Citations for
1PITX2, TFAP2A
A Functional Variant Associated with Atrial Fibrillation Regulates PITX2c Expression through TFAP2a.
Ye J, Tucker NR, Weng LC, Clauss S, Lubitz SA, Ellinor PT.
Am J Hum Genet 99(6):1281-1291. doi: 10.1016/j.ajhg.2016.10.001. 2016
2PITX2
PITX2 Modulates Atrial Membrane Potential and the Antiarrhythmic Effects of Sodium-Channel Blockers.
Syeda F, Holmes AP, Yu TY, Tull S, Kuhlmann SM, Pavlovic D, Betney D, Riley G, Kucera JP, Jousset F, de Groot JR, Rohr S, Brown NA, Fabritz L, Kirchhof P.
J Am Coll Cardiol 68(17):1881-1894. doi: 10.1016/j.jacc.2016.07.766. 2016
3LEF1, PITX2, SOX2
Sox2 and Lef-1 interact with Pitx2 to regulate incisor development and stem cell renewal.
Sun Z, Yu W, Sanz Navarro M, Sweat M, Eliason S, Sharp T, Liu H, Seidel K, Zhang L, Moreno M, Lynch T, Holton NE, Rogers L, Neff T, Goodheart MJ, Michon F, Klein OD, Chai Y, Dupuy A, Engelhardt JF, Chen Z, Amendt BA.
Development 143(22):4115-4126. 2016
4PITX2
PITX2 loss-of-function mutation contributes to tetralogy of Fallot.
Sun YM, Wang J, Qiu XB, Yuan F, Xu YJ, Li RG, Qu XK, Huang RT, Xue S, Yang YQ.
Gene 577(2):258-64. doi: 10.1016/j.gene.2015.12.001. 2016
5PITX2
Pitx2 impairs calcium handling in a dose-dependent manner by modulating Wnt signalling.
Lozano-Velasco E, Hernández-Torres F, Daimi H, Serra SA, Herraiz A, Hove-Madsen L, Aránega A, Franco D.
Cardiovasc Res 109(1):55-66. doi: 10.1093/cvr/cvv207. 2016
6BARX1, ISL1, PITX1, PITX2, SIX2
Control of stomach smooth muscle development and intestinal rotation by transcription factor BARX1.
Jayewickreme CD, Shivdasani RA.
Dev Biol 405(1):21-32. doi: 10.1016/j.ydbio.2015.05.024. Epub 2015 Jun 6. 2015
7PITX2
Expression patterns and immunohistochemical localization of PITX2B transcription factor in the developing mouse heart.
Hernandez-Torres F, Franco D, Aranega AE, Navarro F.
Int J Dev Biol 59(4-6):247-54. doi: 10.1387/ijdb.140224fh. 2015
8ENPEP, PITX2
Long-range regulatory interactions at the 4q25 atrial fibrillation risk locus involve PITX2c and ENPEP.
Aguirre LA, Alonso ME, Badía-Careaga C, Rollán I, Arias C, Fernández-Mińán A, López-Jiménez E, Aránega A, Gómez-Skarmeta JL, Franco D, Manzanares M.
BMC Biol 13:26. doi: 10.1186/s12915-015-0138-0. 2015
9PITX2
Axial level-specific regulation of neuronal development: lessons from PITX2.
Waite MR, Martin DM.
J Neurosci Res 93(2):195-8. doi: 10.1002/jnr.23471. Review. 2015
10DEPDC1B, PITX2
Identification of the GTPase-activating protein DEP domain containing 1B (DEPDC1B) as a transcriptional target of Pitx2
Wu D, Zhu X, Jimenez-Cowell K, Mold AJ, Sollecito CC, Lombana N, Jiao M, Wei Q.
Exp Cell Res. Apr 10;333(1):80-92. doi: 10.1016/j.yexcr.2015.02.008. Epub 2015 Feb 19. P 2015
11GDF1, PITX2
The transcription factor Pitx2 positions the embryonic axis and regulates twinning.
Torlopp A, Khan MA, Oliveira NM, Lekk I, Soto-Jiménez LM, Sosinsky A, Stern CD.
Elife 3:e03743. doi: 10.7554/eLife.03743. 2014
12PITX2
DNA methylation of PITX2 predicts poor survival in men with prostate cancer.
Vasiljević N, Ahmad AS, Carter PD, Fisher G, Berney DM, Foster CS, Cuzick J, Lorincz AT.
Biomark Med 8(9):1143-50. doi: 10.2217/bmm.14.41. 2014
13FOXC1, PITX2
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.
French CR, Seshadri S, Destefano AL, Fornage M, Arnold CR, Gage PJ, Skarie JM, Dobyns WB, Millen KJ, Liu T, Dietz W, Kume T, Hofker M, Emery DJ, Childs SJ, Waskiewicz AJ, Lehmann OJ.
J Clin Invest 124(11):4877-81. doi: 10.1172/JCI75109. 2014
14PITX2
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
Wei D, Gong XH, Qiu G, Wang J, Yang YQ.
Int J Mol Med 33(5):1201-8. doi: 10.3892/ijmm.2014.1689. 2014
15MYF5, PITX2
Pitx2c is reactivated in the failing myocardium and stimulates myf5 expression in cultured cardiomyocytes.
Torrado M, Franco D, Hernández-Torres F, Crespo-Leiro MG, Iglesias-Gil C, Castro-Beiras A, Mikhailov AT.
PLoS One 9(3):e90561. doi: 10.1371/journal.pone.0090561. eCollection 2014. 2014
16PAXIP1, PITX2
PITX2 associates with PTIP-containing histone H3 lysine 4 methyltransferase complex.
Liu Y, Huang Y, Fan J, Zhu GZ.
Biochem Biophys Res Commun 444(4):634-7. doi: 10.1016/j.bbrc.2014.01.143. Epub 2014 Jan 31. 2014
17PITX2, PITX3
Redox regulation by Pitx2 and Pitx3 is critical for fetal myogenesis.
L'honoré A, Commčre PH, Ouimette JF, Montarras D, Drouin J, Buckingham M.
Dev Cell 29(4):392-405. doi: 10.1016/j.devcel.2014.04.006. Erratum in: Dev Cell. 2016 Dec 19;39(6):756. 2014
18LHX6, PITX2
The LIM homeodomain transcription factor LHX6: a transcriptional repressor that interacts with pituitary homeobox 2 (PITX2) to regulate odontogenesis.
Zhang Z, Gutierrez D, Li X, Bidlack F, Cao H, Wang J, Andrade K, Margolis HC, Amendt BA.
J Biol Chem 288(4):2485-500. doi: 10.1074/jbc.M112.402933. Epub 2012 Dec 10. 2013
19PITX2
PITX2c loss-of-function mutations responsible for congenital atrial septal defects.
Yuan F, Zhao L, Wang J, Zhang W, Li X, Qiu XB, Li RG, Xu YJ, Xu L, Qu XK, Fang WY, Yang YQ.
Int J Med Sci 10(10):1422-9. doi: 10.7150/ijms.6809. 2013
20PITX2
Pitx2-mediated cardiac outflow tract remodeling.
Ma HY, Xu J, Eng D, Gross MK, Kioussi C.
Dev Dyn 242(5):456-68. doi: 10.1002/dvdy.23934. 2013
21FGF9, PITX2, TGFB1
Relationship between the localization of fibroblast growth factor 9 in prostate cancer cells and postoperative recurrence.
Teishima J, Shoji K, Hayashi T, Miyamoto K, Ohara S, Matsubara A.
Prostate Cancer Prostatic Dis 15(1):8-14. doi: 10.1038/pcan.2011.48. Epub 2011 Oct 18. 2012
22CITED2, NODAL, PITX2
CITED2 mutation links congenital heart defects to dysregulation of the cardiac gene VEGF and PITX2C expression.
Li Q, Pan H, Guan L, Su D, Ma X.
Biochem Biophys Res Commun 423(4):895-9. doi: 10.1016/j.bbrc.2012.06.099. Epub 2012 Jun 23. 2012
23DEL6PD, FOXC1, PITX2
PITX2 and FOXC1 spectrum of mutations in ocular syndromes.
Reis LM, Tyler RC, Volkmann Kloss BA, Schilter KF, Levin AV, Lowry RB, Zwijnenburg PJ, Stroh E, Broeckel U, Murray JC, Semina EV.
Eur J Hum Genet 20(12):1224-33. doi: 10.1038/ejhg.2012.80. Epub 2012 May 9. 2012
24PITX2
Pitx2 is an upstream activator of extraocular myogenesis and survival.
Zacharias AL, Lewandoski M, Rudnicki MA, Gage PJ.
Dev Biol 349(2):395-405. Epub 2010 Oct 28. 2011
25PITX2, WDR5
WD repeat-containing protein 5, a ubiquitously expressed histone methyltransferase adaptor protein, regulates smooth muscle cell-selective gene activation through interaction with pituitary homeobox 2.
Gan Q, Thiébaud P, Thézé N, Jin L, Xu G, Grant P, Owens GK.
J Biol Chem 286(24):21853-64. Epub 2011 Apr 28. 2011
26PITX2
PITX2 is involved in stress response in cultured human trabecular meshwork cells through regulation of SLC13A3.
Strungaru MH, Footz T, Liu Y, Berry FB, Belleau P, Semina EV, Raymond V, Walter MA.
Invest Ophthalmol Vis Sci. 52(10):7625-33. 2011
27CDH2, PITX2, SHROOM3
Shroom3 and a Pitx2-N-cadherin pathway function cooperatively to generate asymmetric cell shape changes during gut morphogenesis.
Plageman TF Jr, Zacharias AL, Gage PJ, Lang RA.
Dev Biol 357(1):227-34. Epub 2011 Jun 25. 2011
28DEL4Q, PITX2, RIEG1
Longitudinal observation of a patient with Rieger syndrome and interstitial deletion 4 (q25-q31.1).
Moreira L, Schinzel A, Baumer A, Pinto P, Góes F, Falcăo Mde L, Barbosa AL, Riegel M.
Am J Med Genet A 152A(4):977-81.PMID: 20358612 2010
29PITX2
Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous.
Arikawa A, Yoshida S, Yoshikawa H, Ishikawa K, Yamaji Y, Arita RI, Ueno A, Ishibashi T.
Eye (Lond). 24(2):391-3. 2010
30PITX2, SHOX2
Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification.
Wang J, Klysik E, Sood S, Johnson RL, Wehrens XH, Martin JF.
Proc Natl Acad Sci U S A 107(21):9753-8. Epub 2010 May 10.PMID: 20457925 2010
31AXR1, FOXC1, PITX2, RIEG1
Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations.
Tümer Z, Bach-Holm D.
Eur J Hum Genet 17(12):1527-39. Epub 2009 Jun 10. 2009
32PAWR, PITX2, RIEG1
Human PRKC apoptosis WT1 regulator is a novel PITX2-interacting protein that regulates PITX2 transcriptional activity in ocular cells.
Acharya M, Lingenfelter DJ, Huang L, Gage PJ, Walter MA.
J Biol Chem 284(50):34829-38. Epub 2009 Oct 2.PMID: 19801652 2009
33HMGN2, PITX2
Chromatin-associated HMG-17 is a major regulator of homeodomain transcription factor activity modulated by Wnt/beta-catenin signaling.
Amen M, Espinoza HM, Cox C, Liang X, Wang J, Link TM, Brennan RG, Martin JF, Amendt BA.
Nucleic Acids Res 36(2):462-76. Epub 2007 Nov 27. 2008
34PITX2
Pitx2 regulates gonad morphogenesis.
RodrĂ­guez-LeĂłn J, RodrĂ­guez Esteban C, MartĂ­ M, Santiago-Josefat B, Dubova I, Rubiralta X, IzpisĂşa Belmonte JC.
Proc Natl Acad Sci U S A 105(32):11242-7. Epub 2008 Aug 4. 2008
35FOXJ1, PITX2, RIEG1
Novel expression and transcriptional regulation of FoxJ1 during oro-facial morphogenesis.
Venugopalan SR, Amen MA, Wang J, Wong L, Cavender AC, D'Souza RN, Akerlund M, Brody SL, Hjalt TA, Amendt BA.
Hum Mol Genet 17(23):3643-54. Epub 2008 Aug 22. 2008
36PITX2
Pitx2 is functionally important in the early stages of vascular smooth muscle cell differentiation.
Shang Y, Yoshida T, Amendt BA, Martin JF, Owens GK.
J Cell Biol 181(3):461-73.PMID: 18458156 2008
37PITX2, TBX1
Cranial muscle defects of Pitx2 mutants result from specification defects in the first branchial arch.
Shih HP, Gross MK, Kioussi C.
Proc Natl Acad Sci U S A 104(14):5907-12. Epub 2007 Mar 23. 2007
38AXR1, FOXC1, PITX2, RIEG1
Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.
Strungaru MH, Dinu I, Walter MA.
Invest Ophthalmol Vis Sci 48(1):228-37. 2007
39RIEG1, PITX2, ENPEP
Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome.
Engenheiro E, Saraiva J, Carreira I, Ramos L, Ropers HH, Silva E, Tommerup N, TŸmer Z.
Clin Genet 72(5):464-70. Epub 2007 Sep 10. 2007
40ASMD2, ASMD3, ASMD4, ASMD5, ASMFD, AXR1, AXR2, FOXC1, IRID1, MAF, PAX6, PITX2, RIEG1, RIEG2
Molecular and developmental mechanisms of anterior segment dysgenesis.
Sowden JC.
Eye 21(10):1310-8. Review. 2007
41PITX2, PLOD2
Involvement of Pitx2, a homeodomain transcription factor, in hypothyroidism associated reproductive disorders.
Ghosh P, Saha SK, Nandi SS, Bhattacharya S, Roy SS.
Cell Physiol Biochem 20(6):887-98.PMID: 17982271 2007
42PITX2
Haemodynamics determined by a genetic programme govern asymmetric development of the aortic arch.
Yashiro K, Shiratori H, Hamada H.
Nature. 450(7167):180-1. 2007
43PITX2
Pitx2c and Nkx2-5 are required for the formation and identity of the pulmonary myocardium.
Mommersteeg MT, Brown NA, Prall OW, de Gier-de Vries C, Harvey RP, Moorman AF, Christoffels VM.
Circ Res. 101(9):902-9. 2007
44DEL4Q, PITX2, RIEG1
Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome.
Engenheiro E, Saraiva J, Carreira I, Ramos L, Ropers HH, Silva E, Tommerup N, Tümer Z.
Clin Genet 72(5):464-70. Epub 2007 Sep 10.PMID: 17850355 2007
45RIEG1, PITX2, AXRI, FOXC1
Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis.
Berry FB, Lines MA, Oas JM, Footz T, Underhill DA, Gage PJ, Walter MA.
Hum Mol Genet 15(6):905-19. Epub 2006 Jan 31. 2006
46LEFTY1, LEFTY2, PITX2, RTTN
Localization of candidate regions for a novel gene for Kartagener syndrome.
Gutierrez-Roelens I, Sluysmans T, Jorissen M, Amyere M, Vikkula M.
Eur J Hum Genet 14(7):809-15. Epub 2006 Apr 26. 2006
47AXR1, FOXC1, PITX2, RIEG1
Novel Mutations of FOXC1 and PITX2 in Patients with Axenfeld-Rieger Malformations.
Weisschuh N, Dressler P, Schuettauf F, Wolf C, Wissinger B, Gramer E.
Invest Ophthalmol Vis Sci 47(9):3846-52. 2006
48PITX2, RIEG1
A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy.
Kniestedt C, Taralczak M, Thiel MA, Stuermer J, Baumer A, Gloor BP.
Ophthalmology 113(10):1791.e1-8. Epub 2006 Jul 31. 2006
49PITX2
Expression of the homeobox gene Pitx2 in neural crest is required for optic stalk and ocular anterior segment development.
Evans AL, Gage PJ.
Hum Mol Genet 14(22):3347-59. Epub 2005 Oct 3. 2005
50PITX2
PITX2, beta-catenin and LEF-1 interact to synergistically regulate the LEF-1 promoter.
Vadlamudi U, Espinoza HM, Ganga M, Martin DM, Liu X, Engelhardt JF, Amendt BA.
J Cell Sci. 118(Pt 6):1129-37. 2005
51CITED2, PITX2, TFAP2A, NODAL
Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway.
Bamforth SD, Braganca J, Farthing CR, Schneider JE, Broadbent C, Michell AC, Clarke K, Neubauer S, Norris D, Brown NA, Anderson RH, Bhattacharya S.
Nat Genet 36(11):1189-96. Epub 2004 Oct 10. 2004
52PITX2, RIEG1
Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations.
Lines MA, Kozlowski K, Kulak SC, Allingham RR, Heon E, Ritch R, Levin AV, Shields MB, Damji KF, Newlin A, Walter MA.
Invest Ophthalmol Vis Sci 45(3):828-33. 2004
53PITX2, RGDC
Mutation in PITX2 is associated with ring dermoid of the cornea.
Xia K, Wu L, Liu X, Xi X, Liang D, Zheng D, Cai F, Pan Q, Long Z, Dai H, Hu Z, Tang B, Zhang Z, Xia J.
J Med Genet 41(12):e129. No abstract available. 2004
54GCM1, PITX2
Interaction, cooperative promoter modulation, and renal colocalization of GCMa and Pitx2.
Schubert SW, Kardash E, Khan MA, Cheusova T, Kilian K, Wegner M, Hashemolhosseini S.
J Biol Chem. 279(48):50358-65. 2004
55NKX2-5, NPPA, PLOD1, PITX2
PITX2 isoform-specific regulation of atrial natriuretic factor expression: synergism and repression with Nkx2.5.
Ganga M, Espinoza HM, Cox CJ, Morton L, Hjalt TA, Lee Y, Amendt BA.
J Biol Chem 278(25):22437-45. Epub 2003 Apr 11. 2003
56PITX1, PITX2
Pitx factors are involved in basal and hormone-regulated activity of the human prolactin promoter.
Quentien MH, Manfroid I, Moncet D, Gunz G, Muller M, Grino M, Enjalbert A, Pellegrini I.
J Biol Chem 277(46):44408-16. Epub 2002 Sep 9. 2002
57CYP1B1, MYOC, PITX2
Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene.
Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Heon E.
Am J Hum Genet 70(2):448-60. 2002
58PITX2
A molecular basis for differential developmental anomalies in Axenfeld-Rieger syndrome.
Espinoza HM, Cox CJ, Semina EV, Amendt BA.
Hum Mol Genet 11(7):743-53. 2002
59PITX2
Differential regulation of gene expression by PITX2 isoforms.
Cox CJ, Espinoza HM, McWilliams B, Chappell K, Morton L, Hjalt TA, Semina EV, Amendt BA.
J Biol Chem 277(28):25001-10. Epub 2002 Apr 10. 2002
60PITX2
Identification of a Wnt/Dvl/beta-Catenin --> Pitx2 pathway mediating cell-type-specific proliferation during development.
Kioussi C, Briata P, Baek SH, Rose DW, Hamblet NS, Herman T, Ohgi KA, Lin C, Gleiberman A, Wang J, Brault V, Ruiz-Lozano P, Nguyen HD, Kemler R, Glass CK, Wynshaw-Boris A, Rosenfeld MG.
Cell. 111(5):673-85. 2002
61PITX2
Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome.
Priston M, Kozlowski K, Gill D, Letwin K, Buys Y, Levin AV, Walter MA, Heon E.
Hum Mol Genet 10(16):1631-8. 2001
62PITX2
Two-step regulation of left-right asymmetric expression of Pitx2: initiation by nodal signaling and maintenance by Nkx2.
Shiratori H, Sakuma R, Watanabe M, Hashiguchi H, Mochida K, Sakai Y, Nishino J, Saijoh Y, Whitman M, Hamada H.
Mol Cell 7(1):137-49. 2001
63PITX2
Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth development.
Green PD, Hjalt TA, Kirk DE, Sutherland LB, Thomas BL, Sharpe PT, Snead ML, Murray JC, Russo AF, Amendt BA.
Gene Expr. 9(6):265-81. 2001
64PITX2
Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders.
Kozlowski K, Walter MA.
Hum Mol Genet 9(14):2131-9. 2000
65MYL1, MYL2, MYL3, PITX2
Multiple transcriptional domains, with distinct left and right components, in the atrial chambers of the developing heart.
Franco D, Campione M, Kelly R, Zammit PS, Buckingham M, Lamers WH, Moorman AF.
Circ Res 87(11):984-91. 2000
66PITX2, RIEG1
Threading analysis of the Pitx2 homeodomain: Predicted structural effects of mutations causing Rieger syndrome and iridogoniodysgenesis.
Banerjee-Basu S, Baxevanis AD.
Hum Mutat 14(4):312-319 1999
67PITX2
Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis.
Lin CR, Kioussi C, O'Connell S, Briata P, Szeto D, Liu F, Izpisua-Belmonte JC, Rosenfeld MG.
Nature 401(6750):279-82 1999
68PITX2, RIEG1
Function of Rieger syndrome gene in left-right asymmetry and craniofacial development.
Lu MF, Pressman C, Dyer R, Johnson RL, Martin JF.
Nature 401(6750):276-8 1999
69LEFTY2, PITX2
The novel Cer-like protein Caronte mediates the establishment of embryonic left-right asymmetry.
Rodriguez Esteban C, Capdevila J, Economides AN, Pascual J, Ortiz A, Izpisua Belmonte JC.
Nature 401(6750):243-51. 1999
70PITX2
Expression of the members of the Ptx family of transcription factors in human pituitary adenomas.
Pellegrini-Bouiller I, Manrique C, Gunz G, Grino M, Zamora AJ, Figarella-Branger D, Grisoli F, Jaquet P, Enjalbert A.
J Clin Endocrinol Metab. 84(6):2212-20. 1999
71IHG2, PITX2
Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene.
Alward WL, Semina EV, Kalenak JW, Heon E, Sheth BP, Stone EM, Murray JC.
Am J Ophthalmol 125(1):98-100. 1998
72PITX2, RIEG1
Construction and analysis of a sequence-ready map in 4q25 : Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks 90 kb upstream of this gene.
Flomen RH, Vatcheva R, Gorman PA, Baptista PR, Groet J, Barisic I, Ligutic I, Nizetic D.
Genomics 47(3):409-13. 1998
73IHG2, PITX2
Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome.
Kulak SC, Kozlowski K, Semina EV, Pearce WG, Walter MA.
Hum Mol Genet 7(7):1113-7. 1998
74PITX2
Pitx2 participates in the late phase of the pathway controlling left-right asymmetry.
Piedra ME, Icardo JM, Albajar M, Rodriguez-Rey JC, Ros MA.
Cell 94(3):319-24. 1998
75PITX2
The transcription factor Pitx2 mediates situs-specific morphogenesis in response to left-right asymmetric signals.
Logan M, Pagan-Westphal SM, Smith DM, Paganessi L, Tabin CJ.
Cell 94(3):307-17. 1998
76PITX2
Pitx2 determines left-right asymmetry of internal organs in vertebrates.
Ryan AK, Blumberg B, Rodriguez-Esteban C, Yonei-Tamura S, Tamura K, Tsukui T, de la Pena J, Sabbagh W, Greenwald J, Choe S, Norris DP, Robertson EJ, Evans RM, Rosenfeld MG, Izpisua Belmonte JC.
Nature 394(6693):545-51. 1998
77RIEG1, PITX2
The molecular basis of Rieger syndrome. Analysis of Pitx2 homeodomain protein activities.
Amendt BA, Sutherland LB, Semina EV, Russo AF.
J Biol Chem 273(32):20066-72. 1998
78PITX2
Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation.
Gage PJ, Camper SA.
Hum Mol Genet 6(3):457-64. 1997
79RIEG1, PITX2
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome.
Semina EV, Reiter R, Leysens NJ, Alward WL, Small KW, Datson NA, Siegel-Bartelt J, Bierke-Nelson D, Bitoun P, Zabel BU, Carey JC, Murray JC.
Nat Genet 14(4):392-9. 1996