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Items: 1 to 20 of 189

1.

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.

PMID:
9063745
2.

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.

PMID:
9063744
3.

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 15;74(3):320-32.

PMID:
11414760
4.

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 19;249(2):486-91.

PMID:
9712723
5.

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 1;43(3):267-77.

PMID:
9268629
6.

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.

7.

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.

8.

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 15;46(3):364-72.

PMID:
9441739
9.

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 5;84(2):127-35.

10.

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 15;53(2):146-54.

PMID:
9790763
11.
12.

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 26;333:111-9.

PMID:
15177686
13.

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 15;62(1):82-5.

PMID:
10585771
14.

Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region.

Shiohama A, Sasaki T, Noda S, Minoshima S, Shimizu N.

Biochem Biophys Res Commun. 2003 Apr 25;304(1):184-90.

PMID:
12705904
15.

Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.

Sutherland HF, Kim UJ, Scambler PJ.

Genomics. 1998 Aug 15;52(1):37-43.

PMID:
9740669
16.

Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.

Stalmans I.

Verh K Acad Geneeskd Belg. 2005;67(4):229-76. Review.

PMID:
16334858
17.
18.

Expression of Cdcrel-1 (Pnutl1), a gene frequently deleted in velo-cardio-facial syndrome/DiGeorge syndrome.

Maldonado-Saldivia J, Funke B, Pandita RK, Schüler T, Morrow BE, Schorle H.

Mech Dev. 2000 Aug;96(1):121-4.

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