Dr J H Duncan Bassett

Publications


Journals

  • Karunaratne A; Esapa CR; Hiller J; Boyde A; Head R; Bassett JH; Terrill NJ; Williams GR; et alBrown MA; Croucher PI; Brown SD; Cox RD; Barber AH; Thakker RV; Gupta HS. (Apr 2012). Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and backscattered electron imaging. J Bone Miner Res. 27:876-890. DOI.
  • Xing W; Govoni K; Donahue LR; Kesavan C; Wergedal J; Long C; Bassett JH; Gogakos A; et alWojcicka A; Williams GR; Mohan S. (13 Jan 2012). Genetic evidence that thyroid hormone is indispensable for prepubertal IGF-I expression and bone acquisition in mice. J Bone Miner Res. DOI.
  • Waung JA; Bassett JH; Williams GR. (Apr 2012). Thyroid hormone metabolism in skeletal development and adult bone maintenance. Trends Endocrinol Metab. 23:155-162. DOI.
  • Bassett JH; van der Spek A; Gogakos A; Williams GR. (2012). Quantitative X-ray imaging of rodent bone by Faxitron. Methods Mol Biol. 816:499-506. DOI.
  • Esapa CT; Hough TA; Testori S; Head RA; Crane EA; Chan CP; Evans H; Bassett JH; et alTylzanowski P; McNally EG; Carr AJ; Boyde A; Howell PG; Clark A; Williams GR; Brown MA; Croucher PI; Nesbit MA; Brown SD; Cox RD; Cheeseman MT; Thakker RV. (Feb 2012). A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation. J Bone Miner Res. 27:413-428. DOI.
  • Williams GR; Bassett JH. (Jun 2011). Deiodinases: the balance of thyroid hormone: local control of thyroid hormone action: role of type 2 deiodinase. J Endocrinol. 209:261-272. DOI.
  • Hu M; Bassett JH; Danks L; Howell PG; Xu K; Spanoudakis E; Kotsianidis I; Boyde A; et alWilliams GR; Horwood N; Roberts IA; Karadimitris A. (1 Mar 2011). Activated invariant NKT cells regulate osteoclast development and function. J Immunol. 186:2910-2917. DOI.
  • Vanleene M; Saldanha Z; Cloyd KL; Jell G; Bou-Gharios G; Bassett JH; Williams GR; Fisk NM; et alOyen ML; Stevens MM; Guillot PV; Shefelbine SJ. (20 Jan 2011). Transplantation of human fetal blood stem cells in the osteogenesis imperfecta mouse leads to improvement in multiscale tissue properties. Blood. 117:1053-1060. DOI.
  • Combs CE; Nicholls JJ; Bassett JHD; Williams GR. (2011). Thyroid hormones and bone development. Minerva Endocrinologica: a journal on endocrine system diseases. 36:71-85.
  • Gogakos AI; Bassett JHD; Williams GR. (1 Nov 2010). Thyroid and bone. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS. 503:129-136. Author weblink DOI.
  • Bassett JH; Boyde A; Howell PG; Bassett RH; Galliford TM; Archanco M; Evans H; Lawson MA; et alCroucher P; St Germain DL; Galton VA; Williams GR. (20 Apr 2010). Optimal bone strength and mineralization requires the type 2 iodothyronine deiodinase in osteoblasts. Proc Natl Acad Sci U S A. 107:7604-7609. DOI.
  • Bassett JHD. (1 Mar 2010). The skeletal consequences of altered thyroid hormone metabolism. ENDOCRINE JOURNAL. 57:S240-S240.
  • Bassett JH; Williams GR. (Apr 2009). The skeletal phenotypes of TRalpha and TRbeta mutant mice. J Mol Endocrinol. 42:269-282. DOI.
  • Gogakos AI; Cheung MS; Bassett JHD; Williams GR. (2009). Bone signalling pathways and treatment of osteoporosis. Expert review of Endcinology and Metabolism. 4:639-650.
  • Hameed S; Dhillo WS; Patterson M; Bloom SR; Rashid S; Bassett JHD; Williams GR; Gardiner JV. (2009). The Central Regulation of Food Intake and Energy Expenditure by Thyroid Hormones. Hot Thyroidology (www.hotthyroidology.com.
  • Bassett JH; Williams GR. (Sep 2008). Critical role of the hypothalamic-pituitary-thyroid axis in bone. Bone. 43:418-426. DOI.
  • Bassett JHD; Williams AJ; Murphy E; Boyde A; Howell PGT; Swinhoe R; Archanco M; Flamant F; et alSamarut J; Costagliola S; Vassart G; Weiss RE; Refetoff S; Williams GR. (1 Feb 2008). A lack of thyroid hormones rather than excess thyrotropin causes abnormal skeletal development in hypothyroidism. MOLECULAR ENDOCRINOLOGY. 22:501-512. Author weblink DOI.
  • Guillot PV; Abass O; Bassett JH; Shefelbine SJ; Bou-Gharios G; Chan J; Kurata H; Williams GR; et alPolak J; Fisk NM. (1 Feb 2008). Intrauterine transplantation of human fetal mesenchymal stem cells from first-trimester blood repairs bone and reduces fractures in osteogenesis imperfecta mice. Blood. 111:1717-1725. DOI.
  • Ghaffar A; Bassett JHD. (2008). Management of Normocalcaemic Primary Hyperparathyroidism. Review of Endocrinology. 1:1-3.
  • Galliford TM; Bernstein ND; Bassett JHD; Williams GR. (1 Aug 2007). Contrasting roles for thyroid hormone in the developing and adult skeleton. Hot Thyroidology (www.hotthyroidology.com). 1-11.
  • Bassett JH; Nordström K; Boyde A; Howell PG; Kelly S; Vennström B; Williams GR. (Aug 2007). Thyroid status during skeletal development determines adult bone structure and mineralization. Mol Endocrinol. 21:1893-1904. DOI.
  • Bassett JH; O'Shea PJ; Sriskantharajah S; Rabier B; Boyde A; Howell PG; Weiss RE; Roux JP; et alMalaval L; Clement-Lacroix P; Samarut J; Chassande O; Williams GR. (May 2007). Thyroid hormone excess rather than thyrotropin deficiency induces osteoporosis in hyperthyroidism. Mol Endocrinol. 21:1095-1107. DOI.
  • Harvey CB; Bassett JH; Maruvada P; Yen PM; Williams GR. (Apr 2007). The rat thyroid hormone receptor (TR) Deltabeta3 displays cell-, TR isoform-, and thyroid hormone response element-specific actions. Endocrinology. 148:1764-1773. DOI.
  • Murphy E; Bassett JHD; Williams GR. (1 Sep 2006). Disorders of calcium metabolism. Practitioner. 250:4-8.
  • Bassett JHD; O'Shea PJ; Chassande O; Samarut J; Cheng SY; Vennstrom B; Howell PGT; Boyde A; et alWilliams GR. (1 Mar 2006). Analysis of skeletal phenotypes in thyroid hormone receptor mutant mice. SCANNING. 28:91-93. Author weblink.
  • O'Shea PJ; Bassett JH; Cheng SY; Williams GR. (2006). Characterization of skeletal phenotypes of TRalpha1 and TRbeta mutant mice: implications for tissue thyroid status and T3 target gene expression. Nucl Recept Signal. 4:e011. DOI.
  • Bassett JH; Swinhoe R; Chassande O; Samarut J; Williams GR. (Jan 2006). Thyroid hormone regulates heparan sulfate proteoglycan expression in the growth plate. Endocrinology. 147:295-305. DOI.
  • O'Shea PJ; Bassett JH; Sriskantharajah S; Ying H; Cheng SY; Williams GR. (Dec 2005). Contrasting skeletal phenotypes in mice with an identical mutation targeted to thyroid hormone receptor alpha1 or beta. Mol Endocrinol. 19:3045-3059. DOI.
  • Galliford TM; Murphy E; Williams AJ; Bassett JH; Williams GR. (Dec 2005). Effects of thyroid status on bone metabolism: a primary role for thyroid stimulating hormone or thyroid hormone?. Minerva Endocrinol. 30:237-246.
  • Barnard JC; Williams AJ; Rabier B; Chassande O; Samarut J; Cheng SY; Bassett JH; Williams GR. (Dec 2005). Thyroid hormones regulate fibroblast growth factor receptor signaling during chondrogenesis. Endocrinology. 146:5568-5580. DOI.
  • Bladen JC; Moosajee M; Bassett JH. (Nov 2004). A tense case--Carney's triad. J R Soc Med. 97:540-541. DOI.
  • Bassett JH; Harvey CB; Williams GR. (31 Dec 2003). Mechanisms of thyroid hormone receptor-specific nuclear and extra nuclear actions. Mol Cell Endocrinol. 213:1-11. DOI.
  • Bassett JH; Williams GR. (Oct 2003). The molecular actions of thyroid hormone in bone. Trends Endocrinol Metab. 14:356-364.
  • Pannett AA; Kennedy AM; Turner JJ; Forbes SA; Cavaco BM; Bassett JH; Cianferotti L; Harding B; et alShine B; Flinter F; Maidment CG; Trembath R; Thakker RV. (May 2003). Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. Clin Endocrinol (Oxf). 58:639-646.
  • Turner JJ; Leotlela PD; Pannett AA; Forbes SA; Bassett JH; Harding B; Christie PT; Bowen-Jones D; et alEllard S; Hattersley A; Jackson CE; Pope R; Quarrell OW; Trembath R; Thakker RV. (Jun 2002). Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1. J Clin Endocrinol Metab. 87:2688-2693.
  • Bassett JH; O'Halloran DJ; Williams GR; Beardwell CG; Shalet SM; Thakker RV. (Jan 1999). Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism. Clin Endocrinol (Oxf). 50:69-75.
  • Bassett JH; Rashbass P; Harding B; Forbes SA; Pannett AA; Thakker RV. (Jan 1999). Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1. J Bone Miner Res. 14:3-10. DOI.
  • Höppener JW; De Wit MJ; Simarro-Doorten AY; Roijers JF; van Herrewaarden HM; Lips CJ; Parente F; Quincey D; et alGaudray P; Khodaei S; Weber G; Teh B; Farnebo F; Larsson C; Zhang CX; Calender A; Pannett AAJ; Forbes SA; Bassett JHD; Thakker RV; Lemmens I; Van de Ven WJ; Kas K. (1 Jun 1998). A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1. Genomics. 50:251-259.
  • (Jun 1998). The search for the MEN1 gene. The European Consortium on MEN-1. J Intern Med. 243:441-446.
  • Bassett JH; Forbes SA; Pannett AA; Lloyd SE; Christie PT; Wooding C; Harding B; Besser GM; et alEdwards CR; Monson JP; Sampson J; Wass JA; Wheeler MH; Thakker RV. (Feb 1998). Characterization of mutations in patients with multiple endocrine neoplasia type 1. Am J Hum Genet. 62:232-244. DOI.
  • Bassett JHD; Pannett AAJ; Forbes SA; Thakker RV; McCarthy M; Read AP; Teh BT; Larsson C; et alKytola S; Leisti J; Salmela P; Weber G; Giraud S; Zhang CX; Calender A; Hoppener JWM; vanAmstel HKP; Lips CJM; Kas K; VandeVen WJM; Gaudray P. (1 Oct 1997). The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1). HUMAN GENETICS. 100:657-665. Author weblink DOI.
  • Forbes SA; Pannett AA; Bassett JH; Harding B; Wooding C; Thakker RV; Butler R; Ogilvie D; et alAnand R; Gaudray P; Weber G; Larsson C; Zhang CX; Calender A; Höppener JW; Lips CJ; Kas K. (Sep 1997). Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1). Hum Genet. 100:481-485.
  • Lemmens I; Merregaert J; VandeVen WJM; Kas K; Zhang CX; Giraud S; Wautot V; Buisson N; et alDeWitte K; Salandre J; Lenoir G; Calender A; Parente F; Quincey D; Courseaux A; Carle GF; Gaudray P; DeWit MJ; Lips CJM; Hoppener JWM; Khodaei S; Grant AL; Weber G; Kytola S; Teh BT; Farnebo F; Grimmond S; Phelan C; Larsson C; Forbes SA; Bassett JHD; Pannett AAJ; Thakker RV. (15 Aug 1997). Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene - The European consortium on type 1 (MEN1) gene. GENOMICS. 44:94-100. Author weblink DOI.
  • Lemmens I; VandeVen WJM; Kas K; Zhang CX; Giraud S; Wautot V; Buisson N; DeWitte K; et alSalandre J; Lenoir G; Pugeat M; Calender A; Parente F; Quincey D; Gaudray P; DeWit MJ; Lips CJM; Hoppener JWM; Khodaei S; Grant AL; Weber G; Kytola S; Teh BT; Farnebo F; Phelan C; Hayward N; Larsson C; Pannett AAJ; Forbes SA; Bassett JHD; Thakker RV. (1 Jul 1997). Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. HUMAN MOLECULAR GENETICS. 6:1177-1183. Author weblink DOI.
  • Courseaux A; Grosgeorge J; Gaudray P; Pannett AAJ; Forbes SA; Williamson C; Bassett D; Thakker RV; et alTeh BT; Farnebo F; Shepherd J; Skogseid B; Larsson C; Giraud S; Zhang CX; Salandre J; Calender A. (1996). Definition of the Minimal MEN1 Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13. Genomics. 37:345-356.
  • Bassett JH; Thakker RV. (Jul 1995). Molecular genetics of disorders of calcium homeostasis. Baillieres Clin Endocrinol Metab. 9:581-608.
  • Hirst MC; Bassett JHD; Roche A; Davies KE. (1992). Preparation of radiolabelled hybridisation probes by STS labelling. Trends in Genetics. 8:5-6.
  • Hirst MC; Bassett JH; Roche A; Davies KE. (Jan 1992). Preparation of radiolabelled hybridization probes by STS labelling. Trends Genet. 8:6-7.
  • Hirst MC; Roche A; Flint TJ; Bassett JHD; Davies KE. (1991). Linear order of new and established DNA markers around the Fragile site at Xq27.3. Genomics. 10:243-249.

Chapters in books

  • Cheung MS; Gogakos AI; Bassett JHD; Williams GR. Oxford Textbook of Endocrinology and Diabetes. In Oxford Textbook of Endocrinology and Diabetes. 712-730. Wass J (ed); Stewart P (ed). Oxford University Press, USA (1 Aug 2011).
  • Bassett JHD; Thakker RV. Genetic and molecular biological aspects of endocrine disease. In Genetic and molecular biological aspects of endocrine disease. 581-608. Thakker RV (ed). (1995).

Conferences

  • Bassett JHD; Lu Y; Bernstein ND; Archanco M; Galliford TM; Ghaffar A; Yu M; Hernandez R; et alO'Shea PJ; Williams GR. Biological Effects of Thyroid Hormone on Bone. 13th International Congress of Endocrinology, 8 Nov 2008 - 12 Nov 2008. 175-180. MEDIMOND S R L (1 Jan 2008). Author weblink.
  • Bassett JHD; O'Shea PJ; Nordstrom K; Vennstrom B; Williams GR. Disruption of intramembranous and endochondral bone development in TR alpha 2 null mice. 2nd Joint Meeting of the European-Calcified-Tissue-Society/International-Bone-and-Mineral-Society, 25 Jun 2005 - 29 Jun 2005. 36:S225-S225. ELSEVIER SCIENCE INC (1 Jun 2005). Author weblink.
  • Williams GR. Thyroid and bone. 2nd Joint Meeting of the European-Calcified-Tissue-Society/International-Bone-and-Mineral-Society. 36:S111-S111. (Jun 2005).
  • Lemmes I; Van de Ven WJM; Kas K; Zhang CX; Giraud S; Wautot V; Buisson N; Pugeat M; et alPeix JL; Caldener A; Parente F; Quincey D; Courseaux A; Carle GF; Gaudray P; De Wit MJ; Lips CJM; Hoppener JWM; Khodaei S; Grant AL; Weber G; Teh BT; Farnebo F; Kytola S; Grimmond S; Phelan C; Larsson C; Bassett JHD; Forbes DA; Pannett AAJ; Thakker RV. The search for the MEN1 gene. 6th International Workshop on Multiple Endocrine Neoplasia and von Hippel-Lindau Disease, 25 Jun 1997 - 28 Jun 1997. 243:441-446. BLACKWELL SCIENCE LTD (1 Jun 1998). Author weblink.
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