Selected Publications Show all 26 publications

Loss of angiotensin-converting enzyme-related (ACER) peptidase disrupts behavioural and metabolic responses to diet in Drosophila melanogaster
Glover, Z., Hodges, M.D.J., Dravecz, N., Cameron, J., Askwith, H., Shirras, A.D., Broughton, S.J. 25/04/2019 In: Journal of Experimental Biology. 222, 8, 12 p.
Journal article

Intestinal epithelial suppressor of cytokine signaling 3 (SOCS3) impacts on mucosal homeostasis in a model of chronic inflammation.
Shaw, E.J., Smith, E., Whittingham-Dowd, J.K., Hodges, M.D.J., Else, K.J., Rigby, R.J. 09/2017 In: Immunity, Inflammation and Disease. 5, 3, p. 336-345. 10 p.
Journal article

The Drosophila insulin receptor independently modulates lifespan and locomotor senescence
Hodges, M., Haji Ismail, M.Z.B., Boylan, M., Achall , R., Shirras, A., Broughton, S. 28/05/2015 In: PLoS ONE. 10, 5, 21 p.
Journal article

Differential regulation of E-cadherin expression by the soluble ectodomain and intracellular domain of jagged1
Delury, C., Tinker, C., Rivers, S., Hodges, M., Broughton, S., Parkin, E. 2/08/2013 In: International Journal of Biochemistry Research and Review. 3, 4, p. 278-290. 13 p.
Journal article

Combining immunolabeling and surface-enhanced Raman spectroscopy on cell membranes
Hodges, M., Kerns , J., Bentley, A.J., Fogarty, S., Patel, I.I., Martin, F.L., Fullwood, N.J. 12/2011 In: ACS Nano. 5, 12, p. 9535-9541. 7 p.
Journal article

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, M., Gregory-Evans, C.Y. 13/05/2009 In: Molecular Vision. 15, p. 962-973. 12 p.
Journal article

Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region
Wang, C.M., Dixon, P.H., Decordova, S., Hodges, M., Seibre, N.J., Ozalp, S., Fallahian, M., Sensi, A., Ashrafi, F., Repiska, V., Zhao, J., Xiang, Y., Savage, P.M., Seckl, M.J., Fisher, R.A. 25/02/2009 In: Journal of Medical Genetics. 46, 8, p. 569-575. 7 p.
Journal article

Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa
Guerin, K., Gregory-Evans, C.Y., Hodges, M., Moosajee, M., Mackay, D.S., Gregory-Evans, K., Flannery, J.G. 09/2008 In: Experimental Eye Research. 87, 3, p. 197-207. 11 p.
Journal article

A clearer view of stem cells in retinal disease
Hodges, M., Gregory-Evans, C.Y., Gregory-Evans, K. 2008 In: Stem cell repair and regeneration. London : Imperial College Press p. 227-245. 19 p. ISBN: 978-1-86094-980-7 . Electronic ISBN: 978-1-908979-02-5.
Chapter

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, C.Y., Moosajee, M., Hodges, M., Mackay, D.S., Game, L., Vargesson, N., Bloch-Zupan, A., Rüschendorf, F., Santos-Pintos, L., Wackens, G., Gregory-Evans, K. 2007 In: Human Molecular Genetics. 16, 20, p. 2482-2493. 12 p.
Journal article

Evaluation of deletions in 7q11.2 and 8p12-p21 as prognostic indicators of tumour development following molar pregnancy
Burke, B., Sebire, N.J., Moss, J., Hodges, M., Seckl, M.J., Newlands, E.S., Fisher, R.A. 11/2006 In: Gynecologic Oncology. 103, 2, p. 642-648. 7 p.
Journal article

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
Aitman, T.J., Dong, R., Vyse, T.J., Norsworthy, P.J., Johnson, M.D., Smith, J., Mangion, J., Roberton-Lowe, C., Marshall, A.J., Petretto, E., Hodges, M., Bhangal, G., Patel, S.G., Sheehan-Rooney, K., Duda, M., Cook, P.R., Evans, D.J., Domin, J., Flint, J., Boyle, J.J., Pusey, C.D., Cook, H.T. 16/02/2006 In: Nature. 439, p. 851-855. 5 p.
Journal article

Familial recurrent hydatidiform mole: a review
Fisher, R.A., Hodges, M., Newlands, E.S. 08/2004 In: Journal of Reproductive Medicine. 49, 8, p. 595-601. 7 p.
Journal article

Genomic imprinting in gestational trophoblastic disease: a review
Fisher, R.A., Hodges, M. 04/2003 In: Placenta. 24, Suppl. A, p. s111-s118. 8 p.
Journal article

Genetic refinement and physical mapping of a biparental complete hydatidiform mole locus on chromosome 19q13.4.
Hodges, M., Rees, H.C., Seckl, M.J., Newlands, E.S., Fisher, R.A. 2003 In: Journal of Medical Genetics. 40, 8, 6 p.
Journal article

Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouse.
Hodges, M., Vieira, H., Gregory-Evans, K., Gregory-Evans, C.Y. 11/2002 In: Genomics. 80, 5, p. 531-542. 12 p.
Journal article

The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles
Fisher, R.A., Hodges, M., Rees, H.C., Seibre, N.J., Seckl, M.J., Newlands, E.S., Genest, D.R., Castrillon, D.H. 2002 In: Human Molecular Genetics. 11, 26, p. 3267-3272. 6 p.
Journal article

Characterisation of the CRX Gene; Identification of Alternatively Spliced 5’ Exons and 3’ Sequence
Hodges, M., Gregory-Evans, C. 2001 In: New insights into retinal degenerative diseases. New York : Kluwer Academic Publishers p. 71-86. 16 p. ISBN: 0-306-46679-1.
Chapter

Temporal and spatial expression patterns of the CRX gene and its downstream targets: critical differences during human and mouse eye development
Bibb, L.C., Holt, J.K.L., Tarttelin, E.E., Hodges, M., Gregory-Evans, K., Rutherford, A., Lucas, R.J., Sowden, J.C., Gregory-Evans, C.Y. 2001 In: Human Molecular Genetics. 10, 15, p. 1571-1579. 9 p.
Journal article

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.
Alders, M., Ryan, A., Hodges, M., Bliek, J., Feinberg, A.P., Privitera, O., Westerveld, A., Little, P.F.R., Mannens, M. 05/2000 In: American Journal of Human Genetics. 66, 5, p. 1473-1484. 12 p.
Journal article

A human p57KIP2 transgene is not activated by passage through the maternal mouse germline
John, R.M., Hodges, M., Little, P., Barton, S.C., Surani, M.A. 1999 In: Human Molecular Genetics. 8, 12, p. 2211-2219. 9 p.
Journal article

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, M.A., Hodges, M., Campbell, L., de Meulemeester, T.M.A.M.O., Alders, M., Rodriques, N.R., TAlbot, K., Theodosiou, A.M., Mannens, M.A., Nakamura, Y., Little, P.F.R., Davies, K.E. 1/06/1997 In: Genomics. 42, 2, p. 284-294. 11 p.
Journal article

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, A., Postmus, J., van Wijk, I., Bliek, J., de Meulemeester, M., Westerveld, A., Guillemot, F., Oudejans, C., Little, P., Mannens, M. 06/1997 In: Human Molecular Genetics. 6, 6, p. 859-867. 9 p.
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