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Literature DB >> 9354780

Strike three for GLI3.

L G Biesecker.

Abstract

Entities: Gene

Mesh：

Substances：

Year: 1997 PMID： 9354780 DOI： 10.1038/ng1197-259

Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330

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Cited

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16 in total

1. Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.

Authors: J Kohlhase; P E Taschner; P Burfeind; B Pasche; B Newman; C Blanck; M H Breuning; L P ten Kate; P Maaswinkel-Mooy; B Mitulla; J Seidel; S J Kirkpatrick; R M Pauli; D S Wargowski; K Devriendt; W Proesmans; O Gabrielli; G V Coppa; E Wesby-van Swaay; R C Trembath; A A Schinzel; W Reardon; E Seemanova; W Engel
Journal: Am J Hum Genet Date: 1999-02 Impact factor: 11.025

2. A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.

Authors: B C Schutte; B C Bjork; K B Coppage; M I Malik; S G Gregory; D J Scott; L M Brentzell; Y Watanabe; M J Dixon; J C Murray
Journal: Genome Res Date: 2000-01 Impact factor: 9.043

Review 3. Hedgehog signaling in mouse mammary gland development and neoplasia.

Authors: M T Lewis
Journal: J Mammary Gland Biol Neoplasia Date: 2001-01 Impact factor: 2.673

4. 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.

Authors: U Radhakrishna; D Bornholdt; H S Scott; U C Patel; C Rossier; H Engel; A Bottani; D Chandal; J L Blouin; J V Solanki; K H Grzeschik; S E Antonarakis
Journal: Am J Hum Genet Date: 1999-09 Impact factor: 11.025

5. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.

Authors: Jennifer J Johnston; Isabelle Olivos-Glander; Christina Killoran; Emma Elson; Joyce T Turner; Kathryn F Peters; Margaret H Abbott; David J Aughton; Arthur S Aylsworth; Michael J Bamshad; Carol Booth; Cynthia J Curry; Albert David; Mary Beth Dinulos; David B Flannery; Michelle A Fox; John M Graham; Dorothy K Grange; Alan E Guttmacher; Mark C Hannibal; Wolfram Henn; Raoul C M Hennekam; Lewis B Holmes; H Eugene Hoyme; Kathleen A Leppig; Angela E Lin; Patrick Macleod; David K Manchester; Carlo Marcelis; Laura Mazzanti; Emma McCann; Marie T McDonald; Nancy J Mendelsohn; John B Moeschler; Billur Moghaddam; Giovanni Neri; Ruth Newbury-Ecob; Roberta A Pagon; John A Phillips; Laurie S Sadler; Joan M Stoler; David Tilstra; Catherine M Walsh Vockley; Elaine H Zackai; Touran M Zadeh; Louise Brueton; Graeme Charles M Black; Leslie G Biesecker
Journal: Am J Hum Genet Date: 2005-02-28 Impact factor: 11.025

6. The Shh-independent activator function of the full-length Gli3 protein and its role in vertebrate limb digit patterning.

Authors: Chengbing Wang; Ulrich Rüther; Baolin Wang
Journal: Dev Biol Date: 2007-02-28 Impact factor: 3.582

Strike three for GLI3.

1. Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.

2. A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.

Review 3. Hedgehog signaling in mouse mammary gland development and neoplasia.

4. 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.

5. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.

6. The Shh-independent activator function of the full-length Gli3 protein and its role in vertebrate limb digit patterning.

7. Analysis of the polymorphisms in the caprine Gli3 gene and their associations with production traits in goats.

Review 8. Holoprosencephaly: a paradigm for the complex genetics of brain development.

9. GLI-2 modulates retroviral gene expression.

10. Point mutations in GLI3 lead to misregulation of its subcellular localization.