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SIX5 gene

Known as: SIX Homeobox 5 Gene, SINE OCULIS HOMEOBOX, DROSOPHILA, HOMOLOG OF, 5, DMAHP 
This gene is involved in transcription regulation.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Branchio-oto-renal (BOR) syndrome is an autosomal dominantly inherited developmental disorder, which is characterized by… 
2013
2013
La dystrophie myotonique de type I (DM1) constitue la plus frequente des pathologies musculaires hereditaires chez l’adulte. Bien… 
2006
2006
PURPOSE To map and identify the mutated gene for autosomal dominant cataract (ADC) in family ADC4. METHODS Ophthalmic… 
2005
2005
SIX5 is a member of the human SIX family of transcription factors, many of which are involved in eye development. However, SIX5… 
2004
2004
  • M. Eriksson
  • 2004
  • Corpus ID: 1564279
Myotonic dystrophy (DM1) is a neuromuscular disorder caused by a CTGn expansion in the 3'-untranslated region (UTR) of myotonic… 
2001
2001
Myotonic dystrophy results from a trinucleotide repeat expansion between the myotonic dystrophy protein kinase gene (Dmpk), which… 
2000
2000
Aims—To assess the expression of SIX5 (a homeobox gene) mRNA in surface coelomic epithelium, endocervical epithelium, Fallopian… 
1999
1999
Myotonic dystrophy (DM) is the most prevalent form of adult muscular dystrophy and is characterised by myotonia and muscle…