Search Results - Has, Cristina
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1
Mouse models for dominant dystrophic epidermolysis bullosa carrying common human point mutations recapitulate the human disease by Smith, Blake (Author) , Nyström, Alexander (Author) , Nowell, Cameron J. (Author) , Haußer-Siller, Ingrid (Author) , Gretzmeier, Christine (Author) , Robertson, Susan J. (Author) , Varigos, George A. (Author) , Has, Cristina (Author) , Kern, Johannes S. (Author) , Pang, Ken C. (Author) ,
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2
Constitutional absence of epithelial integrin α3 impacts the composition of the cellular microenvironment of ILNEB keratinocytes by He, Yinghong (Author) , Thriene, Kerstin (Author) , Boerries, Melanie (Author) , Haußer-Siller, Ingrid (Author) , Franzke, Claus-Werner (Author) , Busch, Hauke (Author) , Dengjel, Joern (Author) , Has, Cristina (Author) ,
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3
Monoallelic large intragenic KRT5 deletions account for genetically unsolved cases of Epidermolysis bullosa simplex by Has, Cristina (Author) , Haußer-Siller, Ingrid (Author) ,
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Target-sequence capture and high throughput sequencing identify a de novo CARD14 mutation in an infant with erythrodermic pityriasis rubra pilaris by Has, Cristina (Author) , Haußer-Siller, Ingrid (Author) ,
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5
Monoallelic mutations in the translation initiation codon of KLHL24 cause skin fragility by He, Yinghong (Author) , Maier, Kristin (Author) , Leppert, Juna (Author) , Haußer-Siller, Ingrid (Author) , Schwieger-Briel, Agnes (Author) , Weibel, Lisa (Author) , Theiler, Martin (Author) , Kiritsi, Dimitra (Author) , Busch, Hauke (Author) , Boerries, Melanie (Author) , Hannula-Jouppi, Katariina (Author) , Heikkilä, Hannele (Author) , Tasanen, Kaisa (Author) , Castiglia, Daniele (Author) , Zambruno, Giovanna (Author) , Has, Cristina (Author) ,
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6
Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergies by Has, Cristina (Author) , Haußer-Siller, Ingrid (Author) ,
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7
Integrin α3 mutations with kidney, lung, and skin disease by Has, Cristina (Author) , Straub, Beate Katharina (Author) , Haußer-Siller, Ingrid (Author) ,
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8
Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity by Pigors, Manuela (Author) , Kiritsi, Dimitra (Author) , Krümpelmann, Sebastian (Author) , Wagner, Nicola (Author) , He, Yinghong (Author) , Podda, Maurizio (Author) , Kohlhase, Jürgen (Author) , Haußer-Siller, Ingrid (Author) , Bruckner-Tuderman, Leena (Author) , Has, Cristina (Author) ,
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