These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
139 related articles for article (PubMed ID: 1289066)
1. Expression of the zinc finger gene Gli3 is affected in the morphogenetic mouse mutant extra-toes (Xt). Schimmang T; Lemaistre M; Vortkamp A; Rüther U Development; 1992 Nov; 116(3):799-804. PubMed ID: 1289066 [TBL] [Abstract][Full Text] [Related]
2. Birth defects caused by mutations in human GLI3 and mouse Gli3 genes. Naruse I; Ueta E; Sumino Y; Ogawa M; Ishikiriyama S Congenit Anom (Kyoto); 2010 Mar; 50(1):1-7. PubMed ID: 20201963 [TBL] [Abstract][Full Text] [Related]
3. Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt). Vortkamp A; Franz T; Gessler M; Grzeschik KH Mamm Genome; 1992; 3(8):461-3. PubMed ID: 1322743 [No Abstract] [Full Text] [Related]
4. Gli3 expression is affected in the morphogenetic mouse mutants add and Xt. Schimmang T; van der Hoeven F; Rüther U Prog Clin Biol Res; 1993; 383A():153-61. PubMed ID: 8302891 [TBL] [Abstract][Full Text] [Related]
5. A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene. Hui CC; Joyner AL Nat Genet; 1993 Mar; 3(3):241-6. PubMed ID: 8387379 [TBL] [Abstract][Full Text] [Related]
6. Isolation and characterization of a cosmid contig for the GCPS gene region. Vortkamp A; Heid C; Gessler M; Grzeschik KH Hum Genet; 1995 Jan; 95(1):82-8. PubMed ID: 7814032 [TBL] [Abstract][Full Text] [Related]
7. Suppression of polydactyly of the Gli3 mutant (extra toes) by deltaEF1 homozygous mutation. Moribe H; Takagi T; Kondoh H; Higashi Y Dev Growth Differ; 2000 Aug; 42(4):367-76. PubMed ID: 10969736 [TBL] [Abstract][Full Text] [Related]
8. Wnt/β-catenin signaling is disrupted in the extra-toes (Gli3(Xt/Xt) ) mutant from early stages of forebrain development, concomitant with anterior neural plate patterning defects. Fotaki V; Price DJ; Mason JO J Comp Neurol; 2011 Jun; 519(9):1640-57. PubMed ID: 21452227 [TBL] [Abstract][Full Text] [Related]
9. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. Johnston JJ; Olivos-Glander I; Killoran C; Elson E; Turner JT; Peters KF; Abbott MH; Aughton DJ; Aylsworth AS; Bamshad MJ; Booth C; Curry CJ; David A; Dinulos MB; Flannery DB; Fox MA; Graham JM; Grange DK; Guttmacher AE; Hannibal MC; Henn W; Hennekam RC; Holmes LB; Hoyme HE; Leppig KA; Lin AE; Macleod P; Manchester DK; Marcelis C; Mazzanti L; McCann E; McDonald MT; Mendelsohn NJ; Moeschler JB; Moghaddam B; Neri G; Newbury-Ecob R; Pagon RA; Phillips JA; Sadler LS; Stoler JM; Tilstra D; Walsh Vockley CM; Zackai EH; Zadeh TM; Brueton L; Black GC; Biesecker LG Am J Hum Genet; 2005 Apr; 76(4):609-22. PubMed ID: 15739154 [TBL] [Abstract][Full Text] [Related]
10. Expression profile of Gli family members and Shh in normal and mutant mouse limb development. Büscher D; Rüther U Dev Dyn; 1998 Jan; 211(1):88-96. PubMed ID: 9438426 [TBL] [Abstract][Full Text] [Related]
11. Mouse Gli1 mutants are viable but have defects in SHH signaling in combination with a Gli2 mutation. Park HL; Bai C; Platt KA; Matise MP; Beeghly A; Hui CC; Nakashima M; Joyner AL Development; 2000 Apr; 127(8):1593-605. PubMed ID: 10725236 [TBL] [Abstract][Full Text] [Related]
12. Gli3 is required for Emx gene expression during dorsal telencephalon development. Theil T; Alvarez-Bolado G; Walter A; Rüther U Development; 1999 Aug; 126(16):3561-71. PubMed ID: 10409502 [TBL] [Abstract][Full Text] [Related]
13. gli, a zinc finger transcription factor and oncogene, is expressed during normal mouse development. Walterhouse D; Ahmed M; Slusarski D; Kalamaras J; Boucher D; Holmgren R; Iannaccone P Dev Dyn; 1993 Feb; 196(2):91-102. PubMed ID: 8364225 [TBL] [Abstract][Full Text] [Related]
14. Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome. Kalff-Suske M; Wild A; Topp J; Wessling M; Jacobsen EM; Bornholdt D; Engel H; Heuer H; Aalfs CM; Ausems MG; Barone R; Herzog A; Heutink P; Homfray T; Gillessen-Kaesbach G; König R; Kunze J; Meinecke P; Müller D; Rizzo R; Strenge S; Superti-Furga A; Grzeschik KH Hum Mol Genet; 1999 Sep; 8(9):1769-77. PubMed ID: 10441342 [TBL] [Abstract][Full Text] [Related]
15. High-resolution mapping of the Gli3 deletion in the mouse extra-toesH mutant. Genestine M; Robert B; Lallemand Y Genesis; 2007 Mar; 45(3):107-12. PubMed ID: 17304534 [TBL] [Abstract][Full Text] [Related]
16. Evidence for genetic control of Sonic hedgehog by Gli3 in mouse limb development. Büscher D; Bosse B; Heymer J; Rüther U Mech Dev; 1997 Mar; 62(2):175-82. PubMed ID: 9152009 [TBL] [Abstract][Full Text] [Related]
17. Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2). Tanimoto Y; Veistinen L; Alakurtti K; Takatalo M; Rice DP J Biol Chem; 2012 Jun; 287(25):21429-38. PubMed ID: 22547067 [TBL] [Abstract][Full Text] [Related]
18. Extra-toes (Xt) homozygous mutant mice demonstrate a role for the Gli-3 gene in the development of the forebrain. Franz T Acta Anat (Basel); 1994; 150(1):38-44. PubMed ID: 7976186 [TBL] [Abstract][Full Text] [Related]
19. Pax9 and Jagged1 act downstream of Gli3 in vertebrate limb development. McGlinn E; van Bueren KL; Fiorenza S; Mo R; Poh AM; Forrest A; Soares MB; Bonaldo Mde F; Grimmond S; Hui CC; Wainwright B; Wicking C Mech Dev; 2005 Nov; 122(11):1218-33. PubMed ID: 16169709 [TBL] [Abstract][Full Text] [Related]
20. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome. Kang S; Graham JM; Olney AH; Biesecker LG Nat Genet; 1997 Mar; 15(3):266-8. PubMed ID: 9054938 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]