Molecular cloning and characterization of the murine gnathodiaphyseal dysplasia gene GDD1
- 17 June 2005
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 331 (4), 1099-1106
- https://doi.org/10.1016/j.bbrc.2005.03.226
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- GDD1 Is Identical to TMEM16E, a Member of the TMEM16 FamilyAmerican Journal of Human Genetics, 2004
- The Novel Gene Encoding a Putative Transmembrane Protein Is Mutated in Gnathodiaphyseal Dysplasia (GDD)American Journal of Human Genetics, 2004
- hCHL2, a novel chordin-related gene, displays differential expression and complex alternative splicing in human tissues and during myoblast and osteoblast maturationGene, 2004
- NGEP, a gene encoding a membrane protein detected only in prostate cancer and normal prostateProceedings of the National Academy of Sciences, 2004
- Autosomal Dominant Gnathodiaphyseal Dysplasia Maps to Chromosome 11p14.3-15.1Journal of Bone and Mineral Research, 2003
- Gnathodiaphyseal Dysplasia: A Syndrome of Fibro-Osseous Lesions of Jawbones, Bone Fragility, and Long Bone BowingJournal of Bone and Mineral Research, 2001
- Familial florid cemento-osseous dysplasia: A case reportJournal of Oral and Maxillofacial Surgery, 2000
- Bone morphogenetic protein-2 converts the differentiation pathway of C2C12 myoblasts into the osteoblast lineage [published erratum appears in J Cell Biol 1995 Feb;128(4):following 713]The Journal of cell biology, 1994
- Osteogenesis imperfecta with unusual skeletal lesions: Report of three familiesAmerican Journal of Medical Genetics, 1985