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Journal Abstract Search
455 related items for PubMed ID: 16449324
1. Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells. Renvoisé B, Khoobarry K, Gendron MC, Cibert C, Viollet L, Lefebvre S. J Cell Sci; 2006 Feb 15; 119(Pt 4):680-92. PubMed ID: 16449324 [Abstract] [Full Text] [Related]
2. Targeting of SMN to Cajal bodies is mediated by self-association. Morse R, Shaw DJ, Todd AG, Young PJ. Hum Mol Genet; 2007 Oct 01; 16(19):2349-58. PubMed ID: 17635841 [Abstract] [Full Text] [Related]
3. Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy. Sun Y, Grimmler M, Schwarzer V, Schoenen F, Fischer U, Wirth B. Hum Mutat; 2005 Jan 01; 25(1):64-71. PubMed ID: 15580564 [Abstract] [Full Text] [Related]
7. Modulation of SMN nuclear foci and cytoplasmic localization by its C-terminus. Hua Y, Zhou J. Cell Mol Life Sci; 2004 Oct 01; 61(19-20):2658-63. PubMed ID: 15526170 [Abstract] [Full Text] [Related]
8. The survival of motor neurons protein determines the capacity for snRNP assembly: biochemical deficiency in spinal muscular atrophy. Wan L, Battle DJ, Yong J, Gubitz AK, Kolb SJ, Wang J, Dreyfuss G. Mol Cell Biol; 2005 Jul 01; 25(13):5543-51. PubMed ID: 15964810 [Abstract] [Full Text] [Related]
9. Fibroblast growth factor-2(23) binds directly to the survival of motoneuron protein and is associated with small nuclear RNAs. Claus P, Bruns AF, Grothe C. Biochem J; 2004 Dec 15; 384(Pt 3):559-65. PubMed ID: 15222879 [Abstract] [Full Text] [Related]
10. Diverse small-molecule modulators of SMN expression found by high-throughput compound screening: early leads towards a therapeutic for spinal muscular atrophy. Jarecki J, Chen X, Bernardino A, Coovert DD, Whitney M, Burghes A, Stack J, Pollok BA. Hum Mol Genet; 2005 Jul 15; 14(14):2003-18. PubMed ID: 15944201 [Abstract] [Full Text] [Related]
11. Nuclear gems and Cajal (coiled) bodies in fetal tissues: nucleolar distribution of the spinal muscular atrophy protein, SMN. Young PJ, Le TT, Dunckley M, Nguyen TM, Burghes AH, Morris GE. Exp Cell Res; 2001 May 01; 265(2):252-61. PubMed ID: 11302690 [Abstract] [Full Text] [Related]
13. The relationship between SMN, the spinal muscular atrophy protein, and nuclear coiled bodies in differentiated tissues and cultured cells. Young PJ, Le TT, thi Man N, Burghes AH, Morris GE. Exp Cell Res; 2000 May 01; 256(2):365-74. PubMed ID: 10772809 [Abstract] [Full Text] [Related]
14. A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells. Sharma A, Lambrechts A, Hao le T, Le TT, Sewry CA, Ampe C, Burghes AH, Morris GE. Exp Cell Res; 2005 Sep 10; 309(1):185-97. PubMed ID: 15975577 [Abstract] [Full Text] [Related]
15. Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein. Hebert MD, Szymczyk PW, Shpargel KB, Matera AG. Genes Dev; 2001 Oct 15; 15(20):2720-9. PubMed ID: 11641277 [Abstract] [Full Text] [Related]
16. Gemin proteins are required for efficient assembly of Sm-class ribonucleoproteins. Shpargel KB, Matera AG. Proc Natl Acad Sci U S A; 2005 Nov 29; 102(48):17372-7. PubMed ID: 16301532 [Abstract] [Full Text] [Related]
17. Unrip, a factor implicated in cap-independent translation, associates with the cytosolic SMN complex and influences its intracellular localization. Grimmler M, Otter S, Peter C, Müller F, Chari A, Fischer U. Hum Mol Genet; 2005 Oct 15; 14(20):3099-111. PubMed ID: 16159890 [Abstract] [Full Text] [Related]
18. A role for protein phosphatase PP1γ in SMN complex formation and subnuclear localization to Cajal bodies. Renvoisé B, Quérol G, Verrier ER, Burlet P, Lefebvre S. J Cell Sci; 2012 Jun 15; 125(Pt 12):2862-74. PubMed ID: 22454514 [Abstract] [Full Text] [Related]
19. Analysis of mutations in the tudor domain of the survival motor neuron protein SMN. Mohaghegh P, Rodrigues NR, Owen N, Ponting CP, Le TT, Burghes AH, Davies KE. Eur J Hum Genet; 1999 Jul 15; 7(5):519-25. PubMed ID: 10439956 [Abstract] [Full Text] [Related]
20. Genetic conversion of an SMN2 gene to SMN1: a novel approach to the treatment of spinal muscular atrophy. DiMatteo D, Callahan S, Kmiec EB. Exp Cell Res; 2008 Feb 15; 314(4):878-86. PubMed ID: 18078930 [Abstract] [Full Text] [Related] Page: [Next] [New Search]