Biology:LMX1B
From HandWiki
LIM homeobox transcription factor 1-beta, also known as LMX1B, is a protein which in humans is encoded by the LMX1B gene.[1][2]
Function
LMX1B is a LIM homeobox transcription factor which plays a central role in dorso-ventral patterning of the vertebrate limb.[3]
Clinical significance
Loss-of-function mutations in the LMX1B gene are associated with Nail-patella syndrome.[4]
References
- ↑ "Entrez Gene: LMX1B LIM homeobox transcription factor 1, beta". https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=4010.
- ↑ "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. December 1997. doi:10.1006/geno.1997.5075. PMID 9441763.
- ↑ "Characterization of migration behavior of myogenic precursor cells in the limb bud with respect to Lmx1b expression". Anat. Embryol. 208 (1): 7–18. April 2004. doi:10.1007/s00429-003-0373-y. PMID 15007643.
- ↑ "Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome". Nat. Genet. 19 (1): 47–50. May 1998. doi:10.1038/ng0598-47. PMID 9590287.
Further reading
- "Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma.". Mol. Vis. 13: 639–48. 2007. 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. 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. 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. 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.
External links
- GeneReviews/NIH/NCBI/UW entry on Nail-Patella Syndrome
- LIM+homeobox+transcription+factor+1+beta at the US National Library of Medicine Medical Subject Headings (MeSH)
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