Citations for
1LDB1, LMX1B
Ldb1 Is Essential for the Development of Isthmic Organizer and Midbrain Dopaminergic Neurons.
Kim S, Zhao Y, Lee JM, Kim WR, Gorivodsky M, Westphal H, Geum D.
Stem Cells Dev 25(13):986-94. doi: 10.1089/scd.2015.0307. Epub 2016 Jun 16. 2016
2LMX1B, OTX2
Otx2 Requires Lmx1b to Control the Development of Mesodiencephalic Dopaminergic Neurons.
Sherf O, Nashelsky Zolotov L, Liser K, Tilleman H, Jovanovic VM, Zega K, Jukic MM, Brodski C.
PLoS One 10(10):e0139697. doi: 10.1371/journal.pone.0139697. eCollection 2015. 2015
3HOXB8, LMX1B
Hoxb8 intersection defines a role for Lmx1b in excitatory dorsal horn neuron development, spinofugal connectivity, and nociception.
Szabo NE, da Silva RV, Sotocinal SG, Zeilhofer HU, Mogil JS, Kania A.
J Neurosci 35(13):5233-46. doi: 10.1523/JNEUROSCI.4690-14.2015. 2015
4LMX1B, PSPC1, SFPQ
LMX1B is part of a transcriptional complex with PSPC1 and PSF.
Hoekstra EJ, Mesman S, de Munnik WA, Smidt MP.
PLoS One 8(1):e53122. doi: 10.1371/journal.pone.0053122. Epub 2013 Jan 4. 2013
5LMX1A, LMX1B
Lmx1a and lmx1b function cooperatively to regulate proliferation, specification, and differentiation of midbrain dopaminergic progenitors.
Yan CH, Levesque M, Claxton S, Johnson RL, Ang SL.
J Neurosci 31(35):12413-25. doi: 10.1523/JNEUROSCI.1077-11.2011. 2011
6FOXA2, LMX1A, LMX1B
Lmx1a and Lmx1b cooperate with Foxa2 to coordinate the specification of dopaminergic neurons and control of floor plate cell differentiation in the developing mesencephalon.
Nakatani T, Kumai M, Mizuhara E, Minaki Y, Ono Y.
Dev Biol 339(1):101-13. doi: 10.1016/j.ydbio.2009.12.017. Epub 2009 Dec 24. 2010
7LMX1B, NPHS2
The transcriptional regulation of podocin (NPHS2) by Lmx1b and a promoter single nucleotide polymorphism.
Harendza S, Stahl RA, Schneider A.
Cell Mol Biol Lett 14(4):679-91. Epub 2009 Jun 27.PMID: 19562271 2009
8LMX1A, LMX1B
Overlapping function of Lmx1a and Lmx1b in anterior hindbrain roof plate formation and cerebellar growth.
Mishima Y, Lindgren AG, Chizhikov VV, Johnson RL, Millen KJ.
J Neurosci 29(36):11377-84. doi: 10.1523/JNEUROSCI.0969-09.2009. 2009
9LMX1B, NPS1
Identification of entire LMX1B gene deletions in nail patella syndrome: evidence for haploinsufficiency as the main pathogenic mechanism underlying dominant inheritance in man.
Bongers EM, de Wijs IJ, Marcelis C, Hoefsloot LH, Knoers NV.
Eur J Hum Genet 16(10):1240-4. Epub 2008 Apr 16. 2008
10NPS1, LMX1B, NR5A1
Ovotestes and XY sex reversal in a female with an interstitial 9q33.3-q34.1 deletion encompassing NR5A1 and LMX1B causing features of genitopatellar syndrome.
Schlaubitz S, Yatsenko SA, Smith LD, Keller KL, Vissers LE, Scott DA, Cai WW, Reardon W, Abdul-Rahman OA, Lammer EJ, Lifchez CA, Magenis E, Veltman JA, Stankiewicz P, Zabel BU, Lee B.
Am J Med Genet A 143(10):1071-81. 2007
11LMX1B, NPS1
Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma.
Millá E, Hernan I, Gamundi MJ, Martínez-Gimeno M, Carballo M.
Mol Vis 13:639-48. 2007
12NPS1, LMX1B
A neurological phenotype in nail patella syndrome (NPS) patients illuminated by studies of murine Lmx1b expression.
Dunston JA, Reimschisel T, Ding YQ, Sweeney E, Johnson RL, Chen ZF, McIntosh I.
Eur J Hum Genet 13(3):330-5. 2005
13LMX1B, NPS1
Functional Characterization of LMX1B Mutations Associated with Nail-Patella Syndrome.
Sato U, Kitanaka S, Sekine T, Takahashi S, Ashida A, Igarashi T.
Pediatr Res 57(6):783-8. Epub 2005 Mar 17. 2005
14PAX2, LMX1B, NPS1
Interaction of the LMX1B and PAX2 gene products suggests possible molecular basis of differential phenotypes in Nail-Patella syndrome.
Marini M, Giacopelli F, Seri M, Ravazzolo R.
Eur J Hum Genet 13(6):789-92. 2005
15NPS1, LMX1B
Genotype-phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy.
Bongers EM, Huysmans FT, Levtchenko E, de Rooy JW, Blickman JG, Admiraal RJ, Huygen PL, Cruysberg JR, Toolens PA, Prins JB, Krabbe PF, Borm GF, Schoots J, van Bokhoven H, van Remortele AM, Hoefsloot LH, van Kampen A, Knoers NV.
Eur J Hum Genet 13(8):935-46. 2005
16LMX1B, NPS1
The human LMX1B gene: transcription unit, promoter, and pathogenic mutations.
Dunston JA, Hamlington JD, Zaveri J, Sweeney E, Sibbring J, Tran C, Malbroux M, O'Neill JP, Mountford R, McIntosh I.
Genomics 84(3):565-76. 2004
17LMX1B, NKX2-2
Lmx1b is essential for the development of serotonergic neurons.
Ding YQ, Marklund U, Yuan W, Yin J, Wegman L, Ericson J, Deneris E, Johnson RL, Chen ZF.
Nat Neurosci 6(9):933-8. 2003
18LMX1B, NPS1
In vivo expression of putative LMX1B targets in nail-patella syndrome kidneys.
Heidet L, Bongers EM, Sich M, Zhang SY, Loirat C, Meyrier A, Broyer M, Landthaler G, Faller B, Sado Y, Knoers NV, Gubler MC.
Am J Pathol 163(1):145-55. 2003
19LMX1B, NPS1, NPHS2
The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes.
Rohr C, Prestel J, Heidet L, Hosser H, Kriz W, Johnson RL, Antignac C, Witzgall R.
J Clin Invest 109(8):1073-82. 2002
20LMX1B, NPS1
Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome.
Morello R, Zhou G, Dreyer SD, Harvey SJ, Ninomiya Y, Thorner PS, Miner JH, Cole W, Winterpacht A, Zabel B, Oberg KC, Lee B.
Nat Genet 27(2):205-8. 2001
21LDB1, LMX1B, NPS1
LMX1B transactivation and expression in nail-patella syndrome.
Dreyer SD, Morello R, German MS, Zabel B, Winterpacht A, Lunstrum GP, Horton WA, Oberg KC, Lee B.
Hum Mol Genet 9(7):1067-74. 2000
22LMX1A, LMX1B
Coordinate roles for LIM homeobox genes in directing the dorsoventral trajectory of motor axons in the vertebrate limb.
Kania A, Johnson RL, Jessell TM.
Cell 102(2):161-73. 2000
23LMX1B, NPS1
Nail-patella syndrome: identification of mutations in the LMX1B gene in Dutch families.
Knoers NV, Bongers EM, van Beersum SE, Lommen EJ, van Bokhoven H, Hol FA.
J Am Soc Nephrol 11(9):1762-6. 2000
24LMX1B, NPS1
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndrome.
Seri M, et al.
Int J Mol Med 4(3):285-90 1999
25LMX1B, NPS1
Restricted distribution of loss-of-function mutations within the LMX1B genes of nail-patella syndrome patients.
Clough MV, Hamlington JD, McIntosh I.
Hum Mutat 14(6):459-65 1999
26LMX1B, NPS1
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome.
Dreyer SD, et al.
Nat Genet 19 : 47-50. 1998
27LMX1B, NPS1
Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome.
Chen H, et al.
Nat Genet 19 : 51-55. 1998
28LMX1B, NPS1
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome.
Vollrath D, et al.
Hum Mol Genet 7 : 1091-1098. 1998
29LMX1B, NPS1
Mutation analysis of LMX1B gene in Nail-Patella syndrome patients.
McIntosh I, Dreyer SD, Clough MV, Dunston JA, Eyaid W, Roig CM, Montgomery T, Ala-Mello S, Kaitila I, Winterpacht A, Zabel B, Frydman M, Cole WG, Francomano CA, Lee B.
Am J Hum Genet 63 : 1651-1658. 1998
30LMX1B, NPS1
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome.
Vollrath D, Jaramillo-Babb VL, Clough MV, McIntosh I, Scott KM, Lichter PR, Richards JE.
Hum Mol Genet 7(7):1091-8. Erratum in: Hum Mol Genet 1998 Aug;7(8):1333. 1998
31LMX1A, LMX1B
Identification of a human LMX1 (LMX1.1)-related gene, LMX1.2 : tissue-specific expression and linkage mapping on chromosome 9.
Iannotti CA, Inoue H, Bernal E, Aoki M, Liu L, Donis-Keller H, German MS, Permutt MA.
Genomics 46(3):520-4. 1997