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SIX1 gene

Known as: SIX Homeobox 1 Gene, SIX1, SINE OCULIS HOMEOBOX, DROSOPHILA, HOMOLOG OF, 1 
This gene may be involved in limb development.
National Institutes of Health

Related topics

Related topics

7 relations
Cell Differentiation processHomeobox Protein SIX1Homo sapiensLimb Development

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Quantitative Trait Locus Analysis of SIX1-SIX6 With Retinal Nerve Fiber Layer Thickness in Individuals of European Descent.
2014
2014
MicroRNA-30a regulates zebrafish myogenesis through targeting the transcription factor Six1
ABSTRACT Precise spatiotemporal regulation of the SIX1 homeoprotein is required to coordinate vital tissue development, including… 
Highly Cited
2012
Highly Cited
2012
Association between genetic variants associated with vertical cup-to-disc ratio and phenotypic features of primary open-angle glaucoma.
2012
2012
Specificity and prognostic validation of a polyclonal antibody to detect Six1 homeoprotein in ovarian cancer.
2008
2008
Bone morphogenetic protein‐7 regulates differentially the mRNA expression of bone morphogenetic proteins and their receptors in rat achilles and patellar tendon cell cultures
Previous animal studies have suggested that certain bone morphogenetic proteins (BMPs) may be useful therapeutically in treating… 
Highly Cited
2006
Highly Cited
2006
Six1 and Six4 promote survival of sensory neurons during early trigeminal gangliogenesis
2006
2006
Renal hypoplasia and dysplasia: starting to put the puzzle together.
The human metanephros is the direct precursor of the mature kidney: It begins to form in the fifth gestational week, when… 
Highly Cited
2006
Highly Cited
2006
Transcriptional Activation of the SALL1 by the Human SIX1 Homeodomain during Kidney Development*
SALL1 is a member of the SAL gene family that encodes a group of putative developmental transcription factors. SALL1 plays a… 
2006
2006
SIX1 Mutation Associated With Enlargement of the Vestibular Aqueduct in a Patient With Branchio‐Oto Syndrome
Objectives: The objectives of this study were to identify SIX1 gene mutations in a patient with branchio‐oto syndrome (BO) and to… 
2004
2004
SIX 1 mutations cause branchio-oto-renal syndrome by disruption of EYA 1 – SIX 1 – DNA complexes
Rainer G. Rufa,b,c, Pin-Xian Xuc,d,e, Derek Silviusd, Edgar A. Ottoa, Frank Beekmanna, Ulla T. Muerba, Shrawan Kumarf, Thomas J… 
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