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Quoted phrase not found in phrase index: "Trichoepithelioma, multiple familial, 1"
Page 1
Small RNA: can RNA interference be exploited for therapy?
Wall NR, Shi Y. Wall NR, et al. Lancet. 2003 Oct 25;362(9393):1401-3. doi: 10.1016/S0140-6736(03)14637-5. Lancet. 2003. PMID: 14585643 Review.
A collection of RNA interference vectors that suppress 50 human de-ubiquitinating enzymes allowed Thijn Brummelkamp and colleagues to study this gene family and to identify de-ubiquitinating enzymes in cancer-relevant pathways (Nature 2003; 424: 797-801). These researchers found …
A collection of RNA interference vectors that suppress 50 human de-ubiquitinating enzymes allowed Thijn Brummelkamp and colleagues to study …
Skull invaders: when surgical pathology and neuropathology worlds collide.
Serracino HS, Kleinschmidt-Demasters BK. Serracino HS, et al. J Neuropathol Exp Neurol. 2013 Jul;72(7):600-13. doi: 10.1097/NEN.0b013e318299c40f. J Neuropathol Exp Neurol. 2013. PMID: 23771219
Unique tumors included a cutaneous cylindroma invasive of skull convexity occurring in familial cylindromatosis and a ganglioneuroma of the middle ear with massive bilateral skull base extension. ...
Unique tumors included a cutaneous cylindroma invasive of skull convexity occurring in familial cylindromatosis and a ganglion …
Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction.
Rajan N, Langtry JA, Ashworth A, Roberts C, Chapman P, Burn J, Trainer AH. Rajan N, et al. Arch Dermatol. 2009 Nov;145(11):1277-84. doi: 10.1001/archdermatol.2009.262. Arch Dermatol. 2009. PMID: 19917957 Free PMC article.
OBJECTIVES: To comprehensively ascertain the extent and severity of clinical features in affected individuals from 2 large families with proven heterozygous mutations in the CYLD locus and to correlate these findings with the 3 appendageal tumor predisposition syndromes (famil …
OBJECTIVES: To comprehensively ascertain the extent and severity of clinical features in affected individuals from 2 large families with pro …
Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes.
Ponti G, Nasti S, Losi L, Pastorino L, Pollio A, Benassi L, Giudice S, Bertazzoni G, Veratti E, Azzoni P, Bianchi Scarrà G, Seidenari S. Ponti G, et al. J Cutan Pathol. 2012 Mar;39(3):366-71. doi: 10.1111/j.1600-0560.2011.01813.x. Epub 2011 Nov 12. J Cutan Pathol. 2012. PMID: 22077640 Clinical Trial.
We describe two families with Brooke-Spiegler syndrome, one with familial cylindromatosis and one with multiple familial trichoepithelioma, which showed wide inter-family phenotypic variability. ...
We describe two families with Brooke-Spiegler syndrome, one with familial cylindromatosis and one with multiple familial trich …
15 results