(Q81209352)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18454678%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

review article

1 reference

title

Kindler syndrome and periodontal disease: review of the literature and a 12-year follow-up case (English)

1 reference

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6 January 2020

1 reference

1 reference

Colin B Wiebe

1

1 reference

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6 January 2020

Giorgio Petricca

2

1 reference

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6 January 2020

Lari Häkkinen

3

1 reference

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6 January 2020

Guoqiao Jiang

4

1 reference

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6 January 2020

Chuanyue Wu

5

1 reference

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6 January 2020

Hannu S Larjava

6

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6 January 2020

publication date

1 May 2008

1 reference

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Journal of Periodontology

6 January 2020

published in

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6 January 2020

volume

79

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6 January 2020

issue

5

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6 January 2020

page(s)

961-966

1 reference

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ERM proteins: from cellular architecture to cell signaling

6 January 2020

cites work

1 reference

12 December 2020

Specificity in pleckstrin homology (PH) domain membrane targeting: a role for a phosphoinositide-protein co-operative mechanism.

1 reference

12 December 2020

The effect of mechanical force on mRNA levels of collagenase, collagen type I, and tissue inhibitors of metalloproteinases in gingivae of dogs

1 reference

12 December 2020

Exclusion of COL7A1 mutation in Kindler syndrome

1 reference

12 December 2020

The phosphotyrosine binding-like domain of talin activates integrins

1 reference

12 December 2020

Clinical and microbiologic study of periodontitis associated with Kindler syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Hereditary acrokeratotic poikiloderma

1 reference

12 December 2020

Inhibition of gingival fibroblast growth by Bacteroides gingivalis

1 reference

12 December 2020

Kindler syndrome: report of two cases and review of the literature

1 reference

12 December 2020

Changes in cell phenotype during regeneration of junctional epithelium of human gingiva in vitro

1 reference

12 December 2020

Kindler syndrome: report of a case with ultrastructural study and review of the literature

1 reference

12 December 2020

Early-onset periodontitis associated with Weary-Kindler syndrome: a case report

1 reference

12 December 2020

Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa.

1 reference

12 December 2020

Abnormal deposition of type VII collagen in Kindler syndrome

1 reference

12 December 2020

The Talin head domain binds to integrin beta subunit cytoplasmic tails and regulates integrin activation

1 reference

12 December 2020

Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy

1 reference

12 December 2020

Migfilin and its binding partners: from cell biology to human diseases

1 reference

12 December 2020

An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

The Kindlins: subcellular localization and expression during murine development

1 reference

12 December 2020

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

1 reference

12 December 2020

Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.

1 reference

12 December 2020

Identifiers

DOI

10.1902/JOP.2008.070167

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18454678%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18454678%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

1 reference