Biomedical Engineering Reference
In-Depth Information
Stoneley M, Willis AE (2004) Cellular internal ribosome entry segments: structures, trans-acting
factors and regulation of gene expression. Oncogene 23:3200-3207
Tollervey D, Lehtonen H, Carmo-Fonseca M, Hurt EC (1991) The small nucleolar RNP protein
NOP1 (fibrillarin) is required for pre-rRNA processing in yeast. EMBO J 10:573-583
Tollervey D, Lehtonen H, Jansen R, Kern H, Hurt EC (1993) Temperature-sensitive mutations
demonstrate roles for yeast fibrillarin in pre-rRNA processing, pre-rRNA methylation, and
ribosome assembly. Cell 72:443-457
Tortoriello G, de Celis JF, Furia M (2010) Linking pseudouridine synthases to growth, develop-
ment and cell competition. FEBS J 277:3249-3263
Tsukiyama T, Ishida N, Shirane M, Minamishima YA, Hatakeyama S, Kitagawa M, Nakayama K
(2001) Down-regulation of p27Kip1 expression is required for development and function of T
cells. J Immunol 166:304-312
Tycowski KT, Steitz JA (2001) Non-coding snoRNA host genes in Drosophila: expression strate-
gies for modification guide snoRNAs. Eur J Cell Biol 80:119-125
van Riggelen J, Yetil A, Felsher DW (2010) MYC as a regulator of ribosome biogenesis and pro-
tein synthesis. Nat Rev Cancer 10:301-309
Vitali P, Royo H, Seitz H, Bachellerie JP, Huttenhofer A, Cavaille J (2003) Identification of 13
novel human modification guide RNAs. Nucleic Acids Res 31:6543-6551
Vulliamy T, Marrone A, Goldman F, Dearlove A, Bessler M, Mason PJ, Dokal I (2001) The RNA
component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature
413:432-435
Vulliamy TJ, Marrone A, Knight SW, Walne A, Mason PJ, Dokal I (2006) Mutations in dyskerato-
sis congenita: their impact on telomere length and the diversity of clinical presentation. Blood
107:2680-2685
Vulliamy T, Beswick R, Kirwan M, Marrone A, Digweed M, Walne A, Dokal I (2008) Mutations
in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis con-
genita. Proc Natl Acad Sci U S A 105:8073-8078
Walbott H, Machado-Pinilla R, Liger D, Blaud M, Rety S, Grozdanov PN, Godin K, van Tilbeurgh
H, Varani G, Meier UT, Leulliot N (2011) The H/ACA RNP assembly factor SHQ1 functions
as an RNA mimic. Genes Dev 25:2398-2408
Walne AJ, Vulliamy T, Marrone A, Beswick R, Kirwan M, Masunari Y, Al-Qurashi FH, Aljurf M,
Dokal I (2007) Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one
subtype due to mutations in the telomerase-associated protein NOP10. Hum Mol Genet
16:1619-1629
Wang C, Meier UT (2004) Architecture and assembly of mammalian H/ACA small nucleolar and
telomerase ribonucleoproteins. EMBO J 23:1857-1867
Watkins NJ, Gottschalk A, Neubauer G, Kastner B, Fabrizio P, Mann M, Luhrmann R (1998)
Cbf5p, a potential pseudouridine synthase, and Nhp2p, a putative RNA-binding protein, are
present together with Gar1p in all H BOX/ACA-motif snoRNPs and constitute a common
bipartite structure. RNA 4:1549-1568
Watkins NJ, Segault V, Charpentier B, Nottrott S, Fabrizio P, Bachi A, Wilm M, Rosbash M,
Branlant C, Luhrmann R (2000) A common core RNP structure shared between the small
nucleolar box C/D RNPs and the spliceosomal U4 snRNP. Cell 103:457-466
Weber MJ (2006) Mammalian small nucleolar RNAs are mobile genetic elements. PLoS Genet
2:e205
Westman BJ, Verheggen C, Hutten S, Lam YW, Bertrand E, Lamond AI (2010) A proteomic screen
for nucleolar SUMO targets shows SUMOylation modulates the function of Nop5/Nop58. Mol
Cell 39:618-631
Wilson JE, Pestova TV, Hellen CU, Sarnow P (2000a) Initiation of protein synthesis from the A site
of the ribosome. Cell 102:511-520
Wilson JE, Powell MJ, Hoover SE, Sarnow P (2000b) Naturally occurring dicistronic cricket paral-
ysis virus RNA is regulated by two internal ribosome entry sites. Mol Cell Biol 20:4990-4999
Wolfraim LA, Letterio JJ (2005) Cutting edge: p27Kip1 deficiency reduces the requirement for
CD28-mediated costimulation in naive CD8+ but not CD4+ T lymphocytes. J Immunol
174:2481-2484
Search WWH ::
Custom Search