Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton.
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Inhibition of protein kinase B (PKB) and PKCzeta mediates keratin K10-induced cell cycle arrest5-Lipoxygenase expression in Langerhans cells of normal human epidermisCaspase cleavage of keratin 18 and reorganization of intermediate filaments during epithelial cell apoptosisEffects of sulfur mustard on the basal cell adhesion complex.Polycystin-1 interacts with intermediate filaments.Mechanisms mediating the vesicant actions of sulfur mustard after cutaneous exposureTransduction of a preselected population of human epidermal stem cells: consequences for gene therapy.Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene.Type II keratins are phosphorylated on a unique motif during stress and mitosis in tissues and cultured cells.Defining the regulatory factors required for epidermal gene expression.Experimental autoimmune encephalomyelitis in mice lacking glial fibrillary acidic protein is characterized by a more severe clinical course and an infiltrative central nervous system lesionUpregulation of P2Y2 receptors by retinoids in normal human epidermal keratinocytesUpdate on peptidylarginine deiminases and deimination in skin physiology and severe human diseases.Transcription regulation and protein subcellular localization of the truncated basic hair keratin hHb1-DeltaN in human breast cancer cells.Modulation of cell proliferation by cytokeratins K10 and K16Analysis of cultured keratinocytes from a transgenic mouse model of psoriasis: effects of suprabasal integrin expression on keratinocyte adhesion, proliferation and terminal differentiation.The type I keratin 19 possesses distinct and context-dependent assembly properties.Recessive epidermolysis bullosa simplex phenotype reproduced in vitro: ablation of keratin 14 is partially compensated by keratin 17.Differences in the width of the intercellular spaces in the epithelial basal infolding and the renal glomerular filtration site between freeze-substitution and conventional fixation.Cross-linked envelopes in nail plate in lamellar ichthyosis.Molecular basis of non-lethal junctional epidermolysis bullosa: identification of a 38 basepair insertion and a splice site mutation in exon 14 of the LAMB3 gene.Comparative sequence analysis and radiation hybrid mapping of two epidermal type II keratin genes in the dog: keratin 1 and keratin 2e.Identification of the glycine-to-arginine substitution G2043R in type VII collagen in a family with dominant dystrophic epidermolysis bullosa from Hungary.Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13Animal Models for Retinoid Receptor Research: Implications for Epidermal Homeostasis, Skin Barrier Function, Wound Healing, and Atopic Dermatitis
P2860
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P2860
Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton.
@en
type
label
Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton.
@en
prefLabel
Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton.
@en
P2860
P356
P1476
Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton.
@en
P2093
P2860
P304
P356
10.1091/MBC.8.2.189
P577
1997-02-01T00:00:00Z