Nalaganje...
Williams-Beuren Syndrome-associated Transcription Factor TFII-I Regulates Osteogenic Marker Genes
Williams-Beuren syndrome (WBS), an autosomal dominant genetic disorder, is characterized by a unique cognitive profile and craniofacial defects. WBS results from a microdeletion at the chromosomal location 7q11.23 that encompasses the genes encoding the members of TFII-I family of transcription fact...
Shranjeno v:
| Main Authors: | , , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
American Society for Biochemistry and Molecular Biology
2009
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2794739/ https://ncbi.nlm.nih.gov/pubmed/19880526 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.C109.063115 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|