Associated Papers
Decoding the mechanisms of cooperative DNA binding by the Paired-like homeodomain family.
Cain B et al.
Biorxiv : the Preprint Server for Biology, 2025
41279221 (PubMed )
Supplement: media-2.xlsx › SuppTable2
The SHOX region and its mutations.
Capone L et al.
Journal of Endocrinological Investigation, 2010
The novel human SHOX allelic variant database.
Niesler B et al.
Human Mutation, 2007
SHOX at a glance: from gene to protein.
Marchini A et al.
Archives of Physiology and Biochemistry, 2007
Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis.
Schneider KU et al.
Human Mutation, 2005
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis.
Falcinelli C et al.
Journal of Medical Genetics, 2002
SHOX gene in Leri-Weill syndrome and in idiopathic short stature.
Bernasconi S et al.
Journal of Endocrinological Investigation, 2001
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