BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

328 related articles for article (PubMed ID: 11313745)

  • 1. A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region.
    Baysal BE; Willett-Brozick JE; Taschner PE; Dauwerse JG; Devilee P; Devlin B
    Eur J Hum Genet; 2001 Feb; 9(2):121-9. PubMed ID: 11313745
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3.
    Arai Y; Hosoda F; Nakayama K; Ohki M
    Genomics; 1996 Jul; 35(1):196-206. PubMed ID: 8661121
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.
    Badenhop RF; Cherian S; Lord RS; Baysal BE; Taschner PE; Schofield PR
    Genes Chromosomes Cancer; 2001 Jul; 31(3):255-63. PubMed ID: 11391796
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Defining a common region of deletion at 13q21 in human cancers.
    Chen C; Brabham WW; Stultz BG; Frierson HF; Barrett JC; Sawyers CL; Isaacs JT; Dong JT
    Genes Chromosomes Cancer; 2001 Aug; 31(4):333-44. PubMed ID: 11433524
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
    Baysal BE; Ferrell RE; Willett-Brozick JE; Lawrence EC; Myssiorek D; Bosch A; van der Mey A; Taschner PE; Rubinstein WS; Myers EN; Richard CW; Cornelisse CJ; Devilee P; Devlin B
    Science; 2000 Feb; 287(5454):848-51. PubMed ID: 10657297
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An integrated physical and gene map of the 3.5-Mb chromosome 3p21.3 (AP20) region implicated in major human epithelial malignancies.
    Protopopov A; Kashuba V; Zabarovska VI; Muravenko OV; Lerman MI; Klein G; Zabarovsky ER
    Cancer Res; 2003 Jan; 63(2):404-12. PubMed ID: 12543795
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Characterization of the human SDHD gene encoding the small subunit of cytochrome b (cybS) in mitochondrial succinate-ubiquinone oxidoreductase.
    Hirawake H; Taniwaki M; Tamura A; Amino H; Tomitsuka E; Kita K
    Biochim Biophys Acta; 1999 Aug; 1412(3):295-300. PubMed ID: 10482792
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sequence-ready contig for the 1.4-cM ductal carcinoma in situ loss of heterozygosity region on chromosome 8p22-p23.
    Wang JC; Radford DM; Holt MS; Helms C; Goate A; Brandt W; Parik M; Phillips NJ; DeSchryver K; Schuh ME; Fair KL; Ritter JH; Marshall P; Donis-Keller H
    Genomics; 1999 Aug; 60(1):1-11. PubMed ID: 10458905
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Construction of a 5-Mb YAC contig from the putative 10q25 tumor-suppressor region for glioblastomas.
    Albarosa R; Finocchiaro G; Chiariello E; Russo G; Susani L; Vezzoni P; Zucchi I
    Genomics; 1997 May; 41(3):345-9. PubMed ID: 9169131
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytochrome b in human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of the components in liver mitochondria and chromosome assignment of the genes for the large (SDHC) and small (SDHD) subunits to 1q21 and 11q23.
    Hirawake H; Taniwaki M; Tamura A; Kojima S; Kita K
    Cytogenet Cell Genet; 1997; 79(1-2):132-8. PubMed ID: 9533030
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer.
    Hoggard N; Hey Y; Brintnell B; James L; Jones D; Mitchell E; Weissenbach J; Varley JM
    Genomics; 1995 Nov; 30(2):233-43. PubMed ID: 8586422
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases.
    Riemann K; Sotlar K; Kupka S; Braun S; Zenner HP; Preyer S; Pfister M; Pusch CM; Blin N
    Cancer Genet Cytogenet; 2004 Apr; 150(2):128-35. PubMed ID: 15066320
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.
    Dannenberg H; Dinjens WN; Abbou M; Van Urk H; Pauw BK; Mouwen D; Mooi WJ; de Krijger RR
    Clin Cancer Res; 2002 Jul; 8(7):2061-6. PubMed ID: 12114404
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.
    Benn DE; Croxson MS; Tucker K; Bambach CP; Richardson AL; Delbridge L; Pullan PT; Hammond J; Marsh DJ; Robinson BG
    Oncogene; 2003 Mar; 22(9):1358-64. PubMed ID: 12618761
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.
    Taschner PE; Jansen JC; Baysal BE; Bosch A; Rosenberg EH; Bröcker-Vriends AH; van Der Mey AG; van Ommen GJ; Cornelisse CJ; Devilee P
    Genes Chromosomes Cancer; 2001 Jul; 31(3):274-81. PubMed ID: 11391798
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.