517 related articles for article (PubMed ID: 11080588)
1. The murine DSCR1-like (Down syndrome candidate region 1) gene family: conserved synteny with the human orthologous genes.
Strippoli P; Petrini M; Lenzi L; Carinci P; Zannotti M
Gene; 2000 Oct; 257(2):223-32. PubMed ID: 11080588
[TBL] [Abstract][Full Text] [Related]
2. A new gene family including DSCR1 (Down Syndrome Candidate Region 1) and ZAKI-4: characterization from yeast to human and identification of DSCR1-like 2, a novel human member (DSCR1L2).
Strippoli P; Lenzi L; Petrini M; Carinci P; Zannotti M
Genomics; 2000 Mar; 64(3):252-63. PubMed ID: 10756093
[TBL] [Abstract][Full Text] [Related]
3. Proteins encoded by human Down syndrome critical region gene 1-like 2 (DSCR1L2) mRNA and by a novel DSCR1L2 mRNA isoform interact with cardiac troponin I (TNNI3).
Canaider S; Facchin F; Griffoni C; Casadei R; Vitale L; Lenzi L; Frabetti F; D'Addabbo P; Carinci P; Zannotti M; Strippoli P
Gene; 2006 May; 372():128-36. PubMed ID: 16516408
[TBL] [Abstract][Full Text] [Related]
4. Cysteine and tyrosine-rich 1 (CYYR1), a novel unpredicted gene on human chromosome 21 (21q21.2), encodes a cysteine and tyrosine-rich protein and defines a new family of highly conserved vertebrate-specific genes.
Vitale L; Casadei R; Canaider S; Lenzi L; Strippoli P; D'Addabbo P; Giannone S; Carinci P; Zannotti M
Gene; 2002 May; 290(1-2):141-51. PubMed ID: 12062809
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. DSCR1, overexpressed in Down syndrome, is an inhibitor of calcineurin-mediated signaling pathways.
Fuentes JJ; Genescà L; Kingsbury TJ; Cunningham KW; Pérez-Riba M; Estivill X; de la Luna S
Hum Mol Genet; 2000 Jul; 9(11):1681-90. PubMed ID: 10861295
[TBL] [Abstract][Full Text] [Related]
8. Identification of two putative novel folate receptor genes in humans and mouse.
Spiegelstein O; Eudy JD; Finnell RH
Gene; 2000 Nov; 258(1-2):117-25. PubMed ID: 11111049
[TBL] [Abstract][Full Text] [Related]
9. Characterization of mouse Eppin and a gene cluster of similar protease inhibitors on mouse chromosome 2.
Sivashanmugam P; Hall SH; Hamil KG; French FS; O'Rand MG; Richardson RT
Gene; 2003 Jul; 312():125-34. PubMed ID: 12909348
[TBL] [Abstract][Full Text] [Related]
10. A new human gene from the Down syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart.
Fuentes JJ; Pritchard MA; Planas AM; Bosch A; Ferrer I; Estivill X
Hum Mol Genet; 1995 Oct; 4(10):1935-44. PubMed ID: 8595418
[TBL] [Abstract][Full Text] [Related]
11. A cellular retinoic acid-binding protein from zebrafish (Danio rerio): cDNA sequence, phylogenetic analysis, mRNA expression, and gene linkage mapping.
Sharma MK; Denovan-Wright EM; Boudreau ME; Wright JM
Gene; 2003 Jun; 311():119-28. PubMed ID: 12853146
[TBL] [Abstract][Full Text] [Related]
12. TDPOZ, a family of bipartite animal and plant proteins that contain the TRAF (TD) and POZ/BTB domains.
Huang CJ; Chen CY; Chen HH; Tsai SF; Choo KB
Gene; 2004 Jan; 324():117-27. PubMed ID: 14693377
[TBL] [Abstract][Full Text] [Related]
13. The ancient source of a distinct gene family encoding proteins featuring RING and C(3)H zinc-finger motifs with abundant expression in developing brain and nervous system.
Gray TA; Hernandez L; Carey AH; Schaldach MA; Smithwick MJ; Rus K; Marshall Graves JA; Stewart CL; Nicholls RD
Genomics; 2000 May; 66(1):76-86. PubMed ID: 10843807
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5.
Orti R; Rachidi M; Vialard F; Toyama K; Lopes C; Taudien S; Rosenthal A; Yaspo ML; Sinet PM; Delabar JM
Genomics; 2000 Mar; 64(2):203-10. PubMed ID: 10729227
[TBL] [Abstract][Full Text] [Related]
16. Identification of two hERR2-related novel nuclear receptors utilizing bioinformatics and inverse PCR.
Chen F; Zhang Q; McDonald T; Davidoff MJ; Bailey W; Bai C; Liu Q; Caskey CT
Gene; 1999 Mar; 228(1-2):101-9. PubMed ID: 10072763
[TBL] [Abstract][Full Text] [Related]
17. Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue.
Pasteris NG; Nagata K; Hall A; Gorski JL
Gene; 2000 Jan; 242(1-2):237-47. PubMed ID: 10721717
[TBL] [Abstract][Full Text] [Related]
18. Isolation and characterization of two evolutionarily conserved murine kinases (Nek6 and nek7) related to the fungal mitotic regulator, NIMA.
Kandli M; Feige E; Chen A; Kilfin G; Motro B
Genomics; 2000 Sep; 68(2):187-96. PubMed ID: 10964517
[TBL] [Abstract][Full Text] [Related]
19. Identification of human FEM1A, the ortholog of a C. elegans sex-differentiation gene.
Krakow D; Sebald E; King LM; Cohn DH
Gene; 2001 Nov; 279(2):213-9. PubMed ID: 11733146
[TBL] [Abstract][Full Text] [Related]
20. DSCR1 gene expression is dependent on NFATc1 during cardiac valve formation and colocalizes with anomalous organ development in trisomy 16 mice.
Lange AW; Molkentin JD; Yutzey KE
Dev Biol; 2004 Feb; 266(2):346-60. PubMed ID: 14738882
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
