Plectin Missense Mutation p.Leu319Pro in the Pathogenesis of Autosomal Recessive Epidermolysis Bullosa Simplex

Binding of Integrin α6β4 to Plectin Prevents Plectin Association with F-Actin but Does Not Interfere with Intermediate Filament Binding

Dirk Geerts, Lionel Fontao, Mirjam G. Nievers et al. · The Journal of Cell Biology · 1999 · 177 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

Plectin-Isoform-Specific Rescue of Hemidesmosomal Defects in Plectin (–/–) Keratinocytes

Kerstin Andrä, Iris Kornacker, Almut Jörgl et al. · Journal of Investigative Dermatology · 2003 · 112 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +8

Formation of hemidesmosome-like structures in the absence of ligand binding by the α6β4 integrin requires binding of HD1/plectin to the cytoplasmic domain of the β4 integrin subunit

Mirjam G. Nievers, Ingrid Kuikman, Dirk Geerts et al. · Journal of Cell Science · 2000 · 57 citations

Life Sciences, Cell Biology, Molecular Biology +14

A Compound Heterozygous One Amino-Acid Insertion/Nonsense Mutation in the Plectin Gene Causes Epidermolysis Bullosa Simplex with Plectin Deficiency

Johann Bauer, Fatima Rouan, Barbara Kofler et al. · American Journal Of Pathology · 2001 · 54 citations · Full text

Medicine, Genetics, Molecular Genetics +7

Loss of interaction between plectin and type XVII collagen results in epidermolysis bullosa simplex

Ken Natsuga, Wataru Nishie, Machiko Nishimura et al. · Human Mutation · 2017 · 23 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +16