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 *

108 related articles for article (PubMed ID: 7633421)

  • 1. Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3.
    Yamakawa K; Mitchell S; Hubert R; Chen XN; Colbern S; Huo YK; Gadomski C; Kim UJ; Korenberg JR
    Hum Mol Genet; 1995 Apr; 4(4):709-16. PubMed ID: 7633421
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3.
    Yamakawa K; Gao DQ; Korenberg JR
    Cytogenet Cell Genet; 1996; 74(1-2):140-5. PubMed ID: 8893822
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping.
    Lehesjoki AE; Koskiniemi M; Norio R; Tirrito S; Sistonen P; Lander E; de la Chapelle A
    Hum Mol Genet; 1993 Aug; 2(8):1229-34. PubMed ID: 8104628
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Localization of 16 exons to a 450-kb region involved in the autoimmune polyglandular disease type I (APECED) on human chromosome 21q22.3.
    Kudoh J; Nagamine K; Asakawa S; Abe I; Kawasaki K; Maeda H; Tsujimoto S; Minoshima S; Ito F; Shimizu N
    DNA Res; 1997 Feb; 4(1):45-52. PubMed ID: 9179495
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isolation of cDNA for a novel human protein KNP-I that is homologous to the E. coli SCRP-27A protein from the autoimmune polyglandular disease type I (APECED) region of chromosome 21q22.3.
    Nagamine K; Kudoh J; Minoshima S; Kawasaki K; Asakawa S; Ito F; Shimizu N
    Biochem Biophys Res Commun; 1996 Aug; 225(2):608-16. PubMed ID: 8753807
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3.
    Lafrenière RG; de Jong PJ; Rouleau GA
    Genomics; 1995 Sep; 29(1):288-90. PubMed ID: 8530089
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.
    Virtaneva K; Miao J; Träskelin AL; Stone N; Warrington JA; Weissenbach J; Myers RM; Cox DR; Sistonen P; de la Chapelle A
    Am J Hum Genet; 1996 Jun; 58(6):1247-53. PubMed ID: 8651302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy gene.
    Stone NE; Fan JB; Willour V; Pennacchio LA; Warrington JA; Hu A; de la Chapelle A; Lehesjoki AE; Cox DR; Myers RM
    Genome Res; 1996 Mar; 6(3):218-25. PubMed ID: 8963899
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis.
    Scott HS; Kyriakou DS; Peterson P; Heino M; Tähtinen M; Krohn K; Chen H; Rossier C; Lalioti MD; Antonarakis SE
    Genomics; 1998 Jan; 47(1):64-70. PubMed ID: 9465297
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PME of Unverricht-Lundborg type in the Mediterranean region: linkage and linkage disequilibrium confirm the assignment to the EPM1 locus.
    Lehesjoki AE; Tassinari CA; Avanzini G; Michelucci R; Franceschetti S; Antonelli A; Rubboli G; de la Chapelle A
    Hum Genet; 1994 Jun; 93(6):668-74. PubMed ID: 8005591
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lafora disease is not linked to the Unverricht-Lundborg locus.
    Labauge P; Beck C; Bellet H; Coquillat G; Vespignani H; Dulac O; Gilgenkrantz S; Dravet C; Genton P; Pellissier JF
    Am J Med Genet; 1995 Feb; 60(1):80-4. PubMed ID: 7485240
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3.
    Lalioti MD; Gos A; Green MR; Rossier C; Morris MA; Antonarakis SE
    Genomics; 1996 Apr; 33(2):298-300. PubMed ID: 8660980
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1).
    Pennacchio LA; Lehesjoki AE; Stone NE; Willour VL; Virtaneva K; Miao J; D'Amato E; Ramirez L; Faham M; Koskiniemi M; Warrington JA; Norio R; de la Chapelle A; Cox DR; Myers RM
    Science; 1996 Mar; 271(5256):1731-4. PubMed ID: 8596935
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3.
    Lafrenière RG; Kibar Z; Rochefort DL; Han FY; Fon EA; Dubé MP; Kang X; Baird S; Korneluk RG; Rommens JM; Rouleau GA
    Gene; 1997 Oct; 198(1-2):313-21. PubMed ID: 9370297
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Isolation and characterization of the mouse cystatin B gene.
    Pennacchio LA; Myers RM
    Genome Res; 1996 Nov; 6(11):1103-9. PubMed ID: 8938434
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation of a human gene (HES1) with homology to an Escherichia coli and a zebrafish protein that maps to chromosome 21q22.3.
    Scott HS; Chen H; Rossier C; Lalioti MD; Antonarakis SE
    Hum Genet; 1997 May; 99(5):616-23. PubMed ID: 9150728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Isolation and genomic structure of a human homolog of the yeast periodic tryptophan protein 2 (PWP2) gene mapping to 21q22.3.
    Lafrenière RG; Rochefort DL; Chrétien N; Neville CE; Korneluk RG; Zuo L; Wei Y; Lichter J; Rouleau GA
    Genome Res; 1996 Dec; 6(12):1216-26. PubMed ID: 8973917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1.
    Lafrenière RG; Rochefort DL; Chrétien N; Rommens JM; Cochius JI; Kälviäinen R; Nousiainen U; Patry G; Farrell K; Söderfeldt B; Federico A; Hale BR; Cossio OH; Sørensen T; Pouliot MA; Kmiec T; Uldall P; Janszky J; Pranzatelli MR; Andermann F; Andermann E; Rouleau GA
    Nat Genet; 1997 Mar; 15(3):298-302. PubMed ID: 9054946
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3.
    Lalioti MD; Chen H; Rossier C; Shafaatian R; Reid JD; Antonarakis SE
    Genomics; 1996 Jul; 35(2):321-7. PubMed ID: 8661145
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolation and characterization of mouse homologue for the human epilepsy gene, EPM2A.
    Ganesh S; Amano K; Delgado-Escueta AV; Yamakawa K
    Biochem Biophys Res Commun; 1999 Apr; 257(1):24-8. PubMed ID: 10092504
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.