about
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationHEATR2 plays a conserved role in assembly of the ciliary motile apparatusOpposing effects of fructokinase C and A isoforms on fructose-induced metabolic syndrome in miceMutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathyA tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development.Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotypeSimple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data.Identification of genes up-regulated in urothelial tumors: the 67-kd laminin receptor and tumor-associated trypsin inhibitor.An observational study on the expression levels of MDM2 and MDMX proteins, and associated effects on P53 in a series of human liposarcomasEndogenous fructose production and fructokinase activation mediate renal injury in diabetic nephropathy.In vitro studies on the relationship between polyunsaturated fatty acids and cancer: tumour or tissue specific effects?Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.Endogenous fructose production and metabolism in the liver contributes to the development of metabolic syndrome.Illuminator, a desktop program for mutation detection using short-read clonal sequencing.Development of a rapid, small-scale DNA repair assay for use on clinical samplesDNA double strand break repair in human bladder cancer is error prone and involves microhomology-associated end-joining.Role of PPARgamma and EGFR signalling in the urothelial terminal differentiation programme.High-fat and high-sucrose (western) diet induces steatohepatitis that is dependent on fructokinase.Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface.Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome.Developing Hollow-Channel Gold Nanoflowers as Trimodal Intracellular Nanoprobes
P50
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P50
description
research fellow at the University of Leeds
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research fellow at the University of Leeds
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wetenschapper
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name
Christine Diggle
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Christine Diggle
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Christine Diggle
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Christine Diggle
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Christine Diggle
@nl
Christine Diggle
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type
label
Christine Diggle
@ast
Christine Diggle
@en
Christine Diggle
@en-gb
Christine Diggle
@es
Christine Diggle
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Christine Diggle
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altLabel
Christine P. Diggle
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Christine P. Diggle
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prefLabel
Christine Diggle
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Christine Diggle
@en
Christine Diggle
@en-gb
Christine Diggle
@es
Christine Diggle
@nl
Christine Diggle
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P106
P21
P2699
P31
P496
0000-0001-6861-359X