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TUBB3 gene
Known as:
Tubulin, Beta 3 Class III Gene
, TUBULIN, BETA-3
, tubulin beta 3 class III
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This gene is involved in microtubule function and structure.
National Institutes of Health
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Related topics
Related topics
8 relations
Cell Movement
Cytokinesis
Microtubule Process
Muscle Contraction
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Broader (1)
Genes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2016
Highly Cited
2016
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development
M. Whitman
,
C. Andrews
,
+10 authors
E. Engle
American Journal of Medical Genetics. Part A
2016
Corpus ID: 23937797
One set of missense mutations in the neuron specific beta tubulin isotype 3 (TUBB3) has been reported to cause malformations of…
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Review
2015
Review
2015
Mitochondrial dynamics and inherited peripheral nerve diseases
D. Pareyson
,
P. Saveri
,
A. Sagnelli
,
G. Piscosquito
Neuroscience Letters
2015
Corpus ID: 25302759
Highly Cited
2013
Highly Cited
2013
MiR-200c and HuR in ovarian cancer
S. Prislei
,
E. Martinelli
,
+6 authors
C. Ferlini
BMC Cancer
2013
Corpus ID: 16375033
BackgroundMicroRNAs in solid malignancies can behave as predictors of either good or poor outcome. This is the case with members…
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Highly Cited
2013
Highly Cited
2013
Direct binding of TUBB3 with DCC couples netrin-1 signaling to intracellular microtubule dynamics in axon outgrowth and guidance
C. Qu
,
T. Dwyer
,
Q. Shao
,
Tao Yang
,
Huai Huang
,
Guofa Liu
Journal of Cell Science
2013
Corpus ID: 15265912
Summary The coupling of axon guidance cues, such as netrin-1, to microtubule (MT) dynamics is essential for growth cone…
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Highly Cited
2010
Highly Cited
2010
Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects.
K. Poirier
,
Yoann Saillour
,
+14 authors
J. Chelly
Human Molecular Genetics
2010
Corpus ID: 14326711
Mutations in the TUBB3 gene, encoding β-tubulin isotype III, were recently shown to be associated with various neurological…
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Highly Cited
2010
Highly Cited
2010
Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations.
J. Demer
,
R. Clark
,
Max A. Tischfield
,
E. Engle
Investigative Ophthalmology and Visual Science
2010
Corpus ID: 30799102
PURPOSE Orbital magnetic resonance imaging (MRI) was used to investigate the structural basis of motility abnormalities in…
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Highly Cited
2008
Highly Cited
2008
Proteomic characterization of cytoskeletal and mitochondrial class III β-tubulin
L. Cicchillitti
,
Roberta Penci
,
+5 authors
C. Ferlini
Molecular Cancer Therapeutics
2008
Corpus ID: 26212762
Class III β-tubulin (TUBB3) has been discovered as a marker of drug resistance in human cancer. To get insights into the…
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Highly Cited
2007
Highly Cited
2007
Class III β‐tubulin, a marker of resistance to paclitaxel, is overexpressed in pancreatic ductal adenocarcinoma and intraepithelial neoplasia
K. M. Lee
,
Dengfeng Cao
,
+4 authors
Michel M. Ouellette
Histopathology
2007
Corpus ID: 30180518
Aims: Class III β‐tubulin (TUBB3) reduces microtubule stability and confers resistance to microtubule‐stabilizing taxanes…
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2002
2002
Congenital fibrosis of the vertically acting extraocular muscles maps to the FEOM3 locus
D. Mackey
,
Wai-Man Chan
,
+4 authors
E. Engle
Human Genetics
2002
Corpus ID: 1354922
Abstract. The diagnosis of congenital fibrosis of the extraocular muscles (CFEOM) encompasses several different inherited…
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Highly Cited
1999
Highly Cited
1999
CFEOM3: a new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3.
E. Doherty
,
M. Macy
,
Susan M. Wang
,
Catherine P. Dykeman
,
M. Melanson
,
E. Engle
Investigative Ophthalmology and Visual Science
1999
Corpus ID: 33698122
PURPOSE To define the clinical characteristics and determine the gene localization for a previously undescribed form of…
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