A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1
- 1 April 2002
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 70 (4), 943-954
- https://doi.org/10.1086/339689
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- The Ras/Rac Guanine Nucleotide Exchange Factor Mammalian Son-of-sevenless Interacts with PACSIN 1/Syndapin I, a Regulator of Endocytosis and the Actin CytoskeletonPublished by Elsevier BV ,2001
- A New Locus for Hereditary Gingival Fibromatosis (GINGF2) Maps to 5q13–q22Genomics, 2001
- Refinement of the Locus for Autosomal Dominant Hereditary Gingival Fibromatosis (GINGF) to a 3.8-cM Region on 2p21Genomics, 2000
- Direct Interaction of SOS1 Ras Exchange Protein with the SH3 Domain of Phospholipase C-γ1Biochemistry, 2000
- Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in RecombinationAmerican Journal of Human Genetics, 1998
- Gingival recession Reappraisal of an enigmatic condition and a new index for monitoringJournal of Clinical Periodontology, 1997
- The pathogenesis of drug‐induced gingival overgrowthJournal of Clinical Periodontology, 1996
- Membrane targeting of the nucleotide exchange factor Sos is sufficient for activating the Ras signaling pathwayCell, 1994
- Hereditary fibrous hyperplasia of the gingiva with varying penetrance and expressivityEuropean Journal of Oral Sciences, 1978
- Variation in the Inheritance and Expression of Gingival FibromatosisThe Journal of Periodontology, 1974