PubMed for id: 1812533141

Year	Number of Results
2000	2
2002	1
2004	1
2005	2
2018	1
2020	1
2022	1
2023	1
2024	0

1

The association between VSX1 exon3 gene variants and keratoconus in Malaysian patients.

Deva JP, Ngeow YF, Zin T. Deva JP, et al. Indian J Ophthalmol. 2023 Jun;71(6):2443-2447. doi: 10.4103/IJO.IJO_2894_22. Indian J Ophthalmol. 2023. PMID: 37322657 Free PMC article.

2

High VSX1 expression promotes the aggressiveness of clear cell renal cell carcinoma by transcriptionally regulating FKBP10.

Ma W, Li X, Yang L, Pan J, Chen Y, Lu Y, Dong X, Li D, Gan W. Ma W, et al. J Transl Med. 2022 Dec 3;20(1):554. doi: 10.1186/s12967-022-03772-2. J Transl Med. 2022. PMID: 36463181 Free PMC article.

3

Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.

Haenig C, Atias N, Taylor AK, Mazza A, Schaefer MH, Russ J, Riechers SP, Jain S, Coughlin M, Fontaine JF, Freibaum BD, Brusendorf L, Zenkner M, Porras P, Stroedicke M, Schnoegl S, Arnsburg K, Boeddrich A, Pigazzini L, Heutink P, Taylor JP, Kirstein J, Andrade-Navarro MA, Sharan R, Wanker EE. Haenig C, et al. Cell Rep. 2020 Aug 18;32(7):108050. doi: 10.1016/j.celrep.2020.108050. Cell Rep. 2020. PMID: 32814053 Free article.

4

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. Kalasidou G, et al. J Biol Regul Homeost Agents. 2018 Nov-Dec;32(6):1515-1518. J Biol Regul Homeost Agents. 2018. PMID: 30574758

5

Transcriptional activity of the paired-like homeodomain proteins CHX10 and VSX1.

Dorval KM, Bobechko BP, Ahmad KF, Bremner R. Dorval KM, et al. J Biol Chem. 2005 Mar 18;280(11):10100-8. doi: 10.1074/jbc.M412676200. Epub 2005 Jan 12. J Biol Chem. 2005. PMID: 15647262 Free article.

6

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. Bisceglia L, et al. Invest Ophthalmol Vis Sci. 2005 Jan;46(1):39-45. doi: 10.1167/iovs.04-0533. Invest Ophthalmol Vis Sci. 2005. PMID: 15623752

7

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. Mintz-Hittner HA, et al. Ophthalmology. 2004 Apr;111(4):828-36. doi: 10.1016/j.ophtha.2003.07.006. Ophthalmology. 2004. PMID: 15051220

8

VSX1: a gene for posterior polymorphous dystrophy and keratoconus.

Héon 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. Héon E, et al. Hum Mol Genet. 2002 May 1;11(9):1029-36. doi: 10.1093/hmg/11.9.1029. Hum Mol Genet. 2002. PMID: 11978762

9

RINX(VSX1), a novel homeobox gene expressed in the inner nuclear layer of the adult retina.

Hayashi T, Huang J, Deeb SS. Hayashi T, et al. Genomics. 2000 Jul 15;67(2):128-39. doi: 10.1006/geno.2000.6248. Genomics. 2000. PMID: 10903837

10

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. Semina EV, et al. Genomics. 2000 Jan 15;63(2):289-93. doi: 10.1006/geno.1999.6093. Genomics. 2000. PMID: 10673340

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