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120 related items for PubMed ID: 12847076
1. Protein expression changes in spinal muscular atrophy revealed with a novel antibody array technology. Anderson K, Potter A, Baban D, Davies KE. Brain; 2003 Sep; 126(Pt 9):2052-64. PubMed ID: 12847076 [Abstract] [Full Text] [Related]
3. Correlation between severity and SMN protein level in spinal muscular atrophy. Lefebvre S, Burlet P, Liu Q, Bertrandy S, Clermont O, Munnich A, Dreyfuss G, Melki J. Nat Genet; 1997 Jul; 16(3):265-9. PubMed ID: 9207792 [Abstract] [Full Text] [Related]
8. Hypomorphic Smn knockdown C2C12 myoblasts reveal intrinsic defects in myoblast fusion and myotube morphology. Shafey D, Côté PD, Kothary R. Exp Cell Res; 2005 Nov 15; 311(1):49-61. PubMed ID: 16219305 [Abstract] [Full Text] [Related]
9. 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]
10. Synergistic anti-apoptotic activity between Bcl-2 and SMN implicated in spinal muscular atrophy. Iwahashi H, Eguchi Y, Yasuhara N, Hanafusa T, Matsuzawa Y, Tsujimoto Y. Nature; 1997 Nov 27; 390(6658):413-7. PubMed ID: 9389483 [Abstract] [Full Text] [Related]
11. Spinal muscular atrophy: a deficiency in a ubiquitous protein; a motor neuron-specific disease. Monani UR. Neuron; 2005 Dec 22; 48(6):885-96. PubMed ID: 16364894 [Abstract] [Full Text] [Related]
12. Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy. Al-Jumah M, Majumdar R, Al-Rajeh S, Awada A, Chaves-Carbello E, Salih M, Al-Shahwan S, Al-Subiey K, Al-Uthaim S. Saudi Med J; 2003 Oct 22; 24(10):1052-4. PubMed ID: 14578966 [Abstract] [Full Text] [Related]
13. Activation of RNA metabolism-related genes in mouse but not human tissues deficient in SMN. Olaso R, Joshi V, Fernandez J, Roblot N, Courageot S, Bonnefont JP, Melki J. Physiol Genomics; 2006 Jan 12; 24(2):97-104. PubMed ID: 16118268 [Abstract] [Full Text] [Related]
14. Neuronal-specific roles of the survival motor neuron protein: evidence from survival motor neuron expression patterns in the developing human central nervous system. Giavazzi A, Setola V, Simonati A, Battaglia G. J Neuropathol Exp Neurol; 2006 Mar 12; 65(3):267-77. PubMed ID: 16651888 [Abstract] [Full Text] [Related]
15. High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients. Bouhouche A, Benomar A, Birouk N, Bouslam N, Ouazzani R, Yahyaoui M, Chkili T. J Neurol; 2003 Oct 12; 250(10):1209-13. PubMed ID: 14586604 [Abstract] [Full Text] [Related]
16. A non-sequence-specific requirement for SMN protein activity: the role of aminoglycosides in inducing elevated SMN protein levels. Wolstencroft EC, Mattis V, Bajer AA, Young PJ, Lorson CL. Hum Mol Genet; 2005 May 01; 14(9):1199-210. PubMed ID: 15790598 [Abstract] [Full Text] [Related]
17. 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]
18. SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS. Veldink JH, Kalmijn S, Van der Hout AH, Lemmink HH, Groeneveld GJ, Lummen C, Scheffer H, Wokke JH, Van den Berg LH. Neurology; 2005 Sep 27; 65(6):820-5. PubMed ID: 16093455 [Abstract] [Full Text] [Related]
19. A clinical, magnetic resonance imaging, and survival motor neuron gene deletion study of Hirayama disease. Misra UK, Kalita J, Mishra VN, Kesari A, Mittal B. Arch Neurol; 2005 Jan 27; 62(1):120-3. PubMed ID: 15642858 [Abstract] [Full Text] [Related]
20. Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy. Jablonka S, Karle K, Sandner B, Andreassi C, von Au K, Sendtner M. Hum Mol Genet; 2006 Feb 01; 15(3):511-8. PubMed ID: 16396995 [Abstract] [Full Text] [Related] Page: [Next] [New Search]