Colocalization of kindlin-1, kindlin-2, and migfilin at keratinocyte focal adhesion and relevance to the pathophysiology of Kindler syndrome.
暂无分享,去创建一个
J. McGrath | S. Ussar | I. Hart | J. Lai-Cheong | K. Arita | J. McGrath
[1] J. McGrath,et al. Unusual molecular findings in Kindler syndrome , 2007, The British journal of dermatology.
[2] L. Liu,et al. Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome , 2007, The British journal of dermatology.
[3] Vinod K. Sharma,et al. Five new homozygous mutations in the KIND1 gene in Kindler syndrome. , 2007, The Journal of investigative dermatology.
[4] U. Schlötzer-Schrehardt,et al. Kindlin-1 Is a Phosphoprotein Involved in Regulation of Polarity, Proliferation, and Motility of Epidermal Keratinocytes* , 2006, Journal of Biological Chemistry.
[5] Hao-Ven Wang,et al. The Kindlins: subcellular localization and expression during murine development. , 2006, Experimental cell research.
[6] V. Gkretsi,et al. Migfilin Interacts with Vasodilator-stimulated Phosphoprotein (VASP) and Regulates VASP Localization to Cell-Matrix Adhesions and Migration* , 2006, Journal of Biological Chemistry.
[7] J. McGrath,et al. Kindler syndrome: a new mutation and new diagnostic possibilities. , 2006, Archives of dermatology.
[8] J. McGrath,et al. Neonatal diagnosis of Kindler syndrome. , 2005, Journal of dermatological science.
[9] J. McGrath,et al. An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene , 2005, Clinical and experimental dermatology.
[10] Chuanyue Wu. Migfilin and its binding partners: from cell biology to human diseases , 2005, Journal of Cell Science.
[11] M. Hentze,et al. Nonsense-mediated decay approaches the clinic , 2004, Nature Genetics.
[12] M. Beckerle,et al. The Kindler Syndrome Protein Is Regulated by Transforming Growth Factor-β and Involved in Integrin-mediated Adhesion* , 2004, Journal of Biological Chemistry.
[13] L. Maquat. Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics , 2004, Nature Reviews Molecular Cell Biology.
[14] H. Feiler,et al. Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. , 2003, American journal of human genetics.
[15] J. Weissenbach,et al. Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. , 2003, Human molecular genetics.
[16] Y. Tu,et al. Migfilin and Mig-2 Link Focal Adhesions to Filamin and the Actin Cytoskeleton and Function in Cell Shape Modulation , 2003, Cell.
[17] L. Maquat,et al. A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance. , 1998, Trends in biochemical sciences.
[18] J. Hornung,et al. Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line , 1988, The Journal of cell biology.
[19] T. Kindler. CONGENITAL POIKILODERMA WITH TRAUMATIC BULLA FOKMATION AND PROGRESSIVE CUTANEOUS ATROPHY. , 1954, The British journal of dermatology.
[20] C. Herz,et al. Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement. , 2007, Acta dermato-venereologica.
[21] J. McGrath,et al. Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome. , 2004, The Journal of investigative dermatology.
[22] H. Dietz,et al. Nonsense-mediated mRNA decay in health and disease. , 1999, Human molecular genetics.