Advances in understanding the molecular basis of skin fragility

por Has, Cristina
Publicado 2018

Update on Genetic Conditions Affecting the Skin and the Kidneys

por Reimer, Antonia, He, Yinghong, Has, Cristina
Publicado 2018

Molecular Therapeutics in Development for Epidermolysis Bullosa: Update 2020

por Has, Cristina, South, Andrew, Uitto, Jouni
Publicado 2020

Junctional Epidermolysis Bullosa: Allelic Heterogeneity and Mutation Stratification for Precision Medicine

por Condrat, Irina, He, Yinghong, Cosgarea, Rodica, Has, Cristina
Publicado 2019

Betulin-Based Oleogel to Improve Wound Healing in Dystrophic Epidermolysis Bullosa: A Prospective Controlled Proof-of-Concept Study

por Schwieger-Briel, Agnes, Kiritsi, Dimitra, Schempp, Christoph, Has, Cristina, Schumann, Hauke
Publicado 2017

Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome

por Kopp, Julia, Has, Cristina, Hotz, Alrun, Grünert, Sarah C., Fischer, Judith
Publicado 2021

Kindler syndrome: a rare case report from Greece

por Gkaitatzi, Maria, Kalloniati, Evangelia, Has, Cristina, Kiritsi, Dimitra, Spiliopoulos, Theofanis, Georgiou, Sophia
Publicado 2019

Editorial: Skin Blistering Diseases

por Has, Cristina, Amber, Kyle T., Murrell, Dedee F., Musette, Philippe, Ludwig, Ralf J.
Publicado 2019

Targeting epidermal lipids for treatment of Mendelian disorders of cornification

por Kiritsi, Dimitra, Schauer, Franziska, Wölfle, Ute, Valari, Manthoula, Bruckner-Tuderman, Leena, Has, Cristina, Happle, Rudolf
Publicado 2014

Effect of small molecule eRF3 degraders on premature termination codon readthrough

por Baradaran-Heravi, Alireza, Balgi, Aruna D, Hosseini-Farahabadi, Sara, Choi, Kunho, Has, Cristina, Roberge, Michel
Publicado 2021

Variable Outcome of Immunotherapy in Advanced Multiple Cutaneous Squamous Cell Carcinomas in Two Patients with Recessive Dystrophic Epidermolysis Bullosa

por TREFZER, Laura, HESS, Maria E., SCHOLTEN, Lena, TECHNAU-HAFSI, Kristin, MEISS, Frank, BOERRIES, Melanie, HAS, Cristina, RAFEI-SHAMSABADI, David
Publicado 2023

Human Papillomavirus-induced Cutaneous and Mucosal Lesions in a Patient with Rothmund-Thomson Syndrome

por KUNTZ, Thomas, KOUSHK-JALALI, Bijan, TIGGES, Christian, SILLING, Steffi, OELLIG, Frank, HAS, Cristina, HAMPL, Monika, WIELAND, Ulrike, KREUTER, Alexander
Publicado 2020

Case Report: Diagnostic and Therapeutic Challenges in Severe Mechanobullous Epidermolysis Bullosa Acquisita

por Schauer, Franziska, Nyström, Alexander, Kunz, Manfred, Hübner, Stefanie, Scholl, Sarah, Athanasiou, Ioannis, Alter, Svenja, Fischer, Judith, Has, Cristina, Kiritsi, Dimitra
Publicado 2022

Progress Towards Treatment and Cure of Epidermolysis Bullosa: Summary of the DEBRA International Research Symposium EB2015

por Uitto, Jouni, Tuderman, Leena Bruckner, Christiano, Angela M., McGrath, John A., Has, Cristina, South, Andrew P., Kopelan, Brett, Robinson, E. Clare
Publicado 2016

Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases

por Mellerio, Jemima E., El Hachem, Maya, Bellon, Nathalia, Zambruno, Giovanna, Buckova, Hana, Autrata, Rudolf, Salavastru, Carmen, Caldaro, Tamara, Greco, Celine, Has, Cristina, Bodemer, Christine
Publicado 2020

Kindlin-2 Mediates Mechanical Activation of Cardiac Myofibroblasts

por Godbout, Elena, Son, Dong Ok, Hume, Stephanie, Boo, Stellar, Sarrazy, Vincent, Clément, Sophie, Kapus, Andras, Wehrle-Haller, Bernhard, Bruckner-Tuderman, Leena, Has, Cristina, Hinz, Boris
Publicado 2020

Mouse models for dominant dystrophic epidermolysis bullosa carrying common human point mutations recapitulate the human disease

por Smith, Blake R. C., Nyström, Alexander, Nowell, Cameron J., Hausser, Ingrid, Gretzmeier, Christine, Robertson, Susan J., Varigos, George A., Has, Cristina, Kern, Johannes S., Pang, Ken C.
Publicado 2021

Proteasome-mediated degradation of keratins 7, 8, 17 and 18 by mutant KLHL24 in a foetal keratinocyte model: Novel insight in congenital skin defects and fragility of epidermolysis...

por Logli, Elena, Marzuolo, Elisa, D’Agostino, Marco, Conti, Libenzio Adrian, Lena, Anna Maria, Diociaiuti, Andrea, Dellambra, Elena, Has, Cristina, Cianfanelli, Valentina, Zambruno, Giovanna, El Hachem, May, Magenta, Alessandra, Candi, Eleonora, Condorelli, Angelo Giuseppe
Publicado 2021

Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients

por Guerrero-Aspizua, Sara, Conti, Claudio J., Escamez, Maria Jose, Castiglia, Daniele, Zambruno, Giovanna, Youssefian, Leila, Vahidnezhad, Hassan, Requena, Luis, Itin, Peter, Tadini, Gianluca, Yordanova, Ivelina, Martin, Ludovic, Uitto, Jouni, Has, Cristina, Del Rio, Marcela
Publicado 2019

Oxidative stress and mitochondrial dysfunction in Kindler syndrome

por Zapatero-Solana, Elisabeth, García-Giménez, Jose Luis, Guerrero-Aspizua, Sara, García, Marta, Toll, Agustí, Baselga, Eulalia, Durán-Moreno, Maria, Markovic, Jelena, García-Verdugo, Jose Manuel, Conti, Claudio J, Has, Cristina, Larcher, Fernando, Pallardó, Federico V, Del Rio, Marcela
Publicado 2014