Crystal Structure of SEDL and Its Implications for a Genetic Disease Spondyloepiphyseal Dysplasia Tarda
Open Access
- 1 December 2002
- journal article
- Published by Elsevier
- Vol. 277 (51) , 49863-49869
- https://doi.org/10.1074/jbc.m207436200
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia TardaAmerican Journal of Human Genetics, 2001
- A missense mutation in the SEDL gene results in delayed onset of X linked spondyloepiphyseal dysplasia in a large pedigreeJournal of Medical Genetics, 2001
- The TRAPP Complex Is a Nucleotide Exchanger for Ypt1 and Ypt31/32Molecular Biology of the Cell, 2000
- Identification and characterization of five new subunits of TRAPPEuropean Journal of Cell Biology, 2000
- Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardaNature Genetics, 1999
- Membrane Fusion and ExocytosisAnnual Review of Biochemistry, 1999
- Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 Å resolutionNature, 1998
- X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred.Journal of Medical Genetics, 1996
- Ypt1p implicated in v-SNARE activationNature, 1994
- A rab protein is required for the assembly of SNARE complexes in the docking of transport vesiclesCell, 1994