FERMT1
FERMT1 (Fermitin family member 1) هوَ بروتين يُشَفر بواسطة جين FERMT1 في الإنسان.[1][2][3]
المراجع
- "Loss of Kindlin-1, a Human Homolog of the Caenorhabditis elegans Actin–Extracellular-Matrix Linker Protein UNC-112, Causes Kindler Syndrome"، Am J Hum Genet، 73 (1): 174–87، يونيو 2003، doi:10.1086/376609، PMC 1180579، PMID 12789646.
- "Entrez Gene: C20orf42 chromosome 20 open reading frame 42"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "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"، Biochim Biophys Acta، 1637 (3): 207–16، أبريل 2003، doi:10.1016/S0925-4439(03)00035-8، PMID 12697302.
قراءة متعمقة
- "Kindler surprise: mutations in a novel actin-associated protein cause Kindler syndrome"، J. Dermatol. Sci.، 38 (3): 169–75، 2005، doi:10.1016/j.jdermsci.2004.12.026، PMID 15927810.
- "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides"، Gene، 138 (1–2): 171–4، 1994، doi:10.1016/0378-1119(94)90802-8، PMID 8125298.
- "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library"، Gene، 200 (1–2): 149–56، 1997، doi:10.1016/S0378-1119(97)00411-3، PMID 9373149.
- "SRPK2: A Differentially Expressed SR Protein-specific Kinase Involved in Mediating the Interaction and Localization of Pre-mRNA Splicing Factors in Mammalian Cells"، J. Cell Biol.، 140 (4): 737–50، 1998، doi:10.1083/jcb.140.4.737، PMC 2141757، PMID 9472028.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences"، Proc. Natl. Acad. Sci. U.S.A.، 99 (26): 16899–903، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome"، Hum. Mol. Genet.، 12 (8): 925–35، 2004، doi:10.1093/hmg/ddg097، PMID 12668616.
- "The Kindler syndrome protein is regulated by transforming growth factor-beta and involved in integrin-mediated adhesion"، J. Biol. Chem.، 279 (8): 6824–33، 2004، doi:10.1074/jbc.M307978200، PMID 14634021.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs"، Nat. Genet.، 36 (1): 40–5، 2004، doi:10.1038/ng1285، PMID 14702039.
- "Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome"، J. Invest. Dermatol.، 122 (1): 78–83، 2004، doi:10.1046/j.0022-202X.2003.22136.x، PMID 14962093.
- "Neonatal diagnosis of Kindler syndrome"، J. Dermatol. Sci.، 39 (3): 183–5، 2005، doi:10.1016/j.jdermsci.2005.05.007، PMID 16051467.
- "Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene"، J. Invest. Dermatol.، 126 (8): 1776–83، 2006، doi:10.1038/sj.jid.5700339، PMID 16675959.
- "Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes"، J. Biol. Chem.، 281 (47): 36082–90، 2007، doi:10.1074/jbc.M606259200، PMID 17012746.
- "Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement"، Archives of Dermatology، 142 (12): 1619–24، 2007، doi:10.1001/archderm.142.12.1619، PMID 17178989.
- "Five new homozygous mutations in the KIND1 gene in Kindler syndrome"، J. Invest. Dermatol.، 127 (9): 2268–70، 2007، doi:10.1038/sj.jid.5700830، PMID 17460733.
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بوابة الكيمياء الحيوية
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