115 related articles for article (PubMed ID: 9063744)
1. Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome.
Roberts C; Daw SC; Halford S; Scambler PJ
Hum Mol Genet; 1997 Feb; 6(2):237-45. PubMed ID: 9063744
[TBL] [Abstract][Full Text] [Related]
2. The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.
Wilming LG; Snoeren CA; van Rijswijk A; Grosveld F; Meijers C
Hum Mol Genet; 1997 Feb; 6(2):247-58. PubMed ID: 9063745
[TBL] [Abstract][Full Text] [Related]
3. A human homolog of the S. cerevisiae HIR1 and HIR2 transcriptional repressors cloned from the DiGeorge syndrome critical region.
Lamour V; Lécluse Y; Desmaze C; Spector M; Bodescot M; Aurias A; Osley MA; Lipinski M
Hum Mol Genet; 1995 May; 4(5):791-9. PubMed ID: 7633437
[TBL] [Abstract][Full Text] [Related]
4. HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation.
Farrell MJ; Stadt H; Wallis KT; Scambler P; Hixon RL; Wolfe R; Leatherbury L; Kirby ML
Circ Res; 1999 Feb; 84(2):127-35. PubMed ID: 9933243
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.
Halford S; Wadey R; Roberts C; Daw SC; Whiting JA; O'Donnell H; Dunham I; Bentley D; Lindsay E; Baldini A
Hum Mol Genet; 1993 Dec; 2(12):2099-107. PubMed ID: 8111380
[TBL] [Abstract][Full Text] [Related]
7. Structural Organization of the WD repeat protein-encoding gene HIRA in the DiGeorge syndrome critical region of human chromosome 22.
Lorain S; Demczuk S; Lamour V; Toth S; Aurias A; Roe BA; Lipinski M
Genome Res; 1996 Jan; 6(1):43-50. PubMed ID: 8681138
[TBL] [Abstract][Full Text] [Related]
8. Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth.
Jeanne M; Vuillaume ML; Ung DC; Vancollie VE; Wagner C; Collins SC; Vonwill S; Haye D; Chelloug N; Pfundt R; Kummeling J; Moizard MP; Marouillat S; Kleefstra T; Yalcin B; Laumonnier F; Toutain A
Hum Genet; 2021 Jun; 140(6):885-896. PubMed ID: 33417013
[TBL] [Abstract][Full Text] [Related]
9. Core histones and HIRIP3, a novel histone-binding protein, directly interact with WD repeat protein HIRA.
Lorain S; Quivy JP; Monier-Gavelle F; Scamps C; Lécluse Y; Almouzni G; Lipinski M
Mol Cell Biol; 1998 Sep; 18(9):5546-56. PubMed ID: 9710638
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Genomic organization of TUPLE1/HIRA: a gene implicated in DiGeorge syndrome.
Llevadot R; Scambler P; Estivill X; Pritchard M
Mamm Genome; 1996 Dec; 7(12):911-4. PubMed ID: 8995764
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development.
Garg V; Yamagishi C; Hu T; Kathiriya IS; Yamagishi H; Srivastava D
Dev Biol; 2001 Jul; 235(1):62-73. PubMed ID: 11412027
[TBL] [Abstract][Full Text] [Related]
16. HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3.
Magnaghi P; Roberts C; Lorain S; Lipinski M; Scambler PJ
Nat Genet; 1998 Sep; 20(1):74-7. PubMed ID: 9731536
[TBL] [Abstract][Full Text] [Related]
17. Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.
Sutherland HF; Kim UJ; Scambler PJ
Genomics; 1998 Aug; 52(1):37-43. PubMed ID: 9740669
[TBL] [Abstract][Full Text] [Related]
18. [Hira gene and development: from yeast to human].
Wang YF; Du XZ
Yi Chuan; 2005 Nov; 27(6):989-94. PubMed ID: 16378951
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.
Chieffo C; Garvey N; Gong W; Roe B; Zhang G; Silver L; Emanuel BS; Budarf ML
Genomics; 1997 Aug; 43(3):267-77. PubMed ID: 9268629
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
