Items where Author is "Hodges, Matt"

Rohaim, Mohammed and Clayton, Emily and Sahin, Irem and Vilela, Julianne and Khalifa, Manar and Al-Natour, Mohammad and Bayoumi, Mahmoud and Poirier, Aurore C. and Branavan, Manoharanehru and Tharmakulasingam, Makunthan and Choudhry, Mouman S. and Sodi, Ravinder and Brown, Amy and Burkhart, Peter and Hacking, Wendy and Botham, Judy and Boyce, Joe and Wilkinson, Hayley and Williams, Craig and Whittingham-Dowd, Jayde and Shaw, Elisabeth and Hodges, Matt and Butler, Lisa and Bates, Michelle and La Ragione, Roberto and Balachandran, Wamadeva and Fernando, Anil and Munir, Muhammad (2020) Artificial Intelligence-Assisted Loop Mediated Isothermal Amplification (ai-LAMP) for Rapid Detection of SARS-CoV-2. Viruses, 12 (9): 972. ISSN 1999-4915

Hodges, Matt and Haji Ismail, Mohd Zamri Bin and Boylan, Michael and Achall, Rajesh and Shirras, Alan and Broughton, Susan (2015) The Drosophila insulin receptor independently modulates lifespan and locomotor senescence. PLoS ONE, 10 (5): 0125312. ISSN 1932-6203

Delury, Craig and Tinker, Claire and Rivers, Samantha and Hodges, Matt and Broughton, Susan and Parkin, Edward (2013) Differential regulation of E-cadherin expression by the soluble ectodomain and intracellular domain of jagged1. International Journal of Biochemistry Research and Review, 3 (4). pp. 278-290. ISSN 2231-086X

Hodges, Matt and Kerns, Jemma and Bentley, Adam J. and Fogarty, Simon and Patel, Imran I. and Martin, Francis L. and Fullwood, Nigel J. (2011) Combining immunolabeling and surface-enhanced Raman spectroscopy on cell membranes. ACS Nano, 5 (12). pp. 9535-9541. ISSN 1936-0851

Gregory-Evans, Kevin and Chang, Francis and Hodges, Matt and Gregory-Evans, Cheryl Y. (2009) Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degeneration. Molecular Vision, 15. pp. 962-973. ISSN 1090-0535

Wang, C. M. and Dixon, P. H. and Decordova, S. and Hodges, Matt and Seibre, N. J. and Ozalp, S. and Fallahian, M. and Sensi, A. and Ashrafi, F. and Repiska, V. and Zhao, J. and Xiang, Y. and Savage, P. M. and Seckl, M. J. and Fisher, R. A. (2009) Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region. Journal of Medical Genetics, 46 (8). pp. 569-575. ISSN 1468-6244

Guerin, K. and Gregory-Evans, C. Y. and Hodges, Matt and Moosajee, M. and Mackay, D. S. and Gregory-Evans, K. and Flannery, John G. (2008) Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa. Experimental Eye Research, 87 (3). pp. 197-207. ISSN 1096-0007

Hodges, Matt and Gregory-Evans, Cheryl Y. and Gregory-Evans, Kevin (2008) A clearer view of stem cells in retinal disease. In: Stem cell repair and regeneration :. Imperial College Press, London, pp. 227-245. ISBN 978-1-86094-980-7

Gregory-Evans, Cheryl Y. and Moosajee, Mariya and Hodges, Matt and Mackay, Donna S. and Game, Laurence and Vargesson, Neil and Bloch-Zupan, Agnès and Rüschendorf, Franz and Santos-Pintos, Lourdes and Wackens, Georges and Gregory-Evans, Kevin (2007) 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. Human Molecular Genetics, 16 (20). pp. 2482-2493. ISSN 1460-2083

Burke, Beverley and Sebire, Neil J. and Moss, Jill and Hodges, Matt and Seckl, Michael J. and Newlands, Edward S. and Fisher, Rosemary A. (2006) Evaluation of deletions in 7q11.2 and 8p12-p21 as prognostic indicators of tumour development following molar pregnancy. Gynecologic Oncology, 103 (2). pp. 642-648. ISSN 0090-8258

Aitman, Timothy J. and Dong, Rong and Vyse, Timothy J. and Norsworthy, Penny J. and Johnson, Michelle D. and Smith, Jennifer and Mangion, Jonathan and Roberton-Lowe, Cheri and Marshall, Amy J. and Petretto, Enrico and Hodges, Matt and Bhangal, Gurjeet and Patel, Sheetal G. and Sheehan-Rooney, Kelly and Duda, Mark and Cook, Paul R. and Evans, David J. and Domin, Jan and Flint, Jonathan and Boyle, Joseph J. and Pusey, Charles D. and Cook, H. Terence (2006) Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Nature, 439. pp. 851-855. ISSN 0028-0836

Fisher, Rosemary A. and Hodges, Matt and Newlands, Edward S. (2004) Familial recurrent hydatidiform mole : a review. Journal of Reproductive Medicine, 49 (8). pp. 595-601.

Fisher, R. A. and Hodges, Matt (2003) Genomic imprinting in gestational trophoblastic disease : a review. Placenta, 24 (Suppl.). s111-s118. ISSN 0143-4004

Hodges, Matt and Rees, H. C. and Seckl, M. J. and Newlands, E. S. and Fisher, R. A. (2003) Genetic refinement and physical mapping of a biparental complete hydatidiform mole locus on chromosome 19q13.4. Journal of Medical Genetics, 40 (8): e95. ISSN 1468-6244

Hodges, Matt and Vieira, Helena and Gregory-Evans, Kevin and Gregory-Evans, Cheryl Y. (2002) Characterization of the genomic and transcriptional structure of the CRX gene : substantial differences between human and mouse. Genomics, 80 (5). pp. 531-542. ISSN 0888-7543

Fisher, Rosemary A. and Hodges, Matt and Rees, Helene C. and Seibre, Neil J. and Seckl, Michael J. and Newlands, Edward S. and Genest, David R. and Castrillon, Diego H. (2002) The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles. Human Molecular Genetics, 11 (26). pp. 3267-3272. ISSN 1460-2083

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

Bibb, Lindsay C. and Holt, James K. L. and Tarttelin, Emma E. and Hodges, Matt and Gregory-Evans, Kevin and Rutherford, Adam and Lucas, Robert J. and Sowden, Jane C. and Gregory-Evans, Cheryl Y. (2001) Temporal and spatial expression patterns of the CRX gene and its downstream targets : critical differences during human and mouse eye development. Human Molecular Genetics, 10 (15). pp. 1571-1579. ISSN 1460-2083

Alders, M. and Ryan, A. and Hodges, Matt and Bliek, J. and Feinberg, A. P. and Privitera, O. and Westerveld, A. and Little, P. F. R. and Mannens, M. (2000) Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome. American Journal of Human Genetics, 66 (5). pp. 1473-1484. ISSN 0002-9297

John, Rosalind M. and Hodges, Matt and Little, Peter and Barton, Sheila C. and Surani, M. Azim (1999) A human p57KIP2 transgene is not activated by passage through the maternal mouse germline. Human Molecular Genetics, 8 (12). pp. 2211-2219. ISSN 1460-2083

Nesbit, M. A. and Hodges, Matt and Campbell, L. and de Meulemeester, T. M. A. M. O. and Alders, M. and Rodriques, N. R. and TAlbot, K. and Theodosiou, A. M. and Mannens, M. A. and Nakamura, Y. and Little, P. F. R. and Davies, K. E. (1997) 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. Genomics, 42 (2). pp. 284-294. ISSN 0888-7543

Alders, Mariëlle and Hodges, Matt and Hadjantonakis, Anna-Katerina and Postmus, Jan and van Wijk, Inge and Bliek, Jet and de Meulemeester, Maurice and Westerveld, Andries and Guillemot, François and Oudejans, Cees and Little, Peter and Mannens, Marcel (1997) The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts. Human Molecular Genetics, 6 (6). pp. 859-867. ISSN 1460-2083