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Items: 1 to 20 of 131

1.

Massively parallel in vivo enhancer assay reveals that highly local features determine the cis-regulatory function of ChIP-seq peaks.

White MA, Myers CA, Corbo JC, Cohen BA.

Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):11952-7. doi: 10.1073/pnas.1307449110. Epub 2013 Jul 1.

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Developing rods transplanted into the degenerating retina of Crx-knockout mice exhibit neural activity similar to native photoreceptors.

Homma K, Okamoto S, Mandai M, Gotoh N, Rajasimha HK, Chang YS, Chen S, Li W, Cogliati T, Swaroop A, Takahashi M.

Stem Cells. 2013 Jun;31(6):1149-59. doi: 10.1002/stem.1372.

4.

CRX/OTX3: a useful marker in the differential diagnosis of tumors of the pineal region and indicator of photoreceptor differentiation in medulloblastomas and atypical teratoid rhabdoid tumors.

Gielen GH, Gessi M, Denkhaus D, Pietsch T.

Appl Immunohistochem Mol Morphol. 2013 May;21(3):248-53. doi: 10.1097/PAI.0b013e3182649dad.

PMID:
23235340
5.

CRX variants in cone-rod dystrophy and mutation overview.

Huang L, Xiao X, Li S, Jia X, Wang P, Guo X, Zhang Q.

Biochem Biophys Res Commun. 2012 Oct 5;426(4):498-503. doi: 10.1016/j.bbrc.2012.08.110. Epub 2012 Aug 30.

PMID:
22960069
6.

Immunohistochemical expression of CRX in extracranial malignant small round cell tumors.

Terry J, Calicchio ML, Rodriguez-Galindo C, Perez-Atayde AR.

Am J Surg Pathol. 2012 Aug;36(8):1165-9. doi: 10.1097/PAS.0b013e3182601d84.

PMID:
22790857
7.

Spontaneous activity promotes synapse formation in a cell-type-dependent manner in the developing retina.

Soto F, Ma X, Cecil JL, Vo BQ, Culican SM, Kerschensteiner D.

J Neurosci. 2012 Apr 18;32(16):5426-39. doi: 10.1523/JNEUROSCI.0194-12.2012.

8.

Crx broadly modulates the pineal transcriptome.

Rovsing L, Clokie S, Bustos DM, Rohde K, Coon SL, Litman T, Rath MF, Møller M, Klein DC.

J Neurochem. 2011 Oct;119(2):262-74. doi: 10.1111/j.1471-4159.2011.07405.x. Epub 2011 Sep 2.

9.

A neuroanatomical and physiological study of the non-image forming visual system of the cone-rod homeobox gene (Crx) knock out mouse.

Rovsing L, Rath MF, Lund-Andersen C, Klein DC, Møller M.

Brain Res. 2010 Jul 9;1343:54-65. doi: 10.1016/j.brainres.2010.04.066. Epub 2010 May 31.

10.

Anatomical changes in the primary visual cortex of the congenitally blind Crx-/- mouse.

Goldshmit Y, Galley S, Foo D, Sernagor E, Bourne JA.

Neuroscience. 2010 Mar 31;166(3):886-98. doi: 10.1016/j.neuroscience.2009.12.039. Epub 2009 Dec 22.

PMID:
20034544
11.

Robust marking of photoreceptor cells and pinealocytes with several reporters under control of the Crx gene.

Samson M, Emerson MM, Cepko CL.

Dev Dyn. 2009 Dec;238(12):3218-25. doi: 10.1002/dvdy.22138.

12.

CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene.

Langmann T, Lai CC, Weigelt K, Tam BM, Warneke-Wittstock R, Moritz OL, Weber BH.

Nucleic Acids Res. 2008 Nov;36(20):6523-34. doi: 10.1093/nar/gkn737. Epub 2008 Oct 16.

13.

Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation.

Kitiratschky VB, Nagy D, Zabel T, Zrenner E, Wissinger B, Kohl S, Jägle H.

Br J Ophthalmol. 2008 Aug;92(8):1086-91. doi: 10.1136/bjo.2007.133231.

PMID:
18653602
14.

Induction of functional photoreceptor phenotype by exogenous Crx expression in mouse retinal stem cells.

Jomary C, Jones SE.

Invest Ophthalmol Vis Sci. 2008 Jan;49(1):429-37. doi: 10.1167/iovs.07-0812.

PMID:
18172122
15.

Further evidence of autosomal-dominant Leber congenital amaurosis caused by heterozygous CRX mutation.

Wang P, Guo X, Zhang Q.

Graefes Arch Clin Exp Ophthalmol. 2007 Sep;245(9):1401-2. Epub 2007 Mar 9. No abstract available.

PMID:
17347810
16.

Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame.

Paunescu K, Preising MN, Janke B, Wissinger B, Lorenz B.

Ophthalmology. 2007 Jul;114(7):1348-1357.e1. Epub 2007 Feb 22. Review.

PMID:
17320181
17.

Docosahexaenoic acid promotes photoreceptor differentiation without altering Crx expression.

Garelli A, Rotstein NP, Politi LE.

Invest Ophthalmol Vis Sci. 2006 Jul;47(7):3017-27.

PMID:
16799048
18.

Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy.

Itabashi T, Wada Y, Sato H, Kawamura M, Shiono T, Tamai M.

Am J Ophthalmol. 2004 Nov;138(5):876-7.

PMID:
15531334
19.

Inner retinal abnormalities in a mouse model of Leber's congenital amaurosis.

Pignatelli V, Cepko CL, Strettoi E.

J Comp Neurol. 2004 Feb 9;469(3):351-9.

PMID:
14730587
20.

Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.

Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.

Ophthalmology. 2002 Oct;109(10):1862-70.

PMID:
12359607

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