BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 16473310)

  • 1. No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree.
    Curtain R; Tajouri L; Lea R; MacMillan J; Griffiths L
    Eur J Med Genet; 2006; 49(1):57-62. PubMed ID: 16473310
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG.
    Norberg A; Forsgren L; Holmberg D; Holmberg M
    Neurosci Lett; 2006 Mar; 396(2):137-42. PubMed ID: 16378686
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.
    Jones KW; Ehm MG; Pericak-Vance MA; Haines JL; Boyd PR; Peroutka SJ
    Genomics; 2001 Dec; 78(3):150-4. PubMed ID: 11735221
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.
    Cevoli S; Pierangeli G; Monari L; Valentino ML; Bernardoni P; Mochi M; Cortelli P; Montagna P
    Neurol Sci; 2002 Apr; 23(1):7-10. PubMed ID: 12111614
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association analysis of chromosome 1 migraine candidate genes.
    Fernandez F; Curtain RP; Colson NJ; Ovcaric M; MacMillan J; Griffiths LR
    BMC Med Genet; 2007 Aug; 8():57. PubMed ID: 17727731
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [From gene to disease; from CACNA1A to migraine].
    Kors EE; Haan J; Frants RR; Ferrari MD
    Ned Tijdschr Geneeskd; 2001 Feb; 145(6):266-7. PubMed ID: 11236374
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group.
    Ophoff RA; Terwindt GM; Vergouwe MN; van Eijk R; Mohrenweiser H; Litt M; Hofker MH; Haan J; Ferrari MD; Frants RR
    Eur J Hum Genet; 1996; 4(6):321-8. PubMed ID: 9043864
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Replication study of the insulin receptor gene in migraine with aura.
    Netzer C; Freudenberg J; Heinze A; Heinze-Kuhn K; Goebel I; McCarthy LC; Roses AD; Göbel H; Todt U; Kubisch C
    Genomics; 2008 Jun; 91(6):503-7. PubMed ID: 18455362
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
    Ophoff RA; Terwindt GM; Vergouwe MN; Frants RR; Ferrari MD
    Neurologia; 1997 Dec; 12 Suppl 5():31-7. PubMed ID: 9436352
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome 19p13 loci in Finnish migraine with aura families.
    Kaunisto MA; Tikka PJ; Kallela M; Leal SM; Papp JC; Korhonen A; Hämäläinen E; Harno H; Havanka H; Nissilä M; Säkö E; Ilmavirta M; Kaprio J; Färkkilä M; Ophoff RA; Palotie A; Wessman M
    Am J Med Genet B Neuropsychiatr Genet; 2005 Jan; 132B(1):85-9. PubMed ID: 15449251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19].
    Joutel A; Bousser MG; Biousse V; Labauge P; Chabriat H; Nibbio A; Maciazek J; Meyer B; Bach MA; Weissenbach J
    Rev Neurol (Paris); 1994; 150(5):340-5. PubMed ID: 7878319
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The genetic spectrum of a population-based sample of familial hemiplegic migraine.
    Thomsen LL; Kirchmann M; Bjornsson A; Stefansson H; Jensen RM; Fasquel AC; Petursson H; Stefansson M; Frigge ML; Kong A; Gulcher J; Stefansson K; Olesen J
    Brain; 2007 Feb; 130(Pt 2):346-56. PubMed ID: 17142831
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genes on bovine chromosome 18 associated with bilateral convergent strabismus with exophthalmos in German Brown cattle.
    Fink S; Mömke S; Wöhlke A; Distl O
    Mol Vis; 2008 Sep; 14():1737-51. PubMed ID: 18836565
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Is the CACNA1A gene involved in familial migraine with aura?
    Brugnoni R; Leone M; Rigamonti A; Moranduzzo E; Cornelio F; Mantegazza R; Bussone G
    Neurol Sci; 2002 Apr; 23(1):1-5. PubMed ID: 12111613
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility.
    D'Onofrio M; Ambrosini A; Di Mambro A; Arisi I; Santorelli FM; Grieco GS; Nicoletti F; Nappi G; Pierelli F; Schoenen J; Buzzi MG
    Neurosci Lett; 2009 Mar; 453(1):12-5. PubMed ID: 19429006
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility.
    Lea RA; Curtain RP; Hutchins C; Brimage PJ; Griffiths LR
    Am J Med Genet; 2001 Dec; 105(8):707-12. PubMed ID: 11803518
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: no evidence for mutations in familial hyperaldosteronism type II in a large affected kindred.
    Elphinstone MS; Gordon RD; So A; Jeske YW; Stratakis CA; Stowasser M
    Clin Endocrinol (Oxf); 2004 Dec; 61(6):716-23. PubMed ID: 15579186
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.
    Morcuende JA; Minhas R; Dolan L; Stevens J; Beck J; Wang K; Weinstein SL; Sheffield V
    Spine (Phila Pa 1976); 2003 Sep; 28(17):2025-8; discussion 2029. PubMed ID: 12973153
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
    Fernandez DM; Hand CK; Sweeney BJ; Parfrey NA
    Headache; 2008 Jan; 48(1):101-8. PubMed ID: 18184292
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.