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1.

Molecular spectrum of TSHß subunit gene defects in central hypothyroidism in the UK and Ireland.

Nicholas, A K; Jaleel, S; Lyons, G; Schoenmakers, E; Dattani, M T; Crowne, E; Bernhard, B; Kirk, J; Roche, E F; Chatterjee, V K; Schoenmakers, N.

Clin Endocrinol (Oxf); 86(3): 410-418, 2017 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-27362444

2.

Primary amenorrhoea and infertility due to a mutation in the beta-subunit of follicle-stimulating hormone.

Matthews, C H; Borgato, S; Beck-Peccoz, P; Adams, M; Tone, Y; Gambino, G; Casagrande, S; Tedeschini, G; Benedetti, A; Chatterjee, V K.

Nat Genet; 5(1): 83-6, 1993 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-8220432

3.

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia.

Clifton-Bligh, R J; Wentworth, J M; Heinz, P; Crisp, M S; John, R; Lazarus, J H; Ludgate, M; Chatterjee, V K.

Nat Genet; 19(4): 399-401, 1998 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-9697705

4.

Augmentation index in resistance to thyroid hormone (RTH).

Owen, P J D; Chatterjee, V K; John, R; Halsall, D; Lazarus, J H.

Clin Endocrinol (Oxf); 70(4): 650-4, 2009 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-18803680

5.

Rapid disease progression in a patient with mismatch repair-deficient and cortisol secreting adrenocortical carcinoma treated with pembrolizumab.

Casey, R T; Giger, O; Seetho, I; Marker, A; Pitfield, D; Boyle, L H; Gurnell, M; Shaw, A; Tischkowitz, M; Maher, E R; Chatterjee, V K; Janowitz, T; Mells, G; Corrie, P; Challis, B G.

Semin Oncol; 45(3): 151-155, 2018 06.

Artículo en Inglés | MEDLINE | ID: mdl-30262398

6.

Thyroid hormone resistance syndrome. Inhibition of normal receptor function by mutant thyroid hormone receptors.

Chatterjee, V K; Nagaya, T; Madison, L D; Datta, S; Rentoumis, A; Jameson, J L.

J Clin Invest; 87(6): 1977-84, 1991 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-2040690

7.

Activators of peroxisome proliferator-activated receptor gamma have depot-specific effects on human preadipocyte differentiation.

Adams, M; Montague, C T; Prins, J B; Holder, J C; Smith, S A; Sanders, L; Digby, J E; Sewter, C P; Lazar, M A; Chatterjee, V K; O'Rahilly, S.

J Clin Invest; 100(12): 3149-53, 1997 Dec 15.

Artículo en Inglés | MEDLINE | ID: mdl-9399962

8.

Inhibition of cellular proliferation through IkappaB kinase-independent and peroxisome proliferator-activated receptor gamma-dependent repression of cyclin D1.

Wang, C; Fu, M; D'Amico, M; Albanese, C; Zhou, J N; Brownlee, M; Lisanti, M P; Chatterjee, V K; Lazar, M A; Pestell, R G.

Mol Cell Biol; 21(9): 3057-70, 2001 May.

Artículo en Inglés | MEDLINE | ID: mdl-11287611

9.

A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis.

Baris, I; Arisoy, A E; Smith, A; Agostini, M; Mitchell, C S; Park, S M; Halefoglu, A M; Zengin, E; Chatterjee, V K; Battaloglu, E.

J Clin Endocrinol Metab; 91(10): 4183-7, 2006 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-16882747

10.

Influences of age, gender, smoking, and family history on autoimmune thyroid disease phenotype.

Manji, N; Carr-Smith, J D; Boelaert, K; Allahabadia, A; Armitage, M; Chatterjee, V K; Lazarus, J H; Pearce, S H S; Vaidya, B; Gough, S C; Franklyn, J A.

J Clin Endocrinol Metab; 91(12): 4873-80, 2006 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-16968788

11.

Elevated plasma adiponectin in humans with genetically defective insulin receptors.

Semple, R K; Soos, M A; Luan, J; Mitchell, C S; Wilson, J C; Gurnell, M; Cochran, E K; Gorden, P; Chatterjee, V K K; Wareham, N J; O'Rahilly, S.

J Clin Endocrinol Metab; 91(8): 3219-23, 2006 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-16705075

12.

Genetics of congenital hypothyroidism.

Park, S M; Chatterjee, V K K.

J Med Genet; 42(5): 379-89, 2005 May.

Artículo en Inglés | MEDLINE | ID: mdl-15863666

13.

Mild cold effects on hunger, food intake, satiety and skin temperature in humans.

Langeveld, M; Tan, C Y; Soeters, M R; Virtue, S; Ambler, G K; Watson, L P E; Murgatroyd, P R; Chatterjee, V K; Vidal-Puig, A.

Endocr Connect; 5(2): 65-73, 2016 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-26864459

14.

A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism.

Koulouri, O; Nicholas, A K; Schoenmakers, E; Mokrosinski, J; Lane, F; Cole, T; Kirk, J; Farooqi, I S; Chatterjee, V K; Gurnell, M; Schoenmakers, N.

J Clin Endocrinol Metab; 101(3): 847-51, 2016 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-26735259

15.

A dominant negative human peroxisome proliferator-activated receptor (PPAR){alpha} is a constitutive transcriptional corepressor and inhibits signaling through all PPAR isoforms.

Semple, R K; Meirhaeghe, A; Vidal-Puig, A J; Schwabe, J W R; Wiggins, D; Gibbons, G F; Gurnell, M; Chatterjee, V K K; O'Rahilly, S.

Endocrinology; 146(4): 1871-82, 2005 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-15661858

16.

Evidence for gene-nutrient interaction at the PPARgamma locus.

Luan, J; Browne, P O; Harding, A H; Halsall, D J; O'Rahilly, S; Chatterjee, V K; Wareham, N J.

Diabetes; 50(3): 686-9, 2001 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-11246892

17.

Spectrum of transcriptional, dimerization, and dominant negative properties of twenty different mutant thyroid hormone beta-receptors in thyroid hormone resistance syndrome.

Collingwood, T N; Adams, M; Tone, Y; Chatterjee, V K.

Mol Endocrinol; 8(9): 1262-77, 1994 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-7838159

18.

Repression of the human glycoprotein hormone alpha-subunit gene by glucocorticoids: evidence for receptor interactions with limiting transcriptional activators.

Chatterjee, V K; Madison, L D; Mayo, S; Jameson, J L.

Mol Endocrinol; 5(1): 100-10, 1991 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-1708098

19.

Thyroid hormone resistance syndrome manifests as an aberrant interaction between mutant T3 receptors and transcriptional corepressors.

Yoh, S M; Chatterjee, V K; Privalsky, M L.

Mol Endocrinol; 11(4): 470-80, 1997 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-9092799

20.

A novel TR beta mutation (R383H) in resistance to thyroid hormone syndrome predominantly impairs corepressor release and negative transcriptional regulation.

Clifton-Bligh, R J; de Zegher, F; Wagner, R L; Collingwood, T N; Francois, I; Van Helvoirt, M; Fletterick, R J; Chatterjee, V K.

Mol Endocrinol; 12(5): 609-21, 1998 May.

Artículo en Inglés | MEDLINE | ID: mdl-9605924

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