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Mutation of POC1B in a severe syndromic retinal ciliopathy.
Beck BB, Phillips JB, Bartram MP, Wegner J, Thoenes M, Pannes A, Sampson J, Heller R, Göbel H, Koerber F, Neugebauer A, Hedergott A, Nürnberg G, Nürnberg P, Thiele H, Altmüller J, Toliat MR, Staubach S, Boycott KM, Valente EM, Janecke AR, Eisenberger T, Bergmann C, Tebbe L, Wang Y, Wu Y, Fry AM, Westerfield M, Wolfrum U, Bolz HJ. Beck BB, et al. Among authors: sampson j. Hum Mutat. 2014 Oct;35(10):1153-62. doi: 10.1002/humu.22618. Epub 2014 Aug 11. Hum Mutat. 2014. PMID: 25044745 Free PMC article.
Hsp70 proteins in mitosis and disease.
O'Regan L, Sampson J, Fry AM. O'Regan L, et al. Among authors: sampson j. Oncotarget. 2015 Oct 20;6(32):32293-4. doi: 10.18632/oncotarget.5965. Oncotarget. 2015. PMID: 26450908 Free PMC article. No abstract available.
Desmoid tumour: a rare cause of congenital unilateral calf enlargement mimicking calf hypertrophy.
Elseed M, Sampson JN, Polvikoski T, Henderson M, Parkhurst Y, Bertoli M, Schiava M, Lofra RM, Moat D, Wong K, Michell-Sodhi J, Guglieri M, Straub V, Harris E, Marini-Bettolo C. Elseed M, et al. Among authors: sampson jn. Neuromuscul Disord. 2024 Dec 4;47:105258. doi: 10.1016/j.nmd.2024.105258. Online ahead of print. Neuromuscul Disord. 2024. PMID: 39709903
1,559 results