Cambridge University Hospital


Standort der Organisation:
Cambridge, Großbritannien (UK)

Publikationen in Kooperation mit FAU-Wissenschaftern

Mangolini, M., Goette, F., Moore, A., Ammon, T., Oelsner, M., Lutzny-Geier, G.,... Ringshausen, I. (2018). Notch2 controls non-autonomous Wnt-signalling in chronic lymphocytic leukaemia. Nature Communications, 9(1).
Herrick, A.L., Peytrignet, S., Lunt, M., Pan, X., Hesselstrand, R., Mouthon, L.,... Denton, C.P. (2018). Patterns and predictors of skin score change in early diffuse systemic sclerosis from the European Scleroderma Observational Study. Annals of the Rheumatic Diseases.
Van Der Zanden, L.F.M., Vermeulen, S.H., Oskarsdottir, A., Maurits, J.S.F., Diekstra, M.H.M., Ambert, V.,... Oosterwijk, E. (2017). Description of the EuroTARGET cohort: A European collaborative project on TArgeted therapy in renal cell cancer-GEnetic- and tumor-related biomarkers for response and toxicity. Urologic Oncology-Seminars and Original Investigations, 35(8), 529.e9-529.e16.
Peytrignet, S., Denton, C.P., Lunt, M., Hesselstrand, R., Mouthon, L., Silman, A.,... Herrick, A.L. (2017). Disability, fatigue, pain and their associates in early diffuse cutaneous systemic sclerosis: the European Scleroderma Observational Study. Rheumatology.
Horton, S.J., Giotopoulos, G., Yun, H., Vohra, S., Sheppard, O., Bashford-Rogers, R.,... Huntly, B.J.P. (2017). Early loss of Crebbp confers malignant stem cell properties on lymphoid progenitors. Nature Cell Biology, 19(9), 1093-1104.
Jones, D., Boudes, P.F., Swain, M.G., Bowlus, C.L., Galambos, M.R., Bacon, B.R.,... Hirschfield, G.M. (2017). Seladelpar (MBX-8025), a selective PPAR-δ agonist, in patients with primary biliary cholangitis with an inadequate response to ursodeoxycholic acid: a double-blind, randomised, placebo-controlled, phase 2, proof-of-concept study. Lancet Gastroenterology and Hepatology, 2(10), 716-726.
Lehalle, D., Mosca-Boidron, A.-L., Begtrup, A., Boute-Benejean, O., Charles, P., Cho, M.T.,... Faivre, L. (2017). STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability. Journal of Medical Genetics, 54(7), 479-488.
Herrick, A.L., Pan, X., Peytrignet, S., Lunt, M., Hesselstrand, R., Mouthon, L.,... Denton, C.P. (2017). Treatment outcome in early diffuse cutaneous systemic sclerosis: the European Scleroderma Observational Study (ESOS). Annals of the Rheumatic Diseases.
Sifrim, A., Hitz, M.-P., Wilsdon, A., Breckpot, J., Al Turki, S.H., Thienpont, B.,... Hurles, M.E. (2016). Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing. Nature Genetics, 48(9), 1060-5.
Meyer, E., Carss, K.J., Rankin, J., Nichols, J.M.E., Grozeva, D., Joseph, A.P.,... Kurian, M.A. (2016). Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. Nature Genetics.
Pirie, A., Guo, Q., Kraft, P., Canisius, S., Eccles, D.M., Rahman, N.,... Schmidt, M.K. (2015). Common germline polymorphisms associated with breast cancer-specific survival. Breast Cancer Research, 17, 58.
Kramar, A., Negrier, S., Sylvester, R., Joniau, S., Mulders, P., Powles, T.,... Filleron, T. (2015). Guidelines for the definition of time-to-event end points in renal cell cancer clinical trials: results of the DATECAN project+. Annals of Oncology, 26(12), 2392-8.
Palmio, J., Evila, A., Chapon, F., Tasca, G., Xiang, F., Bradvik, B.,... Udd, B. (2014). Hereditary myopathy with early respiratory failure: occurrence in various populations. Journal of Neurology Neurosurgery and Psychiatry, 85(3), 345-53.

Zuletzt aktualisiert 2016-30-06 um 07:00