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CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
Dobson-Stone C, Hallupp M, Shahheydari H, Ragagnin AMG, Chatterton Z, Carew-Jones F, Shepherd CE, Stefen H, Paric E, Fath T, Thompson EM, Blumbergs P, Short CL, Field CD, Panegyres PK, Hecker J, Nicholson G, Shaw AD, Fullerton JM, Luty AA, Schofield PR, Brooks WS, Rajan N, Bennett MF, Bahlo M, Landers JE, Piguet O, Hodges JR, Halliday GM, Topp SD, Smith BN, Shaw CE, McCann E, Fifita JA, Williams KL, Atkin JD, Blair IP, Kwok JB. Dobson-Stone C, et al. Among authors: rajan n. Brain. 2020 Mar 1;143(3):783-799. doi: 10.1093/brain/awaa039. Brain. 2020. PMID: 32185393 Free PMC article.
CYLD in health and disease.
Marín-Rubio JL, Raote I, Inns J, Dobson-Stone C, Rajan N. Marín-Rubio JL, et al. Among authors: rajan n. Dis Model Mech. 2023 Jun 1;16(6):dmm050093. doi: 10.1242/dmm.050093. Epub 2023 Jun 30. Dis Model Mech. 2023. PMID: 37387450 Free PMC article. Review.
Milia: a useful clinical marker of CYLD mutation carrier status.
Bajwa DS, Nasr B, Carmichael AJ, Rajan N. Bajwa DS, et al. Among authors: rajan n. Clin Exp Dermatol. 2018 Mar;43(2):193-195. doi: 10.1111/ced.13296. Epub 2017 Oct 12. Clin Exp Dermatol. 2018. PMID: 29023940 No abstract available.
305 results