Homozygous Mutations in NEUROD1 Are Responsible for a Novel Syndrome of Permanent Neonatal Diabetes and Neurological Abnormalities
RUBIO-CABEZAS, Oscar, MINTON, Jayne A. L, KANTOR, Iren, WILLIAMS, Denise, ELLARD, Sian, HATTERSLEY, Andrew T
Published in Diabetes (New York, N.Y.) (01.09.2010)
Published in Diabetes (New York, N.Y.) (01.09.2010)
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Wolcott-Rallison Syndrome Is the Most Common Genetic Cause of Permanent Neonatal Diabetes in Consanguineous Families
Rubio-Cabezas, Oscar, Patch, Ann-Marie, Minton, Jayne A. L, Flanagan, Sarah E, Edghill, Emma L, Hussain, Khalid, Balafrej, Amina, Deeb, Asma, Buchanan, Charles R, Jefferson, Ian G, Mutair, Angham, Hattersley, Andrew T, Ellard, Sian
Published in The journal of clinical endocrinology and metabolism (01.11.2009)
Published in The journal of clinical endocrinology and metabolism (01.11.2009)
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Clinical Heterogeneity in Patients With FOXP3 Mutations Presenting With Permanent Neonatal Diabetes
Rubio-Cabezas, Oscar, Minton, Jayne A.L, Caswell, Richard, Shield, Julian P, Deiss, Dorothee, Sumnik, Zdenek, Cayssials, Amely, Herr, Mathias, Loew, Anja, Lewis, Vaughan, Ellard, Sian, Hattersley, Andrew T
Published in Diabetes care (2009)
Published in Diabetes care (2009)
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Association Analysis of 6,736 U.K. Subjects Provides Replication and Confirms TCF7L2 as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk
GROVES, Christopher J, ZEGGINI, Eleftheria, MCCARTHY, Mark I, MINTON, Jayne, FRAYLING, Timothy M, WEEDON, Michael N, RAYNER, Nigel W, HITMAN, Graham A, WALKER, Mark, WILTSHIRE, Steven, HATTERSLEY, Andrew T
Published in Diabetes (New York, N.Y.) (01.09.2006)
Published in Diabetes (New York, N.Y.) (01.09.2006)
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Mutation surveyor: software for DNA sequence analysis
Minton, Jayne A L, Flanagan, Sarah E, Ellard, Sian
Published in Methods in molecular biology (Clifton, N.J.) (01.01.2011)
Published in Methods in molecular biology (Clifton, N.J.) (01.01.2011)
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Sodium-potassium ATPase beta 1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress
Zatyka, Malgorzata, Ricketts, Christopher, da Silva Xavier, Gabriela, Minton, Jayne, Fenton, Sarah, Hofmann-Thiel, Sabine, Rutter, Guy A, Barrett, Timothy G
Published in Human molecular genetics (01.01.2008)
Published in Human molecular genetics (01.01.2008)
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Association Studies of Genetic Variation in the WFS1 Gene and Type 2 Diabetes in U.K. Populations
MINTON, Jayne A. L, HATTERSLEY, Andrew T, OWEN, Katharine, MCCARTHY, Mark I, WALKER, Mark, LATIF, Farida, BARRETT, Timothy, FRAYLING, Timothy M
Published in Diabetes (New York, N.Y.) (01.04.2002)
Published in Diabetes (New York, N.Y.) (01.04.2002)
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Thiamine-responsive megaloblastic anaemia syndrome : Long-term follow-up and mutation analysis of seven families
RICKETTS, Christopher J, MINTON, Jayne A, SAMUEL, Jacob, ARIYAWANSA, Indra, WALES, Jerry K, LO, Ivan F, BARRETT, Timothy G
Published in Acta pædiatrica (Oslo) (2006)
Published in Acta pædiatrica (Oslo) (2006)
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Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiology
Edghill, Emma L, Minton, Jayne A L, Groves, Christopher J, Flanagan, Sarah E, Patch, Ann-Marie, Rubio-Cabezas, Oscar, Shepherd, Maggie, Lenzen, Sigurd, McCarthy, Mark I, Ellard, Sian, Hattersley, Andrew T
Published in Journal of the Pancreas (08.01.2010)
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Published in Journal of the Pancreas (08.01.2010)
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Herpesvirus Entry Mediator Ligand (HVEM-L), a Novel Ligand for HVEM/TR2, Stimulates Proliferation of T Cells and Inhibits HT29 Cell Growth
Harrop, Jeremy A., McDonnell, Peter C., Brigham-Burke, Michael, Lyn, Sally D., Minton, Jayne, Tan, K.B., Dede, Kim, Spampanato, Jay, Silverman, Carol, Hensley, Preston, DiPrinzio, Rocco, Emery, John G., Deen, Keith, Eichman, Christopher, Chabot-Fletcher, Marie, Truneh, Alemseged, Young, Peter R.
Published in The Journal of biological chemistry (16.10.1998)
Published in The Journal of biological chemistry (16.10.1998)
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Characterization of [125I]‐SB‐258585 binding to human recombinant and native 5‐HT6 receptors in rat, pig and human brain tissue
Hirst, Warren D, Minton, Jayne A L, Bromidge, Steven M, Moss, Stephen F, Latter, Alison J, Riley, Graham, Routledge, Carol, Middlemiss, Derek N, Price, Gary W
Published in British journal of pharmacology (01.08.2000)
Published in British journal of pharmacology (01.08.2000)
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Wolfram syndrome
Minton, Jayne A L, Rainbow, Lynne A, Ricketts, Christopher, Barrett, Timothy G
Published in Reviews in endocrine & metabolic disorders (01.03.2003)
Published in Reviews in endocrine & metabolic disorders (01.03.2003)
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The impact of the angiotensin-converting enzyme insertion/deletion polymorphism on severe hypoglycemia in Type 2 diabetes
Freathy, Rachel M, Lonnen, Kathryn F, Steele, Anna M, Minton, Jayne A L, Frayling, Timothy M, Hattersley, Andrew T, Macleod, Kenneth M
Published in The review of diabetic studies (01.01.2006)
Published in The review of diabetic studies (01.01.2006)
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Pharmacological characterisation of a cell line expressing GABAB1b and GABAB2 receptor subunits
HIRST, Warren D, BABBS, Adam J, GREEN, Andrew, MINTON, Jayne A. L, SHAW, Tracy E, WISE, Alan, RICE, Simon Q, PANGALOS, Menelas N, PRICE, Gary W
Published in Biochemical pharmacology (01.04.2003)
Published in Biochemical pharmacology (01.04.2003)
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Pharmacological characterisation of a cell line expressing GABA B1b and GABA B2 receptor subunits
Hirst, Warren D., Babbs, Adam J., Green, Andrew, Minton, Jayne A.L., Shaw, Tracy E., Wise, Alan, Rice, Simon Q., Pangalos, Menelas N., Price, Gary W.
Published in Biochemical pharmacology (01.04.2003)
Published in Biochemical pharmacology (01.04.2003)
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Sodium-potassium ATPase β1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress
Zatyka, Malgorzata, Ricketts, Christopher, da Silva Xavier, Gabriela, Minton, Jayne, Fenton, Sarah, Hofmann-Thiel, Sabine, Rutter, Guy A, Barrett, Timothy G.
Published in Human molecular genetics (15.01.2008)
Published in Human molecular genetics (15.01.2008)
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Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes
Torsvik, Janniche, Johansson, Stefan, Johansen, Anders, Ek, Jakob, Minton, Jayne, Ræder, Helge, Ellard, Sian, Hattersley, Andrew, Pedersen, Oluf, Hansen, Torben, Molven, Anders, Njølstad, Pål R
Published in Human genetics (2010)
Published in Human genetics (2010)
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Journal Article
Characterization of [ 125 I]‐SB‐258585 binding to human recombinant and native 5‐HT 6 receptors in rat, pig and human brain tissue
Hirst, Warren D, Minton, Jayne A L, Bromidge, Steven M, Moss, Stephen F, Latter, Alison J, Riley, Graham, Routledge, Carol, Middlemiss, Derek N, Price, Gary W
Published in British journal of pharmacology (29.01.2009)
Published in British journal of pharmacology (29.01.2009)
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Journal Article
Sodium-potassium ATPase 1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress
Zatyka, Malgorzata, Ricketts, Christopher, da Silva Xavier, Gabriela, Minton, Jayne, Fenton, Sarah, Hofmann-Thiel, Sabine, Rutter, Guy A, Barrett, Timothy G
Published in Human molecular genetics (15.01.2008)
Published in Human molecular genetics (15.01.2008)
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Journal Article
Thiamine-responsive megaloblastic anaemia syndrome: Long-term follow-up and mutation analysis of seven families
Ricketts, Christopher J., Minton, Jayne A., Samuel, Jacob, Ariyawansa, Indra, Wales, Jerry K., Lo, Ivan F., Barrett, Timothy G.
Published in Acta Paediatrica (01.01.2006)
Published in Acta Paediatrica (01.01.2006)
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