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Journal Abstract Search

515 related items for PubMed ID: 11080588

  • 21. Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene.
    Egeo A, Mazzocco M, Arrigo P, Vidal-Taboada JM, Oliva R, Pirola B, Giglio S, Rasore-Quartino A, Scartezzini P.
    Biochem Biophys Res Commun; 1998 Jun 18; 247(2):302-6. PubMed ID: 9642120
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  • 22. Gene structure and evolution of Tieg3, a new member of the Tieg family of proteins.
    Wang Z, Peters B, Klussmann S, Bender H, Herb A, Krieglstein K.
    Gene; 2004 Jan 21; 325():25-34. PubMed ID: 14697507
    [Abstract] [Full Text] [Related]

  • 23. Cloning and expression analysis of a novel gene, RP42, mapping to an autism susceptibility locus on 6q16.
    Mas C, Bourgeois F, Bulfone A, Levacher B, Mugnier C, Simonneau M.
    Genomics; 2000 Apr 01; 65(1):70-4. PubMed ID: 10777668
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  • 24. 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 01; 59(1):66-76. PubMed ID: 10395801
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  • 25. Identification and structural analysis of human RBM8A and RBM8B: two highly conserved RNA-binding motif proteins that interact with OVCA1, a candidate tumor suppressor.
    Salicioni AM, Xi M, Vanderveer LA, Balsara B, Testa JR, Dunbrack RL, Godwin AK.
    Genomics; 2000 Oct 01; 69(1):54-62. PubMed ID: 11013075
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  • 29. 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 15; 60(1):78-86. PubMed ID: 10458913
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  • 30. Comparative sequence and expression analyses of four mammalian VPS4 genes.
    Beyer A, Scheuring S, Müller S, Mincheva A, Lichter P, Köhrer K.
    Gene; 2003 Feb 13; 305(1):47-59. PubMed ID: 12594041
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  • 31. mRNA 5' region sequence incompleteness: a potential source of systematic errors in translation initiation codon assignment in human mRNAs.
    Casadei R, Strippoli P, D'Addabbo P, Canaider S, Lenzi L, Vitale L, Giannone S, Frabetti F, Facchin F, Carinci P, Zannotti M.
    Gene; 2003 Dec 04; 321():185-93. PubMed ID: 14637006
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  • 33. Molecular evolution of epididymal lipocalin genes localized on mouse chromosome 2.
    Suzuki K, Lareyre JJ, Sánchez D, Gutierrez G, Araki Y, Matusik RJ, Orgebin-Crist MC.
    Gene; 2004 Sep 15; 339():49-59. PubMed ID: 15363845
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  • 35. Restoration of DSCR1 to disomy in the trisomy 16 mouse model of Down syndrome does not correct cardiac or craniofacial development anomalies.
    Lange AW, Rothermel BA, Yutzey KE.
    Dev Dyn; 2005 Jul 15; 233(3):954-63. PubMed ID: 15906378
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  • 36. Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes.
    Pappano WN, Scott IC, Clark TG, Eddy RL, Shows TB, Greenspan DS.
    Genomics; 1998 Sep 01; 52(2):236-9. PubMed ID: 9782094
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  • 38. Structure and evolution of the mouse pregnancy-specific glycoprotein (Psg) gene locus.
    McLellan AS, Fischer B, Dveksler G, Hori T, Wynne F, Ball M, Okumura K, Moore T, Zimmermann W.
    BMC Genomics; 2005 Jan 12; 6():4. PubMed ID: 15647114
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  • 39. Genomic organization, alternative splicing, and expression patterns of the DSCR1 (Down syndrome candidate region 1) gene.
    Fuentes JJ, Pritchard MA, Estivill X.
    Genomics; 1997 Sep 15; 44(3):358-61. PubMed ID: 9325060
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  • 40. Identification and analysis of human RCAN3 (DSCR1L2) mRNA and protein isoforms.
    Facchin F, Canaider S, Vitale L, Frabetti F, Griffoni C, Lenzi L, Casadei R, Strippoli P.
    Gene; 2008 Jan 15; 407(1-2):159-68. PubMed ID: 18022329
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