The Kindlins: subcellular localization and expression during murine development (Q28513797)

25 January 2017

title

The Kindlins: subcellular localization and expression during murine development (English)

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25 January 2017

main subject

Fermitin family member 1

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GOA release 2020-03-11

Fermitin family member 3

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GOA release 2020-03-11

Fermitin family member 2

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GOA release 2020-03-11

author

Reinhard Fässler

4

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Siegfried Ussar

1

object named as

Siegfried Ussar

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25 January 2017

Hao-Ven Wang

2

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25 January 2017

Stefan Linder

3

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25 January 2017

Markus Moser

5

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25 January 2017

language of work or name

English

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publication date

1 October 2006

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Experimental Cell Research

25 January 2017

published in

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25 January 2017

volume

312

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25 January 2017

issue

16

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25 January 2017

page(s)

3142–3151

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

25 January 2017

cites work

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URP1: a member of a novel family of PH and FERM domain-containing membrane-associated proteins is significantly over-expressed in lung and colon carcinomas

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Proteomic analysis of the cell-surface membrane in chronic lymphocytic leukemia: identification of two novel proteins, BCNP1 and MIG2B.

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

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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 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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Kindler syndrome complicated by squamous cell carcinoma of the hard palate: successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor

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Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy

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Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.

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

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Expression of the mitogen-inducible gene-2 (mig-2) is elevated in human uterine leiomyomas but not in leiomyosarcomas.

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A novel LIM protein Cal promotes cardiac differentiation by association with CSX/NKX2-5

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Podosomes at a glance

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