkendorf, S., Cotsarelis, G., Mill, P., Hui, C., Ortonne, N., Ortonne, J. P., & Schedl, A. (2005) · Current Biology · doi:10.1016/j.cub.2005.06.064 · Cited by 427 · see citing works

Lef1 expression is activated by BMP-4 and regulates inductive tissue interactions in tooth and hair development.Preprint

Kratochwil, K., Dull, M., Fariñas, I., Galcerán, J., & Grosschedl, R. (1996) · Genes & Development · doi:10.1101/gad.10.11.1382 · Cited by 425 · see citing works

Noggin is a mesenchymally derived stimulator of hair-follicle induction

Botchkarev, V. A., Botchkareva, N. V., Roth, W., Nakamura, M., Chen, L.-H., Herzog, W., Lindner, G., McMahon, J. A., Peters, C., Lauster, R., et al. (1999) · Nature Cell Biology · doi:10.1038/11078 · Cited by 414 · see citing works

β-catenin Activity in the Dermal Papilla Regulates Morphogenesis and Regeneration of Hair

Enshell‐Seijffers, D., Lindon, C., Kashiwagi, M., & Morgan, B. A. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.01.016 · Cited by 408 · see citing works

β-catenin activation is necessary and sufficient to specify the dorsal dermal fate in the mouse

Atit, R., Sgaier, S. K., Mohamed, O. A., Taketo, M. M., Dufort, D., Joyner, A. L., Niswander, L., & Conlon, R. A. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.04.449 · Cited by 400 · cited 5× · see citing works

Cell lineage in mammalian craniofacial mesenchyme.

Yoshida, T., Vivatbutsiri, P., Morriss-Kay, G., Saga, Y., & Iseki, S. (2008) · Mechanisms of Development · doi:10.1016/j.mod.2008.06.007 · Cited by 384 · see citing works

Involvement of a novel Tnf receptor homologue in hair follicle induction.

Headon, D. J., & Overbeek, P. A. (1999) · Nature Genetics · doi:10.1038/11943 · Cited by 379 · see citing works

Reciprocal Requirements for EDA/EDAR/NF-κB and Wnt/β-Catenin Signaling Pathways in Hair Follicle Induction

Zhang, Y., Tomann, P., Andl, T., Gallant, N. M., Huelsken, J., Jerchow, B., Birchmeier, W., Paus, R., Piccolo, S., Mikkola, M. L., et al. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.05.011 · Cited by 363 · see citing works

Two lineage boundaries coordinate vertebrate apical ectodermal ridge formationPreprint

Kimmel, R. A., Turnbull, D. H., Blanquet, V., Wurst, W., Loomis, C. A., & Joyner, A. L. (2000) · Genes & Development · doi:10.1101/gad.14.11.1377 · Cited by 341 · see citing works

Sox2-positive dermal papilla cells specify hair follicle type in mammalian epidermis

Driskell, R. R., Giangreco, A., Jensen, K. B., Mulder, K. W., & Watt, F. M. (2009) · Development · doi:10.1242/dev.038620 · Cited by 331 · see citing works

Onset of Keratin 17 Expression Coincides with the Definition of Major Epithelial Lineages during Skin Development

McGowan, K. M., & Coulombe, P. A. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.2.469 · Cited by 319 · see citing works

Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia

Wang, X., Sutton, V. R., Peraza-Llanes, J. O., Yu, Z., Rosetta, R., Kou, Y.-C., Eble, T. N., Patel, A., Christina Thaller, B., Fang, P., et al. (2007) · Nature Genetics · doi:10.1038/ng2057 · Cited by 283 · see citing works

Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia

Grzeschik, K., Bornholdt, D., Oeffner, F., König, A., Boente, M. D. C., Enders, H., Fritz, B., Hertl, M., Grasshoff, U., Höfling, K., et al. (2007) · Nature Genetics · doi:10.1038/ng2052 · Cited by 283 · see citing works

Dermo-1: A Novel Twist-Related bHLH Protein Expressed in the Developing Dermis

Li, L., Cserjesi, P., & Olson, E. N. (1995) · Developmental Biology · doi:10.1006/dbio.1995.0023 · Cited by 258 · see citing works

The secret life of the hair follicle

Hardy, M. (1992) · Trends in Genetics · doi:10.1016/0168-9525(92)90044-5 · Cited by 238 · see citing works

Self-organization of periodic patterns by dissociated feather mesenchymal cells and the regulation of size, number and spacing of primordia

Jiang, T., Jung, H.-S., Widelitz, R. B., & Chuong, C. (1999) · Development · doi:10.1242/dev.126.22.4997 · Cited by 237 · see citing works

Sprinter: a novel transmembrane protein required for Wg secretion and signaling

Goodman, R. M., Thombre, S., Karagonlar, Z. F., Gray, D., Betts, D., Roebuck, J., Spana, E. P., & Selva, E. M. (2006) · Development · doi:10.1242/dev.02674 · Cited by 222 · see citing works

Skin-Nervous System Interactions

Ansel, J. C., Kaynard, A. H., Armstrong, C. A., Olerud, J. E., Bunnett, N. W., & Payan, D. G. (1996) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12330326 · Cited by 209 · see citing works

Characterization of Wnt signaling components and activation of the Wnt canonical pathway in the murine retina

Liu, H. S., Mohamed, O. A., Dufort, D., & Wallace, V. A. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10315 · Cited by 203 · see citing works

Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate

Zhang, Y., Andl, T., Yang, S. H., Teta, M., Liu, F., Seykora, J. T., Tobias, J. W., Piccolo, S., Schmidt‐Ullrich, R., Nagy, A., et al. (2008) · Development · doi:10.1242/dev.017459 · Cited by 193 · see citing works

Paracrine regulation of keratinocyte proliferation and differentiation

Werner, S., & Smola, H. (2001) · Trends in Cell Biology · doi:10.1016/s0962-8924(01)01955-9 · Cited by 183 · see citing works

Reprogramming adult dermis to a neonatal state through epidermal activation of β-catenin

Collins, C. A., Kretzschmar, K., & Watt, F. M. (2011) · Development · doi:10.1242/dev.064592 · Cited by 152 · see citing works

Generation of mice with a conditional null allele for Wntless

Carpenter, A. C., Rao, S., Wells, J. M., Campbell, K., & Lang, R. A. (2010) · genesis · doi:10.1002/dvg.20651 · Cited by 148 · see citing works

Increased Expression of Wnt2 and SFRP4 in Tsk Mouse Skin: Role of Wnt Signaling in Altered Dermal Fibrillin Deposition and Systemic Sclerosis

Bayle, J., Fitch, J. L., Jacobsen, K. A., Kumar, R., Lafyatis, R., & Lemaire, R. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5701101 · Cited by 135 · see citing works

Murine Wnt-11 and Wnt-12 have temporally and spatially restricted expression patterns during embryonic development

Christiansen, J. H., Dennis, C. L., Wicking, C., Monkley, S. J., Wilkinson, D. G., & Wainwright, B. J. (1995) · Mechanisms of Development · doi:10.1016/0925-4773(95)00383-5 · Cited by 134 · see citing works

Induction of Hair Growth in Ear Wounds by Cultured Dermal Papilla Cells

Jahoda, C. A. B., Reynolds, A. J., & OLIVER, R. F. (1993) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12366039 · Cited by 118 · see citing works

Whisker growth induced by implantation of cultured vibrissa dermal papilla cells in the adult rat

Horne, K. A., Jahoda, C. A. B., & OLIVER, R. F. (1986) · Development · doi:10.1242/dev.97.1.111 · Cited by 117 · see citing works

Distinct Wnt members regulate the hierarchical morphogenesis of skin regions (spinal tract) and individual feathers

Chang, C., Jiang, T., Lin, C., Burrus, L. W., Chuong, C., & Widelitz, R. B. (2004) · Mechanisms of Development · doi:10.1016/j.mod.2003.12.004 · Cited by 117 · see citing works

β-Catenin Signaling in Fibroproliferative Disease

Bowley, E., O’Gorman, D. B., & Gan, B. S. (2006) · Journal of Surgical Research · doi:10.1016/j.jss.2006.07.026 · Cited by 106 · see citing works

Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axisPreprint

Hu, B., Lefort, K., Qiu, W., Nguyen, B.-C., Rajaram, R. D., Castillo, E., He, F., Chen, Y., Angel, P. E., Brisken, C., et al. (2010) · Genes & Development · doi:10.1101/gad.1886910 · Cited by 106 · see citing works

The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis

Bazzi, H., Fantauzzo, K. A., Richardson, G. D., Jahoda, C. A. B., & Christiano, A. M. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.02.035 · Cited by 98 · see citing works

Compartmentalization of the Somite and Myogenesis in Chick Embryos Are Influenced by Wnt Expression

Wagner, J., Schmidt, C., Nikowits, W., & Christ, B. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9921 · Cited by 96 · see citing works

Goosecoid acts cell autonomously in mesenchyme-derived tissues during craniofacial development

Rivera‐Pérez, J. A., Wakamiya, M., & Behringer, R. R. (1999) · Development · doi:10.1242/dev.126.17.3811 · Cited by 85 · see citing works

Molecular Regulation of Angiogenesis in the Skin

Detmar, M. J. (1996) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12340457 · Cited by 83 · see citing works

Dorsal dermis development depends on a signal from the dorsal neural tube, which can be substituted by Wnt-1

Olivera-Martínez, I., Thélu, J., Teillet, M., & Dhouailly, D. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(00)00540-2 · Cited by 77 · see citing works

β-Catenin has sequential roles in the survival and specification of ventral dermis

Ohtola, J. A., Myers, J., Akhtar‐Zaidi, B., Zuzindlak, D., Sandesara, P. B., Yeh, K., Mackem, S., & Atit, R. P. (2008) · Development · doi:10.1242/dev.021170 · Cited by 75 · see citing works

Peridermal cell patterning in the feather-forming skin of the chick embryo

Sengel, P., & Mauger, A. (1976) · Developmental Biology · doi:10.1016/0012-1606(76)90132-9 · Cited by 74 · see citing works

Inductive Properties of Hair Follicle Cells

Reynolds, A. J., & Jahoda, C. A. B. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb24390.x · Cited by 72 · see citing works

Role of canonical Wnt signaling/β-catenin viaDermo1in cranial dermal cell development

Trần, T. H., Jarrell, A. S., Zentner, G. E., Welsh, A. L., Brownell, I., Scacheri, P. C., & Atit, R. P. (2010) · Development · doi:10.1242/dev.056473 · Cited by 69 · see citing works

Dkk4 and Eda Regulate Distinctive Developmental Mechanisms for Subtypes of Mouse Hair

Cui, C., Kunisada, M., Piao, Y., Childress, V., Ko, M. S. H., & Schlessinger, D. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010009 · Cited by 46 · see citing works

Tamoxifen‐dependent, inducible Hoxb6CreERT recombinase function in lateral plate and limb mesoderm, CNS isthmic organizer, posterior trunk neural crest, hindgut, and tailbud

Nguyen, M., Zhu, J., Nakamura, E., Bao, X., & Mackem, S. (2009) · Developmental Dynamics · doi:10.1002/dvdy.21846 · Cited by 41 · see citing works

Skin field formation: morphogenetic events.

Dhouailly, D., Olivera-Martínez, I., Fliniaux, I., Missier, S., Viallet, J. P., & Thélu, J. (2004) · The International Journal of Developmental Biology · doi:10.1387/ijdb.15272373 · Cited by 39 · see citing works

The role of BMP-2 and BMP-4 in follicle initiation and the murine hair cycle.

Wilson, N., Hynd, P., & Powell, B. C. (1999) · PubMed · Cited by 31 · see citing works

Temporal and spatial protease nexin 1 expression during chick development

Rodríguez‐Niedenführ, M. (2003) · Gene Expression Patterns · doi:10.1016/s1567-133x(03)00117-0 · Cited by 6 · see citing works

Inference and analysis of cell-cell communication using CellChat

Jin, S., Guerrero-Juarez, C. F., Zhang, L., Chang, I., Ramos, R., Kuan, C.-H., Myung, P., Plikus, M. V., & Nie, Q. (2021) · Nature Communications · doi:10.1038/s41467-021-21246-9 · Cited by 8,409 · see citing works

Mesenchymal Stem/Stromal Cell-Derived Exosomes for Immunomodulatory Therapeutics and Skin Regeneration

Ha, D. H., Kim, H.-K., Lee, J., Kwon, H. H., Park, G., Yang, S. H., Jung, J. Y., Choi, H., Lee, J. H., Sung, S., et al. (2020) · Cells · doi:10.3390/cells9051157 · Cited by 545 · see citing works

Microenvironmental reprogramming by three-dimensional culture enables dermal papilla cells to induce de novo human hair-follicle growth

Higgins, C. A., Chen, J. C., Cerise, J. E., Jahoda, C. A. B., & Christiano, A. M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1309970110 · Cited by 396 · see citing works

Signaling Involved in Hair Follicle Morphogenesis and Development

Pisal, R. V., Dev, K., Diaz, D. C., Qureshi, W. M. S., Filip, S., & Mokrý, J. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15011647 · Cited by 391 · see citing works

Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling

Sennett, R., & Rendl, M. (2012) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2012.08.011 · Cited by 387 · see citing works

Fgf9 from dermal γδ T cells induces hair follicle neogenesis after wounding

Gay, D. L., Kwon, O., Zhang, Z., Spata, M., Plikus, M. V., Holler, P. D., Ito, M., Yang, Z., Treffeisen, E. R., Kim, C. D., et al. (2013) · Nature Medicine · doi:10.1038/nm.3181 · Cited by 319 · see citing works

Molecular mechanisms of viral oncogenesis in humans

Krump, N. A., & You, J. (2018) · Nature Reviews Microbiology · doi:10.1038/s41579-018-0064-6 · Cited by 300 · see citing works

Androgenetic Alopecia: An Update of Treatment Options

Kelly, Y., Blanco, A., & Tosti, A. (2016) · Drugs · doi:10.1007/s40265-016-0629-5 · Cited by 279 · see citing works

Regenerative Scar-Free Skin Wound Healing

Monavarian, M., Kader, S. I., Moeinzadeh, S., & Jabbari, E. (2019) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2018.0350 · Cited by 293 · see citing works

A randomized evaluator blinded study of effect of microneedling in androgenetic alopecia: A pilot study

Dhurat, R. S., Sukesh, M. S., Avhad, G., Dandale, A., Pal, A., & Pund, P. (2013) · International Journal of Trichology · doi:10.4103/0974-7753.114700 · Cited by 262 · see citing works

Targeting Wnt/β-Catenin Pathway for Developing Therapies for Hair Loss

Choi, B. Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144915 · Cited by 263 · see citing works

Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing

Lim, C. H., Sun, Q., Ratti, K., Lee, S.-H., Zheng, Y., Takeo, M., Lee, W., Rabbani, P. S., Plikus, M. V., Cain, J. E., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07142-9 · Cited by 247 · see citing works

Epithelial Wnt Ligand Secretion Is Required for Adult Hair Follicle Growth and Regeneration

Myung, P. S., Takeo, M., Ito, M., & Atit, R. P. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.230 · Cited by 242 · see citing works

An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin

Sennett, R., Wang, Z., Rezza, A., Grisanti, L., Roitershtein, N., Sicchio, C., Mok, K. W., Heitman, N. J., Clavel, C., Ma’ayan, A., et al. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.06.023 · Cited by 211 · see citing works

Macrophages induce AKT/β-catenin-dependent Lgr5+ stem cell activation and hair follicle regeneration through TNF

Wang, X.-S., Chen, H.-Y., Tian, R.-Y., Zhang, Y., Drutskaya, M., Wang, C., Ge, J.-F., Fan, Z., Kong, D., Wang, X.-X., et al. (2017) · Nature Communications · doi:10.1038/ncomms14091 · Cited by 208 · see citing works

Dermal fibroblast in cutaneous development and healing

Thulabandu, V., Chen, D.-M., & Atit, R. (2017) · Wiley Interdisciplinary Reviews: Developmental Biology · doi:10.1002/wdev.307 · Cited by 194 · see citing works

Understanding the impact of fibroblast heterogeneity on skin fibrosis

Griffin, M., desJardins-Park, H. E., Mascharak, S., Borrelli, M. R., & Longaker, M. T. (2020) · Disease Models & Mechanisms · doi:10.1242/dmm.044164 · Cited by 194 · see citing works

Early inductive events in ectodermal appendage morphogenesis

Biggs, L. C., & Mikkola, M. L. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.01.007 · Cited by 184 · see citing works

Extracellular vesicles derived from MSCs activates dermal papilla cell in vitro and promotes hair follicle conversion from telogen to anagen in mice

Rajendran, R. L., Gangadaran, P., Bak, S., Oh, J. M., Kalimuthu, S., Lee, H., Baek, S. H., Zhu, L., Sung, Y. K., Jeong, S. Y., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-15505-3 · Cited by 188 · see citing works

Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish

Wehner, D., Tsarouchas, T. M., Michael, A., Haase, C., Weidinger, G., Reimer, M. M., Becker, T., & Becker, C. G. (2017) · Nature Communications · doi:10.1038/s41467-017-00143-0 · Cited by 175 · see citing works

Identifying the Target Cells and Mechanisms of Merkel Cell Polyomavirus Infection

Liu, W., Yang, R., Payne, A. S., Schowalter, R. M., Spurgeon, M. E., Lambert, P. F., Xu, X., Buck, C. B., & You, J. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.04.024 · Cited by 173 · see citing works

Lef1 expression in fibroblasts maintains developmental potential in adult skin to regenerate wounds

Phan, Q. M., Fine, G. M., Salz, L., Herrera, G. G., Wildman, B., Driskell, I. M., & Driskell, R. R. (2020) · eLife · doi:10.7554/elife.60066 · Cited by 170 · see citing works

Fgf20 governs formation of primary and secondary dermal condensations in developing hair folliclesPreprint

Huh, S., Närhi, K. M., Lindfors, P. H., Häärä, O., Yang, L. M., Ornitz, D. M., & Mikkola, M. L. (2013) · Genes & Development · doi:10.1101/gad.198945.112 · Cited by 155 · see citing works

Hierarchical patterning modes orchestrate hair follicle morphogenesis

Glover, J. D., Wells, K. L., Matthäus, F., Painter, K. J., Ho, W., Riddell, J., Johansson, J. A., Ford, M. J., Jahoda, C. A. B., Klika, V., et al. (2017) · PLOS Biology · doi:10.1371/journal.pbio.2002117 · Cited by 155 · see citing works

An updated classification of hair follicle morphogenesis

Saxena, N., Mok, K., & Rendl, M. (2019) · Experimental Dermatology · doi:10.1111/exd.13913 · Cited by 147 · see citing works

Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells

Veltri, A., Lang, C. M. R., & Lien, W. (2017) · Stem Cells · doi:10.1002/stem.2723 · Cited by 147 · see citing works

Wnt/β-catenin signaling in dermal condensates is required for hair follicle formation

Tsai, S., Sennett, R., Rezza, A., Clavel, C., Grisanti, L., Zemla, R., Najam, S., & Rendl, M. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.11.023 · Cited by 138 · see citing works

Bone Marrow Mesenchymal Stem Cell-Derived CD63 + Exosomes Transport Wnt3a Exteriorly and Enhance Dermal Fibroblast Proliferation, Migration, and Angiogenesis In Vitro

McBride, J. D., Rodriguez-Menocal, L., Guzman, W., Candanedo, A., García-Contreras, M., & Badiavas, E. V. (2017) · Stem Cells and Development · doi:10.1089/scd.2017.0087 · Cited by 141 · see citing works

Inhibition of β-catenin signalling in dermal fibroblasts enhances hair follicle regeneration during wound healing

Rognoni, E., Gomez, C., Pisco, A. O., Rawlins, E. L., Simons, B. D., Watt, F. M., & Driskell, R. R. (2016) · Development · doi:10.1242/dev.131797 · Cited by 137 · see citing works

Self-Organization in Pattern Formation

Schweisguth, F., & Corson, F. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.05.019 · Cited by 124 · see citing works

PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration

Chen, Y., Fan, Z., Wang, X., Mo, M., Zeng, S. B., Xu, R.-H., Wang, X., & Wu, Y. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01650-6 · Cited by 130 · see citing works

Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture

Villeneuve, C., Hashmi, A., Ylivinkka, I., Lawson-Keister, E., Miroshnikova, Y. A., Gonzalez, C. P., Myllymäki, S.-M., Bertillot, F., Yadav, B., Zhang, T., et al. (2024) · Nature Cell Biology · doi:10.1038/s41556-023-01332-4 · Cited by 121 · see citing works

Single-Cell Analysis Reveals a Hair Follicle Dermal Niche Molecular Differentiation Trajectory that Begins Prior to Morphogenesis

Gupta, K., Levinsohn, J. L., Linderman, G. C., Chen, D., Sun, T. Y., Dong, D., Taketo, M. M., Bosenberg, M., Kluger, Y., Choate, K. A., et al. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.11.032 · Cited by 115 · see citing works

Epidermal Wnt Controls Hair Follicle Induction by Orchestrating Dynamic Signaling Crosstalk between the Epidermis and Dermis

Fu, J., & Hsu, W. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.407 · Cited by 120 · see citing works

Dermal Condensate Niche Fate Specification Occurs Prior to Formation and Is Placode Progenitor Dependent

Mok, K., Saxena, N., Heitman, N., Grisanti, L., Srivastava, D., Muraro, M. J., Jacob, T., Sennett, R., Wang, Z., Su, Y., et al. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.11.034 · Cited by 110 · see citing works

Phagocytosis of Wnt inhibitor SFRP4 by late wound macrophages drives chronic Wnt activity for fibrotic skin healing

Gay, D., Ghinatti, G., Guerrero-Juarez, C., Ferrer, R. A., Ferri, F., Lim, C., Murakami, S., Gault, N., Barroca, V., Rombeau, I., et al. (2020) · Science Advances · doi:10.1126/sciadv.aay3704 · Cited by 95 · see citing works

Immune modulation of hair follicle regeneration

Rahmani, W. M., Sinha, S., & Biernaskie, J. A. (2020) · npj Regenerative Medicine · doi:10.1038/s41536-020-0095-2 · Cited by 113 · see citing works

Epidermal Development in Mammals: Key Regulators, Signals from Beneath, and Stem Cells

Liu, S., Zhang, H., & Duan, E. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140610869 · Cited by 110 · see citing works

Scalable production of controllable dermal papilla spheroids on PVA surfaces and the effects of spheroid size on hair follicle regeneration

Huang, Y., Chan, C., Lin, W., Chiu, H., Tsai, R., Tsai, T., Chan, J. L., & Lin, S. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.09.083 · Cited by 105 · see citing works

Long non-coding RNA HoxA-AS3 interacts with EZH2 to regulate lineage commitment of mesenchymal stem cells

Zhu, X., Yan, Y., Chen, D., Ai, C., Lu, X., Xu, S., Jiang, S., Zhong, G., Chen, D., & Jiang, Y. (2016) · Oncotarget · doi:10.18632/oncotarget.11538 · Cited by 102 · see citing works

Development of the Mouse Dermal Adipose Layer Occurs Independently of Subcutaneous Adipose Tissue and Is Marked by Restricted Early Expression of FABP4

Wojciechowicz, K., Gledhill, K., Ambler, C. A., Manning, C. B., & Jahoda, C. A. B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059811 · Cited by 98 · see citing works

Apoptotic extracellular vesicles are metabolized regulators nurturing the skin and hair

Ma, L., Chen, C., Liu, D., Huang, Z., Li, J., Liu, H., Kwok, R. T. K., Tang, B. Z., Sui, B., Zhang, X., et al. (2022) · Bioactive Materials · doi:10.1016/j.bioactmat.2022.04.022 · Cited by 93 · see citing works

Single-cell Transcriptome Profiling reveals Dermal and Epithelial cell fate decisions during Embryonic Hair Follicle Development

Ge, W., Tan, S., Wang, S.-H., Li, L., Sun, X.-F., Shen, W., & Wang, X. (2020) · Theranostics · doi:10.7150/thno.44306 · Cited by 92 · see citing works

A Beginner’s Introduction to Skin Stem Cells and Wound Healing

Garcia, D. D., Filipová, A., Veloz, I. G., & Martínez‐Fierro, M. L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011030 · Cited by 92 · see citing works

BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin

Zhu, X.-J., Liu, Y., Dai, Z.-M., Zhang, X., Yang, X., Li, Y., Qiu, M., Fu, J., Hsu, W., Chen, Y., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004687 · Cited by 89 · see citing works

Involvement of Wnt, Eda and Shh at defined stages of sweat gland development

Cui, C.-Y., Yin, M., Sima, J., Childress, V., Michel, M., Piao, Y., & Schlessinger, D. (2014) · Development · doi:10.1242/dev.109231 · Cited by 80 · see citing works

Differentiated Daughter Cells Regulate Stem Cell Proliferation and Fate through Intra-tissue Tension

Ning, W., Muroyama, A., Li, H., & Lechler, T. (2020) · Cell stem cell · doi:10.1016/j.stem.2020.11.002 · Cited by 79 · see citing works

Establishment of an in vitro organoid model of dermal papilla of human hair follicle

Gupta, A., Chawla, S., Hegde, A., Singh, D., Bandyopadhyay, B., Lakshmanan, C. C., Kalsi, G., & Ghosh, S. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26853 · Cited by 80 · see citing works

Molecular and spatial landmarks of early mouse skin development

Jacob, T., Annusver, K., Czarnewski, P., Dalessandri, T., Kalk, C., Levron, C. L., Sanz, N. C., Kastriti, M. E., Mikkola, M. L., Rendl, M., et al. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.07.015 · Cited by 75 · see citing works

Exploring Differentially Expressed Genes by RNA-Seq in Cashmere Goat (Capra hircus) Skin during Hair Follicle Development and Cycling

Geng, R., Yuan, C., & Chen, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062704 · Cited by 76 · see citing works

Reprogramming of three-dimensional microenvironments for in vitro hair follicle induction

Kageyama, T., Shimizu, A., Anakama, R., Nakajima, R., Suzuki, K., Okubo, Y., & Fukuda, J. (2022) · Science Advances · doi:10.1126/sciadv.add4603 · Cited by 73 · see citing works

Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions

Tsutsui, K., Machida, H., Nakagawa, A., Ahn, K., Morita, R., Sekiguchi, K., Miner, J. H., & Fujiwara, H. (2021) · Nature Communications · doi:10.1038/s41467-021-22881-y · Cited by 73 · see citing works

Single Cell and Open Chromatin Analysis Reveals Molecular Origin of Epidermal Cells of the Skin

Fan, X., Wang, D., Burgmaier, J. E., Teng, Y., Romano, R., Sinha, S., & Yi, R. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.08.010 · Cited by 68 · see citing works

Evaluating the Efficacy of Different Platelet-Rich Plasma Regimens for Management of Androgenetic Alopecia: A Single-Center, Blinded, Randomized Clinical Trial

Hausauer, A. K., & Jones, D. (2018) · Dermatologic Surgery · doi:10.1097/dss.0000000000001567 · Cited by 68 · see citing works

A Single-Cell Transcriptome Atlas of Cashmere Goat Hair Follicle Morphogenesis

Ge, W., Zhang, W., Zhang, Y., Zheng, Y., Li, F., Wang, S., Liu, J., Tan, S., Yan, Z., Wang, L., et al. (2021) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2021.07.003 · Cited by 67 · see citing works

New investigational drugs for androgenetic alopecia

de Sousa, I. C. V. D., & Tosti, A. (2013) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2013.784743 · Cited by 67 · see citing works

Sox2 modulates the function of two distinct cell lineages in mouse skin

Lesko, M. H., Driskell, R. R., Kretzschmar, K., Goldie, S. J., & Watt, F. M. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.08.004 · Cited by 66 · see citing works

Treatment of Androgenetic Alopecia Using PRP to Target Dysregulated Mechanisms and Pathways

Abdin, R., Zhang, Y., & Jimenez, J. J. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.843127 · Cited by 71 · see citing works

Spontaneous tumour regression in keratoacanthomas is driven by Wnt/retinoic acid signalling cross-talk

Zito, G., Saotome, I., Liu, Z. Z., Ferro, E. G., Sun, T. Y., Nguyen, D. X., Bilgüvar, K., Ko, C. J., & Greco, V. (2014) · Nature Communications · doi:10.1038/ncomms4543 · Cited by 63 · see citing works

Augmenting Endogenous Wnt Signaling Improves Skin Wound Healing

Whyte, J. L., Smith, A. A., Liu, B., Manzano, W., Evans, N. D., Dhamdhere, G. R., Fang, M. Y., Chang, H. Y., Oro, A. E., & Helms, J. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076883 · Cited by 61 · see citing works

The G protein-coupled receptor Gpr161 regulates forelimb formation, limb patterning and skeletal morphogenesis in a primary cilium-dependent manner

Hwang, S.-H., White, K. A., Somatilaka, B. N., Shelton, J. M., Richardson, J. A., & Mukhopadhyay, S. (2018) · Development · doi:10.1242/dev.154054 · Cited by 60 · see citing works

Principles and mechanisms of regeneration in the mouse model for wound‐induced hair follicle neogenesis

Wang, X., Hsi, T., Guerrero‐Juarez, C. F., Pham, K., Cho, K., McCusker, C., Monuki, E. S., Cho, K. W. Y., Gay, D. L., & Plikus, M. V. (2015) · Regeneration · doi:10.1002/reg2.38 · Cited by 59 · see citing works

Morroniside regulates hair growth and cycle transition via activation of the Wnt/β-catenin signaling pathway

Zhou, L., Wang, H., Jing, J., Yu, L., Wu, X., & Lu, Z. (2018) · Scientific Reports · doi:10.1038/s41598-018-32138-2 · Cited by 58 · see citing works

DNA N6-methyladenine demethylase ALKBH1 enhances osteogenic differentiation of human MSCs

Zhou, C., Liu, Y., Li, X., Zou, J., & Zou, S. (2016) · Bone Research · doi:10.1038/boneres.2016.33 · Cited by 59 · see citing works

Integrative Analysis of Methylome and Transcriptome Reveals the Regulatory Mechanisms of Hair Follicle Morphogenesis in Cashmere Goat

Wang, S., Li, F., Liu, J., Zhang, Y., Zheng, Y., Ge, W., Qu, L., & Wang, X. (2020) · Cells · doi:10.3390/cells9040969 · Cited by 57 · see citing works

Secretion and extracellular space travel of Wnt proteins.

Gross, J. C., & Boutros, M. (2013) · Current Opinion in Genetics and Development · doi:10.1016/j.gde.2013.02.017 · Cited by 57 · see citing works

Dermal Fibroblast Heterogeneity and Its Contribution to the Skin Repair and Regeneration

Xue, M., Zhao, R., MARCH, L. M., & Jackson, C. (2021) · Advances in Wound Care · doi:10.1089/wound.2020.1287 · Cited by 55 · see citing works

Fibroblasts in Diabetic Foot Ulcers

Voza, F. A., Huerta, C. T., Le, N., Shao, H., Ribieras, A. J., Ortiz, Y. Y., Atkinson, C., Machuca, T., Liu, Z., & Velazquez, O. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25042172 · Cited by 55 · see citing works

Tbx18 Targets Dermal Condensates for Labeling, Isolation, and Gene Ablation during Embryonic Hair Follicle Formation

Grisanti, L., Clavel, C., Cai, X., Rezza, A., Tsai, S., Sennett, R., Mumau, M. D., Cai, C., & Rendl, M. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.329 · Cited by 55 · see citing works

Stroma as an Active Player in the Development of the Tumor Microenvironment

Vannucci, L. E. (2014) · Cancer Microenvironment · doi:10.1007/s12307-014-0150-x · Cited by 55 · see citing works

Elevated NF-κB signaling in Asherman syndrome patients and animal models

Wang, X., Ma, N., Sun, Q., Huang, C., Liu, Y., & Luo, X. (2017) · Oncotarget · doi:10.18632/oncotarget.14853 · Cited by 55 · see citing works

Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis

Augustin, I., Gross, J. C., Baumann, D., Korn, C., Kerr, G., Grigoryan, T., Mauch, C., Birchmeier, W., & Boutros, M. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20121871 · Cited by 54 · see citing works

Gene trajectory inference for single-cell data by optimal transport metrics

Qu, R., Cheng, X., Sefik, E., Stanley, J. S., Landa, B., Strino, F., Platt, S., Garritano, J., Odell, I. D., Coifman, R. R., et al. (2024) · Nature Biotechnology · doi:10.1038/s41587-024-02186-3 · Cited by 52 · see citing works

Conditional ablation of TGF-β signaling inhibits tumor progression and invasion in an induced mouse bladder cancer model

Yu, L., Zhu, F., Zhang, H., Chen, D., Zhang, X., Gao, Q., & Li, Y. (2016) · Scientific Reports · doi:10.1038/srep29479 · Cited by 52 · see citing works

Microneedling for Hair Loss

Gupta, A. K., Quinlan, E. M., Venkataraman, M., & Bamimore, M. A. (2021) · Journal of Cosmetic Dermatology · doi:10.1111/jocd.14525 · Cited by 50 · see citing works

The Roles of WNT Signaling Pathways in Skin Development and Mechanical-Stretch-Induced Skin Regeneration

Bai, R., Guo, Y., Liu, W., Song, Y., Yu, Z., & Ma, X. (2023) · Biomolecules · doi:10.3390/biom13121702 · Cited by 51 · see citing works

An investigation of crosstalk between Wnt/β-catenin and transforming growth factor-β signaling in androgenetic alopecia

Lu, G. Y., Wu, Z.-B., Chu, X.-Y., Bi, Z., & Fan, W. (2016) · Medicine · doi:10.1097/md.0000000000004297 · Cited by 48 · see citing works

LHX2 is a direct NF-κB target gene that promotes primary hair follicle placode down-growth

Tomann, P., Paus, R., Millar, S. E., Scheidereit, C., & Schmidt‐Ullrich, R. (2016) · Development · doi:10.1242/dev.130898 · Cited by 46 · see citing works

Molecular Mechanisms of Merkel Cell Polyomavirus Transformation and Replication

Liu, W., & You, J. (2020) · Annual Review of Virology · doi:10.1146/annurev-virology-011720-121757 · Cited by 46 · see citing works

Lack of Collagen VI Promotes Wound-Induced Hair Growth

Chen, P., Cescon, M., & Bonaldo, P. (2015) · Journal of Investigative Dermatology · doi:10.1038/jid.2015.187 · Cited by 46 · see citing works

Morphogenesis of chimeric hair follicles in engineered skin substitutes with human keratinocytes and murine dermal papilla cells

Sriwiriyanont, P., Lynch, K. A., Maier, E. A., Hahn, J. M., Supp, D. M., & Boyce, S. T. (2012) · Experimental Dermatology · doi:10.1111/exd.12003 · Cited by 46 · see citing works

Wnt10b promotes hair follicles growth and dermal papilla cells proliferation via Wnt/β-Catenin signaling pathway in Rex rabbits

Wu, Z., Zhu, Y., Liu, H., Liu, G., & Li, F. (2020) · Bioscience Reports · doi:10.1042/bsr20191248 · Cited by 46 · see citing works

Ubiquitin specific peptidase 21 regulates interleukin-8 expression, stem-cell like property of human renal cell carcinoma

Peng, L., Hu, Y., Chen, D., Jiao, S., & Sun, S. (2016) · Oncotarget · doi:10.18632/oncotarget.9751 · Cited by 45 · see citing works

Distinct Requirements for Cranial Ectoderm and Mesenchyme-Derived Wnts in Specification and Differentiation of Osteoblast and Dermal Progenitors

Goodnough, L. H., Dinuoscio, G. J., Ferguson, J. W., Williams, T., Lang, R. A., & Atit, R. P. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004152 · Cited by 44 · see citing works

Exosomes derived from mouse vibrissa dermal papilla cells promote hair follicle regeneration during wound healing by activating Wnt/β-catenin signaling pathway

Shang, Y., Li, M., Zhang, L., Han, C., Shen, K., Wang, K., Li, Y., Zhang, Y., Luo, L., Jia, Y., et al. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02689-w · Cited by 43 · see citing works

Tuning Wnt Signals for More or Fewer Hairs

Lei, M., Chuong, C., & Widelitz, R. B. (2013) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.446 · Cited by 43 · see citing works

GINS2 regulates matrix metallopeptidase 9 expression and cancer stem cell property in human triple negative Breast cancer

Peng, L., Song, Z., Chen, D., Linghu, R., Wang, Y., Zhang, X., Kou, X., Yang, J., & Jiao, S. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.10.032 · Cited by 42 · see citing works

Wls Is Expressed in the Epidermis and Regulates Embryonic Hair Follicle Induction in Mice

Huang, S., Zhu, X., Liu, Y., Tao, Y., Feng, G., He, L., Guo, X., & Ma, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045904 · Cited by 41 · see citing works

Genome-Wide Scan Reveals LEMD3 and WIF1 on SSC5 as the Candidates for Porcine Ear Size

Zhang, L., Liang, J., Luo, W., Liu, X., Yan, H., Zhao, K., Shi, H., Zhang, Y., Wang, L., & Wang, L. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102085 · Cited by 40 · see citing works

Regional Control of Hairless versus Hair-Bearing Skin by Dkk2

Song, Y., Boncompagni, A. C., Kim, S.-S., Gochnauer, H. R., Zhang, Y., Loots, G. G., Wu, D., Li, Y., Xu, M., & Millar, S. E. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.11.017 · Cited by 40 · see citing works

Dermal Papilla Cells: From Basic Research to Translational Applications

Zhang, H.-L., Qiu, X.-X., & Liao, X. (2024) · Biology · doi:10.3390/biology13100842 · Cited by 39 · see citing works

The protective effects of Zhen-Wu-Tang against cisplatin-induced acute kidney injury in rats

Liu, Q., Shou-yu, H., He, Y., Zhang, J., Zeng, X., Gong, F., & Liang, L. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179137 · Cited by 39 · see citing works

A Cascade of Wnt, Eda, and Shh Signaling Is Essential for Touch Dome Merkel Cell Development

Xiao, Y., Thoresen, D. T., Miao, L., Williams, J. S., Wang, C., Atit, R. P., Wong, S. Y., & Brownell, I. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006150 · Cited by 39 · see citing works

Signaling in Tooth, Hair, and Mammary Placodes

Ahn, Y. (2015) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2014.11.013 · Cited by 37 · see citing works

Wnt/β-catenin Signaling Pathway Regulates Specific lncRNAs That Impact Dermal Fibroblasts and Skin Fibrosis

Mullin, N. K., Mallipeddi, N., Hamburg‐Shields, E., Ibarra, B. A., Khalil, A. M., & Atit, R. P. (2017) · Frontiers in Genetics · doi:10.3389/fgene.2017.00183 · Cited by 38 · see citing works

Hair Follicle Morphogenesis During Embryogenesis, Neogenesis, and Organogenesis

Park, S. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.933370 · Cited by 37 · see citing works

Inducing hair follicle neogenesis with secreted proteins enriched in embryonic skin

Fan, S. M.-Y., Tsai, C.-F., Yen, C.-M., Lin, M.-H., Wang, W.-H., Chan, C.-C., Chen, C.-L., Phua, K. K. L., Pan, S.-H., Plikus, M. V., et al. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.03.003 · Cited by 36 · see citing works

Chitosan/LiCl composite scaffolds promote skin regeneration in full-thickness loss

Yuan, J., Hou, Q., Chen, D., Zhong, L., Dai, X., Zhu, Z., Li, M., & Fu, X. (2019) · Science China Life Sciences · doi:10.1007/s11427-018-9389-6 · Cited by 36 · see citing works

Decomposing a deterministic path to mesenchymal niche formation by two intersecting morphogen gradients

Qu, R., Gupta, K., Dong, D., Jiang, Y., Landa, B., Saez, C., Strickland, G., Levinsohn, J. L., Weng, P., Taketo, M. M., et al. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.03.011 · Cited by 35 · see citing works

Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth*

Okano, J., Lévy, C., Lichti, U., Sun, H.-W., Yuspa, S., Sakai, Y., & Morasso, M. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.397273 · Cited by 33 · see citing works

1338 Dermal Wnt/β-catenin activation tunably controls hair follicle initiation

Gupta, K., Chen, D., Levinsohn, J. L., Choate, K. A., Taketo, M. M., & Myung, P. S. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2018.03.1355

Wnt/β-catenin signaling in dermal condensates is required for hair follicle formation

Tsai, S., Sennett, R., Rezza, A., Clavel, C., Grisanti, L., Zemla, R., Najam, S., & Rendl, M. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.11.023 · Cited by 138 · see citing works

872 Dermal Wnt/β-catenin signaling controls hair follicle dermal condensate size during development

Chen, D., Sun, T. Y., Gupta, K., & Myung, P. S. (2017) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2017.02.898

β-catenin activation in hair follicle dermal stem cells induces ectopic hair outgrowth and skin fibrosis

Tao, Y., Yang, Q., Wang, L., Zhang, J., Zhu, X., Sun, Q., Han, Y., Luo, Q., Wang, Y., Guo, X., et al. (2018) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjy032 · Cited by 26 · see citing works

LB822 β-catenin activation in hair follicle dermal sheath induces ectopic hair outgrowth and skin fibrosis

Tao, Y., Wang, L., Zhang, J., He, L., & Ma, G. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.05.080