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T Dwight

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Articles 38
Citations 155
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Recent Articles
1.
Kim E, Rath E, Tsang V, Duff A, Robinson B, Church W, et al.
Endocr Relat Cancer . 2015 May; 22(3):387-97. PMID: 25972245
Mitochondrial dysfunction, due to mutations of the gene encoding succinate dehydrogenase (SDH), has been implicated in the development of adrenal phaeochromocytomas, sympathetic and parasympathetic paragangliomas, renal cell carcinomas, gastrointestinal stromal...
2.
Tsang V, Dwight T, Benn D, Meyer-Rochow G, Gill A, Sywak M, et al.
Endocr Relat Cancer . 2014 Mar; 21(3):415-26. PMID: 24623741
miR-210 is a key regulator of response to hypoxia. Pheochromocytomas (PCs) and paragangliomas (PGLs) with germline SDHx or VHL mutations have pseudohypoxic gene expression signatures. We hypothesised that PC/PGLs containing...
3.
Dwight T
J Med Res . 2009 Dec; 12(1):17-40.9. PMID: 19971625
No abstract available.
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Dwight T
J Med Res . 2009 Dec; 9(3):324-8. PMID: 19971538
No abstract available.
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Dwight T
J Med Res . 2009 Dec; 7(1):113-114.1. PMID: 19971446
No abstract available.
6.
Cardinal J, Bergman L, Hayward N, Sweet A, Warner J, Marks L, et al.
J Med Genet . 2005 Jan; 42(1):69-74. PMID: 15635078
Introduction: Mutation testing for the MEN1 gene is a useful method to diagnose and predict individuals who either have or will develop multiple endocrine neoplasia type 1 (MEN 1). Clinical...
7.
Dwight T, Kytola S, Teh B, Theodosopoulos G, Richardson A, Philips J, et al.
Eur J Endocrinol . 2002 May; 146(5):619-27. PMID: 11980616
Objective: The aim of this study was to determine the primary genetic events that may underlie the formation of parathyroid tumors in patients with lithium-associated hyperparathyroidism (HPT). Methods: Comparative genomic...
8.
Benn D, Dwight T, Richardson A, Delbridge L, Bambach C, Stowasser M, et al.
Cancer Res . 2001 Jan; 60(24):7048-51. PMID: 11156410
Pheochromocytomas are tumors of the adrenal medulla originating in the chromaffin cells derived from the neural crest. Ten % of these tumors are associated with the familial cancer syndromes multiple...
9.
Capes-Davis A, Andrew S, Hyland V, Twigg S, Learoyd D, Dwight T, et al.
Gene Expr . 2000 Aug; 8(5-6):311-26. PMID: 10947080
The RET proto-oncogene encodes a receptor tyrosine kinase activated by the binding of factors from the glial cell line-derived neurotrophic factor (GDNF) family to receptor-alpha components such as GDNF family...
10.
Dwight T, Twigg S, Delbridge L, Wong F, Farnebo F, Richardson A, et al.
Clin Endocrinol (Oxf) . 2000 Aug; 53(1):85-92. PMID: 10931084
Objective: Hyperparathyroidism (HPT) is a common endocrine disorder. Several loci of genetic interest have been identified in parathyroid tumours, including the MEN1 gene locus at 11q13; the HPT-JT region at...