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 *

83 related articles for article (PubMed ID: 8651652)

  • 1. Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: homozygous NAIP deletion in a sporadic case.
    Jackson M; Morrison KE; Al-Chalabi A; Bakker M; Leigh PN
    Ann Neurol; 1996 Jun; 39(6):796-800. PubMed ID: 8651652
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Deletions causing spinal muscular atrophy do not predispose to amyotrophic lateral sclerosis.
    Parboosingh JS; Meininger V; McKenna-Yasek D; Brown RH; Rouleau GA
    Arch Neurol; 1999 Jun; 56(6):710-2. PubMed ID: 10369311
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic mapping of a mouse modifier gene that can prevent ALS onset.
    Kunst CB; Messer L; Gordon J; Haines J; Patterson D
    Genomics; 2000 Dec; 70(2):181-9. PubMed ID: 11112346
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.
    Watihayati MS; Fatemeh H; Marini M; Atif AB; Zahiruddin WM; Sasongko TH; Tang TH; Zabidi-Hussin ZA; Nishio H; Zilfalil BA
    Brain Dev; 2009 Jan; 31(1):42-5. PubMed ID: 18842367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Application of DNA-based tests for diagnosis of spinal muscular atrophy in Saudi Arabia.
    al-Rajeh S; Majumdar R; Awada A; al-Jumah M
    East Mediterr Health J; 1999 Nov; 5(6):1225-9. PubMed ID: 11924116
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of deletional damage in SMN1, SMN2, and NAIP genes in patients with spinal muscular atrophy in the northwestern region of Russia].
    Glotov AS; Kiselev AV; Ivashchenko TE; Baranov VS
    Genetika; 2001 Aug; 37(8):1156-9. PubMed ID: 11642117
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy.
    Taylor JE; Thomas NH; Lewis CM; Abbs SJ; Rodrigues NR; Davies KE; Mathew CG
    Eur J Hum Genet; 1998; 6(5):467-74. PubMed ID: 9801871
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS.
    Orrell RW; Habgood JJ; de Belleroche JS; Lane RJ
    J Neurol Sci; 1997 Jan; 145(1):55-61. PubMed ID: 9073029
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Survival motor neuron gene and neuronal apoptosis inhibitory protein gene deletion in patients with spinal muscular atrophy].
    Ma S; Yuan L; Liu T; Yang T; Zhou W; Wu H
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2000 Dec; 22(6):551-4. PubMed ID: 12903402
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 250(10):1209-13. PubMed ID: 14586604
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and molecular genetic features of congenital spinal muscular atrophy.
    Devriendt K; Lammens M; Schollen E; Van Hole C; Dom R; Devlieger H; Cassiman JJ; Fryns JP; Matthijs G
    Ann Neurol; 1996 Nov; 40(5):731-8. PubMed ID: 8957014
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A molecular genetic analysis of spinal muscular atrophy (SMA) in families at high risk from different regions of Ukraine].
    Ekshiian AIu; Livshits LA; Bychkova AM; Afanas'eva NA; Bariliak IR
    Tsitol Genet; 1997; 31(6):75-81. PubMed ID: 9591348
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deletion analysis of Bulgarian SMA families.
    Jordanova A; Stoyanova V; Uzunova M; Litvinenko I; Kremensky I
    Hum Mutat; 1998; 12(1):33-8. PubMed ID: 9633817
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis.
    Vechio JD; Bruijn LI; Xu Z; Brown RH; Cleveland DW
    Ann Neurol; 1996 Oct; 40(4):603-10. PubMed ID: 8871580
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene.
    Gambardella A; Mazzei R; Toscano A; Annesi G; Pasqua A; Annesi F; Quattrone F; Oliveri RL; Valentino P; Bono F; Aguglia U; Zappia M; Vita G; Quattrone A
    Ann Neurol; 1998 Nov; 44(5):836-9. PubMed ID: 9818944
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.
    Jackson M; Al-Chalabi A; Enayat ZE; Chioza B; Leigh PN; Morrison KE
    Ann Neurol; 1997 Nov; 42(5):803-7. PubMed ID: 9392581
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.