[cite web | title = Entrez Gene: C20orf42 chromosome 20 open reading frame 42| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55612| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=White SJ, McLean WH |title=Kindler surprise: mutations in a novel actin-associated protein cause Kindler syndrome. |journal=J. Dermatol. Sci. |volume=38 |issue= 3 |pages= 169–75 |year= 2005 |pmid= 15927810 |doi= 10.1016/j.jdermsci.2004.12.026
*cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=
*cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, "et al." |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=
*cite journal | author=Wang HY, Lin W, Dyck JA, "et al." |title=SRPK2: a differentially expressed SR protein-specific kinase involved in mediating the interaction and localization of pre-mRNA splicing factors in mammalian cells. |journal=J. Cell Biol. |volume=140 |issue= 4 |pages= 737–50 |year= 1998 |pmid= 9472028 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Jobard F, Bouadjar B, Caux F, "et al." |title=Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. |journal=Hum. Mol. Genet. |volume=12 |issue= 8 |pages= 925–35 |year= 2004 |pmid= 12668616 |doi=
*cite journal | author=Weinstein EJ, Bourner M, Head R, "et al." |title=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. |journal=Biochim. Biophys. Acta |volume=1637 |issue= 3 |pages= 207–16 |year= 2003 |pmid= 12697302 |doi=
*cite journal | author=Siegel DH, Ashton GH, Penagos HG, "et al." |title=Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. |journal=Am. J. Hum. Genet. |volume=73 |issue= 1 |pages= 174–87 |year= 2003 |pmid= 12789646 |doi=
*cite journal | author=Kloeker S, Major MB, Calderwood DA, "et al." |title=The Kindler syndrome protein is regulated by transforming growth factor-beta and involved in integrin-mediated adhesion. |journal=J. Biol. Chem. |volume=279 |issue= 8 |pages= 6824–33 |year= 2004 |pmid= 14634021 |doi= 10.1074/jbc.M307978200
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Ashton GH, McLean WH, South AP, "et al." |title=Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome. |journal=J. Invest. Dermatol. |volume=122 |issue= 1 |pages= 78–83 |year= 2004 |pmid= 14962093 |doi= 10.1046/j.0022-202X.2003.22136.x
*cite journal | author=Fassihi H, Wessagowit V, Jones C, "et al." |title=Neonatal diagnosis of Kindler syndrome. |journal=J. Dermatol. Sci. |volume=39 |issue= 3 |pages= 183–5 |year= 2005 |pmid= 16051467 |doi= 10.1016/j.jdermsci.2005.05.007
*cite journal | author=Has C, Wessagowit V, Pascucci M, "et al." |title=Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene. |journal=J. Invest. Dermatol. |volume=126 |issue= 8 |pages= 1776–83 |year= 2006 |pmid= 16675959 |doi= 10.1038/sj.jid.5700339
*cite journal | author=Herz C, Aumailley M, Schulte C, "et al." |title=Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes. |journal=J. Biol. Chem. |volume=281 |issue= 47 |pages= 36082–90 |year= 2007 |pmid= 17012746 |doi= 10.1074/jbc.M606259200
*cite journal | author=Sadler E, Klausegger A, Muss W, "et al." |title=Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement. |journal=Archives of dermatology |volume=142 |issue= 12 |pages= 1619–24 |year= 2007 |pmid= 17178989 |doi= 10.1001/archderm.142.12.1619
*cite journal | author=Lai-Cheong JE, Liu L, Sethuraman G, "et al." |title=Five new homozygous mutations in the KIND1 gene in Kindler syndrome. |journal=J. Invest. Dermatol. |volume=127 |issue= 9 |pages= 2268–70 |year= 2007 |pmid= 17460733 |doi= 10.1038/sj.jid.5700830
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