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 *

203 related articles for article (PubMed ID: 21821450)

  • 21. Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III.
    Zheleznyakova GY; Kiselev AV; Vakharlovsky VG; Rask-Andersen M; Chavan R; Egorova AA; Schiöth HB; Baranov VS
    BMC Med Genet; 2011 Jul; 12():96. PubMed ID: 21762474
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patients.
    Watihayati MS; Zabidi-Hussin AM; Tang TH; Matsuo M; Nishio H; Zilfalil BA
    Pediatr Int; 2007 Feb; 49(1):11-4. PubMed ID: 17250498
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A comprehensive overview of SMN and NAIP copy numbers in Iranian SMA patients.
    Savad S; Ashrafi MR; Samadaian N; Heidari M; Modarressi MH; Zamani G; Amidi S; Younesi S; Amin MMT; Saadati P; Ronagh A; Ardakani HS; Eslami S; Ghafouri-Fard S
    Sci Rep; 2023 Feb; 13(1):3202. PubMed ID: 36828874
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Modification of phenotype by SMN2 copy numbers in two Chinese families with SMN1 deletion in two continuous generations.
    Chen WJ; He J; Zhang QJ; Lin QF; Chen YF; Lin XZ; Lin MT; Murong SX; Wang N
    Clin Chim Acta; 2012 Nov; 413(23-24):1855-60. PubMed ID: 22884440
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity.
    Harada Y; Sutomo R; Sadewa AH; Akutsu T; Takeshima Y; Wada H; Matsuo M; Nishio H
    J Neurol; 2002 Sep; 249(9):1211-9. PubMed ID: 12242541
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.
    Miskovic M; Lalic T; Radivojevic D; Cirkovic S; Vlahovic G; Zamurovic D; Guc-Scekic M
    Tohoku J Exp Med; 2011 Nov; 225(3):153-9. PubMed ID: 21971302
    [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. Gender Effects on the Clinical Phenotype in Japanese Patients with Spinal Muscular Atrophy.
    Ar Rochmah M; Shima A; Harahap NIF; Niba ETE; Morisada N; Yanagisawa S; Saito T; Kaneko K; Saito K; Morioka I; Iijima K; Lai PS; Bouike Y; Nishio H; Shinohara M
    Kobe J Med Sci; 2017 Oct; 63(2):E41-E44. PubMed ID: 29434173
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic findings of Cypriot spinal muscular atrophy patients.
    Theodorou L; Nicolaou P; Koutsou P; Georghiou A; Anastasiadou V; Tanteles G; Kyriakides T; Zamba-Papanicolaou E; Christodoulou K
    Neurol Sci; 2015 Oct; 36(10):1829-34. PubMed ID: 26017350
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Real-world evidence: Risdiplam in a patient with spinal muscular atrophy type I with a novel splicing mutation and one SMN2 copy.
    Ma K; Zhang K; Chen D; Wang C; Abdalla M; Zhang H; Tian R; Liu Y; Song L; Zhang X; Liu F; Liu G; Wang D
    Hum Mol Genet; 2024 Jun; 33(13):1120-1130. PubMed ID: 38520738
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases.
    Cuscó I; Barceló MJ; del Rio E; Martín Y; Hernández-Chico C; Bussaglia E; Baiget M; Tizzano EF
    Hum Genet; 2001 Mar; 108(3):222-9. PubMed ID: 11354634
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 24(10):1052-4. PubMed ID: 14578966
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients.
    Mrad R; Dorboz I; Ben Jemaa L; Maazoul F; Trabelsi M; Chaabouni M; Mlaiki B; Miladi N; Hentati F; Chaabouni H
    Tunis Med; 2006 Aug; 84(8):465-9. PubMed ID: 17175684
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients.
    Yamamoto T; Sato H; Lai PS; Nurputra DK; Harahap NI; Morikawa S; Nishimura N; Kurashige T; Ohshita T; Nakajima H; Yamada H; Nishida Y; Toda S; Takanashi J; Takeuchi A; Tohyama Y; Kubo Y; Saito K; Takeshima Y; Matsuo M; Nishio H
    Brain Dev; 2014 Nov; 36(10):914-20. PubMed ID: 24359787
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Deletions in the SMN and NAIP genes in patients with spinal muscular atrophy in Croatia.
    Sertić J; Barisić N; Sostarko M; Bosnjak N; Culić V; Cvitanović L; Ferencak G; Brzović Z; Stavljenić-Rukavina A
    Coll Antropol; 1997 Dec; 21(2):487-92. PubMed ID: 9439064
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Quantitative analysis of the genes determining spinal muscular atrophy].
    Nagymihály M; Herczegfalvi A; Tímár L; Karcagi V
    Ideggyogy Sz; 2009 Nov; 62(11-12):390-7. PubMed ID: 20025129
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Association of copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein gene with the natural history in a Chinese spinal muscular atrophy cohort.
    Qu YJ; Ge XS; Bai JL; Wang LW; Cao YY; Lu YY; Jin YW; Wang H; Song F
    J Child Neurol; 2015 Mar; 30(4):429-36. PubMed ID: 25330799
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Spinal muscular atrophy patient detection and carrier screening using dried blood spots on filter paper.
    Harahap NI; Harahap IS; Kaszynski RH; Nurputra DK; Hartomo TB; Pham HT; Yamamoto T; Morikawa S; Nishimura N; Rusdi I; Widiastuti R; Nishio H
    Genet Test Mol Biomarkers; 2012 Feb; 16(2):123-9. PubMed ID: 21942573
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.