Search Results - "TURNER, Jeremy J. O"

Nonsteroidal anti-inflammatory drugs increase TNF production in rheumatoid synovial membrane cultures and whole blood by Page, Theresa H, Turner, Jeremy J O, Brown, Anthony C, Timms, Emma M, Inglis, Julia J, Brennan, Fionula M, Foxwell, Brian M J, Ray, Keith P, Feldmann, Marc

“…Nonsteroidal anti-inflammatory drugs (NSAIDs) inhibit cyclooxygenase activity and hence PG production. However, the ability of NSAIDs to ameliorate pain and…”
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Constitutive P2Y2 receptor activity regulates basal lipolysis in human adipocytes by Ali, Seema B., Turner, Jeremy J. O., Fountain, Samuel J.

“…ABSTRACT White adipocytes are key regulators of metabolic homeostasis, which release stored energy as free fatty acids via lipolysis. Adipocytes possess both…”
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Assessing Glycemic Control in Maintenance Hemodialysis Patients With Type 2 Diabetes by Kazempour-Ardebili, Sara, Lecamwasam, Varunika L, Dassanyake, Thushara, Frankel, Andrew H, Tam, Frederick W.K, Dornhorst, Anne, Frost, Gary, Turner, Jeremy J.O

“…OBJECTIVE: Optimizing glycemic control in diabetic patients undergoing maintenance hemodialysis requires accurate assessment. We hypothesize that 1) 48-h…”
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Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1) by Turner, Jeremy J.O, Christie, Paul T, Pearce, Simon H.S, Turnpenny, Peter D, Thakker, Rajesh V

“…Phenocopies may confound the clinical diagnoses of hereditary disorders. We report phenocopies in Multiple Endocrine Neoplasia type 1 (MEN1), an autosomal…”
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Hypercalcaemia – presentation and management by Turner, Jeremy J O

“…Hypercalcaemia is a common disorder normally caused by primary hyperparathyroidism (PHPT) or malignancy. A proportion of cases present as an emergency, which…”
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Functional characterization of calcium sensing receptor polymorphisms and absence of association with indices of calcium homeostasis and bone mineral density by Harding, Brian, Curley, Alan J., Hannan, Fadil M., Christie, Paul T., Bowl, Michael R., Turner, Jeremy J. O., Barber, Mathew, Gillham-Nasenya, Irina, Hampson, Geeta, Spector, Tim D., Thakker, Rajesh V.

“…Summary Objectives  Associations between calcium‐sensing receptor (CaSR) polymorphisms and serum calcium, PTH and bone mineral density (BMD) have been reported…”
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UK national chronic hypoparathyroidism audit by Kiam, Jian Shen, Sharma, Vivek, Glenister, Liz, Fraser, William D., Turner, Jeremy J. O.

“…Objectives Individuals with chronic hypoparathyroidism may experience suboptimal medical care with high frequency of unplanned hospitalisation and iatrogenic…”
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Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites by HANNAN, Fadil M, NESBIT, M. Andrew, LEMOS, Manuel C, BOWL, Michael R, BOUILLON, Roger, BRAIN, Caroline, BRIDGES, Nicola, BURREN, Christine, CONNELL, John M, HEIKE JUNG, MARKS, Eileen, MCCREDIE, David, CHEN ZHANG, MUGHAL, Zulf, RODDA, Christine, TOLLEFSEN, Sherida, BROWN, Edward M, YANG, Jenny J, THAKKER, Rajesh V, CRANSTON, Treena, CURLEY, Alan J, HARDING, Brian, FRATTER, Carl, RUST, Nigel, CHRISTIE, Paul T, TURNER, Jeremy J. O

“…The calcium-sensing receptor (CaSR) is a G-protein-coupled receptor that has an extracellular bilobed venus flytrap domain (VFTD) predicted to contain five…”
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Genetic Mapping Studies of Familial Juvenile Hyperuricemic Nephropathy on Chromosome 16p11-p13 by Stacey, Joanna M., Turner, Jeremy J. O., Harding, Brian, Nesbit, M. Andrew, Kotanko, Peter, Lhotta, Karl, Puig, Juan G., Torres, Rosa J., Thakker, Rajesh V.

“…Familial juvenile hyperuricemic nephropathy (FJHN), which is inherited as an autosomal dominant disorder, is characterized by hyperuricemia, a low fractional…”
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Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3 by Hannan, Fadil M, Nesbit, M Andrew, Turner, Jeremy J O, Stacey, Joanna M, Cianferotti, Luisella, Christie, Paul T, Conigrave, Arthur D, Whyte, Michael P, Thakker, Rajesh V

“…Familial benign hypocalciuric hypercalcaemia (FBHH) is a genetically heterogeneous disorder that consists of three designated types, FBHH1, FBHH2 and FBHH3,…”
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Hypercalcaemia and primary hyperparathyroidism by Kiam, Jian Shen, Turner, Jeremy J O

“…Hypercalcaemia is most commonly caused by primary hyperparathyroidism (PHPT) or malignancy. PHPT is common, affects women more than men, and is usually caused…”
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Hypercalcaemia and primary hyperparathyroidism by Turner, Jeremy J O

“…Hypercalcaemia is most commonly caused by primary hyperparathyroidism (PHPT) or malignancy. PHPT is common, affects women more than men, and is usually caused…”
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Constitutive P2Y 2 receptor activity regulates basal lipolysis in human adipocytes by Ali, Seema B, Turner, Jeremy J O, Fountain, Samuel J

“…White adipocytes are key regulators of metabolic homeostasis, which release stored energy as free fatty acids via lipolysis. Adipocytes possess both basal and…”
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Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3 by HANNAN, Fadil M, NESBIT, M. Andrew, TURNER, Jeremy Jo, STACEY, Joanna M, CIANFEROTTI, Luisella, CHRISTIE, Paul T, CONIGRAVE, Arthur D, WHYTE, Michael P, THAKKER, Rajesh V

“…Familial benign hypocalciuric hypercalcaemia (FBHH) is a genetically heterogeneous disorder that consists of three designated types, FBHH1, FBHH2 and FBHH3,…”
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Frequent Occurrence of an Intron 4 Mutation in Multiple Endocrine Neoplasia Type 1 by Turner, Jeremy J. O., Leotlela, Poloko D., Pannett, Anna A. J., Forbes, Simon A., Bassett, J. H. Duncan, Harding, Brian, Christie, Paul T., Bowen-Jones, David, Ellard, Sian, Hattersley, Andrew, Jackson, Charles E., Pope, Richard, Quarrell, Oliver W., Trembath, Richard, Thakker, Rajesh V.

“…MEN1 is an autosomal dominant disorder characterized by parathyroid, pituitary, and pancreatic tumors. The MEN1 gene is located on chromosome 11q13 and encodes…”
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Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1 by Turner, Jeremy J O, Leotlela, Poloko D, Pannett, Anna A J, Forbes, Simon A, Bassett, J H Duncan, Harding, Brian, Christie, Paul T, Bowen-Jones, David, Ellard, Sian, Hattersley, Andrew, Jackson, Charles E, Pope, Richard, Quarrell, Oliver W, Trembath, Richard, Thakker, Rajesh V

“…MEN1 is an autosomal dominant disorder characterized by parathyroid, pituitary, and pancreatic tumors. The MEN1 gene is located on chromosome 11q13 and encodes…”
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Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1 : The impact of the human genome on endocrinology: Special features by TURNER, Jeremy J. O, LEOTLELA, Poloko D, JACKSON, Charles E, POPE, Richard, QUARRELL, Oliver W, TREMBATH, Richard, THAKKER, Rajesh V, PANNETT, Anna A. J, FORBES, Simon A, BASSETT, J. H, HARDING, Brian, CHRISTIE, Paul T, BOWEN-JONES, David, ELLARD, Sian, HATTERSLEY, Andrew

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ORIGINAL ARTICLE: Functional characterization of calcium sensing receptor polymorphisms and absence of association with indices of calcium homeostasis and bone mineral density by Harding, Brian, Curley, Alan J, Hannan, Fadil M, Christie, Paul T, Bowl, Michael R, Turner, Jeremy JO, Barber, Mathew, Gillham-Nasenya, Irina, Hampson, Geeta, Spector, Tim D, Thakker, Rajesh V

“…Objectives: Associations between calcium-sensing receptor (CaSR) polymorphisms and serum calcium, PTH and bone mineral density (BMD) have been reported by six…”
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Free radicals, myocytes and reperfusion injury by Turner, J J, Rice-Evans, C A, Davies, M J, Newman, E S

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