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Daniel Hohl

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TOP 3
Magdalini Kypriotou; Marcel Huber; Daniel Hohl
The human epidermal differentiation complex: cornified envelope precursors, S100 proteins and the 'fused genes' family.
Christophe Chapard; Daniel Hohl; Marcel Huber
The role of the TRAF-interacting protein in proliferation and differentiation.
Matthias Schäfer; Ann-Helen Willrodt; Wilhelm Bloch; Hany Farwanah; Daniel Hohl; Aaron J Huebner; Dennis Roop; Konrad Sandhoff; Sabine Werner
Nrf2 links epidermal barrier function with antioxidant defense.

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All Publications

2012: Magdalini Kypriotou; Marcel Huber; Daniel Hohl
The human epidermal differentiation complex: cornified envelope precursors, S100 proteins and the 'fused genes' family.
Experimental dermatology 2012;21(9):643-9.
2012: Christophe Chapard; Daniel Hohl; Marcel Huber
The role of the TRAF-interacting protein in proliferation and differentiation.
Experimental dermatology 2012;21(5):321-6.
2012: Matthias Schäfer; Ann-Helen Willrodt; Wilhelm Bloch; Hany Farwanah; Daniel Hohl; Aaron J Huebner; Dennis Roop; Konrad Sandhoff; Sabine Werner
Nrf2 links epidermal barrier function with antioxidant defense.
EMBO molecular medicine 2012;4(5):364-79.
2011: Magdalena Obarzanek-Fojt; Bertrand Favre; Magdalini Kypriotou; Stephan Ryser; Marcel Huber; Daniel Hohl
Homeodomain-only protein HOP is a novel modulator of late differentiation in keratinocytes.
European journal of cell biology 2011;90(4):279-90.
2011: Stéphanie Almeida; Stephan Ryser; Magdalena Obarzanek-Fojt; Daniel Hohl; Marcel Huber
The TRAF-interacting protein (TRIP) is a regulator of keratinocyte proliferation.
The Journal of investigative dermatology 2011;131(2):349-57.
2011: Maria Antsiferova; Reinhard Dummer; Wendy L Havran; Daniel Hohl; Marcel Huber; Amanda S MacLeod; Michael Meyer; Aleksandra Piwko-Czuchra; Tamara Ramadan; Sabine Werner
Activin enhances skin tumourigenesis and malignant progression by inducing a pro-tumourigenic immune cell response.
Nature communications 2011;2():576.
2009: Massimo C R Lurati; Daniel Hohl
Multiple comedonelike lesions encircling the anal orifice--quiz case.
Archives of dermatology 2009;145(12):1447-52.
2009: Gionata Marazza; H C Pham; L Schärer; P P Pedrazzetti; Thomas Hunziker; R M Trüeb; Daniel Hohl; P Itin; S Lautenschlager; luigi naldi; Luca Borradori
Incidence of bullous pemphigoid and pemphigus in Switzerland: a 2-year prospective study.
The British journal of dermatology 2009;161(4):861-8.
2009: Heidi Koegel; Lukas von Tobel; Matthias Schäfer; Siegfried Alberti; Elisabeth Kremmer; Cornelia Mauch; Daniel Hohl; Xiao-Jing Wang; Hans-Dietmar Beer; Wilhelm Bloch; Alfred Nordheim; Sabine Werner
Loss of serum response factor in keratinocytes results in hyperproliferative skin disease in mice.
The Journal of clinical investigation 2009;119(4):899-910.
2008: Stéphanie Almeida; Caroline Maillard; Peter Itin; Daniel Hohl; Marcel Huber
Five new CYLD mutations in skin appendage tumors and evidence that aspartic acid 681 in CYLD is essential for deubiquitinase activity.
The Journal of investigative dermatology 2008;128(3):587-93.
2007: Laurence Feldmeyer; Martin Keller; Gisela Niklaus; Daniel Hohl; Sabine Werner; Hans-Dietmar Beer
The inflammasome mediates UVB-induced activation and secretion of interleukin-1beta by keratinocytes.
Current biology : CB 2007;17(13):1140-5.
2007: Bertrand Favre; Laure Plantard; Lorène Aeschbach; Noureddine Brakch; Stephanie Christen-Zaech; Pierre A de Viragh; Ann Sergeant; Marcel Huber; Daniel Hohl
SLURP1 is a late marker of epidermal differentiation and is absent in Mal de Meleda.
The Journal of investigative dermatology 2007;127(2):301-8.
2006: Romuald Contzler; Alexandre Regamey; Bertrand Favre; Thierry Roger; Daniel Hohl; Marcel Huber
Histone acetyltransferase HBO1 inhibits NF-kappaB activity by coactivator sequestration.
Biochemical and biophysical research communications 2006;350(1):208-13.
2006: Ulrich auf dem Keller; Marcel Huber; Tobias A Beyer; Angelika Kümin; Christina Siemes; Susanne Braun; Philippe Bugnon; Varvara Mitropoulos; Delinda A Johnson; Jeffrey A Johnson; Daniel Hohl; Sabine Werner
Nrf transcription factors in keratinocytes are essential for skin tumor prevention but not for wound healing.
Molecular and cellular biology 2006;26(10):3773-84.
2006: Laurence Feldmeyer; Marcel Huber; F Fellmann; Jacques Beckmann; E Frenk; Daniel Hohl
Confirmation of the origin of NISCH syndrome.
Human mutation 2006;27(5):408-10.
2006: Laurence Feldmeyer; Barukh Mevorah; K H Grzeschik; Marcel Huber; Daniel Hohl
Clinical variation in X-linked dominant chondrodysplasia punctata (X-linked dominant ichthyosis).
The British journal of dermatology 2006;154(4):766-9.
2006: Felix B Müller; Marcel Huber; Tamar Kinaciyan; Ingrid Hausser; Christina Schaffrath; Thomas Krieg; Daniel Hohl; Bernhard P Korge; Meral J Arin
A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.
Human molecular genetics 2006;15(7):1133-41.
2005: Laurence Feldmeyer; Laure Plantard; Barukh Mevorah; Marcel Huber; Daniel Hohl
Novel mutation of connexin 31 causing erythrokeratoderma variabilis.
The British journal of dermatology 2005;152(5):1072-4.
2005: Marcel Huber; Georges Siegenthaler; Nicolae Mirancea; Ingo Marenholz; Dean Nizetic; Dirk Breitkreutz; Dietmar Mischke; Daniel Hohl
Isolation and characterization of human repetin, a member of the fused gene family of the epidermal differentiation complex.
The Journal of investigative dermatology 2005;124(5):998-1007.
2005: Romuald Contzler; Bertrand Favre; Marcel Huber; Daniel Hohl
Cornulin, a new member of the "fused gene" family, is expressed during epidermal differentiation.
The Journal of investigative dermatology 2005;124(5):990-7.
2004: Tao Yang; Dongcai Liang; Peter J Koch; Daniel Hohl; Farrah Kheradmand; Paul A Overbeek
Epidermal detachment, desmosomal dissociation, and destabilization of corneodesmosin in Spink5-/- mice.
Genes & development 2004;18(19):2354-8.
2004: Lionel Fontao; Kaisa Tasanen; Marcel Huber; Daniel Hohl; Jan Koster; Leena Bruckner-Tuderman; Arnoud Sonnenberg; Luca Borradori
Molecular consequences of deletion of the cytoplasmic domain of bullous pemphigoid 180 in a patient with predominant features of epidermolysis bullosa simplex.
The Journal of investigative dermatology 2004;122(1):65-72.
2003: Alexandre Regamey; Daniel Hohl; Jia Wei Liu; Thierry Roger; Priit Kogerman; Rune Toftgard; Marcel Huber
The tumor suppressor CYLD interacts with TRIP and regulates negatively nuclear factor kappaB activation by tumor necrosis factor.
The Journal of experimental medicine 2003;198(12):1959-64.
2003: Laure Plantard; Marcel Huber; Francoise Macari; Paolo Meda; Daniel Hohl
Molecular interaction of connexin 30.3 and connexin 31 suggests a dominant-negative mechanism associated with erythrokeratodermia variabilis.
Human molecular genetics 2003;12(24):3287-94.
2003: Fabrice CHIMIENTI; Ronald C Hogg; Laure Plantard; Caroline Lehmann; Noureddine Brakch; Judith Fischer; Marcel Huber; Daniel Bertrand; Daniel Hohl
Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda.
Human molecular genetics 2003;12(22):3017-24.
2003: Robert H Rice; Debra Crumrine; Daniel Hohl; Colin S Munro; P M Elias
Cross-linked envelopes in nail plate in lamellar ichthyosis.
The British journal of dermatology 2003;149(5):1050-4.
2003: Susan M Morley; Mariella D'Alessandro; C Sexton; Elizabeth L Rugg; Harshad A Navsaria; Carrie S Shemanko; Marcel Huber; Daniel Hohl; A I Heagerty; Irene M Leigh; E Birgitte Lane
Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutations.
The British journal of dermatology 2003;149(1):46-58.
2003: Slaheddine Marrakchi; Stéphanie Audebert; Bakar Bouadjar; Christina Has; Caroline Lefèvre; Colin Munro; Susan Cure; Florence Jobard; Susanne Morlot; Daniel Hohl; Jean-François Prud'homme; Abdelmajid Zahaf; Hamida Turki; Judith Fischer
Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda.
The Journal of investigative dermatology 2003;120(3):351-5.
2002: Meytal Landau; Meirav Cohen-Bar-Dayan; Daniel Hohl; Joseph Ophir; Charles R Wolf; Andrea Gat; Barukh Mevorah
Erythrokeratodermia variabilis with erythema gyratum repens-like lesions.
Pediatric dermatology 2002;19(4):285-92.
2002: Hans-Dietmar Beer; Christine Munding; Nicole Dubois; Celine Mamie; Daniel Hohl; Sabine Werner
The estrogen-responsive B box protein: a novel regulator of keratinocyte differentiation.
The Journal of biological chemistry 2002;277(23):20740-9.
2002: ana bakija-konsuo; Aleksandra Basta-Juzbasic; I Rudan; Mirna Situm; Magdalena Nardelli-Kovacic; Sonja Levanat; Judith Fischer; Daniel Hohl; Davorin Loncaric; Sven Seiwert; Harry Campbell
Mal de Meleda: genetic haplotype analysis and clinicopathological findings in cases originating from the island of Mljet (Meleda), Croatia.
Dermatology (Basel, Switzerland) 2002;205(1):32-9.
2002: Marcel Huber; Michaela Floeth; Luca Borradori; Heike Schäcke; Elizabeth L Rugg; E Birgitte Lane; Edgar Frenk; Daniel Hohl; Leena Bruckner-Tuderman
Deletion of the cytoplasmatic domain of BP180/collagen XVII causes a phenotype with predominant features of epidermolysis bullosa simplex.
The Journal of investigative dermatology 2002;118(1):185-92.
2001: Alessandro Terrinoni; Frances J D Smith; Biagio Didona; F Canzona; Mauro Paradisi; M Huber; Daniel Hohl; A David; Alain Verloes; I M Leigh; Colin S Munro; Gerry Melino; W H Irwin McLean
Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.
The Journal of investigative dermatology 2001;117(6):1391-6.
2001: Roland Böni; H Xin; Daniel Hohl; Renato G Panizzon; Guenter Burg
Syringocystadenoma papilliferum: a study of potential tumor suppressor genes.
The American Journal of dermatopathology 2001;23(2):87-9.
2001: Judith Fischer; Bakar Bouadjar; Roland Heilig; Marcel Huber; Caroline Lefèvre; Florence Jobard; Francoise Macari; ana bakija-konsuo; F Ait-Belkacem; Jean Weissenbach; Mark Lathrop; Daniel Hohl; Jean-François Prud'homme
Mutations in the gene encoding SLURP-1 in Mal de Meleda.
Human molecular genetics 2001;10(8):875-80.
2000: Francoise Macari; Meytal Landau; Pascal Cousin; Barukh Mevorah; Sarah Brenner; Renato G Panizzon; D F Schorderet; Daniel Hohl; Marcel Huber
Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis.
American journal of human genetics 2000;67(5):1296-301.
2000: Peter J Koch; Pierre A de Viragh; E Scharer; Donnie Bundman; Mary A Longley; Jackie R Bickenbach; Y Kawachi; Y Suga; Zhijian Zhou; Marcel Huber; Daniel Hohl; T Kartasova; Michal Jarnik; Alasdair C Steven; Dennis R Roop
Lessons from loricrin-deficient mice: compensatory mechanisms maintaining skin barrier function in the absence of a major cornified envelope protein.
The Journal of cell biology 2000;151(2):389-400.
2000: M De Heller-Milev; M Huber; R Panizzon; Daniel Hohl
Expression of small proline rich proteins in neoplastic and inflammatory skin diseases.
The British journal of dermatology 2000;143(4):733-40.
1999: Victor L Ruiz-Perez; S A Carter; E Healy; C Todd; Jonathan L Rees; P M Steijlen; A J Carmichael; H M Lewis; Daniel Hohl; P Itin; A Vahlquist; Tommaso Gobello; Cinzia Mazzanti; R Reggazini; G Nagy; Colin S Munro; Tom Strachan
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.
Human molecular genetics 1999;8(9):1621-30.
1999: Robert H Rice; Viviana J Wong; M L Williams; V H Price; Daniel Hohl; J P Sundberg; Kent E Pinkerton
Hair shaft defects visualized after detergent extraction.
Experimental dermatology 1999;8(4):308-10.
1999: Meral J Arin; Mary A Longley; Wolfgang Küster; Marcel Huber; Daniel Hohl; Joseph A Rothnagel; Dennis R Roop
An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis.
Experimental dermatology 1999;8(2):124-7.
1999: Meral J Arin; Mary A Longley; I Anton-Lamprecht; G Kurze; Marcel Huber; Daniel Hohl; Joseph A Rothnagel; Dennis R Roop
A novel substitution in keratin 10 in epidermolytic hyperkeratosis.
The Journal of investigative dermatology 1999;112(4):506-8.
1998: Gabriele Richard; LE Smith; R A Bailey; P Itin; Daniel Hohl; E H Epstein; John J DiGiovanna; John G Compton; Sherri J Bale
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis.
Nature genetics 1998;20(4):366-9.
1997: Gabriele Richard; J P Lin; L Smith; Y M Whyte; P Itin; Uwe Wollina; E Epstein; Daniel Hohl; J M Giroux; L Charnas; Sherri J Bale; John J DiGiovanna
Linkage studies in erythrokeratodermias: fine mapping, genetic heterogeneity and analysis of candidate genes.
The Journal of investigative dermatology 1997;109(5):666-71.
1997: Marcel Huber; V C Yee; N Burri; E Vikerfors; A P Lavrijsen; A S Paller; Daniel Hohl
Consequences of seven novel mutations on the expression and structure of keratinocyte transglutaminase.
The Journal of biological chemistry 1997;272(34):21018-26.
1997: D F Schorderet; M Huber; Ricardo Laurini; G Von Moos; B Gianadda; G Délèze; Daniel Hohl
Prenatal diagnosis of lamellar ichthyosis by direct mutational analysis of the keratinocyte transglutaminase gene.
Prenatal diagnosis 1997;17(5):483-6.
1997: G Y Joh; H Traupe; D Metze; D Nashan; Marcel Huber; Daniel Hohl; Mary A Longley; Joseph A Rothnagel; Dennis R Roop
A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma.
The Journal of investigative dermatology 1997;108(3):357-61.
1997: Frances J D Smith; Laura D Corden; Elizabeth L Rugg; R Ratnavel; Irene M Leigh; Celia Moss; Michael J Tidman; Daniel Hohl; Marcel Huber; L Kunkeler; Colin S Munro; E Birgitte Lane; W H Irwin McLean
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex.
The Journal of investigative dermatology 1997;108(2):220-3.
1996: Daniel Hohl; I Rettler; M Huber
Specificity of B.C1 for TGK after renaturation prior to transfer of proteins.
The Journal of investigative dermatology 1996;106(4):801-3.
1996: B Mevorah; D Salomon; G Siegenthaler; Daniel Hohl; M L Meier; J H Saurat; E Frenk
Ichthyosiform dermatosis with superficial blister formation and peeling: evidence for a desmosomal anomaly and altered epidermal vitamin A metabolism.
Journal of the American Academy of Dermatology 1996;34(2 Pt 2):379-85.
1996: E Frenk; David Guggisberg; B Mevorah; Daniel Hohl
Meleda disease: report of two cases investigated by electron microscopy.
Dermatology (Basel, Switzerland) 1996;193(4):358-61.
1995: M Huber; I Rettler; K Bernasconi; M Wyss; Daniel Hohl
Lamellar ichthyosis is genetically heterogeneous--cases with normal keratinocyte transglutaminase.
The Journal of investigative dermatology 1995;105(5):653-4.
1995: M Krasovec; B Gianadda; Daniel Hohl
Giant recurrence of a multiple agminated Spitz nevus.
Journal of the American Academy of Dermatology 1995;33(2 Pt 2):386-8.
1995: Daniel Hohl; P A de Viragh; F Amiguet-Barras; Susan Gibbs; Claude Backendorf; M Huber
The small proline-rich proteins constitute a multigene family of differentially regulated cornified cell envelope precursor proteins.
The Journal of investigative dermatology 1995;104(6):902-9.
1995: Joseph A Rothnagel; SM Wojcik; K M Liefer; A M Dominey; Marcel Huber; Daniel Hohl; Dennis R Roop
Mutations in the 1A domain of keratin 9 in patients with epidermolytic palmoplantar keratoderma.
The Journal of investigative dermatology 1995;104(3):430-3.
1995: M Huber; I Rettler; K Bernasconi; E Frenk; S P Lavrijsen; M Ponec; A Bon; S Lautenschlager; D F Schorderet; Daniel Hohl
Mutations of keratinocyte transglutaminase in lamellar ichthyosis.
Science (New York, N.Y.) 1995;267(5197):525-8.
1995: David Guggisberg; Daniel Hohl
Intraepidermal IgA pustulosis preceding a CD30+ anaplastic large T-cell lymphoma.
Dermatology (Basel, Switzerland) 1995;191(4):352-4.
1994: P A de Viragh; M Huber; Daniel Hohl
Involucrin mRNA is more abundant in human hair follicles than in normal epidermis.
The Journal of investigative dermatology 1994;103(6):815-9.
1994: Joseph A Rothnagel; H Traupe; SM Wojcik; Marcel Huber; Daniel Hohl; Mark Pittelkow; H Saeki; Y Ishibashi; Dennis R Roop
Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens.
Nature genetics 1994;7(4):485-90.
1994: M Huber; Corinne Scaletta; M Benathan; E Frenk; DA Greenhalgh; Joseph A Rothnagel; D R Roop; Daniel Hohl
Abnormal keratin 1 and 10 cytoskeleton in cultured keratinocytes from epidermolytic hyperkeratosis caused by keratin 10 mutations.
The Journal of investigative dermatology 1994;102(5):691-4.
1993: Joseph A Rothnagel; M P Fisher; S M Axtell; Mark Pittelkow; I Anton-Lamprecht; Marcel Huber; Daniel Hohl; Dennis R Roop
A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis.
Human molecular genetics 1993;2(12):2147-50.
1993: Luca Borradori; Daniel Hohl; P Rochat; E Frenk
Annular bullous eruption in a patient with the CREST syndrome, primary biliary cirrhosis, and Sjögren's syndrome.
Journal of the American Academy of Dermatology 1993;29(4):648-50.
1993: Daniel Hohl; B Ruf Olano; P A de Viragh; M Huber; C J Detrisac; U W Schnyder; D R Roop
Expression patterns of loricrin in various species and tissues.
Differentiation; research in biological diversity 1993;54(1):25-34.
1993: Daniel Hohl; M Huber; E Frenk
Analysis of the cornified cell envelope in lamellar ichthyosis.
Archives of dermatology 1993;129(5):618-24.
1993: Daniel Hohl
Expression patterns of loricrin in dermatological disorders.
The American Journal of dermatopathology 1993;15(1):20-7.
1993: Luca Borradori; Daniel Hohl; M Monteil; E Frenk
Bullous systemic lupus erythematosus. Report of a case with lupus erythematosus cells in the dermis.
Dermatology (Basel, Switzerland) 1993;187(4):306-8.
1993: E Frenk; B Mevorah; Daniel Hohl
The Nägeli-Franceschetti-Jadassohn syndrome: A hereditary ectodermal defect leading to colloid-amyloid formation in the dermis.
Dermatology (Basel, Switzerland) 1993;187(3):169-73.
1992: Claude Backendorf; Daniel Hohl
A common origin for cornified envelope proteins?
Nature genetics 1992;2(2):91.
1992: Joseph A Rothnagel; A M Dominey; L D Dempsey; Mary A Longley; DA Greenhalgh; T A Gagne; Marcel Huber; E Frenk; Daniel Hohl; Dennis R Roop
Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis.
Science (New York, N.Y.) 1992;257(5073):1128-30.
1992: Daniel Hohl; F Pelloni; C Sigg; S Gilardi; T Jung
A prospective study of skeletal changes during short-term acitretin therapy.
Dermatology (Basel, Switzerland) 1992;185(1):23-6.
1991: Daniel Hohl; T Mehrel; U Lichti; M L Turner; D R Roop; Peter M Steinert
Characterization of human loricrin. Structure and function of a new class of epidermal cell envelope proteins.
The Journal of biological chemistry 1991;266(10):6626-36.
1991: Daniel Hohl; U Lichti; D Breitkreutz; P M Steinert; D R Roop
Transcription of the human loricrin gene in vitro is induced by calcium and cell density and suppressed by retinoic acid.
The Journal of investigative dermatology 1991;96(4):414-8.
1990: T Mehrel; Daniel Hohl; Joseph A Rothnagel; M A Longley; Donnie Bundman; C Cheng; U Lichti; M E Bisher; Alasdair C Steven; Peter M Steinert
Identification of a major keratinocyte cell envelope protein, loricrin.
Cell 1990;61(6):1103-12.