Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
June 4, 2003Human Molecular GeneticsOpen Access

Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia

View Full Paper
Ask AI
Bookmark
Share

Authors

ESElisabeth SockFriedrich-Alexander-Universität Erlangen-Nürnberg

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Elisabeth Sock (2003) studied this question.

synapsesocial.com/papers/6aa5b65166012019823a53aehttps://doi.org/10.1093/hmg/ddg158
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Protein Stability and Domain Topology Determine the Transcriptional Activity of the Mammalian Glial Cells Missing Homolog, GCMb2000 · 45 citations
  2. 2Three High Mobility Group-like Sequences within a 48-Base Pair Enhancer of the Col2a1 Gene Are Required for Cartilage-specific Expression in Vivo1998 · 171 citations
  3. 3SOX9 Enhances Aggrecan Gene Promoter/Enhancer Activity and Is Up-regulated by Retinoic Acid in a Cartilage-derived Cell Line, TC62000 · 500 citations
  4. 4Sox10 Is an Active Nucleocytoplasmic Shuttle Protein, and Shuttling Is Crucial for Sox10-Mediated Transactivation2002 · 106 citations
  5. 5Adjacent DNA sequences modulate Sox9 transcriptional activation at paired Sox sites in three chondrocyte-specific enhancer elements2003 · 76 citations