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Marcel Huber

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Magdalini Kypriotou; Marcel Huber; Daniel Hohl
The human epidermal differentiation complex: cornified envelope precursors, S100 proteins and the 'fused genes' family.
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.
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.

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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.
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: 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.
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: 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: 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.
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.
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.
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: 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.
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.
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.
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.
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.