Browsing Centre for Endocrinology by Issue Date

ERG K+ channel blockade enhances firing and epinephrine secretion in rat chromaffin cells: the missing link to LQT2-related sudden death?

Gullo, F; Ales, E; Rosati, B; Lecchi, M; Masi, A; Guasti, L; Cano-Abad, MF; Arcangeli, A; Lopez, MG; Wanke, E (2002-12)

A HIF1 alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas

Dahia, PLM; Ross, KN; Wright, ME; Hayashida, CY; Santagata, S; Barontini, M; Kung, AL; Sanso, G; Powers, JF; Tischler, AS (2005-07)

Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasia

Lin, L; Hindmarsh, PC; Metherell, LA; Alzyoud, M; Al-Ali, M; Brain, CE; Clark, AJL; Dattani, MT; Achermann, JC (2007-02)

The Orexigenic Effect of Ghrelin Is Mediated through Central Activation of the Endogenous Cannabinoid System

Kola, B; Farkas, I; Christ-Crain, M; Wittmann, G; Lolli, F; Amin, F; Harvey-White, J; Liposits, Z; Kunos, G; Grossman, AB (2008-03-12)

Distinct monocyte gene-expression profiles in autoimmune diabetes

Padmos, RC; Schloot, NC; Beyan, H; Ruwhof, C; Staal, FJT; de Ridder, D; Aanstoot, HJ; Lam-Tse, WK; de Wit, H; de Herder, C (2008-10)

Intergenerational Transmission of Glucose Intolerance and Obesity by In Utero Undernutrition in Mice

Jimenez-Chillaron, JC; Isganaitis, E; Charalambous, M; Gesta, S; Pentinat-Pelegrin, T; Faucette, RR; Otis, JP; Chow, A; Diaz, R; Ferguson-Smith, A (2009-02)

Gene Dosage Effects of the Imprinted Delta-Like Homologue 1 (Dlk1/Pref1) in Development: Implications for the Evolution of Imprinting

da Rocha, ST; Charalambous, M; Lin, S-P; Gutteridge, I; Ito, Y; Gray, D; Dean, W; Ferguson-Smith, AC (2009-02)

Functional consequence of a novel Y129C mutation in a patient with two contradictory melanocortin-2-receptor mutations

Chan, LF; Chung, TT; Massoud, AF; Metherell, LA; Clark, AJL (2009-04)

Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency

Chan, LF; Metherell, LA; Krude, H; Ball, C; O'Riordan, SMP; Costigan, C; Lynch, SA; Savage, MO; Cavarzere, P; Clark, AJL (2009-08)

Adenovirus-based virotherapy enabled by cellular YB-1 expression in vitro and in vivo

Rognoni, E; Widmaier, M; Haczek, C; Mantwill, K; Holzmüller, R; Gansbacher, B; Kolk, A; Schuster, T; Schmid, RM; Saur, D (Springer Science and Business Media LLC, 2009-10)

Cannabinoids for clinicians: the rise and fall of the cannabinoid antagonists

Butler, H; Korbonits, M (2009-11)

Identification and characterisation of a novel GHR defect disrupting the polypyrimidine tract and resulting in GH insensitivity

David, A; Miraki-Moud, F; Shaw, NJ; Savage, MO; Clark, AJL; Metherell, LA (2010-01)

Predicting adult-onset autoimmune diabetes: clarity from complexity.

Leslie, RD (2010-02)

Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency

Dias, RP; Chan, LF; Metherell, LA; Pearce, SHS; Clark, AJL (2010-02)

Trials within trials? Researcher, funder and ethical perspectives on the practicality and acceptability of nesting trials of recruitment methods in existing primary care trials

Graffy, J; Bower, P; Ward, E; Wallace, P; Delaney, B; Kinmonth, AL; Collier, D; Miller, J (2010-04-30)

Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2

Chung, TTLL; Chan, LF; Metherell, LA; Clark, AJL (2010-05)

Characterization of Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutations in Familial Isolated Pituitary Adenoma Families

Igreja, S; Chahal, HS; King, P; Bolger, GB; Srirangalingam, U; Guasti, L; Chapple, JP; Trivellin, G; Gueorguiev, M; Guegan, K (2010-08)