| 1 | KTCN1, VSX1
|
| Contributions of VSX1 gene to keratoconus.
|
| Kalasidou G, Frydas I, Kozei A, Syrmakesi P, Loukovitis E, Sfakianakis K, Balidis M, Zachariadis Z, Tranos P, Kozeis N, Anogeianakis G.
|
| J Biol Regul Homeost Agents 32(6):1515-1518.
2018
|
| 2 | KTCN1, VSX1
|
| Analysis of VSX1 Variations in Brazilian Subjects with Keratoconus.
|
| da Silva DC, Gadelha BNB, Feitosa AFB, da Silva RG, Albuquerque TLPE, Santos DCPF, Gadelha DNB, Fonseca Schamber-Reis BL.
|
| J Ophthalmic Vis Res 13(3):266-273. doi: 10.4103/jovr.jovr_116_17.
2018
|
| 3 | CHED1, OVOL2, PPCD1, PPCD3, VSX1, ZEB1
|
| Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2.
|
| Davidson AE, Liskova P, Evans CJ, Dudakova L, Nosková L, Pontikos N, Hartmannová H, Hodaňová K, Stránecký V, Kozmík Z, Levis HJ, Idigo N, Sasai N, Maher GJ, Bellingham J, Veli N, Ebenezer ND, Cheetham ME, Daniels JT, Thaung CM, Jirsova K, Plagnol V, Filipec M, Kmoch S, Tuft SJ, Hardcastle AJ.
|
| Am J Hum Genet 98(1):75-89. doi: 10.1016/j.ajhg.2015.11.018. Epub 2015 Dec 31. 2016
|
| 4 | VSX1
|
| Maternal Vsx1 plays an essential role in regulating prechordal mesendoderm and forebrain formation in zebrafish.
|
| Xu X, He Y, Sun L, Ma S, Luo C.
|
| Dev Biol 394(2):264-76. doi: 10.1016/j.ydbio.2014.08.011. Epub 2014 Aug 21.
2014
|
| 5 | KTCN1, VSX1
|
| Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.
|
| Verma A, Das M, Srinivasan M, Prajna NV, Sundaresan P.
|
| BMC Res Notes 6:103. doi: 10.1186/1756-0500-6-103.
2013
|
| 6 | HCN4, IRX6, RCVRN, TACR3, VSX1
|
| Regulation of retinal interneuron subtype identity by the Iroquois homeobox gene Irx6.
|
| Star EN, Zhu M, Shi Z, Liu H, Pashmforoush M, Sauve Y, Bruneau BG, Chow RL.
|
| Development 139(24):4644-55. doi: 10.1242/dev.081729.
2012
|
| 7 | VSX1
|
| Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.
|
| Paliwal P, Tandon R, Dube D, Kaur P, Sharma A.
|
| Mol Vis. 17:481-5. 2011
|
| 8 | KTCN1, VSX1
|
| Mutational screening of VSX1 in keratoconus patients from the European population.
|
| Dash DP, George S, O'Prey D, Burns D, Nabili S, Donnelly U, Hughes AE, Silvestri G, Jackson J, Frazer D, Héon E, Willoughby CE.
|
| Eye (Lond) 24(6):1085-92. Epub 2009 Sep 18.PMID: 19763142 2010
|
| 9 | KTCN1, VSX1
|
| A novel VSX1 mutation identified in an individual with keratoconus in India.
|
| Paliwal P, Singh A, Tandon R, Titiyal JS, Sharma A.
|
| Mol Vis 15:2475-9.PMID: 19956409 2009
|
| 10 | KTCN1, VSX1
|
| VSX1 gene variants are associated with keratoconus in unrelated Korean patients.
|
| Mok JW, Baek SJ, Joo CK.
|
| J Hum Genet 53(9):842-9. Epub 2008 Jul 15.
2008
|
| 11 | IRX5, VSX1
|
| Genetic control of circuit function: Vsx1 and Irx5 transcription factors regulate contrast adaptation in the mouse retina.
|
| Kerschensteiner D, Liu H, Cheng CW, Demas J, Cheng SH, Hui CC, Chow RL, Wong RO.
|
| J Neurosci 28(10):2342-52.PMID: 1832208 2008
|
| 12 | VSX1, VSX2
|
| Negative regulation of Vsx1 by its paralog Chx10/Vsx2 is conserved in the vertebrate retina.
|
| Clark AM, Yun S, Veien ES, Wu YY, Chow RL, Dorsky RI, Levine EM.
|
| Brain Res 1192:99-113. Epub 2007 Jun 18.
2008
|
| 13 | VSX1
|
| No VSX1 gene mutations associated with keratoconus.
|
| Aldave AJ, Yellore VS, Salem AK, Yoo GL, Rayner SA, Yang H, Tang GY, Piconell Y, Rabinowitz YS.
|
| Invest Ophthalmol Vis Sci 47(7):2820-2. 2006
|
| 14 | VSX1
|
| Expression of VSX1 in human corneal keratocytes during differentiation into myofibroblasts in response to wound healing.
|
| Barbaro V, Di Iorio E, Ferrari S, Bisceglia L, Ruzza A, De Luca M, Pellegrini G.
|
| Invest Ophthalmol Vis Sci 47(12):5243-50. 2006
|
| 15 | ALX4, PFM1, MNX1, SCRA, VSX1, KTCN1, VSX2, MCIA, SOPT, HESX1, HOXD13, PSDY2, MSX2, PFM2, SIX3, HPE2, DCS, SHOX
|
| Homeodomain revisited: a lesson from disease-causing mutations.
|
| Chi YI.
|
| Hum Genet 116(6):433-44. Epub 2005 Feb 23. 2005
|
| 16 | KTCN1, KTCN4, VSX1
|
| VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation.
|
| Bisceglia L, Ciaschetti M, De Bonis P, Campo PA, Pizzicoli C, Scala C, Grifa M, Ciavarella P, Delle Noci N, Vaira F, Macaluso C, Zelante L.
|
| Invest Ophthalmol Vis Sci 46(1):39-45. 2005
|
| 17 | VSX1
|
| Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1.
|
| Chow RL, Volgyi B, Szilard RK, Ng D, McKerlie C, Bloomfield SA, Birch DG, McInnes RR.
|
| Proc Natl Acad Sci U S A 101(6):1754-9. Epub 2004 Jan 26. 2004
|
| 18 | VSX1
|
| VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells.
|
| Mintz-Hittner HA, Semina EV, Frishman LJ, Prager TC, Murray JC.
|
| Ophthalmology 111(4):828-36.
2004
|
| 19 | CAASDS, VSX1
|
| VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells.
|
| Mintz-Hittner HA, Semina EV, Frishman LJ, Prager TC, Murray JC.
|
| Ophthalmology 111(4):828-36.
2004
|
| 20 | KTCN1, VSX1
|
| VSX1: a gene for posterior polymorphous dystrophy and keratoconus.
|
| Heon E, Greenberg A, Kopp KK, Rootman D, Vincent AL, Billingsley G, Priston M, Dorval KM, Chow RL, McInnes RR, Heathcote G, Westall C, Sutphin JE, Semina E, Bremner R, Stone EM.
|
| Hum Mol Genet 11(9):1029-36. 2002
|
| 21 | VSX1
|
| Isolation and Characterization of a Novel Human paired-like Homeodomain-Containing Transcription Factor Gene, VSX1, Expressed in Ocular Tissues.
|
| Semina EV, Mintz-Hittner HA, Murray JC.
|
| Genomics 63(2):289-293. 2000
|
| 22 | VSX1
|
| RINX(VSX1), a novel homeobox gene expressed in the inner nuclear layer of the adult retina.
|
| Hayashi T, Huang J, Deeb SS.
|
| Genomics 67(2):128-39. 2000
|