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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 15987103)

  • 21. Targeting of SMN to Cajal bodies is mediated by self-association.
    Morse R; Shaw DJ; Todd AG; Young PJ
    Hum Mol Genet; 2007 Oct; 16(19):2349-58. PubMed ID: 17635841
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical and genetic study of spinal muscular atrophies in Oman.
    Koul R; Al Futaisi A; Chacko A; Rao V; Simsek M; Muralitharan S; Ganguly SS; Bayoumi R
    J Child Neurol; 2007 Oct; 22(10):1227-30. PubMed ID: 17940251
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Stimulating full-length SMN2 expression by delivering bifunctional RNAs via a viral vector.
    Baughan T; Shababi M; Coady TH; Dickson AM; Tullis GE; Lorson CL
    Mol Ther; 2006 Jul; 14(1):54-62. PubMed ID: 16580882
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis of spinal muscular atrophy in Chinese by genetic analysis of fetal cells.
    Wu T; Ding XS; Li WL; Yao J; Deng XX
    Chin Med J (Engl); 2005 Aug; 118(15):1274-7. PubMed ID: 16117881
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene.
    Moutou C; Machev N; Gardes N; Viville S
    Prenat Diagn; 2006 Nov; 26(11):1037-41. PubMed ID: 16941715
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fabrication and validation of a multi-channel type microfluidic chip for electrokinetic streaming potential devices.
    Chun MS; Shim MS; Choi NW
    Lab Chip; 2006 Feb; 6(2):302-9. PubMed ID: 16450042
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.
    Chen WJ; Wu ZY; Lin MT; Su JF; Lin Y; Murong SX; Wang N
    Arch Neurol; 2007 Feb; 64(2):225-31. PubMed ID: 17296838
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Spinal muscular atrophy: clinical classification and disease heterogeneity.
    Russman BS
    J Child Neurol; 2007 Aug; 22(8):946-51. PubMed ID: 17761648
    [TBL] [Abstract][Full Text] [Related]  

  • 29. DNA mutation detection with chip-based temperature gradient capillary electrophoresis using a slantwise radiative heating system.
    Zhang HD; Zhou J; Xu ZR; Song J; Dai J; Fang J; Fang ZL
    Lab Chip; 2007 Sep; 7(9):1162-70. PubMed ID: 17713615
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy.
    Zapletalová E; Hedvicáková P; Kozák L; Vondrácek P; Gaillyová R; Maríková T; Kalina Z; Jüttnerová V; Fajkus J; Fajkusová L
    Neuromuscul Disord; 2007 Jun; 17(6):476-81. PubMed ID: 17475491
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy.
    Vezain M; Saugier-Veber P; Melki J; Toutain A; Bieth E; Husson M; Pedespan JM; Viollet L; Pénisson-Besnier I; Fehrenbach S; Bou J; Frébourg T; Tosi M
    Eur J Hum Genet; 2007 Oct; 15(10):1054-62. PubMed ID: 17609673
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of a battery of tests for drug candidate evaluation in the SMNDelta7 neonate model of spinal muscular atrophy.
    El-Khodor BF; Edgar N; Chen A; Winberg ML; Joyce C; Brunner D; Suárez-Fariñas M; Heyes MP
    Exp Neurol; 2008 Jul; 212(1):29-43. PubMed ID: 18455159
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Pinched flow fractionation devices for detection of single nucleotide polymorphisms.
    Larsen AV; Poulsen L; Birgens H; Dufva M; Kristensen A
    Lab Chip; 2008 May; 8(5):818-21. PubMed ID: 18432355
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Rapid genetic diagnosis and prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography.
    Zhu HY; Wu LQ; Pan Q; Tang BS; Liang DS; Long ZG; Dai HP; Xia K; Xia JH
    Chin Med J (Engl); 2006 Jul; 119(14):1222-5. PubMed ID: 16863617
    [No Abstract]   [Full Text] [Related]  

  • 35. Axonal-SMN (a-SMN), a protein isoform of the survival motor neuron gene, is specifically involved in axonogenesis.
    Setola V; Terao M; Locatelli D; Bassanini S; Garattini E; Battaglia G
    Proc Natl Acad Sci U S A; 2007 Feb; 104(6):1959-64. PubMed ID: 17261814
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Microfluidic probe: a new tool for integrating microfluidic environments and electronic wafer-probing.
    Routenberg DA; Reed MA
    Lab Chip; 2010 Jan; 10(1):123-7. PubMed ID: 20024060
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Enhancement of electrokinetically driven microfluidic T-mixer using frequency modulated electric field and channel geometry effects.
    Yan D; Yang C; Miao J; Lam Y; Huang X
    Electrophoresis; 2009 Sep; 30(18):3144-52. PubMed ID: 19764063
    [TBL] [Abstract][Full Text] [Related]  

  • 38. In vivo activation of SMN in spinal muscular atrophy carriers and patients treated with valproate.
    Brichta L; Holker I; Haug K; Klockgether T; Wirth B
    Ann Neurol; 2006 Jun; 59(6):970-5. PubMed ID: 16607616
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 65(3):267-77. PubMed ID: 16651888
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Spinal muscular atrophy: from gene to therapy.
    Wirth B; Brichta L; Hahnen E
    Semin Pediatr Neurol; 2006 Jun; 13(2):121-31. PubMed ID: 17027862
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.