FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Cristina Has

Research Profile

Physiology

Disorders

Chemicals & Drugs

Anatomy

Procedures

DNA Mutational Analysis

Living Beings

Newborn Infant

Co-author Network

Publications

TOP 3
E Piccinni; Massimo Teson; Giovanna Zambruno; Elena Dellambra; Giovanni Di Zenzo; Cristina Has; Riccardo Maurelli; Daniele Castiglia
Induction of senescence pathways in Kindler syndrome primary keratinocytes.
Cristina Has; D Kiritsi
Molecular therapies for epidermolysis bullosa.
Cristina Has; Cassian Sitaru
Molecular dermatology comes of age.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Cristina Has (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: E Piccinni; Massimo Teson; Giovanna Zambruno; Elena Dellambra; Giovanni Di Zenzo; Cristina Has; Riccardo Maurelli; Daniele Castiglia
Induction of senescence pathways in Kindler syndrome primary keratinocytes.
The British journal of dermatology 2013;168(5):1019-26.
2013: Cristina Has; D Kiritsi
Molecular therapies for epidermolysis bullosa.
Giornale italiano di dermatologia e venereologia : organo ufficiale, Società italiana di dermatologia e sifilografia 2013;148(1):65-72.
2013: Cristina Has; Cassian Sitaru
Molecular dermatology comes of age.
Methods in molecular biology (Clifton, N.J.) 2013;961():1-16.
2013: Dimitra Kiritsi; Cristina Has; Leena Bruckner-Tuderman
Laminin 332 in junctional epidermolysis bullosa.
Cell adhesion & migration 2013;7(1):135-41.
2013: Dimitra Kiritsi; Juergen Kohlhase; Manuela Pigors; Iliana Tantcheva-Poor; Cordula Wessel; Meral J Arin; Leena Bruckner-Tuderman; Cristina Has
Epidermolysis bullosa simplex ogna revisited.
The Journal of investigative dermatology 2013;133(1):270-3.
2012: Larissa Lennartz; Cristina Has; Percy Lehmann
Congenital bullous poikiloderma (Kindler syndrome) - new mutation.
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2012;10(12):919-20.
2012: Jouni Uitto; Cristina Has; Leena Bruckner-Tuderman
Cell-based therapies for epidermolysis bullosa - from bench to bedside.
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2012;10(11):803-7.
2012: Hauke Schumann; A Volz; C Erfurt-Berge; Cristina Has; T M Magin; W Roth; Leena Bruckner-Tuderman
Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 gene.
The British journal of dermatology 2012;167(4):929-36.
2012: Manuela Pigors; Agnes Schwieger-Briel; Jose Suárez; Johannes S Kern; Dimitra Kiritsi; Leeni Mäkelä; Heikki Aho; Leena Bruckner-Tuderman; Cristina Cobzaru; Flavio Faletra; Cristina Has
TGM5 mutations impact epidermal differentiation in acral peeling skin syndrome.
The Journal of investigative dermatology 2012;132(10):2422-9.
2012: Andreas W Arnold; Leena Bruckner-Tuderman; Rudolf Happle; Cristina Has; Ingrid Hausser; Dimitra Kiritsi; Juergen Kohlhase; Peter H Itin
Type 1 segmental Galli-Galli disease resulting from a previously unreported keratin 5 mutation.
The Journal of investigative dermatology 2012;132(8):2100-3.
2012: A W Arnold; Leena Bruckner-Tuderman; Cristina Has; Rudolf Happle
Conradi-Hünermann-Happle syndrome in males vs. MEND syndrome (male EBP disorder with neurological defects).
The British journal of dermatology 2012;166(6):1309-13.
2012: Dimitra Kiritsi; Meltem Onder; Anna M G Pasmooij; Leena Bruckner-Tuderman; Rudolf Happle; Yinghong He; Marcel F Jonkman; Cristina Has
Revertant mosaicism in a human skin fragility disorder results from slipped mispairing and mitotic recombination.
The Journal of clinical investigation 2012;122(5):1742-6.
2012: Cristina Has; Ingrid Hausser; Yinghong He; Friedhelm Hildebrandt; Dimitra Kiritsi; Yair Anikster; Detlef Bockenhauer; Leena Bruckner-Tuderman; Benjamin Dekel; Philipp Esser; Alexander Moeller; Giuseppina Spartà; Beate K Straub; Virginia Vega-Warner; Aoife Waters; Lisa Weibel; Guido F Laube
Integrin α3 mutations with kidney, lung, and skin disease.
The New England journal of medicine 2012;366(16):1508-14.
2012: B Burger; Cristina Has; M Schubert; I Spoerri; Peter H Itin
Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutation.
The British journal of dermatology 2012;166(2):434-9.
2012: Leena Bruckner-Tuderman; Cristina Has
Molecular heterogeneity of blistering disorders: the paradigm of epidermolysis bullosa.
The Journal of investigative dermatology 2012;132(E1):E2-5.
2012: A W Arnold; Rudolf Happle; P H Itin; Johannes S Kern; M Pigors; Cristina Has
Acromelanosis albo-punctata: a distinct inherited dermatosis with acral spotty dyspigmentation without systemic involvement.
Dermatology (Basel, Switzerland) 2012;224(4):331-9.
2011: Cristina Has; Peter Itin; Dimitra Kiritsi; Jürgen Kohlhase; Ludovic Martin; Eugenia Piccinni; Giovanna Zambruno; Marta Garcia Diez; Daniele Castiglia; Marcela del Rio; Judith Fischer; Leena Bruckner-Tuderman
Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.
Human mutation 2011;32(11):1204-12.
2011: Peter C van den Akker; Anthonie J van Essen; Giovanna Zambruno; Johann W Bauer; Leena Bruckner-Tuderman; Daniele Castiglia; Cristina Has; Robert M W Hofstra; Marcel F Jonkman; Alfred Klausegger; John A McGrath; Jemima E Mellerio; Trebor Rengaw; Morris A Swertz
The international dystrophic epidermolysis bullosa patient registry: an online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations.
Human mutation 2011;32(10):1100-7.
2011: Cristina Has
Mosaicism in the skin: the importance of mild or minimal skin lesions.
Archives of dermatology 2011;147(9):1094-6.
2011: Dimitra Kiritsi; Juergen Kohlhase; Hauke Schumann; Cristina Has; Johannes S Kern; Leena Bruckner-Tuderman
Molecular mechanisms of phenotypic variability in junctional epidermolysis bullosa.
Journal of medical genetics 2011;48(7):450-7.
2011: Manuela Pigors; Dimitra Kiritsi; Sebastian Krümpelmann; Nicola Wagner; Yinghong He; Maurizio Podda; Jürgen Kohlhase; Ingrid Hausser; Leena Bruckner-Tuderman; Cristina Has
Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity.
Human molecular genetics 2011;20(9):1811-9.
2011: Martin Leverkus; Andreas Ambach; M Hoefeld-Fegeler; Juergen Kohlhase; E Schmidt; Hauke Schumann; Cristina Has; Harald Gollnick
Late-onset inversa recessive dystrophic epidermolysis bullosa caused by glycine substitutions in collagen type VII.
The British journal of dermatology 2011;164(5):1104-6.
2011: Anja Heinemann; Yinghong He; Elena Zimina; Melanie Boerries; Hauke Busch; Nadja Chmel; Thorsten Kurz; Leena Bruckner-Tuderman; Cristina Has
Induction of phenotype modifying cytokines by FERMT1 mutations.
Human mutation 2011;32(4):397-406.
2011: Wibke von Bartenwerffer; Meral J Arin; Tarek Arshah; Leena Bruckner-Tuderman; Sabine A Eming; Cristina Has; Michael Hoffmann; Juergen Kohlhase; Kim Kremer; Alexander Kreuter; Thomas Krieg; I Tantcheva-Poór; Karin Hartmann
Mild recessive dystrophic epidermolysis bullosa associated with two compound heterozygous COL7A1 mutations.
European journal of dermatology : EJD 2011;21(2):170-2.
2011: Yinghong He; Philipp Esser; Anja Heinemann; Leena Bruckner-Tuderman; Cristina Has
Kindlin-1 and -2 have overlapping functions in epithelial cells implications for phenotype modification.
The American journal of pathology 2011;178(3):975-82.
2011: Yinghong He; Philipp Esser; Vivien Schacht; Leena Bruckner-Tuderman; Cristina Has
Role of kindlin-2 in fibroblast functions: implications for wound healing.
The Journal of investigative dermatology 2011;131(1):245-56.
2010: A W Arnold; Peter H Itin; M Pigors; Juergen Kohlhase; Leena Bruckner-Tuderman; Cristina Has
Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria.
The British journal of dermatology 2010;163(4):866-9.
2010: Adrian Sprenger; Victoria Küttner; Martin L Biniossek; Christine Gretzmeier; Melanie Boerries; Claudia Mack; Cristina Has; Leena Bruckner-Tuderman; Jörn Dengjel
Comparative quantitation of proteome alterations induced by aging or immortalization in primary human fibroblasts and keratinocytes for clinical applications.
Molecular bioSystems 2010;6(9):1579-82.
2010: Meral J Arin; Gundula Grimberg; Hauke Schumann; H De Almeida; Y-R Chang; Gianluca Tadini; Juergen Kohlhase; Thomas Krieg; Leena Bruckner-Tuderman; Cristina Has
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.
The British journal of dermatology 2010;162(6):1365-9.
2010: Dimitra Kiritsi; Ioana Cosgarea; Claus-Werner Franzke; Hauke Schumann; Vinzenz Oji; Juergen Kohlhase; Leena Bruckner-Tuderman; Cristina Has
Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals.
The Journal of investigative dermatology 2010;130(6):1741-6.
2010: Cristina Has; Johannes S Kern
Collagen XVII.
Dermatologic clinics 2010;28(1):61-6.
2009: Johannes S Kern; G Grüninger; R Imsak; Marcel Lucas Müller; Hauke Schumann; D Kiritsi; S Emmert; W Borozdin; Juergen Kohlhase; Leena Bruckner-Tuderman; Cristina Has
Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohort.
The British journal of dermatology 2009;161(5):1089-97.
2009: Cristina Has; Corinna Herz; Elena Zimina; Hai-Yan Qu; Yinghong He; Zhi-Gang Zhang; Ting-Ting Wen; Yannick Gache; Monique Aumailley; Leena Bruckner-Tuderman
Kindlin-1 Is required for RhoGTPase-mediated lamellipodia formation in keratinocytes.
The American journal of pathology 2009;175(4):1442-52.
2008: Cristina Has; Ivelina Yordanova; Maria Balabanova; Jana Kazandjieva; Corinna Herz; Juergen Kohlhase; Leena Bruckner-Tuderman
A novel large FERMT1 (KIND1) gene deletion in Kindler syndrome.
Journal of dermatological science 2008;52(3):209-12.
2008: Cristina Has; R J Ludwig; Corinna Herz; Johannes S Kern; Siegfried Ussar; F R Ochsendorf; R Kaufmann; Hauke Schumann; Juergen Kohlhase; Leena Bruckner-Tuderman
C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes.
The British journal of dermatology 2008;159(5):1192-6.
2008: Hauke Schumann; Cristina Has; Juergen Kohlhase; Leena Bruckner-Tuderman
Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutations.
The British journal of dermatology 2008;159(2):464-9.
2007: Johannes S Kern; Corinna Herz; E Haan; D Moore; S Nottelmann; T von Lilien; P Greiner; A Schmitt-Graeff; O G Opitz; Leena Bruckner-Tuderman; Cristina Has
Chronic colitis due to an epithelial barrier defect: the role of kindlin-1 isoforms.
The Journal of pathology 2007;213(4):462-70.
2007: Andreas Volz; Cristina Has; Hauke Schumann; Leena Bruckner-Tuderman
Network epidermolysis bullosa: molecular pathomechanisms and novel therapeutic approaches.
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2007;5(4):274-9.
2007: Cristina Has; S Danescu; A Volz; F Nöh; K Technau; Leena Bruckner-Tuderman
Incontinentia pigmenti in a newborn with a novel nonsense mutation in the NEMO gene.
The British journal of dermatology 2007;156(2):392-3.
2007: Ayse Tülin Mansur; Nursel Elcioglu; Ikbal Esen Aydingöz; A Deniz Akkaya; Zehra Asiran Serdar; Corinna Herz; Leena Bruckner-Tuderman; Cristina Has
Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement.
Acta dermato-venereologica 2007;87(6):563-5.
2006: Pamela Poblete Gutiérrez; W H C Burgdorf; Cristina Has; Mark Berneburg; Jorge Frank
[Hereditary photodermatoses].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2006;57(12):1067-82.
2006: Cristina Has; Leena Bruckner-Tuderman
Molecular and diagnostic aspects of genetic skin fragility.
Journal of dermatological science 2006;44(3):129-44.
2006: Corinna Herz; Monique Aumailley; Carsten Schulte; Ursula Schlötzer-Schrehardt; Leena Bruckner-Tuderman; Cristina Has
Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes.
The Journal of biological chemistry 2006;281(47):36082-90.
2006: Claus-Werner Franzke; Cristina Has; Carsten Schulte; Laura Huilaja; Kaisa Tasanen; Monique Aumailley; Leena Bruckner-Tuderman
C-terminal truncation impairs glycosylation of transmembrane collagen XVII and leads to intracellular accumulation.
The Journal of biological chemistry 2006;281(40):30260-8.
2006: Cristina Has; Vesarat Wessagowit; Monica Pascucci; Corinna Baer; Biagio Didona; Christian Wilhelm; Cristina Pedicelli; Andrea Locatelli; Juergen Kohlhase; G H S Ashton; Gianluca Tadini; Giovanna Zambruno; Leena Bruckner-Tuderman; John A McGrath; Daniele Castiglia
Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.
The Journal of investigative dermatology 2006;126(8):1776-83.
2006: Cristina Has; Yow-Ren Chang; Andreas Volz; Doris Hoeping; Juergen Kohlhase; Leena Bruckner-Tuderman
Novel keratin 14 mutations in patients with severe recessive epidermolysis bullosa simplex.
The Journal of investigative dermatology 2006;126(8):1912-4.
2006: Johannes S Kern; Juergen Kohlhase; Leena Bruckner-Tuderman; Cristina Has
Expanding the COL7A1 mutation database: novel and recurrent mutations and unusual genotype-phenotype constellations in 41 patients with dystrophic epidermolysis bullosa.
The Journal of investigative dermatology 2006;126(5):1006-12.
2006: Sigrid M C Broekaert; Evelin Knauss-Scherwitz; Tilo Biedermann; Gisela Metzler; Cristina Has; Juergen Kohlhase; Martin Röcken; Martin Schaller
Epidermolysis bullosa pruriginosa due to a glycine substitution mutation in the COL7A1-gene.
Acta dermato-venereologica 2006;86(6):556-7.
2006: Monique Aumailley; Cristina Has; Lucy Tunggal; Leena Bruckner-Tuderman
Molecular basis of inherited skin-blistering disorders, and therapeutic implications.
Expert reviews in molecular medicine 2006;8(24):1-21.
2005: Laura Väisänen; Cristina Has; Claus-Werner Franzke; Tiina Hurskainen; Marja-Leena Tuomi; Leena Bruckner-Tuderman; Kaisa Tasanen
Molecular mechanisms of junctional epidermolysis bullosa: Col 15 domain mutations decrease the thermal stability of collagen XVII.
The Journal of investigative dermatology 2005;125(6):1112-8.
2005: Margarita Stefanova; Katrin Zemke; Boyan Dimitrov; Cristina Has; Johannes S Kern; Leena Bruckner-Tuderman; Kerstin Kutsche
Disruption of ERBB2IP is not associated with dystrophic epidermolysis bullosa in both father and son carrying a balanced 5;13 translocation.
The Journal of investigative dermatology 2005;125(4):700-4.
2004: Cristina Has; Johannes S Kern; Leena Bruckner-Tuderman
[Hereditary blistering disorders].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2004;55(10):920, 922-30.
2004: Christine Herzog; Cristina Has; Claus-Werner Franzke; Frank Echtermeyer; Ursula Schlötzer-Schrehardt; Stephan Kröger; Erika Elisabet Gustafsson; Reinhard Fässler; Leena Bruckner-Tuderman
Dystroglycan in skin and cutaneous cells: beta-subunit is shed from the cell surface.
The Journal of investigative dermatology 2004;122(6):1372-80.
2002: Laurent Misery; Jean-Christophe Antoine; Renaud Touraine; Ronald Wanders; Séverine Maitre; Cristina Has; Jean-Luc Perrot; Frédéric Cambazard
[Sjogren-Larsson syndrome: two cases with delayed diagnosis].
Annales de médecine interne 2002;153(4):280-2.
2002: Cristina Has; Laurent Misery; Louis David; Frédéric Cambazard
Recurring staphylococcal scalded skin syndrome-like bullous mastocytosis: the utility of cytodiagnosis and the rapid regression with steroids.
Pediatric dermatology 2002;19(3):220-3.
2002: Cristina Has; Udo Seedorf; Frank Kannenberg; Leena Bruckner-Tuderman; Elzo Folkers; Regina Fölster-Holst; Ivo Baric; Heiko Traupe
Gas chromatography-mass spectrometry and molecular genetic studies in families with the Conradi-Hünermann-Happle syndrome.
The Journal of investigative dermatology 2002;118(5):851-8.
2000: Cristina Has; Leena Bruckner-Tuderman; D Müller; Michaela Floeth; E Folkers; D Donnai; Heiko Traupe
The Conradi-Hünermann-Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicism.
Human molecular genetics 2000;9(13):1951-5.
2000: Heiko Traupe; Cristina Has
The Conradi-Hünermann-Happle syndrome is caused by mutations in the gene that encodes a 8- 7 sterol isomerase and is biochemically related to the CHILD syndrome.
European journal of dermatology : EJD 2000;10(6):425-8.