Hodges MD - Search Results

1

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

2

The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts.

Alders M, Hodges M, Hadjantonakis AK, Postmus J, van Wijk I, Bliek J, de Meulemeester M, Westerveld A, Guillemot F, Oudejans C, Little P, Mannens M. Alders M, et al. Hum Mol Genet. 1997 Jun;6(6):859-67. doi: 10.1093/hmg/6.6.859. Hum Mol Genet. 1997. PMID: 9175731

3

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.

4

A human p57(KIP2) transgene is not activated by passage through the maternal mouse germline.

John RM, Hodges M, Little P, Barton SC, Surani MA. John RM, et al. Hum Mol Genet. 1999 Nov;8(12):2211-9. doi: 10.1093/hmg/8.12.2211. Hum Mol Genet. 1999. PMID: 10545601

5

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

6

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.

7

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

8

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

9

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

10

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

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