168 related articles for article (PubMed ID: 10072440)
1. Isolation and embryonic expression of the novel mouse gene Hic1, the homologue of HIC1, a candidate gene for the Miller-Dieker syndrome.
Grimm C; Spörle R; Schmid TE; Adler ID; Adamski J; Schughart K; Graw J
Hum Mol Genet; 1999 Apr; 8(4):697-710. PubMed ID: 10072440
[TBL] [Abstract][Full Text] [Related]
2. Identification and developmental expression of the zebrafish orthologue of the tumor suppressor gene HIC1.
Bertrand S; Pinte S; Stankovic-Valentin N; Deltour-Balerdi S; Guérardel C; Bégue A; Laudet V; Leprince D
Biochim Biophys Acta; 2004 Apr; 1678(1):57-66. PubMed ID: 15093138
[TBL] [Abstract][Full Text] [Related]
3. Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller-Dieker syndrome.
Carter MG; Johns MA; Zeng X; Zhou L; Zink MC; Mankowski JL; Donovan DM; Baylin SB
Hum Mol Genet; 2000 Feb; 9(3):413-9. PubMed ID: 10655551
[TBL] [Abstract][Full Text] [Related]
4. A L225A substitution in the human tumour suppressor HIC1 abolishes its interaction with the corepressor CtBP.
Stankovic-Valentin N; Verger A; Deltour-Balerdi S; Quinlan KG; Crossley M; Leprince D
FEBS J; 2006 Jul; 273(13):2879-90. PubMed ID: 16762039
[TBL] [Abstract][Full Text] [Related]
5. Characterization of HRG22, a human homologue of the putative tumor suppressor gene HIC1.
Deltour S; Pinte S; Guérardel C; Leprince D
Biochem Biophys Res Commun; 2001 Sep; 287(2):427-34. PubMed ID: 11554746
[TBL] [Abstract][Full Text] [Related]
6. [Chromosome arm 17p13.3: could HIC1 be the one ?].
Chopin V; Leprince D
Med Sci (Paris); 2006 Jan; 22(1):54-61. PubMed ID: 16386221
[TBL] [Abstract][Full Text] [Related]
7. Identification of a second G-C-rich promoter conserved in the human, murine and rat tumor suppressor genes HIC1.
Pinte S; Guérardel C; Deltour-Balerdi S; Godwin AK; Leprince D
Oncogene; 2004 May; 23(22):4023-31. PubMed ID: 15007385
[TBL] [Abstract][Full Text] [Related]
8. The tumor suppressor gene HIC1 (hypermethylated in cancer 1) is a sequence-specific transcriptional repressor: definition of its consensus binding sequence and analysis of its DNA binding and repressive properties.
Pinte S; Stankovic-Valentin N; Deltour S; Rood BR; Guérardel C; Leprince D
J Biol Chem; 2004 Sep; 279(37):38313-24. PubMed ID: 15231840
[TBL] [Abstract][Full Text] [Related]
9. Generation of two modified mouse alleles of the Hic1 tumor suppressor gene.
Pospichalova V; Tureckova J; Fafilek B; Vojtechova M; Krausova M; Lukas J; Sloncova E; Takacova S; Divoky V; Leprince D; Plachy J; Korinek V
Genesis; 2011 Mar; 49(3):142-51. PubMed ID: 21309068
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.
Chong SS; Pack SD; Roschke AV; Tanigami A; Carrozzo R; Smith AC; Dobyns WB; Ledbetter DH
Hum Mol Genet; 1997 Feb; 6(2):147-55. PubMed ID: 9063734
[TBL] [Abstract][Full Text] [Related]
12. Physical and transcriptional mapping of the 17p13.3 region that is frequently deleted in human cancer.
Hoff C; Seranski P; Mollenhauer J; Korn B; Detzel T; Reinhardt R; Ramser J; Poustka A
Genomics; 2000 Nov; 70(1):26-33. PubMed ID: 11087658
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. The Reelin receptors ApoER2 and VLDLR are direct target genes of HIC1 (Hypermethylated In Cancer 1).
Dubuissez M; Faiderbe P; Pinte S; Dehennaut V; Rood BR; Leprince D
Biochem Biophys Res Commun; 2013 Oct; 440(3):424-30. PubMed ID: 24076391
[TBL] [Abstract][Full Text] [Related]
17. Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant.
Lee J; Prohaska JR; Dagenais SL; Glover TW; Thiele DJ
Gene; 2000 Aug; 254(1-2):87-96. PubMed ID: 10974539
[TBL] [Abstract][Full Text] [Related]
18. Identification of the p53 family-responsive element in the promoter region of the tumor suppressor gene hypermethylated in cancer 1.
Britschgi C; Rizzi M; Grob TJ; Tschan MP; Hügli B; Reddy VA; Andres AC; Torbett BE; Tobler A; Fey MF
Oncogene; 2006 Mar; 25(14):2030-9. PubMed ID: 16301995
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Characterization and in silico mapping of a novel murine zinc finger transcription factor.
Wride MA; Mansergh FC; Somani JM; Winkfein RJ; Rancourt DE
Gene; 2002 May; 289(1-2):49-59. PubMed ID: 12036583
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
