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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.
2018
2018
Cystic Kidney Disease Panel Plus
Referring Healthcare
2018
Corpus ID: 53490377
The Blueprint Genetics Cystic Kidney Disease Panel (version 2, Mar 01, 2018) Plus Analysis includes sequence analysis and copy…
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2017
2017
The Fusarium oxysporum effector pair Avr2 & Six5 in action
L. Cao
2017
Corpus ID: 89866576
Plants are continuously challenged by pathogenic microbes lurking in the environment. Successful pathogens can overcome plant…
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2017
2017
Branchiootorenal Syndrome (BOR)-3 Very Illustrative Cases
Oliveira Ca
2017
Corpus ID: 79289844
Although the association of hearing loss, preauricular pits and branchial fistulae occurring in families was known since 1932 it…
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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
Review
2015
Review
2015
Myotonic Dystrophy and the Heart - A Review
S. Thampi
,
J. Chithra
,
S. Surendran
2015
Corpus ID: 6363391
Myotonic Dystrophy (Dystrophia Myotonica, DM) is the most frequently inherited neuromuscular disease of adult life. DM is a…
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2003
2003
Identification of SIX5 binding site, target genes, and functional links with myotonic dystophy (DM1) symptoms.
J. Ra
2003
Corpus ID: 79096217
2002
2002
Identification, isolation and characterisation of the Drosophila othologue of human SIX5.
G. Hamilton
2002
Corpus ID: 78391372
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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1996
1996
Identification and characterisation of two human homeodomain encoding genes : DMAHP and Six1.
Boucher Ca
1996
Corpus ID: 57012063