These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
25. Structural and functional characterization of human telomerase RNA processing and cajal body localization signals. Theimer CA; Jády BE; Chim N; Richard P; Breece KE; Kiss T; Feigon J Mol Cell; 2007 Sep; 27(6):869-81. PubMed ID: 17889661 [TBL] [Abstract][Full Text] [Related]
26. U4 snRNA nucleolar localization requires the NHPX/15.5-kD protein binding site but not Sm protein or U6 snRNA association. Gerbi SA; Borovjagin AV; Odreman FE; Lange TS J Cell Biol; 2003 Sep; 162(5):821-32. PubMed ID: 12939253 [TBL] [Abstract][Full Text] [Related]
27. [A role for Cajal bodies in assembly of the nuclear transcription machinery]. Gall JG Tsitologiia; 2003; 45(10):971-5. PubMed ID: 14989168 [TBL] [Abstract][Full Text] [Related]
28. Non-canonical Cajal bodies form in the nucleus of late stage avian oocytes lacking functional nucleolus. Khodyuchenko T; Gaginskaya E; Krasikova A Histochem Cell Biol; 2012 Jul; 138(1):57-73. PubMed ID: 22382586 [TBL] [Abstract][Full Text] [Related]
29. Architecture of human telomerase RNA. Zhang Q; Kim NK; Feigon J Proc Natl Acad Sci U S A; 2011 Dec; 108(51):20325-32. PubMed ID: 21844345 [TBL] [Abstract][Full Text] [Related]
30. A common sequence motif determines the Cajal body-specific localization of box H/ACA scaRNAs. Richard P; Darzacq X; Bertrand E; Jády BE; Verheggen C; Kiss T EMBO J; 2003 Aug; 22(16):4283-93. PubMed ID: 12912925 [TBL] [Abstract][Full Text] [Related]
31. Immunoprecipitation analysis to study RNA-protein interactions in Xenopus oocytes. Mabuchi N; Masuyama K; Ohno M Methods Mol Biol; 2008; 488():257-65. PubMed ID: 18982297 [TBL] [Abstract][Full Text] [Related]
33. hNaf1 is required for accumulation of human box H/ACA snoRNPs, scaRNPs, and telomerase. Hoareau-Aveilla C; Bonoli M; Caizergues-Ferrer M; Henry Y RNA; 2006 May; 12(5):832-40. PubMed ID: 16601202 [TBL] [Abstract][Full Text] [Related]
34. In vivo analysis of Cajal body movement, separation, and joining in live human cells. Platani M; Goldberg I; Swedlow JR; Lamond AI J Cell Biol; 2000 Dec; 151(7):1561-74. PubMed ID: 11134083 [TBL] [Abstract][Full Text] [Related]
35. PHAX and CRM1 are required sequentially to transport U3 snoRNA to nucleoli. Boulon S; Verheggen C; Jady BE; Girard C; Pescia C; Paul C; Ospina JK; Kiss T; Matera AG; Bordonné R; Bertrand E Mol Cell; 2004 Dec; 16(5):777-87. PubMed ID: 15574332 [TBL] [Abstract][Full Text] [Related]
36. Signal recognition particle assembly in relation to the function of amplified nucleoli of Xenopus oocytes. Sommerville J; Brumwell CL; Politz JC; Pederson T J Cell Sci; 2005 Mar; 118(Pt 6):1299-307. PubMed ID: 15741230 [TBL] [Abstract][Full Text] [Related]
37. Nuclear RanGTP is not required for targeting small nucleolar RNAs to the nucleolus. Narayanan A; Eifert J; Marfatia KA; Macara IG; Corbett AH; Terns RM; Terns MP J Cell Sci; 2003 Jan; 116(Pt 1):177-86. PubMed ID: 12456727 [TBL] [Abstract][Full Text] [Related]
39. Role of the box C/D motif in localization of small nucleolar RNAs to coiled bodies and nucleoli. Narayanan A; Speckmann W; Terns R; Terns MP Mol Biol Cell; 1999 Jul; 10(7):2131-47. PubMed ID: 10397754 [TBL] [Abstract][Full Text] [Related]
40. Cell cycle-dependent recruitment of telomerase RNA and Cajal bodies to human telomeres. Jády BE; Richard P; Bertrand E; Kiss T Mol Biol Cell; 2006 Feb; 17(2):944-54. PubMed ID: 16319170 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]