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 *

107 related articles for article (PubMed ID: 11054561)

  • 1. C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5.
    Zhu X; Higashimoto K; Soejima H; Yatsuki H; Sugihara H; Mukai T; Joh K
    Gene; 2000 Oct; 256(1-2):311-7. PubMed ID: 11054561
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesis.
    Gaitanou M; Buanne P; Pappa C; Georgopoulou N; Mamalaki A; Tirone F; Matsas R
    Biochem J; 2001 May; 355(Pt 3):715-24. PubMed ID: 11311134
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues.
    Hu RJ; Lee MP; Johnson LA; Feinberg AP
    Hum Mol Genet; 1996 Nov; 5(11):1743-8. PubMed ID: 8923002
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification and characterization of a novel human cDNA encoding a 21 kDa pRb-associated protein.
    Wen H; Ao S
    Gene; 2001 Jan; 263(1-2):85-92. PubMed ID: 11223246
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The identification of a novel human homologue of the SH3 binding glutamic acid-rich (SH3BGR) gene establishes a new family of highly conserved small proteins related to Thioredoxin Superfamily.
    Mazzocco M; Maffei M; Egeo A; Vergano A; Arrigo P; Di Lisi R; Ghiotto F; Scartezzini P
    Gene; 2002 May; 291(1-2):233-9. PubMed ID: 12095696
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification and characterization of human ZNF274 cDNA, which encodes a novel kruppel-type zinc-finger protein having nucleolar targeting ability.
    Yano K; Ueki N; Oda T; Seki N; Masuho Y; Muramatsu M
    Genomics; 2000 Apr; 65(1):75-80. PubMed ID: 10777669
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification and cellular localization of human PFTAIRE1.
    Yang T; Chen JY
    Gene; 2001 Apr; 267(2):165-72. PubMed ID: 11313143
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.
    Cooper PR; Smilinich NJ; Day CD; Nowak NJ; Reid LH; Pearsall RS; Reece M; Prawitt D; Landers J; Housman DE; Winterpacht A; Zabel BU; Pelletier J; Weissman BE; Shows TB; Higgins MJ
    Genomics; 1998 Apr; 49(1):38-51. PubMed ID: 9570947
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.
    Paulsen M; Davies KR; Bowden LM; Villar AJ; Franck O; Fuermann M; Dean WL; Moore TF; Rodrigues N; Davies KE; Hu RJ; Feinberg AP; Maher ER; Reik W; Walter J
    Hum Mol Genet; 1998 Jul; 7(7):1149-59. PubMed ID: 9618174
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cloning and characterization of the mouse and human TUSP gene, a novel member of the tubby superfamily.
    Li QZ; Wang CY; Shi JD; Ruan QG; Eckenrode S; Davoodi-Semiromi A; Kukar T; Gu Y; Lian W; Wu D; She JX
    Gene; 2001 Aug; 273(2):275-84. PubMed ID: 11595174
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression.
    Prawitt D; Enklaar T; Klemm G; Gärtner B; Spangenberg C; Winterpacht A; Higgins M; Pelletier J; Zabel B
    Hum Mol Genet; 2000 Jan; 9(2):203-16. PubMed ID: 10607831
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.
    Alders M; Ryan A; Hodges M; Bliek J; Feinberg AP; Privitera O; Westerveld A; Little PF; Mannens M
    Am J Hum Genet; 2000 May; 66(5):1473-84. PubMed ID: 10762538
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type.
    Crider-Miller SJ; Reid LH; Higgins MJ; Nowak NJ; Shows TB; Futreal PA; Weissman BE
    Genomics; 1997 Dec; 46(3):355-63. PubMed ID: 9441738
    [TBL] [Abstract][Full Text] [Related]  

  • 14. EHD1--an EH-domain-containing protein with a specific expression pattern.
    Mintz L; Galperin E; Pasmanik-Chor M; Tulzinsky S; Bromberg Y; Kozak CA; Joyner A; Fein A; Horowitz M
    Genomics; 1999 Jul; 59(1):66-76. PubMed ID: 10395801
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.
    Mannens M; Alders M; Redeker B; Bliek J; Steenman M; Wiesmeyer C; de Meulemeester M; Ryan A; Kalikin L; Voûte T; De Kraker J; Hoovers J; Slater R; Feinberg A; Little P; Westerveld A
    Med Pediatr Oncol; 1996 Nov; 27(5):490-4. PubMed ID: 8827079
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular cloning and characterization of a novel human BTB domain-containing gene, BTBD10, which is down-regulated in glioma.
    Chen J; Xu J; Ying K; Cao G; Hu G; Wang L; Luo C; Lou M; Mao Y; Xie Y; Lu Y
    Gene; 2004 Sep; 340(1):61-9. PubMed ID: 15556295
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization and tissue-specific expression of human LRIG2.
    Holmlund C; Nilsson J; Guo D; Starefeldt A; Golovleva I; Henriksson R; Hedman H
    Gene; 2004 May; 332():35-43. PubMed ID: 15145052
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human FRAG1 encodes a novel membrane-spanning protein that localizes to chromosome 11p15.5, a region of frequent loss of heterozygosity in cancer.
    Lorenzi MV; Castagnino P; Aaronson DC; Lieb DC; Lee CC; Keck CL; Popescu NC; Miki T
    Genomics; 1999 Nov; 62(1):59-66. PubMed ID: 10585768
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cloning and characterization of a novel endoplasmic reticulum localized G-patch domain protein, IER3IP1.
    Yiu WH; Poon JW; Tsui SK; Fung KP; Waye MM
    Gene; 2004 Aug; 337():37-44. PubMed ID: 15276200
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development.
    Weksberg R; Smith AC; Squire J; Sadowski P
    Hum Mol Genet; 2003 Apr; 12 Spec No 1():R61-8. PubMed ID: 12668598
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.