Hodges MD - Search Results

1

Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degeneration.

Gregory-Evans K, Chang F, Hodges MD, Gregory-Evans CY. Gregory-Evans K, et al. Among authors: hodges md. Mol Vis. 2009 May 13;15:962-73. Mol Vis. 2009. PMID: 19461934 Free PMC article.

2

Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouse.

Hodges MD, Vieira H, Gregory-Evans K, Gregory-Evans CY. Hodges MD, et al. Genomics. 2002 Nov;80(5):531-42. doi: 10.1006/geno.2002.6854. Genomics. 2002. PMID: 12408971

3

SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.

Gregory-Evans CY, Moosajee M, Hodges MD, Mackay DS, Game L, Vargesson N, Bloch-Zupan A, Rüschendorf F, Santos-Pinto L, Wackens G, Gregory-Evans K. Gregory-Evans CY, et al. Among authors: hodges md. Hum Mol Genet. 2007 Oct 15;16(20):2482-93. doi: 10.1093/hmg/ddm204. Epub 2007 Jul 25. Hum Mol Genet. 2007. PMID: 17656375

4

Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development.

Bibb LC, Holt JK, Tarttelin EE, Hodges MD, Gregory-Evans K, Rutherford A, Lucas RJ, Sowden JC, Gregory-Evans CY. Bibb LC, et al. Among authors: hodges md. Hum Mol Genet. 2001 Jul 15;10(15):1571-9. doi: 10.1093/hmg/10.15.1571. Hum Mol Genet. 2001. PMID: 11468275

5

Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa.

Guerin K, Gregory-Evans CY, Hodges MD, Moosajee M, Mackay DS, Gregory-Evans K, Flannery JG. Guerin K, et al. Among authors: hodges md. Exp Eye Res. 2008 Sep;87(3):197-207. doi: 10.1016/j.exer.2008.05.016. Epub 2008 Jun 3. Exp Eye Res. 2008. PMID: 18644591

6

The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles.

Fisher RA, Hodges MD, Rees HC, Sebire NJ, Seckl MJ, Newlands ES, Genest DR, Castrillon DH. Fisher RA, et al. Among authors: hodges md. Hum Mol Genet. 2002 Dec 15;11(26):3267-72. doi: 10.1093/hmg/11.26.3267. Hum Mol Genet. 2002. PMID: 12471053

7

Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2.

Nesbit MA, Hodges MD, Campbell L, de Meulemeester TM, Alders M, Rodrigues NR, Talbot K, Theodosiou AM, Mannens MA, Nakamura Y, Little PF, Davies KE. Nesbit MA, et al. Among authors: hodges md. Genomics. 1997 Jun 1;42(2):284-94. doi: 10.1006/geno.1997.4737. Genomics. 1997. PMID: 9192849

8

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.

Alders M, Ryan A, Hodges M, Bliek J, Feinberg AP, Privitera O, Westerveld A, Little PF, Mannens M. Alders M, et al. Am J Hum Genet. 2000 May;66(5):1473-84. doi: 10.1086/302892. Epub 2000 Apr 10. Am J Hum Genet. 2000. PMID: 10762538 Free PMC article.

9

Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region.

Wang CM, Dixon PH, Decordova S, Hodges MD, Sebire NJ, Ozalp S, Fallahian M, Sensi A, Ashrafi F, Repiska V, Zhao J, Xiang Y, Savage PM, Seckl MJ, Fisher RA. Wang CM, et al. Among authors: hodges md. J Med Genet. 2009 Aug;46(8):569-75. doi: 10.1136/jmg.2008.064196. Epub 2009 Feb 25. J Med Genet. 2009. PMID: 19246479

10

Evaluation of deletions in 7q11.2 and 8p12-p21 as prognostic indicators of tumour development following molar pregnancy.

Burke B, Sebire NJ, Moss J, Hodges MD, Seckl MJ, Newlands ES, Fisher RA. Burke B, et al. Among authors: hodges md. Gynecol Oncol. 2006 Nov;103(2):642-8. doi: 10.1016/j.ygyno.2006.04.015. Epub 2006 Jun 27. Gynecol Oncol. 2006. PMID: 16806440

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