LMX1B
LMX1B (LIM homeobox transcription factor 1 beta) هوَ بروتين يُشَفر بواسطة جين LMX1B في الإنسان.[1][2]
المراجع
- "Entrez Gene: LMX1B LIM homeobox transcription factor 1, beta"، مؤرشف من الأصل في 06 مارس 2010.
- "Identification of a human LMX1 (LMX1.1)-related gene, LMX1.2: tissue-specific expression and linkage mapping on chromosome 9"، Genomics، 46 (3): 520–4، ديسمبر 1997، doi:10.1006/geno.1997.5075، PMID 9441763.
قراءة متعمقة
- "Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma."، Mol. Vis.، 13: 639–48، 2007، PMC 2669506، PMID 17515884.
- "A novel LMX1B nonsense mutation in a family with nail-patella syndrome."، J. Dermatol. Sci.، 52 (1): 57–60، 2008، doi:10.1016/j.jdermsci.2008.04.014، PMID 18562181.
- "A synonymous genetic alteration of LMX1B in a family with nail-patella syndrome."، The Korean Journal of Internal Medicine، 24 (3): 274–8، 2009، doi:10.3904/kjim.2009.24.3.274، PMC 2732789، PMID 19721866.
- "Association analysis of 15 polymorphisms within 10 candidate genes for antisocial behavioural traits."، Psychiatr. Genet.، 17 (5): 299–303، 2007، doi:10.1097/YPG.0b013e32816ebc9e، PMID 17728669.
- "Phenotype severity and genetic variation at the disease locus: an investigation of nail dysplasia in the nail patella syndrome."، Ann. Hum. Genet.، 69 (Pt 1): 1–8، 2005، doi:10.1046/j.1529-8817.2004.00133.x، PMID 15638822.
- "Identification of entire LMX1B gene deletions in nail patella syndrome: evidence for haploinsufficiency as the main pathogenic mechanism underlying dominant inheritance in man."، Eur. J. Hum. Genet.، 16 (10): 1240–4، 2008، doi:10.1038/ejhg.2008.83، PMID 18414507.
- "Insight into podocyte differentiation from the study of human genetic disease: nail-patella syndrome and transcriptional regulation in podocytes."، Pediatr. Res.، 51 (5): 551–8، 2002، doi:10.1203/00006450-200205000-00002، PMID 11978876.
- "[The nail-patella syndrome: rare genetically determined cause of proteinuria]"، Pol. Arch. Med. Wewn.، 116 (6): 1192–9، 2006، PMID 18634531.
- "The LIM-homeodomain transcription factor LMX1B regulates expression of NF-kappa B target genes."، Exp. Cell Res.، 315 (1): 76–96، 2009، doi:10.1016/j.yexcr.2008.10.012، PMID 18996370.
- "A novel mutation in LMX1B gene causes nail-patella syndrome in a large Chinese family."، Bone، 43 (3): 591–5، 2008، doi:10.1016/j.bone.2008.04.025، PMID 18595794.
- "In vivo expression of putative LMX1B targets in nail-patella syndrome kidneys."، Am. J. Pathol.، 163 (1): 145–55، 2003، doi:10.1016/S0002-9440(10)63638-3، PMC 1868155، PMID 12819019.
- "Do polymorphisms in transcription factors LMX1A and LMX1B influence the risk for Parkinson's disease?"، J Neural Transm، 116 (3): 333–8، 2009، doi:10.1007/s00702-009-0187-z، PMID 19189040.
- "Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypes."، Invest. Ophthalmol. Vis. Sci.، 50 (4): 1522–30، 2009، doi:10.1167/iovs.08-2483، PMID 18952915.
- "The transcriptional regulation of podocin (NPHS2) by Lmx1b and a promoter single nucleotide polymorphism."، Cell. Mol. Biol. Lett.، 14 (4): 679–91، 2009، doi:10.2478/s11658-009-0026-0، PMID 19562271.
- "Overlapping function of Lmx1a and Lmx1b in anterior hindbrain roof plate formation and cerebellar growth."، J. Neurosci.، 29 (36): 11377–84، 2009، doi:10.1523/JNEUROSCI.0969-09.2009، PMC 2765661، PMID 19741143.
- "Genotype-phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy."، Eur. J. Hum. Genet.، 13 (8): 935–46، 2005، doi:10.1038/sj.ejhg.5201446، PMID 15928687.
- "The transcription factor PITX3 is associated with sporadic Parkinson's disease."، Neurobiol. Aging، 30 (5): 731–8، 2009، doi:10.1016/j.neurobiolaging.2007.08.014، PMID 17905480.
- "LMX1B 17-bp deletion and A3243G mtDNA transition in a previously described patient."، Eur. Neurol.، 49 (3): 186–7، 2003، doi:10.1159/000069078، PMID 12646768.
- "Confirmation of CLIM2/LMX1B interaction by yeast two-hybrid screening and analysis of its involvement in nail-patella syndrome."، Int. J. Mol. Med.، 12 (1): 79–82، 2003، doi:10.3892/ijmm.12.1.79، PMID 12792813.
- "Co-occurrence of familial Mediterranean fever (FMF) heterozygote mutation and nail-patella syndrome (NPS) in 3 members of a family with LMX1B mutation analysis."، Genet. Couns.، 18 (2): 259–62، 2007، PMID 17710881.
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بوابة الكيمياء الحيوية
بوابة علم الأحياء الخلوي والجزيئي
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