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SIX5 gene
Known as:
SIX Homeobox 5 Gene
, SINE OCULIS HOMEOBOX, DROSOPHILA, HOMOLOG OF, 5
, DMAHP
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This gene is involved in transcription regulation.
National Institutes of Health
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Related topics
Related topics
6 relations
Cell Differentiation process
Homeobox Protein SIX5, human
Homo sapiens
Pattern Formation
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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
Masanori Takahashi
,
Masaru Tamura
,
K. Kawakami
2016
Corpus ID: 90270586
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
T. Schmidt
,
T. Bierhals
,
+7 authors
K. Kutsche
Cytogenetic and Genome Research
2013
Corpus ID: 5606903
Branchio-oto-renal (BOR) syndrome is an autosomal dominantly inherited developmental disorder, which is characterized by…
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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
G. Sicot
2013
Corpus ID: 160123328
La dystrophie myotonique de type I (DM1) constitue la plus frequente des pathologies musculaires hereditaires chez l’adulte. Bien…
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2006
2006
A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
J. Bateman
,
J. Bateman
,
+10 authors
M. Spence
Investigative Ophthalmology and Visual Science
2006
Corpus ID: 1134331
PURPOSE To map and identify the mutated gene for autosomal dominant cataract (ADC) in family ADC4. METHODS Ophthalmic…
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2005
2005
Characterisation of the transcription factor, SIX5, using a new panel of monoclonal antibodies
Y. Pham
,
N. Man
,
+4 authors
G. Morris
Journal of Cellular Biochemistry
2005
Corpus ID: 918981
SIX5 is a member of the human SIX family of transcription factors, many of which are involved in eye development. However, SIX5…
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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…
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2001
2001
Skeletal muscle Na currents in mice heterozygous for Six5 deficiency.
D. Mistry
,
J. Moorman
,
S. Reddy
,
J. Mounsey
Physiological Genomics
2001
Corpus ID: 35308222
Myotonic dystrophy results from a trinucleotide repeat expansion between the myotonic dystrophy protein kinase gene (Dmpk), which…
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2000
2000
Expression of a homeobox gene (SIX5) in borderline ovarian tumours
C. Winchester
,
S. Robertson
,
T. Macleod
,
K. Johnson
,
M. Thomas
Journal of Clinical Pathology
2000
Corpus ID: 1198551
Aims—To assess the expression of SIX5 (a homeobox gene) mRNA in surface coelomic epithelium, endocervical epithelium, Fallopian…
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1999
1999
Expression and functional analysis of the transcription factor DMAHP
S. E. Harris
1999
Corpus ID: 63315124
Myotonic dystrophy (DM) is the most prevalent form of adult muscular dystrophy and is characterised by myotonia and muscle…
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Review
1998
Review
1998
Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes.
S. Tapscott
,
T. Klesert
,
R. J. Widrow
,
R. Stöger
,
C. Laird
Current Opinion in Genetics and Development
1998
Corpus ID: 23329607
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