Literature DB >> 1322743

Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt).

A Vortkamp1, T Franz, M Gessler, K H Grzeschik.   

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Year:  1992        PMID： 1322743     DOI： 10.1007/bf00356157

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  14 in total

1.  GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity.

Authors:  J M Ruppert; B Vogelstein; K Arheden; K W Kinzler
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

2.  A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p.

Authors:  A Vortkamp; U Thias; M Gessler; W Rosenkranz; P M Kroisel; N Tommerup; G Krüger; J Götz; L Pelz; K H Grzeschik
Journal:  Genomics       Date:  1991-11       Impact factor: 5.736

3.  Extra-toes: anew mutant gene causing multiple abnormalities in the mouse.

Authors:  D R Johnson
Journal:  J Embryol Exp Morphol       Date:  1967-06

4.  Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.

Authors:  L M Kunkel; U Tantravahi; M Eisenhard; S A Latt
Journal:  Nucleic Acids Res       Date:  1982-03-11       Impact factor: 16.971

5.  A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome.

Authors:  N Tommerup; F Nielsen
Journal:  Am J Med Genet       Date:  1983-11

6.  GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.

Authors:  A Vortkamp; M Gessler; K H Grzeschik
Journal:  Nature       Date:  1991-08-08       Impact factor: 49.962

Review 7.  The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.

Authors:  T R Gollop; L R Fontes
Journal:  Am J Med Genet       Date:  1985-09

8.  Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes).

Authors:  R M Winter; S M Huson
Journal:  Am J Med Genet       Date:  1988-12

9.  Transcription of H-2 and Qa genes in embryonic and adult mice.

Authors:  K Fahrner; B L Hogan; R A Flavell
Journal:  EMBO J       Date:  1987-05       Impact factor: 11.598

10.  Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt).

Authors:  T M Pohl; M G Mattei; U Rüther
Journal:  Development       Date:  1990-12       Impact factor: 6.868
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  24 in total

1.  Cell signaling regulation of vertebrate limb growth and patterning.

Authors:  Yingzi Yang; Scott H Kozin
Journal:  J Bone Joint Surg Am       Date:  2009-07       Impact factor: 5.284

2.  Physical mapping of the beige critical region on mouse chromosome 13.

Authors:  S F Kingsmore; M D Barbosa; Q A Nguyen; J A Ashley; S M Blaydes; V T Tchernev; J C Detter; M Lovett
Journal:  Mamm Genome       Date:  1996-10       Impact factor: 2.957

3.  Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

Authors:  U Radhakrishna; J L Blouin; H Mehenni; U C Patel; M N Patel; J V Solanki; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

4.  Musculoskeletal integration at the wrist underlies the modular development of limb tendons.

Authors:  Alice H Huang; Timothy J Riordan; Brian Pryce; Jennifer L Weibel; Spencer S Watson; Fanxin Long; Veronique Lefebvre; Brian D Harfe; H Scott Stadler; Haruhiko Akiyama; Sara F Tufa; Douglas R Keene; Ronen Schweitzer
Journal:  Development       Date:  2015-06-10       Impact factor: 6.868

5.  Cilia-dependent GLI processing in neural crest cells is required for tongue development.

Authors:  Grethel Millington; Kelsey H Elliott; Ya-Ting Chang; Ching-Fang Chang; Andrzej Dlugosz; Samantha A Brugmann
Journal:  Dev Biol       Date:  2017-03-09       Impact factor: 3.582

6.  Molecular linkage of the morphogenetic mutation add and the zinc finger gene Gli3.

Authors:  F van der Hoeven; T Schimmang; A Vortkamp; U Rüther
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

7.  The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling.

Authors:  Derek E Gildea; Erin S Luetkemeier; Xiaozhong Bao; Stacie K Loftus; Susan Mackem; Yingzi Yang; William J Pavan; Leslie G Biesecker
Journal:  FASEB J       Date:  2011-02-03       Impact factor: 5.191

8.  The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene.

Authors:  Jeffrey O Bush; Yu Lan; Rulang Jiang
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-26       Impact factor: 11.205

9.  A new mouse limb mutation identifies a Twist allele that requires interacting loci on chromosome 4 for its phenotypic expression.

Authors:  Isabelle Blanc; Antoine Bach; Yvan Lallemand; Fabienne Perrin-Schmitt; Jean-Louis Guénet; Benoît Robert
Journal:  Mamm Genome       Date:  2003-12       Impact factor: 2.957

10.  The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3.

Authors:  T Schimmang; S I Oda; U Rüther
Journal:  Mamm Genome       Date:  1994-06       Impact factor: 2.957
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