The DOI matches its Crossref record; 213 of the 216 references it cites were found in a registry or an index.
The cornified envelope: a model of cell death in the skin
Abstract
The epidermis functions as a barrier against the environment by means of several layers of terminally differentiated, dead keratinocytes - the cornified layer, which forms the endpoint of epidermal differentiation and death. The cornified envelope replaces the plasma membrane of differentiating keratinocytes and consists of keratins that are enclosed within an insoluble amalgam of proteins, which are crosslinked by transglutaminases and surrounded by a lipid envelope. New insights into the molecular mechanisms and the physiological endpoints of cornification are increasing our understanding of the pathological defects of this unique form of programmed cell death, which is associated with barrier malfunctions and ichthyosis.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“A portion of EO ceramides are converted into protein-bound hydroxy (P-O) ceramides (Fig. 1B), which are connected to cross-linked proteins constituting the cornified envelope, a structure located beneath the surface of corneocytes (20)(21)(22).”
From Comparative profiling and comprehensive quantification of stratum corneum ceramides in humans and mice by LC/MS/MS (2020) · cites this paper as [20]
In the citing paper
“Unlike plasma membranes in general, which are constituted by a lipid bilayer, corneocytes are covered by a lipid monolayer mainly composed of P-O ceramides (20), which are presumed to link corneocytes to the lipid lamellae.”
From Comparative profiling and comprehensive quantification of stratum corneum ceramides in humans and mice by LC/MS/MS (2020) · cites this paper as [20]
In the citing paper
“The latter process, which is commonly known as cornification (or keratinization) and critically relies on CASP14 [1026, 1027] and multiple isoforms of transglutaminase [1025, 1028, 1029], has long been considered as a form of PCD [1025, 1030].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [1025]
Citations
Cites
Nuclear receptor that identifies a novel retinoic acid response pathway
Mangelsdorf, D. J., Ong, E. S., Dyck, J. A., & Evans, R. M. (1990) · Nature · doi:10.1038/345224a0 · Cited by 1,491
Transglutaminases: crosslinking enzymes with pleiotropic functions
Lorand, L., & Graham, R. M. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1014 · Cited by 1,439
INTERMEDIATE FILAMENTS: Structure, Dynamics, Function and Disease
Fuchs, E. V., & Weber, K. (1994) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.63.070194.002021 · Cited by 1,427
MOLECULAR AND CELLULAR BIOLOGY OF INTERMEDIATE FILAMENTS
Steinert, P. M., & Roop, D. R. (1988) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.57.070188.003113 · Cited by 1,386
Nuclear Receptor Repression Mediated by a Complex Containing SMRT, mSin3A, and Histone Deacetylase
Nagy, L., Kao, H.-Y., Chakravarti, D., Lin, R. J., Hassig, C. A., Ayer, D. E., Schreiber, S. L., & Evans, R. M. (1997) · Cell · doi:10.1016/s0092-8674(00)80218-4 · Cited by 1,230
Barrier Function of the Skin: “La Raison d'Être” of the Epidermis
Madison, K. C. (2003) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2003.12359.x · Cited by 1,192
Leid, M. E., Kastner, P., Lyons, R., Nakshatri, H., Saunders, M., Zacharewski, T. R., Chen, J.-Y., Staub, A., Garnier, J., Mader, S., et al. (1992) · Cell · doi:10.1016/0092-8674(92)90478-u · Cited by 1,144
A Structural Scaffolding of Intermediate Filaments in Health and Disease
Fuchs, E. V., & Cleveland, D. W. (1998) · Science · doi:10.1126/science.279.5350.514 · Cited by 1,013
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome
Chavanas, S., Bodemer, C., Rochat, A., Hamel‐Teillac, D., Ali, M., Irvine, A. D., Bonafé, J., WILKINSON, J. D., Taı̈eb, A., Barrandon, Y., et al. (2000) · Nature Genetics · doi:10.1038/75977 · Cited by 851
Regulation of terminal differentiation of cultured human keratinocytes by vitamin A
Fuchs, E., & Green, H. (1981) · Cell · doi:10.1016/0092-8674(81)90169-0 · Cited by 750
Flagged first, then by citations
3 of the 216 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Konig, A., Happle, R., Bornholdt, D., Engel, H. & Grzeschik, K. H. Mutations in the NSDHL gene, encoding a 3β-hydroxysteroid dehydrogenase, cause CHILD syndrome. Am. J. Med. Genet. 90, 339–346 (2000). · DOI
Cited by
Sorted by citations
Items 401–500 of 1,002
Greisenegger, E. K., Novak, N., Maintz, L., Bieber, T. R. M., Zimprich, F., Haubenberger, D., Gleiß, A., Stingl, G., Kopp, T., & Zimprich, A. A. (2009) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/j.1468-3083.2009.03469.x · Cited by 61
Vávrová, K., Kováčik, A., & Opálka, L. (2017) · European Pharmaceutical Journal · doi:10.1515/afpuc-2017-0004 · Cited by 61
Nickel Sensitization, Hand Eczema, and Loss-of-Function Mutations in the Filaggrin Gene
Thyssen, J. P., Carlsen, B. C., & Menné, T. (2008) · Dermatitis · doi:10.2310/6620.2008.08022 · Cited by 61
Lemberg, C., Vicente, K. M. D. S., Fróis-Martins, R., Altmeier, S., Tran, V. D. T., Mertens, S., Amorim-Vaz, S., Rai, L. S., d’Enfert, C., Pagni, M., et al. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010012 · Cited by 63
Warters, R. L., Packard, A. T., Kramer, G. F., Gaffney, D. K., & Moos, P. J. (2009) · Radiation Research · doi:10.1667/rr1677.1 · Cited by 60
Redox Imbalance in T Cell-Mediated Skin Diseases
Pastore, S., & Korkina, L. G. (2010) · Mediators of Inflammation · doi:10.1155/2010/861949 · Cited by 62
Entrapment of Conjunctival Goblet Cells by Desiccation-Induced Cornification
Corrales, R. M., de Paiva, C. S., Li, D., Farley, W. J., Henriksson, J. T., Bergmanson, J. P. G., & Pflugfelder, S. C. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-5782 · Cited by 60
Nobre, R. J., Herráez-Hernández, E., Fei, J.-W., Langbein, L., Kaden, S., Gröne, H., & de Villiers, E. (2009) · Journal of Virology · doi:10.1128/jvi.02490-08 · Cited by 60
Cellular Changes that Accompany Shedding of Human Corneocytes
Lin, T., Crumrine, D. A., Ackerman, L. D., Santiago, J.-L., Roelandt, T., Uchida, Y., Hupe, M., Fabriàs, G., Abad, J. L., Rice, R. H., et al. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.173 · Cited by 60
Zeng, Y., Nguyen, G. H., & Jin, H. (2016) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-016-2696-z · Cited by 59
Skin immunity and its dysregulation in psoriasis
Lanna, C., Mancini, M., Gaziano, R., Cannizzaro, M. V., Galluzzo, M., Talamonti, M., Rovella, V., Annicchiarico‐Petruzzelli, M., Melino, G., Wang, Y., et al. (2019) · Cell Cycle · doi:10.1080/15384101.2019.1653099 · Cited by 59
Self-citationCohen, I., Birnbaum, R. Y., Liani-Leibson, K., Taube, R., Sivan, S., & Birk, O. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042628 · Cited by 60
Jiang, R., Shi, Z., Johnson, J. J., Liu, Y., & Stack, M. S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.191361 · Cited by 59
Cellular Stress and General Pathological Processes
Gusev, E. Y., & Zotova, N. V. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190319114641 · Cited by 64
Dual targeting of mTOR/IL-17A and autophagy by fisetin alleviates psoriasis-like skin inflammation
Roy, T., Banang‐Mbeumi, S., Boateng, S. T., Ruiz, E. M., Chamcheu, R. N., Kang, L., King, J. A. C., Walker, A. L., Nagalo, B. M., Kousoulas, K. G., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1075804 · Cited by 61
Cytokines and Epidermal Lipid Abnormalities in Atopic Dermatitis: A Systematic Review
Upadhyay, P. R., Seminario‐Vidal, L., Abe, B. T., Ghobadi, C., & Sims, J. T. (2023) · Cells · doi:10.3390/cells12242793 · Cited by 60
The Coordinated Response of the Physical and Antimicrobial Peptide Barriers of the Skin
Borkowski, A. W., & Gallo, R. L. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2010.360 · Cited by 58
Filaggrin gene variants and atopic diseases in early childhood assessed longitudinally from birth
Bønnelykke, K., Pipper, C. B., Tavendale, R., Palmer, C. N. A., & Bisgaard, H. F. (2010) · Pediatric Allergy and Immunology · doi:10.1111/j.1399-3038.2010.01073.x · Cited by 58
Controlling the hydration of the skin though the application of occluding barrier creams
Sparr, E., Millecamps, D., Isoir, M., Burnier, V., Larsson, Å., & Cabane, B. (2012) · Journal of The Royal Society Interface · doi:10.1098/rsif.2012.0788 · Cited by 58
Review: cornification, morphogenesis and evolution of feathers
Alibardi, L. (2016) · PROTOPLASMA · doi:10.1007/s00709-016-1019-2 · Cited by 58
Li, H., Wu, N., Pu, C., Hsiao, C., Chang, D., & Hung, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-60050-1 · Cited by 59
Towell, A. M., Feuillie, C., Vitry, P., da Costa, T. M., Mathelié‐Guinlet, M., Kežić, S., Fleury, O. M., McAleer, M. A., Dufrêne, Y. F., Irvine, A. D., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2014444118 · Cited by 58
Gunnarsson, M., Mojumdar, E. H., Topgaard, D., & Sparr, E. (2021) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2021.07.012 · Cited by 57
The role of filaggrin loss-of-function mutations in atopic dermatitis
O’Regan, G. M., & Irvine, A. D. (2008) · Current Opinion in Allergy and Clinical Immunology · doi:10.1097/aci.0b013e32830e6fb2 · Cited by 57
John, S., Thiebach, L., Frie, C., Mokkapati, S., Bechtel, M., Nischt, R., Rosser-Davies, S. J., Paulsson, M., & Smyth, N. R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034252 · Cited by 57
The Role of Filaggrin in the Skin Barrier and Disease Development
Armengot‐Carbó, M., Hernández‐Martín, A., & Torrelo, A. (2015) · Actas Dermo-Sifiliográficas · doi:10.1016/j.adengl.2014.12.007 · Cited by 56
Recombinant Filaggrin Is Internalized and Processed to Correct Filaggrin Deficiency
Stout, T. E., McFarland, T. J., Mitchell, J. C., Appukuttan, B., & Stout, J. T. (2013) · Journal of Investigative Dermatology · doi:10.1038/jid.2013.284 · Cited by 56
Aberdam, D., Candi, E., Knight, R. A., & Melino, G. (2008) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2008.09.002 · Cited by 59
Self-citationOverexpression of Psoriasin (S100A7) Contributes to Dysregulated Differentiation in Psoriasis
Ekman, A., Vegfors, J., Eding, C., & Enerbäck, C. (2016) · Acta Dermato Venereologica · doi:10.2340/00015555-2596 · Cited by 56
Pichery, M., Huchenq, A., Sandhoff, R., Severino‐Freire, M., Zaafouri, S., Opálka, L., Levade, T., Soldan, V., Bertrand‐Michel, J., Lhuillier, É., et al. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx079 · Cited by 56
Niche-Specific Factors Dynamically Regulate Sebaceous Gland Stem Cells in the Skin
Veniaminova, N. A., Grachtchouk, M. A., Doane, O. J., Peterson, J. K., Quigley, D. A., Lull, M. V., Pyrozhenko, D. V., Nair, R. R., Patrick, M. T., Balmain, A., et al. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.08.015 · Cited by 55
The epidermal lipid barrier in microbiome–skin interaction
Tchoupa, A. K., Kretschmer, D., Schittek, B., & Peschel, A. (2023) · Trends in Microbiology · doi:10.1016/j.tim.2023.01.009 · Cited by 55
Kizawa, K., Takahara, H., Unno, M., & Heizmann, C. W. (2011) · Biochimie · doi:10.1016/j.biochi.2011.05.028 · Cited by 55
Ligand Targeting of EphA2 Enhances Keratinocyte Adhesion and Differentiation via Desmoglein 1
Lin, S. Y., Gordon, K., Kaplan, N., & Getsios, S. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-03-0242 · Cited by 55
Differentiation of epidermal keratinocytes is dependent on glucosylceramide:ceramide processing
Amen, N., Mathow, D., Rabionet, M., Sandhoff, R., Langbein, L., Gretz, N., Jäckel, C., Gröne, H., & Jennemann, R. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt264 · Cited by 56
Scott, C. A., Rajpopat, S., & Di, W. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1474-9 · Cited by 56
Comparative Genomics Identifies Epidermal Proteins Associated with the Evolution of the Turtle Shell
Holthaus, K. B., Strasser, B., Sipos, W., Schmidt, H. A., Mlitz, V., Sukseree, S., Weissenbacher, A., Tschachler, E., Alibardi, L., & Eckhart, L. (2015) · Molecular Biology and Evolution · doi:10.1093/molbev/msv265 · Cited by 55
dos Santos, J. F., Borçari, N. R., Araújo, M. S., & Nunes, V. A. (2019) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28589 · Cited by 55
Modifications of the Innate Immune System in Atopic Dermatitis
Maintz, L., & Novak, N. (2011) · Journal of Innate Immunity · doi:10.1159/000323963 · Cited by 55
HIF-1α controls keratinocyte proliferation by up-regulating p21(WAF1/Cip1)
Cho, Y.-S., Bae, J.-M., Chun, Y., Chung, J., Jeon, Y., Kim, I., Kim, M., & Park, J. (2007) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2007.11.017 · Cited by 59
Programmed cell death in the skin
Costanzo, A., Fausti, F., Spallone, G., Moretti, F., Narcisi, A., & Botti, E. (2015) · The International Journal of Developmental Biology · doi:10.1387/ijdb.150050ac · Cited by 55
Su, D., Li-ping, H., Shi, C., Li, Y., Qian, S., Feng, Z., & Yu, L. (2024) · Virulence · doi:10.1080/21505594.2024.2425744 · Cited by 59
Interleukin-1 alpha blockade prevents hyperkeratosis in an in vitro model of lamellar ichthyosis
O’Shaughnessy, R. F. L., Choudhary, I., & Harper, J. I. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq145 · Cited by 54
Zanetti, F., Titz, B., Sewer, A., Sasso, G. L., Scotti, E., Schlage, W. K., Mathis, C., Leroy, P., Majeed, S., Torres, L. O., et al. (2016) · Food and Chemical Toxicology · doi:10.1016/j.fct.2016.12.027 · Cited by 54
Molecular basis of the skin barrier structures revealed by electron microscopy
Ishida‐Yamamoto, A., Igawa, S., & Kishibe, M. (2018) · Experimental Dermatology · doi:10.1111/exd.13674 · Cited by 54
The role of PNPLA1 in ω-O-acylceramide synthesis and skin barrier function
Hirabayashi, T., Murakami, M., & Kihara, A. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2018.09.010 · Cited by 54
Arabzadeh, A., Troy, T., & Turksen, K. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.02342-05 · Cited by 54
Regulation of stem cell function by protein ubiquitylation
Strikoudis, A., Guillamot, M., & Aifantis, I. (2014) · EMBO Reports · doi:10.1002/embr.201338373 · Cited by 55
MicroRNAs in human skin ageing
Mancini, M., Lena, A. M., Saintigny, G., Mahé, C., Daniele, N. D., Melino, G., & Candi, E. (2014) · Ageing Research Reviews · doi:10.1016/j.arr.2014.04.003 · Cited by 53
Self-citationThree-Dimensional In Vitro Skin and Skin Cancer Models Based on Human Fibroblast-Derived Matrix
Berning, M., Praetzel‐Wunder, S., Bickenbach, J. R., & Boukamp, P. (2015) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2014.0698 · Cited by 53
Sugimura, Y., Hosono, M., Kitamura, M., Tsuda, T., Yamanishi, K., Maki, M., & Hitomi, K. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06692.x · Cited by 53
Cathepsin H: Molecular characteristics and clues to function and mechanism
Wang, Y., Zhao, J., Gu, Y., Wang, H., Jiang, M., Zhao, S., Qing, H., & Ni, J. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115585 · Cited by 52
Xue, M., Chow, S., Dervish, S., Chan, Y.-K. A., Julovi, S. M., & Jackson, C. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.181388 · Cited by 52
Deciphering the functions of the hair follicle infundibulum in skin physiology and disease
Schneider, M. R., & Paus, R. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-1999-1 · Cited by 52
Kazrin regulates keratinocyte cytoskeletal networks, intercellular junctions and differentiation
Sevilla, L. M., Nachat, R., Groot, K. R., & Watt, F. M. (2008) · Journal of Cell Science · doi:10.1242/jcs.029538 · Cited by 53
Evaluation of the relation between lipid coat, transepidermal water loss, and skin pH
Algiert‐Zielińska, B., Batory, M., Skubalski, J., & Rotsztejn, H. (2017) · International Journal of Dermatology · doi:10.1111/ijd.13726 · Cited by 51
Vitamin D Receptor Activation Improves Allergen-Triggered Eczema in Mice
Hartmann, B., Riedel, R., Jörß, K., Loddenkemper, C., Steinmeyer, A., Zügel, U., Babina, M., Radbruch, A., & Worm, M. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.296 · Cited by 51
Kim, B. E., Leung, D. Y. M., Streib, J. E., Boguniewicz, M., Hamid, Q. A., & Howell, M. D. (2006) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2006.10.005 · Cited by 51
Hatano, Y., & Elias, P. M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1239251 · Cited by 50
Basu, K., Palmer, C. N. A., Lipworth, B. J., McLean, W. H. I., Terron‐Kwiatkowski, A., Zhao, Y., Liao, H., Smith, F. J. D., Mitra, A. A., & Mukhopadhyay, S. (2008) · Allergy · doi:10.1111/j.1398-9995.2008.01660.x · Cited by 50
Wollenberg, A., Fölster‐Holst, R., Aroman, M. S., Sampogna, F., & Vestergaard, C. (2018) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/jdv.14846 · Cited by 50
Hon, K. E., Pong, N. H., Wang, S. S., Lee, V. W. Y., Luk, N. M., & Leung, T. F. (2013) · Drugs in R&D · doi:10.1007/s40268-013-0004-x · Cited by 50
Programmed cell death: similarities and differences in animals and plants. A flower paradigm
Mea, M. D., Serafini‐Fracassini, D., & Duca, S. D. (2007) · Amino Acids · doi:10.1007/s00726-007-0530-3 · Cited by 50
Filaggrin Null Alleles Are Not Associated with Psoriasis
Zhao, Y., Terron-Kwiatkowski, A., Liao, H., Lee, S. P., Allen, M. H., Hull, P. R., Campbell, L., Trembath, R. C., Capon, F., Griffiths, C. E. M., et al. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700817 · Cited by 50
Recent advances on application of polysaccharides in cosmetics
Wu, Q., Cheng, N., Fang, D., Wang, H., Rahman, F., Hao, H., & Zhang, Y. (2024) · Journal of Dermatologic Science and Cosmetic Technology · doi:10.1016/j.jdsct.2024.100004 · Cited by 51
Skin barrier-inflammatory pathway is a driver of the psoriasis-atopic dermatitis transition
Dong, S., Li, D., & Shi, D. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1335551 · Cited by 54
Beckham, S. A., Boyd, S. E., Reynolds, S. L., Willis, C., Johnstone, M., Mika, A., Simerská, P., Wijeyewickrema, L. C., Smith, A. I., Kemp, D. J., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.061911 · Cited by 49
Mea, M. D., Filippis, F. D., Genovesi, V., Fracassini, D. S., & Duca, S. D. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.092072 · Cited by 49
Liu, S., Kam, W. R., Ding, J., Hatton, M. P., & Sullivan, D. A. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.12-11221 · Cited by 49
Hereditary Palmoplantar Keratodermas
Braun‐Falco, M. (2009) · JDDG Journal der Deutschen Dermatologischen Gesellschaft · doi:10.1111/j.1610-0387.2009.07058.x · Cited by 49
Kongsuwan, K., Josh, P., Colgrave, M. L., Bagnall, N. H., Gough, J., Burns, B., & Pearson, R. (2010) · International Journal for Parasitology · doi:10.1016/j.ijpara.2009.10.013 · Cited by 48
Pirh2 E3 Ubiquitin Ligase Modulates Keratinocyte Differentiation through p63
Jung, Y.-S., Qian, Y., Yan, W., & Chen, X. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.466 · Cited by 48
Yanagi, T., Akiyama, M., Nishihara, H., Ishikawa, J., Sakai, K., Miyamura, Y., Naoe, A., Kitahara, T., Tanaka, S., & Shimizu, H. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.091120 · Cited by 48
Yeo, J., Jung, G. S., Tarakanova, A., Martín‐Martínez, F. J., Zhao Qin, A., Cheng, Y., Zhang, Y., & Buehler, M. J. (2018) · Extreme Mechanics Letters · doi:10.1016/j.eml.2018.01.009 · Cited by 48
Crumrine, D. A., Khnykin, D., Krieg, P., Man, M., Celli, A., Mauro, T. M., Wakefield, J. S., Menon, G. K., Mauldin, E. A., Miner, J. H., et al. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2018.11.005 · Cited by 48
Smirnov, A., Lena, A. M., Cappello, A., Panatta, E., Anemona, L., Bischetti, S., Annicchiarico‐Petruzzelli, M., Mauriello, A., Melino, G., & Candi, E. (2018) · Oncogene · doi:10.1038/s41388-018-0509-4 · Cited by 48
Self-citationThe occurrence and development mechanisms of esophageal stricture: state of the art review
Yang, F., Hu, Y., Shi, Z., Liu, M., Hu, K., Ye, G., Pang, Q., Hou, R., Tang, K., & Zhu, Y. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-04932-2 · Cited by 48
Italian legumes: effect of sourdough fermentation on lunasin-like polypeptides
Rizzello, C. G., Hernández‐Ledesma, B., Fernández‐Tomé, S., Curiel, J. A., Pinto, D., Marzani, B., Coda, R., & Gobbetti, M. (2015) · Microbial Cell Factories · doi:10.1186/s12934-015-0358-6 · Cited by 47
Allende, M. L., Sipe, L. M., Tuymetova, G., Wilson-Henjum, K. L., Chen, W., & Proia, R. L. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.478420 · Cited by 47
Ictiosis congénitas autosómicas recesivas
Rodríguez‐Pazos, L., Ginarte, M., Vega, A. I., & Toribio, J. (2012) · Actas Dermo-Sifiliográficas · doi:10.1016/j.ad.2011.11.015 · Cited by 47
Pham, Q. D., Topgaard, D., & Sparr, E. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608739114 · Cited by 47
Non-animal models in dermatological research
Dellambra, E. (2018) · ALTEX · doi:10.14573/altex.1808022 · Cited by 49
Filaggrin and the great epidermal barrier grief
McGrath, J. A. (2008) · Australasian Journal of Dermatology · doi:10.1111/j.1440-0960.2008.00443.x · Cited by 47
Distinct epidermal stem cell compartments are maintained by independent niche microenvironments
Braun, K. M., & Prowse, D. M. (2006) · Stem Cell Reviews and Reports · doi:10.1007/s12015-006-0050-7 · Cited by 47
The Role of Contact Allergy in Atopic Dermatitis
Fonacier, L. S., & Aquino, M. (2010) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2010.06.001 · Cited by 47
Ras signaling is essential for skin development
Drosten, M., Lechuga, C. G., & Barbacid, M. (2014) · Oncogene · doi:10.1038/onc.2013.254 · Cited by 46
Ipponjima, S., Umino, Y., Nagayama, M., & Denda, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-62240-3 · Cited by 46
Zhang, Y., Heinemann, N., Rademacher, F., Darvin, M. E., Raab, C., Keck, C. M., Vollert, H., Fluhr, J. W., Gläser, R., Harder, J., et al. (2022) · Antioxidants · doi:10.3390/antiox11061071 · Cited by 46
Regulation of Involucrin in Psoriatic Epidermal Keratinocytes: The Roles of ERK1/2 and GSK-3β
Chen, J., Man, X., Li, W., Zhou, J., Landeck, L., Cai, S., & Zheng, M. (2013) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-012-9499-y · Cited by 46
Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
Fischer, H., Langbein, L., Reichelt, J., Praetzel‐Wunder, S., Buchberger, M., Ghannadan, M., Tschachler, E., & Eckhart, L. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.197 · Cited by 48
Cramer, C., Link, E., Horster, M., Koletzko, S., Bauer, C.-P., Berdel, D., Berg, A. V., Lehmann, I., Herbarth, O., Borte, M., et al. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2010.03.036 · Cited by 46
iASPP is a novel autophagy inhibitor in keratinocytes
Chikh, A., Sanzà, P., Raimondi, C., Akinduro, O., Warnes, G., Chiorino, G., Byrne, C. R., Harwood, C. A., & Bergamaschi, D. (2014) · Journal of Cell Science · doi:10.1242/jcs.144816 · Cited by 46
RetractedHuang, K., Ma, K., Liu, P., Chen, B., & Chueh, S. (2016) · Experimental Dermatology · doi:10.1111/exd.13024 · Cited by 46
Nygaard, U., van den Bogaard, E. H. J., Niehues, H., Hvid, M., Deleuran, M. S., Johansen, C., & Vestergaard, C. (2016) · Acta Dermato Venereologica · doi:10.2340/00015555-2552 · Cited by 46
Choi, H. K., Cho, Y. H., Lee, E. O., Kim, J. W., & Park, C. S. (2017) · Archives of Dermatological Research · doi:10.1007/s00403-017-1782-8 · Cited by 46
Harland, D. P., & Plowman, J. E. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-10-8195-8_10 · Cited by 46
Zalenskaya, I. A., Chandra, N., Yousefieh, N., Fang, X., Adedipe, O. E., Jackson, S. S., Anderson, S. M., Mauck, C. K., Schwartz, J. L., Thurman, A. R., et al. (2018) · Journal of Clinical Investigation · doi:10.1172/jci120583 · Cited by 46
Bamai, Y. A., Araki, A., Nomura, T., Kawai, T., Tsuboi, T., Kobayashi, S., Miyashita, C., Takeda, M., Shimizu, H., & Kishi, R. (2018) · Environment International · doi:10.1016/j.envint.2018.08.046 · Cited by 46
Regulation of ERK-MAPK signaling in human epidermis
Cursons, J., Gao, J., Hurley, D., Print, C. G., Dunbar, P. R., Jacobs, M. D., & Crampin, E. J. (2015) · BMC Systems Biology · doi:10.1186/s12918-015-0187-6 · Cited by 46
Thyssen, J. P., Linneberg, A. R., Carlsen, B. C., Johansen, J. D., Engkilde, K., Hansen, T. F., Pociot, F., Pedersen, O. B., Meldgaard, M., Szecsi, P. B., et al. (2011) · BMJ Open · doi:10.1136/bmjopen-2011-000062 · Cited by 46
Metadata
- Authors
- Candi, E., Schmidt, R., & Melino, G.
- Affiliations
- University of Rome Tor Vergata (IT)
- L'Oréal (France) (FR)
- Corresponding author
- Melino, Gerry
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2005-04
- Volume
- 6
- Issue
- 4
- Pages
- 328-340
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- OpenAlex
- W2005630031
- Cited by
- 1,776
- References
- 216
- Citations by year
- 2026: 58 · 2025: 68 · 2024: 85 · 2023: 99 · 2022: 77 · 2021: 96 · 2020: 107 · 2019: 74 · 2018: 97 · 2017: 86 · 2016: 94 · 2015: 83 · 2014: 95 · 2013: 110 · 2012: 98
- FWCI
- 5.07
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Cineca Institutional Research Information System (Tor Vergata University) (submittedVersion)
- Funders
- National Institutes of Health
- Medical Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Health Sciences › Medicine › Dermatology › Genetic and rare skin diseases.
- Keywords
- cornified envelope, keratinization, keratinocytes, epidermal differentiation, programmed cell death, keratin, transglutaminase cross-linking, skin barrier, ichthyosis, skin barrier dysfunction
- MeSH terms
- Epidermal Cells, Filaggrin Proteins, Animals, Cell Adhesion, Cell Differentiation, Epidermis, Humans, Intermediate Filament Proteins, Membrane Proteins, Protein Precursors, Transglutaminases, Substrate Specificity, Apoptosis, Genetic Diseases, Inborn
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review