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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

Related topics

Related topics

6 relations
Cell Differentiation processHomeobox Protein SIX5, humanHomo sapiensPattern Formation

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Mice defective of Six4 and Six5 , show abnormal growth and epithelialization of the primary body wall, resulting in omphalocele with no severe defects in abdominal muscle differentiation
2013
2013
Branchio-Otic Syndrome Caused by a Genomic Rearrangement: Clinical Findings and Molecular Cytogenetic Studies in a Patient with a Pericentric Inversion of Chromosome 8
Branchio-oto-renal (BOR) syndrome is an autosomal dominantly inherited developmental disorder, which is characterized by… 
2013
2013
Conséquences pathologiques des expansions CTG sur le système nerveux central d’un modèle murin de la dystrophie myotonique de Steinert : approches moléculaires, protéomiques et cellulaires
La dystrophie myotonique de type I (DM1) constitue la plus frequente des pathologies musculaires hereditaires chez l’adulte. Bien… 
2006
2006
A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
PURPOSE To map and identify the mutated gene for autosomal dominant cataract (ADC) in family ADC4. METHODS Ophthalmic… 
2005
2005
Characterisation of the transcription factor, SIX5, using a new panel of monoclonal antibodies
SIX5 is a member of the human SIX family of transcription factors, many of which are involved in eye development. However, SIX5… 
2004
2004
Real-time RT-PCR for CTG repeat-containing genes.
  • M. Eriksson
  • Methods in molecular biology
  • 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
Skeletal muscle Na currents in mice heterozygous for Six5 deficiency.
Myotonic dystrophy results from a trinucleotide repeat expansion between the myotonic dystrophy protein kinase gene (Dmpk), which… 
2000
2000
Expression of a homeobox gene (SIX5) in borderline ovarian tumours
Aims—To assess the expression of SIX5 (a homeobox gene) mRNA in surface coelomic epithelium, endocervical epithelium, Fallopian… 
1999
1999
Expression and functional analysis of the transcription factor DMAHP
Myotonic dystrophy (DM) is the most prevalent form of adult muscular dystrophy and is characterised by myotonia and muscle… 
Review
1998
Review
1998
Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes.
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