Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes (Q24305400)

establishment of epithelial cell polarity

GOA release 2020-03-11

1 reference

Ursula Schlötzer-Schrehardt

GOA release 2020-03-11

1 reference

4

object named as

Ursula Schlötzer-Schrehardt

0 references

Leena Bruckner-Tuderman

5

object named as

Leena Bruckner-Tuderman

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author name string

Corinna Herz

1

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Monique Aumailley

2

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Carsten Schulte

3

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Cristina Has

Journal of Biological Chemistry

6

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language of work or name

English

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publication date

24 November 2006

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published in

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volume

281

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issue

47

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page(s)

36082-90

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cites work

Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome

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The UNC-112 gene in Caenorhabditis elegans encodes a novel component of cell-matrix adhesion structures required for integrin localization in the muscle cell membrane

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ERM proteins and merlin: integrators at the cell cortex

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Inositol-lipid binding motifs: signal integrators through protein-lipid and protein-protein interactions

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Physical and functional association of migfilin with cell-cell adhesions

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Migfilin and Mig-2 link focal adhesions to filamin and the actin cytoskeleton and function in cell shape modulation

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The Kindler syndrome protein is regulated by transforming growth factor-beta and involved in integrin-mediated adhesion.

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Kindler surprise: mutations in a novel actin-associated protein cause Kindler syndrome.

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Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome

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A role for alphabeta1 integrins in focal adhesion function and polarized cytoskeletal dynamics

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Keratinocytes from patients lacking collagen XVII display a migratory phenotype

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Two forms of collagen XVII in keratinocytes. A full-length transmembrane protein and a soluble ectodomain

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Collagen XVII is destabilized by a glycine substitution mutation in the cell adhesion domain Col15

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A novel nonsense mutation in Kindler syndrome.

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Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.

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Laminin 5 deposition regulates keratinocyte polarization and persistent migration

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Protein kinase CK2 inhibitor 4,5,6,7-tetrabromobenzotriazole (TBB) induces apoptosis and caspase-dependent degradation of haematopoietic lineage cell-specific protein 1 (HS1) in Jurkat cells

21 January 2018

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The shape of things to come: an emerging role for protein kinase CK2 in the regulation of cell morphology and the cytoskeleton

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α3β1 Integrin Is Required for Normal Development of the Epidermal Basement Membrane

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Conditional ablation of beta1 integrin in skin. Severe defects in epidermal proliferation, basement membrane formation, and hair follicle invagination

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Skin and hair follicle integrity is crucially dependent on beta 1 integrin expression on keratinocytes

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beta 1 integrin function in vivo: adhesion, migration and more

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Integrins: bidirectional, allosteric signaling machines

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