Hodges MD - Search Results

1

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

2

Familial recurrent hydatidiform mole: a review.

Fisher RA, Hodges MD, Newlands ES. Fisher RA, et al. Among authors: hodges md. J Reprod Med. 2004 Aug;49(8):595-601. J Reprod Med. 2004. PMID: 15457849 Review.

3

Genomic imprinting in gestational trophoblastic disease--a review.

Fisher RA, Hodges MD. Fisher RA, et al. Among authors: hodges md. Placenta. 2003 Apr;24 Suppl A:S111-8. doi: 10.1053/plac.2002.0939. Placenta. 2003. PMID: 12842422 Review.

4

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

5

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

6

Genetic refinement and physical mapping of a biparental complete hydatidiform mole locus on chromosome 19q13.4.

Hodges MD, Rees HC, Seckl MJ, Newlands ES, Fisher RA. Hodges MD, et al. J Med Genet. 2003 Aug;40(8):e95. doi: 10.1136/jmg.40.8.e95. J Med Genet. 2003. PMID: 12920087 Free PMC article. No abstract available.

7

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

8

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

9

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

10

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.

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