65 related articles for article (PubMed ID: 15051220)
1. 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; 2004 Apr; 111(4):828-36. PubMed ID: 15051220
[TBL] [Abstract][Full Text] [Related]
2. 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; 2004 Feb; 101(6):1754-9. PubMed ID: 14745032
[TBL] [Abstract][Full Text] [Related]
3. Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy.
Meyer E; Michaelides M; Tee LJ; Robson AG; Rahman F; Pasha S; Luxon LM; Moore AT; Maher ER
Mol Vis; 2010 Apr; 16():650-64. PubMed ID: 20405026
[TBL] [Abstract][Full Text] [Related]
4. Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
Krafchak CM; Pawar H; Moroi SE; Sugar A; Lichter PR; Mackey DA; Mian S; Nairus T; Elner V; Schteingart MT; Downs CA; Kijek TG; Johnson JM; Trager EH; Rozsa FW; Mandal MN; Epstein MP; Vollrath D; Ayyagari R; Boehnke M; Richards JE
Am J Hum Genet; 2005 Nov; 77(5):694-708. PubMed ID: 16252232
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of the VSX1 gene in familial keratoconus.
Liskova P; Ebenezer ND; Hysi PG; Gwilliam R; El-Ashry MF; Moodaley LC; Hau S; Twa M; Tuft SJ; Bhatacharya SS
Mol Vis; 2007 Oct; 13():1887-91. PubMed ID: 17960127
[TBL] [Abstract][Full Text] [Related]
6. 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; 2018; 13(3):266-273. PubMed ID: 30090183
[TBL] [Abstract][Full Text] [Related]
7. Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus.
De Bonis P; Laborante A; Pizzicoli C; Stallone R; Barbano R; Longo C; Mazzilli E; Zelante L; Bisceglia L
Mol Vis; 2011; 17():2482-94. PubMed ID: 21976959
[TBL] [Abstract][Full Text] [Related]
8. Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass.
Munroe RJ; Prabhu V; Acland GM; Johnson KR; Harris BS; O'Brien TP; Welsh IC; Noden DM; Schimenti JC
BMC Dev Biol; 2009 Apr; 9():27. PubMed ID: 19379485
[TBL] [Abstract][Full Text] [Related]
9. Magnetic Resonance Imaging Findings and Genetic Testing Results in Children With Congenital Corneal Opacities.
Xia JL; Kadom N; Mansukhani SA; Couser NL; Lenhart PD
Am J Ophthalmol; 2024 Mar; 259():62-70. PubMed ID: 37907146
[TBL] [Abstract][Full Text] [Related]
10. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.
Twigg SR; Versnel SL; Nürnberg G; Lees MM; Bhat M; Hammond P; Hennekam RC; Hoogeboom AJ; Hurst JA; Johnson D; Robinson AA; Scambler PJ; Gerrelli D; Nürnberg P; Mathijssen IM; Wilkie AO
Am J Hum Genet; 2009 May; 84(5):698-705. PubMed ID: 19409524
[TBL] [Abstract][Full Text] [Related]
11. Mutation of
Letelier J; Buono L; Almuedo-Castillo M; Zang J; Mounieres C; González-Díaz S; Polvillo R; Sanabria-Reinoso E; Corbacho J; Sousa-Ortega A; Diez Del Corral R; Neuhauss SCF; Martínez-Morales JR
Elife; 2023 May; 12():. PubMed ID: 37227126
[TBL] [Abstract][Full Text] [Related]
12. Inherited Eye Diseases with Retinal Manifestations through the Eyes of Homeobox Genes.
Markitantova Y; Simirskii V
Int J Mol Sci; 2020 Feb; 21(5):. PubMed ID: 32111086
[TBL] [Abstract][Full Text] [Related]
13. Expression of visual system homeobox 1 in human keratoconus.
Wang YN; Liu XN; Wang XD; Yin Y; Chen Y; Xiao XH; Xu K; Zhu XP
Int J Ophthalmol; 2019; 12(2):201-206. PubMed ID: 30809473
[TBL] [Abstract][Full Text] [Related]
14. Genetic Aspects of Keratoconus: A Literature Review Exploring Potential Genetic Contributions and Possible Genetic Relationships with Comorbidities.
Loukovitis E; Sfakianakis K; Syrmakesi P; Tsotridou E; Orfanidou M; Bakaloudi DR; Stoila M; Kozei A; Koronis S; Zachariadis Z; Tranos P; Kozeis N; Balidis M; Gatzioufas Z; Fiska A; Anogeianakis G
Ophthalmol Ther; 2018 Dec; 7(2):263-292. PubMed ID: 30191404
[TBL] [Abstract][Full Text] [Related]
15. Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing.
Matías-Pérez D; García-Montaño LA; Cruz-Aguilar M; García-Montalvo IA; Nava-Valdéz J; Barragán-Arevalo T; Villanueva-Mendoza C; Villarroel CE; Guadarrama-Vallejo C; la Cruz RV; Chacón-Camacho O; Zenteno JC
J Hum Genet; 2018 Nov; 63(11):1169-1180. PubMed ID: 30181649
[TBL] [Abstract][Full Text] [Related]
16.
Nejabat M; Naghash P; Dastsooz H; Mohammadi S; Alipour M; Fardaei M
J Ophthalmic Vis Res; 2017; 12(2):135-140. PubMed ID: 28540003
[TBL] [Abstract][Full Text] [Related]
17. The genetic and environmental factors for keratoconus.
Gordon-Shaag A; Millodot M; Shneor E; Liu Y
Biomed Res Int; 2015; 2015():795738. PubMed ID: 26075261
[TBL] [Abstract][Full Text] [Related]
18. Gene therapy in keratoconus.
Farjadnia M; Naderan M; Mohammadpour M
Oman J Ophthalmol; 2015; 8(1):3-8. PubMed ID: 25709266
[TBL] [Abstract][Full Text] [Related]
19. The Genetics of Keratoconus: A Review.
Wheeler J; Hauser MA; Afshari NA; Allingham RR; Liu Y
Reprod Syst Sex Disord; 2012 Jun; (Suppl 6):. PubMed ID: 23795306
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]