145 related articles for article (PubMed ID: 11773971)
1. High-resolution mapping of the Gli3 mutation extra-toes reveals a 51.5-kb deletion.
Maynard TM; Jain MD; Balmer CW; LaMantia AS
Mamm Genome; 2002 Jan; 13(1):58-61. PubMed ID: 11773971
[No Abstract] [Full Text] [Related]
2. 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]
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. The mouse mutation Pdn (Polydactyly Nagoya) is caused by the integration of a retrotransposon into the Gli3 gene.
Thien H; Rüther U
Mamm Genome; 1999 Mar; 10(3):205-9. PubMed ID: 10051311
[TBL] [Abstract][Full Text] [Related]
5. Cloning and sequence analysis of the murine Gli3 cDNA.
Thien H; Büscher D; Rüther U
Biochim Biophys Acta; 1996 Jul; 1307(3):267-9. PubMed ID: 8688459
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. The XtJ allele generates a Gli3 fusion transcript.
Büscher D; Grotewold L; Rüther U
Mamm Genome; 1998 Aug; 9(8):676-8. PubMed ID: 9680393
[No Abstract] [Full Text] [Related]
8. Expression pattern of Irx1 and Irx2 during mouse digit development.
Zülch A; Becker MB; Gruss P
Mech Dev; 2001 Aug; 106(1-2):159-62. PubMed ID: 11472848
[TBL] [Abstract][Full Text] [Related]
9. Hedgehog-regulated processing of Gli3 produces an anterior/posterior repressor gradient in the developing vertebrate limb.
Wang B; Fallon JF; Beachy PA
Cell; 2000 Feb; 100(4):423-34. PubMed ID: 10693759
[TBL] [Abstract][Full Text] [Related]
10. De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and overlap with murine models.
Elson E; Perveen R; Donnai D; Wall S; Black GC
J Med Genet; 2002 Nov; 39(11):804-6. PubMed ID: 12414818
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Lumping and splitting: molecular biology in the genetics clinic.
Biesecker LG
Clin Genet; 1998 Jan; 53(1):3-7. PubMed ID: 9550355
[No Abstract] [Full Text] [Related]
13. GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity.
Ruppert JM; Vogelstein B; Arheden K; Kinzler KW
Mol Cell Biol; 1990 Oct; 10(10):5408-15. PubMed ID: 2118997
[TBL] [Abstract][Full Text] [Related]
14. The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.
Radhakrishna U; Bornholdt D; Scott HS; Patel UC; Rossier C; Engel H; Bottani A; Chandal D; Blouin JL; Solanki JV; Grzeschik KH; Antonarakis SE
Am J Hum Genet; 1999 Sep; 65(3):645-55. PubMed ID: 10441570
[TBL] [Abstract][Full Text] [Related]
15. Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene region.
Vortkamp A; Gessler M; Le Paslier D; Elaswarapu R; Smith S; Grzeschik KH
Genomics; 1994 Aug; 22(3):563-8. PubMed ID: 8001967
[TBL] [Abstract][Full Text] [Related]
16. Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes.
Mégarbané A; Le Lorc'H M; Elghezal H; Joly G; Gosset P ; Souraty N; Samaras L; Prieur M; Vekemans M; Turleau C; Romana SP
J Med Genet; 2001 Mar; 38(3):178-82. PubMed ID: 11303510
[No Abstract] [Full Text] [Related]
17. Gene structure and allelic expression assay of the human GLI3 gene.
Kang S; Rosenberg M; Ko VD; Biesecker LG
Hum Genet; 1997 Dec; 101(2):154-7. PubMed ID: 9402960
[TBL] [Abstract][Full Text] [Related]
18. Pallister-Hall syndrome phenotype in mice mutant for Gli3.
Böse J; Grotewold L; Rüther U
Hum Mol Genet; 2002 May; 11(9):1129-35. PubMed ID: 11978771
[TBL] [Abstract][Full Text] [Related]
19. The amino-terminal region of Gli3 antagonizes the Shh response and acts in dorsoventral fate specification in the developing spinal cord.
Meyer NP; Roelink H
Dev Biol; 2003 May; 257(2):343-55. PubMed ID: 12729563
[TBL] [Abstract][Full Text] [Related]
20. GLI3 mutations in human disorders mimic Drosophila cubitus interruptus protein functions and localization.
Shin SH; Kogerman P; Lindström E; Toftgárd R; Biesecker LG
Proc Natl Acad Sci U S A; 1999 Mar; 96(6):2880-4. PubMed ID: 10077605
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
