BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 10510981)

  • 1. Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24.
    Morita R; Miyazaki E; Shah PU; Castroviejo IP; Delgado-Escueta AV; Yamakawa K
    Epilepsy Res; 1999 Nov; 37(2):151-8. PubMed ID: 10510981
    [TBL] [Abstract][Full Text] [Related]  

  • 2. JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24.
    Morita R; Miyazaki E; Fong CY; Chen XN; Korenberg JR; Delgado-Escueta AV; Yamakawa K
    Biochem Biophys Res Commun; 1998 Jul; 248(2):307-14. PubMed ID: 9675132
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME.
    Moore T; Hecquet S; McLellann A; Ville D; Grid D; Picard F; Moulard B; Asherson P; Makoff AJ; McCormick D; Nashef L; Froguel P; Arzimanoglou A; LeGuern E; Bailleul B
    Epilepsy Res; 2001 Aug; 46(2):157-67. PubMed ID: 11463517
    [TBL] [Abstract][Full Text] [Related]  

  • 4. T-STAR gene: fine mapping in the candidate region for childhood absence epilepsy on 8q24 and mutational analysis in patients.
    Sugimoto Y; Morita R; Amano K; Shah PU; Pascual-Castroviejo I; Khan S; Delgado-Escueta AV; Yamakawa K
    Epilepsy Res; 2001 Aug; 46(2):139-44. PubMed ID: 11463515
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map.
    Sugimoto Y; Morita R; Amano K; Fong CY; Shah PU; Castroviejo IP; Khan S; Delgado-Escueta AV; Yamakawa K
    Genomics; 2000 Sep; 68(3):264-72. PubMed ID: 10995568
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.
    Delgado-Escueta AV; Medina MT; Serratosa JM; Castroviejo IP; Gee MN; Weissbecker K; Westling BW; Fong CY; Alonso ME; Cordova S; Shah P; Khan S; Sainz J; Rubio-Donnadieu F; Sparkes RS
    Adv Neurol; 1999; 79():351-74. PubMed ID: 10514826
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Analysis of haplotype-based haplotype relative risk and transmission disequilibrium test in childhood absence epilepsy].
    Ge X; Wang ZP; Zhang YF; Shao XH; Bao KR
    Zhonghua Er Ke Za Zhi; 2003 Sep; 41(9):675-9. PubMed ID: 14733810
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.
    Robinson R; Taske N; Sander T; Heils A; Whitehouse W; Goutières F; Aicardi J; Lehesjoki AE; Siren A; Laue Friis M; Kjeldsen MJ; Panayiotopoulos C; Kennedy C; Ferrie C; Rees M; Gardiner RM
    Epilepsy Res; 2002 Feb; 48(3):169-79. PubMed ID: 11904235
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Complex regulation and nuclear localization of JRK protein.
    Waldron R; Moore T
    Biochem Soc Trans; 2004 Dec; 32(Pt 6):920-3. PubMed ID: 15506925
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.
    Fong GC; Shah PU; Gee MN; Serratosa JM; Castroviejo IP; Khan S; Ravat SH; Mani J; Huang Y; Zhao HZ; Medina MT; Treiman LJ; Pineda G; Delgado-Escueta AV
    Am J Hum Genet; 1998 Oct; 63(4):1117-29. PubMed ID: 9758624
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolation and characterization of a Jerky and JRK/JH8 like gene, tigger transposable element derived 7, TIGD7.
    Dou T; Gu S; Zhou Z; Ji C; Zeng L; Ye X; Xu J; Ying K; Xie Y; Mao Y
    Biochem Genet; 2004 Aug; 42(7-8):279-85. PubMed ID: 15487591
    [No Abstract]   [Full Text] [Related]  

  • 12. Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation.
    Marini C; Harkin LA; Wallace RH; Mulley JC; Scheffer IE; Berkovic SF
    Brain; 2003 Jan; 126(Pt 1):230-40. PubMed ID: 12477709
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial occurrence of early-onset childhood absence epilepsy.
    Titomanlio L; Romano A; Bellini G; Pascotto A; Iuliano R; Miraglia Del Giudice E; Del Giudice E
    Eur J Paediatr Neurol; 2007 May; 11(3):178-80. PubMed ID: 17267250
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutational screening of GABRG2 gene in Pakistani population of Punjab with generalized tonic clonic seizures and children with childhood absence epilepsy.
    Iqbal MJ; Wasim M; Rashid U; Zeeshan N; Ali R; Nayyab S; Habib S; Manzoor B; Zahid N
    J Chin Med Assoc; 2018 Aug; 81(8):665-669. PubMed ID: 29929832
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of childhood absence epilepsy using haplotype-based haplotype relative risk and transmission disequilibrium test.
    Zhiping W; Xin G; Xiaoqing L; Yafen Z
    Brain Dev; 2004 Sep; 26(6):367-72. PubMed ID: 15275697
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p.
    Nabbout R; Baulac S; Desguerre I; Bahi-Buisson N; Chiron C; Ruberg M; Dulac O; LeGuern E
    Neurology; 2007 Apr; 68(17):1374-81. PubMed ID: 17452582
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic and physical maps of the stargazer locus on mouse chromosome 15.
    Letts VA; Valenzuela A; Kirley JP; Sweet HO; Davisson MT; Frankel WN
    Genomics; 1997 Jul; 43(1):62-8. PubMed ID: 9226373
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy.
    Delgado-Escueta AV; Greenberg D; Weissbecker K; Liu A; Treiman L; Sparkes R; Park MS; Barbetti A; Terasaki PI
    Epilepsia; 1990; 31 Suppl 3():S19-29. PubMed ID: 2121470
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tandem pore domain K(+)-channel TASK-3 (KCNK9) and idiopathic absence epilepsies.
    Kananura C; Sander T; Rajan S; Preisig-Müller R; Grzeschik KH; Daut J; Derst C; Steinlein OK
    Am J Med Genet; 2002 Mar; 114(2):227-9. PubMed ID: 11857586
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [T-type calcium channel gene-CACNA1H is a susceptibility gene to childhood absence epilepsy].
    Lü JJ; Zhang YH; Chen YC; Pan H; Wang JL; Zhang L; Wu HS; Xu KM; Liu XY; Tao LD; Shen Y; Wu XR
    Zhonghua Er Ke Za Zhi; 2005 Feb; 43(2):133-6. PubMed ID: 15833171
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.