BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 9921902)

  • 21. A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes.
    Kuhlenbäumer G; Schirmacher A; Meuleman J; Tissir F; Del-Favero J; Stögbauer F; Young P; Ringelstein B; Van Broeckhoven C; Timmerman V
    Genomics; 1999 Dec; 62(2):242-50. PubMed ID: 10610718
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.
    Del-Favero J; Krols L; Michalik A; Theuns J; Löfgren A; Goossens D; Wehnert A; Van den Bossche D; Van Zand K; Backhovens H; van Regenmorter N; Martin JJ; Van Broeckhoven C
    Hum Mol Genet; 1998 Feb; 7(2):177-86. PubMed ID: 9425224
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12.
    Xie YG; Han FY; Peyrard M; Ruttledge MH; Fransson I; DeJong P; Collins J; Dunham I; Nordenskjöld M; Dumanski JP
    Hum Mol Genet; 1993 Sep; 2(9):1361-8. PubMed ID: 8242058
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.
    Pang JT; Lloyd SE; Wooding C; Farren B; Pottinger B; Harding B; Leigh SE; Pook MA; Benham FJ; Gillett GT; Taggart RT; Thakker RV
    Hum Genet; 1996 Jun; 97(6):732-41. PubMed ID: 8641689
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Physical and cDNA mapping in the DBH region of human chromosome 9q34.
    Gilbert JR; Kumar A; Newey S; Rao N; Ioannou P; Qiu H; Lin D; Xu P; Pettenati MJ; Pericak-Vance MA
    Hum Hered; 2000; 50(3):151-7. PubMed ID: 10686491
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A high-resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23.
    Baysal BE; van Schothorst EM; Farr JE; James MR; Devilee P; Richard CW
    Genomics; 1997 Sep; 44(2):214-21. PubMed ID: 9299238
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Isolation and characterization of a novel gene close to the human phosphoinositide-specific phospholipase C beta 3 gene on chromosomal region 11q13.
    Lagercrantz J; Carson E; Larsson C; Nordenskjöld M; Weber G
    Genomics; 1996 Feb; 31(3):380-4. PubMed ID: 8838322
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A high-resolution PAC and BAC map of the SCA2 region.
    Nechiporuk T; Nechiporuk A; Sahba S; Figueroa K; Shibata H; Chen XN; Korenberg JR; de Jong P; Pulst SM
    Genomics; 1997 Sep; 44(3):321-9. PubMed ID: 9325053
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Description of a 700-kb yeast artificial chromosome contig containing the BCL1 translocation breakpoint region at 11q13.
    Szepetowski P; Perucca-Lostanlen D; Grosgeorge J; LePaslier D; Brownstein BH; Carle GF; Gaudray P
    Cytogenet Cell Genet; 1995; 69(1-2):101-7. PubMed ID: 7835075
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Detailed transcript map of a 810-kb region at 11p14 involving identification of 10 novel human 3' exons.
    Guillemot F; Auffray C; Devignes MD
    Eur J Hum Genet; 1999; 7(4):487-95. PubMed ID: 10352939
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A sequence-ready BAC clone contig of human chromosome 10p15 spanning the loss of heterozygosity region in glioma.
    Harada K; Nishizaki T; Maekawa K; Kubota H; Harada K; Suzuki M; Ohno T; Sasaki K; Soeda E
    Genomics; 2000 Aug; 67(3):268-72. PubMed ID: 10936048
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families.
    Beales PL; Warner AM; Hitman GA; Thakker R; Flinter FA
    J Med Genet; 1997 Feb; 34(2):92-8. PubMed ID: 9039982
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1).
    Courseaux A; Grosgeorge J; Gaudray P; Pannett AA; Forbes SA; Williamson C; Bassett D; Thakker RV; Teh BT; Farnebo F; Shepherd J; Skogseid B; Larsson C; Giraud S; Zhang CX; Salandre J; Calender A
    Genomics; 1996 Nov; 37(3):354-65. PubMed ID: 8938448
    [TBL] [Abstract][Full Text] [Related]  

  • 36. High-resolution physical map and transcript identification of a prostate cancer deletion interval on 8p22.
    Arbieva ZH; Banerjee K; Kim SY; Edassery SL; Maniatis VS; Horrigan SK; Westbrook CA
    Genome Res; 2000 Feb; 10(2):244-57. PubMed ID: 10673282
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).
    Forbes SA; Pannett AA; Bassett JH; Harding B; Wooding C; Thakker RV; Butler R; Ogilvie D; Anand R; Gaudray P; Weber G; Larsson C; Zhang CX; Calender A; Höppener JW; Lips CJ; Kas K
    Hum Genet; 1997 Sep; 100(3-4):481-5. PubMed ID: 9272177
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characterization of five novel human genes in the 11q13-q22 region.
    O'Brien KP; Tapia-Páez I; Ståhle-Bäckdahl M; Kedra D; Dumanski JP
    Biochem Biophys Res Commun; 2000 Jun; 273(1):90-4. PubMed ID: 10873569
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKN1B: hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p).
    Baens M; Wlodarska I; Corveleyn A; Hoornaert I; Hagemeijer A; Marynen P
    Genomics; 1999 Feb; 56(1):40-50. PubMed ID: 10036184
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene.
    Irobi J; Tissir F; De Jonghe P; De Vriendt E; Van Broeckhoven C; Timmerman V; Beuten J
    Genomics; 2000 Apr; 65(1):34-43. PubMed ID: 10777663
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.