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Items: 1 to 20 of 207

1.

Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4.

Dunn NR, Winnier GE, Hargett LK, Schrick JJ, Fogo AB, Hogan BL.

Dev Biol. 1997 Aug 15;188(2):235-47.

2.

Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse.

Masuya H, Sagai T, Moriwaki K, Shiroishi T.

Dev Biol. 1997 Feb 1;182(1):42-51.

3.

Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development.

Mo R, Freer AM, Zinyk DL, Crackower MA, Michaud J, Heng HH, Chik KW, Shi XM, Tsui LC, Cheng SH, Joyner AL, Hui C.

Development. 1997 Jan;124(1):113-23.

4.

Pallister-Hall syndrome phenotype in mice mutant for Gli3.

Böse J, Grotewold L, Rüther U.

Hum Mol Genet. 2002 May 1;11(9):1129-35.

PMID:
11978771
5.

Bmp4 in limb bud mesoderm regulates digit pattern by controlling AER development.

Selever J, Liu W, Lu MF, Behringer RR, Martin JF.

Dev Biol. 2004 Dec 15;276(2):268-79.

6.

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.

7.

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 16;96(6):2880-4.

8.

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.

9.

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.

PMID:
10441342
10.
11.

Levels of Gli3 repressor correlate with Bmp4 expression and apoptosis during limb development.

Bastida MF, Delgado MD, Wang B, Fallon JF, Fernandez-Teran M, Ros MA.

Dev Dyn. 2004 Sep;231(1):148-60. Erratum in: Dev Dyn. 2005 Aug;233(4):1613.

12.

Direct interaction with Hoxd proteins reverses Gli3-repressor function to promote digit formation downstream of Shh.

Chen Y, Knezevic V, Ervin V, Hutson R, Ward Y, Mackem S.

Development. 2004 May;131(10):2339-47. Epub 2004 Apr 21.

13.

Genetic interaction of Gli3 and Alx4 during limb development.

Panman L, Drenth T, Tewelscher P, Zuniga A, Zeller R.

Int J Dev Biol. 2005;49(4):443-8.

14.

A hypermorphic mouse Gli3 allele results in a polydactylous limb phenotype.

Wang C, Pan Y, Wang B.

Dev Dyn. 2007 Mar;236(3):769-76.

16.

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.

Kang S, Graham JM Jr, Olney AH, Biesecker LG.

Nat Genet. 1997 Mar;15(3):266-8.

PMID:
9054938
17.

Noggin antagonism of BMP4 signaling controls development of the axial skeleton in the mouse.

Wijgerde M, Karp S, McMahon J, McMahon AP.

Dev Biol. 2005 Oct 1;286(1):149-57.

18.

Paired-related homeobox genes cooperate in handplate and hindlimb zeugopod morphogenesis.

Lu MF, Cheng HT, Lacy AR, Kern MJ, Argao EA, Potter SS, Olson EN, Martin JF.

Dev Biol. 1999 Jan 1;205(1):145-57.

20.

Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly.

Qu S, Tucker SC, Ehrlich JS, Levorse JM, Flaherty LA, Wisdom R, Vogt TF.

Development. 1998 Jul;125(14):2711-21.

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