BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1271 related articles for article (PubMed ID: 11414760)

  • 1. Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.
    Berti L; Mittler G; Przemeck GK; Stelzer G; Günzler B; Amati F; Conti E; Dallapiccola B; Hrabé de Angelis M; Novelli G; Meisterernst M
    Genomics; 2001 Jun; 74(3):320-32. PubMed ID: 11414760
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11.
    Funke B; Saint-Jore B; Puech A; Sirotkin H; Edelmann L; Carlson C; Raft S; Pandita RK; Kucherlapati R; Skoultchi A; Morrow BE
    Genomics; 1997 Dec; 46(3):364-72. PubMed ID: 9441739
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.
    Funke B; Pandita RK; Morrow BE
    Genomics; 2001 May; 73(3):264-71. PubMed ID: 11350118
    [TBL] [Abstract][Full Text] [Related]  

  • 4. cDNA isolation, genomic structure, regulation, and chromosomal localization of human lung Kruppel-like factor.
    Wani MA; Conkright MD; Jeffries S; Hughes MJ; Lingrel JB
    Genomics; 1999 Aug; 60(1):78-86. PubMed ID: 10458913
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.
    Funke B; Puech A; Saint-Jore B; Pandita R; Skoultchi A; Morrow B
    Genomics; 1998 Oct; 53(2):146-54. PubMed ID: 9790763
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular cloning, structure, expression, and chromosomal localization of the human Osterix (SP7) gene.
    Gao Y; Jheon A; Nourkeyhani H; Kobayashi H; Ganss B
    Gene; 2004 Oct; 341():101-10. PubMed ID: 15474293
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A novel human amino acid transporter, hNAT3: cDNA cloning, chromosomal mapping, genomic structure, expression, and functional characterization.
    Gu S; Adan-Rice D; Leach RJ; Jiang JX
    Genomics; 2001 Jun; 74(3):262-72. PubMed ID: 11414754
    [TBL] [Abstract][Full Text] [Related]  

  • 9. cDNA cloning and characterization of the human THRAP2 gene which maps to chromosome 12q24, and its mouse ortholog Thrap2.
    Musante L; Bartsch O; Ropers HH; Kalscheuer VM
    Gene; 2004 May; 332():119-27. PubMed ID: 15145061
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cloning, genomic structure, and expression analysis of the mouse transcriptional intermediary factor 1 gamma gene.
    Yan KP; Dollé P; Mark M; Lerouge T; Wendling O; Chambon P; Losson R
    Gene; 2004 Jun; 334():3-13. PubMed ID: 15256250
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phemx, a novel mouse gene expressed in hematopoietic cells maps to the imprinted cluster on distal chromosome 7.
    Nicholson RH; Pantano S; Eliason JF; Galy A; Weiler S; Kaplan J; Hughes MR; Ko MS
    Genomics; 2000 Aug; 68(1):13-21. PubMed ID: 10950922
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome.
    Wang YK; Spörle R; Paperna T; Schughart K; Francke U
    Genomics; 1999 Apr; 57(2):235-48. PubMed ID: 10198163
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular cloning, expression and chromosomal localization of a novel human REG family gene, REG III.
    Nata K; Liu Y; Xu L; Ikeda T; Akiyama T; Noguchi N; Kawaguchi S; Yamauchi A; Takahashi I; Shervani NJ; Onogawa T; Takasawa S; Okamoto H
    Gene; 2004 Sep; 340(1):161-70. PubMed ID: 15556304
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
    Pasteris NG; Gorski JL
    Genomics; 1999 Aug; 60(1):57-66. PubMed ID: 10458911
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene.
    Budarf ML; Collins J; Gong W; Roe B; Wang Z; Bailey LC; Sellinger B; Michaud D; Driscoll DA; Emanuel BS
    Nat Genet; 1995 Jul; 10(3):269-78. PubMed ID: 7670464
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Altered replication timing of the HIRA/Tuple1 locus in the DiGeorge and Velocardiofacial syndromes.
    D'Antoni S; Mattina T; Di Mare P; Federico C; Motta S; Saccone S
    Gene; 2004 May; 333():111-9. PubMed ID: 15177686
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cloning, chromosome mapping and expression analysis of the HIRA gene from Drosophila melanogaster.
    Llevadot R; Marqués G; Pritchard M; Estivill X; Ferrús A; Scambler P
    Biochem Biophys Res Commun; 1998 Aug; 249(2):486-91. PubMed ID: 9712723
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cloning and characterization of the human CLOCK gene: expression in the suprachiasmatic nuclei.
    Steeves TD; King DP; Zhao Y; Sangoram AM; Du F; Bowcock AM; Moore RY; Takahashi JS
    Genomics; 1999 Apr; 57(2):189-200. PubMed ID: 10198158
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ZNF74, a gene deleted in DiGeorge syndrome, is expressed in human neural crest-derived tissues and foregut endoderm epithelia.
    Ravassard P; Côté F; Grondin B; Bazinet M; Mallet J; Aubry M
    Genomics; 1999 Nov; 62(1):82-5. PubMed ID: 10585771
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.
    Lindsay EA; Rizzu P; Antonacci R; Jurecic V; Delmas-Mata J; Lee CC; Kim UJ; Scambler PJ; Baldini A
    Genomics; 1996 Feb; 32(1):104-12. PubMed ID: 8786095
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 64.