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krishna chatterjee
krishna chatterjee
未知所在单位机构
在 medschl.cam.ac.uk 的电子邮件经过验证
标题
引用次数
引用次数
年份
Induction of adipocyte complement-related protein of 30 kilodaltons by PPARγ agonists: a potential mechanism of insulin sensitization
TP Combs, JA Wagner, J Berger, T Doebber, WJ Wang, BB Zhang, ...
Endocrinology 143 (3), 998-1007, 2002
8492002
Hypothalamic AMPK and fatty acid metabolism mediate thyroid regulation of energy balance
M López, L Varela, MJ Vázquez, S Rodríguez-Cuenca, CR González, ...
Nature medicine 16 (9), 1001-1008, 2010
7752010
Safety and immunogenicity of seven COVID-19 vaccines as a third dose (booster) following two doses of ChAdOx1 nCov-19 or BNT162b2 in the UK (COV-BOOST): a blinded, multicentre …
APS Munro, L Janani, V Cornelius, PK Aley, G Babbage, D Baxter, M Bula, ...
The Lancet 398 (10318), 2258-2276, 2021
7312021
Prevalence and relative risk of other autoimmune diseases in subjects with autoimmune thyroid disease
K Boelaert, PR Newby, MJ Simmonds, RL Holder, JD Carr-Smith, ...
The American journal of medicine 123 (2), 183. e1-183. e9, 2010
5712010
Mechanism of corepressor binding and release from nuclear hormone receptors
L Nagy, HY Kao, JD Love, C Li, E Banayo, JT Gooch, V Krishna, ...
Genes & development 13 (24), 3209-3216, 1999
5201999
Paracrine regulation of angiogenesis and adipocyte differentiation during in vivo adipogenesis
D Fukumura, A Ushiyama, DG Duda, L Xu, J Tam, V Krishna, K Chatterjee, ...
Circulation research 93 (9), e88-e97, 2003
4512003
A mutation in the thyroid hormone receptor alpha gene
E Bochukova, N Schoenmakers, M Agostini, E Schoenmakers, ...
New England Journal of Medicine 366 (3), 243-249, 2012
4332012
Pitfalls in the measurement and interpretation of thyroid function tests
O Koulouri, C Moran, D Halsall, K Chatterjee, M Gurnell
Best practice & research Clinical endocrinology & metabolism 27 (6), 745-762, 2013
3532013
Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans
E Schoenmakers, M Agostini, C Mitchell, N Schoenmakers, L Papp, ...
The Journal of clinical investigation 120 (12), 4220-4235, 2010
3322010
Genetic analysis of 29 kindreds with generalized and pituitary resistance to thyroid hormone. Identification of thirteen novel mutations in the thyroid hormone receptor beta gene.
M Adams, C Matthews, TN Collingwood, Y Tone, P Beck-Peccoz, ...
The Journal of clinical investigation 94 (2), 506-515, 1994
2901994
Clonal dynamics of haematopoiesis across the human lifespan
E Mitchell, M Spencer Chapman, N Williams, KJ Dawson, N Mende, ...
Nature 606 (7913), 343-350, 2022
2842022
2013 European thyroid association guidelines for the diagnosis and treatment of thyrotropin-secreting pituitary tumors
P Beck-Peccoz, A Lania, A Beckers, K Chatterjee, JL Wemeau
European thyroid journal 2 (2), 76-82, 2013
2652013
Initial thyroid status and cardiovascular risk factors: the EPIC‐Norfolk prospective population study
SM Boekholdt, SM Titan, WM Wiersinga, K Chatterjee, DCG Basart, ...
Clinical endocrinology 72 (3), 404-410, 2010
2592010
Prospective functional classification of all possible missense variants in PPARG
AR Majithia, B Tsuda, M Agostini, K Gnanapradeepan, R Rice, G Peloso, ...
Nature genetics 48 (12), 1570-1575, 2016
2472016
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement
Y Sun, B Bak, N Schoenmakers, ASP van Trotsenburg, W Oostdijk, ...
Nature genetics 44 (12), 1375-1381, 2012
2332012
A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate
M Castanet, SM Park, A Smith, M Bost, J Leger, S Lyonnet, A Pelet, ...
Human molecular genetics 11 (17), 2051-2059, 2002
2302002
Hypothalamic AMPK-ER stress-JNK1 axis mediates the central actions of thyroid hormones on energy balance
N Martínez-Sánchez, P Seoane-Collazo, C Contreras, L Varela, ...
Cell metabolism 26 (1), 212-229. e12, 2017
2212017
Non-DNA binding, dominant-negative, human PPARγ mutations cause lipodystrophic insulin resistance
M Agostini, E Schoenmakers, C Mitchell, I Szatmari, D Savage, A Smith, ...
Cell metabolism 4 (4), 303-311, 2006
2212006
Follitropin (FSH) deficiency in an infertile male due to FSHβ gene mutation. A syndrome of normal puberty and virilization but under-developed testicles with azoospermia, low …
G Lindstedt, E Nyström, C Matthews, I Ernest, PO Janson, K Chatterjee
Walter de Gruyter 36 (8), 663-665, 1998
2081998
Retardation of post‐natal development caused by a negatively acting thyroid hormone receptor α1
A Tinnikov, K Nordström, P Thorén, JM Kindblom, S Malin, B Rozell, ...
The EMBO journal, 2002
2002002
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