BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

652 related articles for article (PubMed ID: 14578966)

  • 21. Correlation between deletion patterns of SMN and NAIP genes and the clinical features of spinal muscular atrophy in Indian patients.
    Dastur RS; Gaitonde PS; Khadilkar SV; Udani VP; Nadkarni JJ
    Neurol India; 2006 Sep; 54(3):255-9. PubMed ID: 16936383
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Correlation between genotype and phenotype in Korean patients with spinal muscular atrophy.
    Cho K; Ryu K; Lee E; Won S; Kim J; Yoo OJ; Hahn S
    Mol Cells; 2001 Feb; 11(1):21-7. PubMed ID: 11266116
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families.
    Savas S; Eraslan S; Kantarci S; Karaman B; Acarsoz D; Tükel T; Cogulu O; Ozkinay F; Basaran S; Aydinli K; Yuksel-Apak M; Kirdar B
    Prenat Diagn; 2002 Aug; 22(8):703-9. PubMed ID: 12210580
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].
    Spiegel R; Hagmann A; Boltshauser E; Moser H
    Schweiz Med Wochenschr; 1996 May; 126(21):907-14. PubMed ID: 8693311
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [A study of survival motor neuron and neuronal apoptosis inhibitory protein gene in spinal muscular atrophy].
    Zhang L; Yang X; Xiao B
    Zhonghua Nei Ke Za Zhi; 2001 Jun; 40(6):401-4. PubMed ID: 11798607
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A genetic and phenotypic analysis in Spanish spinal muscular atrophy patients with c.399_402del AGAG, the most frequently found subtle mutation in the SMN1 gene.
    Cuscó I; López E; Soler-Botija C; Jesús Barceló M; Baiget M; Tizzano EF
    Hum Mutat; 2003 Aug; 22(2):136-43. PubMed ID: 12872254
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular analysis of the SMN1 and NAIP genes in Iranian patients with spinal muscular atrophy.
    Derakhshandeh-Peykar P; Esmaili M; Ousati-Ashtiani Z; Rahmani M; Babrzadeh F; Farshidi S; Attaran E; Sajedifar MM; Farhud DD
    Ann Acad Med Singap; 2007 Nov; 36(11):937-41. PubMed ID: 18071605
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 25(1):64-71. PubMed ID: 15580564
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophy.
    Arkblad EL; Darin N; Berg K; Kimber E; Brandberg G; Lindberg C; Holmberg E; Tulinius M; Nordling M
    Neuromuscul Disord; 2006 Dec; 16(12):830-8. PubMed ID: 17049859
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Sequence of a 131-kb region of 5q13.1 containing the spinal muscular atrophy candidate genes SMN and NAIP.
    Chen Q; Baird SD; Mahadevan M; Besner-Johnston A; Farahani R; Xuan J; Kang X; Lefebvre C; Ikeda JE; Korneluk RG; MacKenzie AE
    Genomics; 1998 Feb; 48(1):121-7. PubMed ID: 9503025
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic testing and risk assessment for spinal muscular atrophy (SMA).
    Ogino S; Wilson RB
    Hum Genet; 2002 Dec; 111(6):477-500. PubMed ID: 12436240
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis of spinal muscular atrophy in Turkish families.
    Erdem H; Dayangaç D; Pehlivan S; Topaloglu H
    Cent Eur J Public Health; 2001 Feb; 9(1):35-7. PubMed ID: 11243588
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes.
    Haider MZ; Moosa A; Dalal H; Habib Y; Reynold L
    J Biomed Sci; 2001; 8(2):191-6. PubMed ID: 11287750
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular analysis of SMA patients without homozygous SMN1 deletions using a new strategy for identification of SMN1 subtle mutations.
    Clermont O; Burlet P; Benit P; Chanterau D; Saugier-Veber P; Munnich A; Cusin V
    Hum Mutat; 2004 Nov; 24(5):417-27. PubMed ID: 15459957
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular analysis of the SMN and NAIP genes in Saudi spinal muscular atrophy patients.
    Al Rajeh S; Majumdar R; Awada A; Adeyokunnu A; Al Jumah M; Al Bunyan M; Snellen A
    J Neurol Sci; 1998 Jun; 158(1):43-6. PubMed ID: 9667776
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Spinal muscular atrophy carrier screening by multiplex polymerase chain reaction using dried blood spot on filter paper.
    Majumdar R; Rehana Z; Al Jumah M; Fetaini N
    Ann Hum Genet; 2005 Mar; 69(Pt 2):216-21. PubMed ID: 15720302
    [TBL] [Abstract][Full Text] [Related]  

  • 38. SMA type 2 unrelated to chromosome 5q13.
    Nevo Y; Kramer U; Legum C; Shomrat R; Fatal A; Soffer D; Harel S; Shapira Y
    Am J Med Genet; 1998 Jan; 75(2):193-5. PubMed ID: 9450884
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Survival motor neuron SMN1 and SMN2 gene promoters: identical sequences and differential expression in neurons and non-neuronal cells.
    Boda B; Mas C; Giudicelli C; Nepote V; Guimiot F; Levacher B; Zvara A; Santha M; LeGall I; Simonneau M
    Eur J Hum Genet; 2004 Sep; 12(9):729-37. PubMed ID: 15162126
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 33.