Literature DB >> 8528259

A two-hit model for developmental defects in Gorlin syndrome.

S Levanat1, R J Gorlin, S Fallet, D R Johnson, J E Fantasia, A E Bale.   

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Year:  1996        PMID： 8528259     DOI： 10.1038/ng0196-85

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


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  34 in total

1.  Confirmation of a double-hit model for the NF1 gene in benign neurofibromas.

Authors:  E Serra; S Puig; D Otero; A Gaona; H Kruyer; E Ars; X Estivill; C Lázaro
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

2.  Neuropilin-2 contributes to tumorigenicity in a mouse model of Hedgehog pathway medulloblastoma.

Authors:  Melanie G Hayden Gephart; YouRong Sophie Su; Samuel Bandara; Feng-Chiao Tsai; Jennifer Hong; Nicholas Conley; Helen Rayburn; Ljiljana Milenkovic; Tobias Meyer; Matthew P Scott
Journal:  J Neurooncol       Date:  2013-09-12       Impact factor: 4.130

3.  Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation.

Authors:  N K Ragge; A Salt; J R O Collin; A Michalski; P A Farndon
Journal:  Br J Ophthalmol       Date:  2005-08       Impact factor: 4.638

4.  Surgery for cystic lymphangioma in Gorlin-Goltz syndrome.

Authors:  C Kayser; G Kayser; P Baier; U T Hopt; S Eggstein
Journal:  Langenbecks Arch Surg       Date:  2007-01-13       Impact factor: 3.445

5.  Impaired skin and hair follicle development in Runx2 deficient mice.

Authors:  Donald J Glotzer; Elazar Zelzer; Bjorn R Olsen
Journal:  Dev Biol       Date:  2008-01-16       Impact factor: 3.582

6.  Variable expressivity of patched mutations in flies and humans.

Authors:  A E Bale
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

7.  Two modifications in the treatment of keratocystic odontogenic tumors (KCOT) and the use of Carnoy's solution (CS)--a retrospective study lasting between 2 and 10 years.

Authors:  Martin Gosau; Florian G Draenert; Steffen Müller; Bernhard Frerich; Ralf Bürgers; Thorsten E Reichert; Oliver Driemel
Journal:  Clin Oral Investig       Date:  2009-03-18       Impact factor: 3.573

8.  Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report.

Authors:  Giovanni Ponti; Annamaria Pollio; Lorenza Pastorino; Giovanni Pellacani; Cristina Magnoni; Sabina Nasti; Giulio Fortuna; Aldo Tomasi; Giovanna Bianchi Scarrà; Stefania Seidenari
Journal:  Oncol Lett       Date:  2012-05-08       Impact factor: 2.967

Review 9.  Nevoid basal cell carcinoma syndrome (Gorlin syndrome).

Authors:  Lorenzo Lo Muzio
Journal:  Orphanet J Rare Dis       Date:  2008-11-25       Impact factor: 4.123

Review 10.  Nevoid Basal Cell Carcinoma Syndrome (Gorlin Syndrome).

Authors:  Scott C Bresler; Bonnie L Padwa; Scott R Granter
Journal:  Head Neck Pathol       Date:  2016-03-14
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