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The Journal of Reproductive Medicine|October 2, 2004
Familial recurrent hydatidiform mole: a reviewRosemary A Fisher, Matthew D Hodges, Edward S Newlands
Plos One|January 13, 2022
The orphan drug dichloroacetate reduces amyloid beta-peptide production whilst promoting non-amyloidogenic proteolysis of the amyloid precursor proteinEdward T Parkin, Jessica E Hammond, Lauren Owens, et al.
Genomics|November 1, 2002
Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouseMatthew D Hodges, Helena Vieira, Kevin Gregory-Evans, et al.
Molecular Vision|May 23, 2009
Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degenerationKevin Gregory-Evans, Francis Chang, Matthew D Hodges, et al.
The Journal of Experimental Biology|April 4, 2019
Loss of angiotensin-converting enzyme-related (ACER) peptidase disrupts behavioural and metabolic responses to diet in Drosophila melanogasterZoe Glover, Matthew D Hodges, Nikolett Dravecz, et al.
Immunity, Inflammation and Disease|May 17, 2017
Intestinal epithelial suppressor of cytokine signaling 3 (SOCS3) impacts on mucosal homeostasis in a model of chronic inflammationElisabeth J Shaw, Emily E Smith, Jayde Whittingham-Dowd, et al.
Gynecologic Oncology|June 30, 2006
Evaluation of deletions in 7q11.2 and 8p12-p21 as prognostic indicators of tumour development following molar pregnancyBeverley Burke, Neil J Sebire, Jill Moss, et al.
ACS Nano|November 10, 2011
Combining immunolabeling and surface-enhanced Raman spectroscopy on cell membranesMatthew D Hodges, Jemma G Kelly, Adam J Bentley, et al.
Human Molecular Genetics|December 10, 2002
The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform molesRosemary A Fisher, Matthew D Hodges, Helene C Rees, et al.
Human Molecular Genetics|July 28, 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 colobomaCheryl Y Gregory-Evans, Mariya Moosajee, Matthew D Hodges, et al.
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