受强制性开放获取政策约束的文章 - Cristina Has了解详情
无法在其他位置公开访问的文章：23 篇
Epidermolysis bullosa: Molecular pathology of connective tissue components in the cutaneous basement membrane zone
C Has, A Nyström, AH Saeidian, L Bruckner-Tuderman, J Uitto
Matrix Biology 71, 313-329, 2018
强制性开放获取政策： US National Institutes of Health, German Research Foundation
Molecular and diagnostic aspects of genetic skin fragility
C Has, L Bruckner-Tuderman
Journal of dermatological science 44 (3), 129-144, 2006
强制性开放获取政策： German Research Foundation
Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutations
H Schumann, C Has, J Kohlhase, L Bruckner‐Tuderman
British Journal of Dermatology 159 (2), 464-469, 2008
强制性开放获取政策： German Research Foundation
Collagen XVII
C Has, JS Kern
Dermatologic clinics 28 (1), 61-66, 2010
强制性开放获取政策： German Research Foundation
Under‐recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations
W Szczecinska, D Nesteruk, K Wertheim‐Tysarowska, DT Greenblatt, ...
British Journal of Dermatology 171 (5), 1206-1210, 2014
强制性开放获取政策： German Research Foundation
Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for …
AD Zimmer, GJ Kim, A Hotz, E Bourrat, I Hausser, C Has, V Oji, K Stieler, ...
British Journal of Dermatology 177 (2), 445-455, 2017
强制性开放获取政策： German Research Foundation
Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancer
C Has, B Burger, A Volz, J Kohlhase, L Bruckner-Tuderman, P Itin
Dermatology 221 (4), 309-312, 2010
强制性开放获取政策： German Research Foundation
Profound immunodeficiency with severe skin disease explained by concomitant novel CARMIL2 and PLEC1 loss-of-function mutations
ME Maccari, C Speckmann, M Heeg, A Reimer, F Casetti, C Has, S Ehl, ...
Clinical Immunology 208, 108228, 2019
强制性开放获取政策： Federal Ministry of Education and Research, Germany
A unique LAMB3 splice‐site mutation with founder effect from the Balkans causes lethal epidermolysis bullosa in several European countries
B Mayer, P Silló, M Mazán, D Pintér, M Medvecz, C Has, D Castiglia, ...
British Journal of Dermatology 175 (4), 721-727, 2016
强制性开放获取政策： Hungarian Scientific Research Fund
RhoA activation by CNFy restores cell–cell adhesion in kindlin‐2‐deficient keratinocytes
Y He, T Sonnenwald, A Sprenger, U Hansen, J Dengjel, ...
The Journal of pathology 233 (3), 269-280, 2014
强制性开放获取政策： German Research Foundation
Blaschko line acne on pre‐existent hypomelanosis reflecting a mosaic FGFR2 mutation
D Kiritsi, AI Lorente, R Happle, J Bernabeu Wittel, C Has
British Journal of Dermatology 172 (4), 1125-1127, 2015
强制性开放获取政策： German Research Foundation
Effect of DNA repair host factors on temozolomide or dacarbazine melanoma treatment in Caucasians
L Boeckmann, M Schirmer, A Rosenberger, D Struever, KM Thoms, ...
Pharmacogenetics and genomics 19 (10), 760-769, 2009
强制性开放获取政策： German Research Foundation
Natural history and clinical outcome of junctional epidermolysis bullosa generalized intermediate due to a LAMA3 mutation
A Reimer, A Schwieger‐Briel, Y He, J Leppert, F Schauer, D Kiritsi, ...
British Journal of Dermatology 178 (4), 973-975, 2018
强制性开放获取政策： German Research Foundation
Therapies for inherited skin fragility disorders
C Has, D Kiritsi
Experimental Dermatology 24 (5), 325-331, 2015
强制性开放获取政策： German Research Foundation
Molecular dermatology comes of age
C Has, C Sitaru
Molecular Dermatology: Methods and Protocols, 1-16, 2013
强制性开放获取政策： German Research Foundation
Renal-skin syndromes
C Has, Y He
Cell and Tissue Research 369, 63-73, 2017
强制性开放获取政策： German Research Foundation
Chronic tissue damage: a common pathomechanism of genodermatoses.
C Has
British Journal of Dermatology 181 (3), 2019
强制性开放获取政策： Federal Ministry of Education and Research, Germany
Focal adhesions in the skin: lessons learned from skin fragility disorders
C Has, Y He
European Journal of Dermatology 27, 8-11, 2017
强制性开放获取政策： German Research Foundation
‘Double trouble’: diagnostic challenges in genetic skin disorders
D Kiritsi, M Valari, K Mileounis, L Bruckner‐Tuderman, C Has
British Journal of Dermatology 172 (1), 276-278, 2015
强制性开放获取政策： German Research Foundation
Flightless I, a contributing factor to skin blistering in Kindler syndrome patients?
Z Kopecki, C Has, G Yang, L Bruckner‐Tuderman, A Cowin
Journal of Cutaneous Pathology 47 (2), 2020
强制性开放获取政策： National Health and Medical Research Council, Australia
出版信息和资助信息由计算机程序自动确定