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Cancer research funding data to drive collaboration and inform action.
Garton EM, Cheetham M, Cira MK, Davies L, Mitrou P, Perin DP, Ross AL, Zafar SN, Duncan K. Garton EM, et al. Among authors: cheetham m. Lancet Oncol. 2023 Jun;24(6):584-586. doi: 10.1016/S1470-2045(23)00153-5. Lancet Oncol. 2023. PMID: 37269838 No abstract available.
World RePORT: a database for mapping biomedical research funding.
Adam T, Akuffo H, Carter JG, Charat Z, Cheetham MJ, Crisafulli A, Danielson CM, Gunning J, Haugen B, Jajkowicz D, Kay S, Kilmarx PH, López JM, Olesen OF, Peñas-Jiménez I, Tesfagiorgis K, Wallick SK, Glass RI. Adam T, et al. Among authors: cheetham mj. Lancet Glob Health. 2020 Jan;8(1):e27-e29. doi: 10.1016/S2214-109X(19)30459-0. Lancet Glob Health. 2020. PMID: 31839135 Free article. No abstract available.
Increasing Effectiveness and Equity in Strengthening Health Research Capacity Using Data and Metrics: Recent Advances of the ESSENCE Mechanism.
Kilmarx PH, Maitin T, Adam T, Aslanyan G, Cheetham M, Cruz J, Eigbike M, Gaye O, Jones CM, Kupfer L, Lindo J, Mijumbi R, Nachega JB, Nishi JB, Pantelidou I, Sarker M, Swaminathan S. Kilmarx PH, et al. Among authors: cheetham m. Ann Glob Health. 2023 Jun 2;89(1):38. doi: 10.5334/aogh.3948. eCollection 2023. Ann Glob Health. 2023. PMID: 37273490 Free PMC article.
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease.
Bhattacharyya N, Chai N, Hafford-Tear NJ, Sadan AN, Szabo A, Zarouchlioti C, Jedlickova J, Leung SK, Liao T, Dudakova L, Skalicka P, Parekh M, Moghul I, Jeffries AR, Cheetham ME, Muthusamy K, Hardcastle AJ, Pontikos N, Liskova P, Tuft SJ, Davidson AE. Bhattacharyya N, et al. Among authors: cheetham me. PLoS Genet. 2024 May 7;20(5):e1011230. doi: 10.1371/journal.pgen.1011230. eCollection 2024 May. PLoS Genet. 2024. PMID: 38713708 Free article.
Home versus in-centre haemodialysis for people with kidney failure.
Cheetham MS, Ethier I, Krishnasamy R, Cho Y, Palmer SC, Johnson DW, Craig JC, Stroumza P, Frantzen L, Hegbrant J, Strippoli GF. Cheetham MS, et al. Cochrane Database Syst Rev. 2024 Apr 8;4(4):CD009535. doi: 10.1002/14651858.CD009535.pub3. Cochrane Database Syst Rev. 2024. PMID: 38588450 Review.
Practicalities of Cell Sorting.
Cheetham M, Davies D, Hall C, Petersen CC, Schulte R, Walker R. Cheetham M, et al. Methods Mol Biol. 2024;2779:125-143. doi: 10.1007/978-1-0716-3738-8_7. Methods Mol Biol. 2024. PMID: 38526785
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability.
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, Nikolopoulos G, Rigby A, Black GC, Watson CM, Mansour S, Inglehearn CF, Mighell AJ, Bloch-Zupan A; UK Inherited Retinal Disease Consortium, Genomics England Research Consortium. Smith CEL, et al. J Med Genet. 2024 Apr 8:jmg-2023-109728. doi: 10.1136/jmg-2023-109728. Online ahead of print. J Med Genet. 2024. PMID: 38458752 Free article.
306 results