User profiles for CHRISTINE P. DIGGLE
Christine P DiggleUniversity of Leeds Verified email at leeds.ac.uk Cited by 3873 |
Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy
Digital clubbing, recognized by Hippocrates in the fifth century BC, is the outward hallmark
of pulmonary hypertrophic osteoarthropathy, a clinical constellation that develops secondary …
of pulmonary hypertrophic osteoarthropathy, a clinical constellation that develops secondary …
[PDF][PDF] High‐fat and high‐sucrose (western) diet induces steatohepatitis that is dependent on fructokinase
…, MR Jackman, PS MacLean, CP Diggle… - …, 2013 - Wiley Online Library
Fructose intake from added sugars has been implicated as a cause of nonalcoholic fatty
liver disease. Here we tested the hypothesis that fructose may interact with a high‐fat diet to …
liver disease. Here we tested the hypothesis that fructose may interact with a high‐fat diet to …
Opposing effects of fructokinase C and A isoforms on fructose-induced metabolic syndrome in mice
…, MPT Le, GE Garcia, CP Diggle… - Proceedings of the …, 2012 - National Acad Sciences
Fructose intake from added sugars correlates with the epidemic rise in obesity, metabolic
syndrome, and nonalcoholic fatty liver disease. Fructose intake also causes features of …
syndrome, and nonalcoholic fatty liver disease. Fructose intake also causes features of …
[HTML][HTML] Endogenous fructose production and metabolism in the liver contributes to the development of metabolic syndrome
…, CA Roncal-Jimenez, ES Bales, CP Diggle… - Nature …, 2013 - nature.com
Carbohydrates with high glycaemic index are proposed to promote the development of
obesity, insulin resistance and fatty liver, but the mechanism by which this occurs remains …
obesity, insulin resistance and fatty liver, but the mechanism by which this occurs remains …
Ketohexokinase: expression and localization of the principal fructose-metabolizing enzyme
CP Diggle, M Shires, D Leitch… - … of Histochemistry & …, 2009 - journals.sagepub.com
Ketohexokinase (KHK, also known as fructokinase) initiates the pathway through which
most dietary fructose is metabolized. Very little is known about the cellular localization of this …
most dietary fructose is metabolized. Very little is known about the cellular localization of this …
Endogenous fructose production and fructokinase activation mediate renal injury in diabetic nephropathy
…, DT Bonthron, A Asipu, CP Diggle… - Journal of the …, 2014 - journals.lww.com
Diabetes is associated with activation of the polyol pathway, in which glucose is converted
to sorbitol by aldose reductase. Previous studies focused on the role of sorbitol in mediating …
to sorbitol by aldose reductase. Previous studies focused on the role of sorbitol in mediating …
[PDF][PDF] CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation
…, M Kurkowiak, NT Loges, CP Diggle… - The American Journal of …, 2014 - cell.com
A diverse family of cytoskeletal dynein motors powers various cellular transport systems,
including axonemal dyneins generating the force for ciliary and flagellar beating essential to …
including axonemal dyneins generating the force for ciliary and flagellar beating essential to …
[HTML][HTML] HEATR2 Plays a Conserved Role in Assembly of the Ciliary Motile Apparatus
Cilia are highly conserved microtubule-based structures that perform a variety of sensory
and motility functions during development and adult homeostasis. In humans, defects …
and motility functions during development and adult homeostasis. In humans, defects …
DNA double strand break repair in human bladder cancer is error prone and involves microhomology-associated end-joining
J Bentley, CP Diggle, P Harnden… - Nucleic acids …, 2004 - academic.oup.com
In human cells DNA double strand breaks (DSBs) can be repaired by the non-homologous
end-joining (NHEJ) pathway. In a background of NHEJ deficiency, DSBs with mismatched …
end-joining (NHEJ) pathway. In a background of NHEJ deficiency, DSBs with mismatched …
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
Infantile myopathies with diaphragmatic paralysis are genetically heterogeneous, and
clinical symptoms do not assist in differentiating between them. We used phased haplotype …
clinical symptoms do not assist in differentiating between them. We used phased haplotype …