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TUBA8 gene

Known as: TUBA8, TUBULIN, ALPHA-8, TUBULIN, ALPHA-LIKE 2 
National Institutes of Health

Related topics

Related topics

2 relations
TUBA4A genebeta-Tubulin

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Alpha-syntrophin dependent expression of tubulin alpha 8 protein in hepatocytes
The scaffold protein alpha-syntrophin (SNTA) is a component of the dystrophin glycoprotein complex and has been comprehensively… 
Review
2018
Review
2018
Manifestation of recessive combined D‐2‐, L‐2‐hydroxyglutaric aciduria in combination with 22q11.2 deletion syndrome
22q11.2 deletion syndrome is one of the most common human microdeletion syndromes. The clinical phenotype of 22q11.2 deletion… 
2018
2018
Transcriptome analysis of adherens junction pathway-related genes after peripheral nerve injury
The neural regeneration process is driven by a wide range of molecules and pathways. Adherens junctions are critical cellular… 
Review
2017
Review
2017
A unique case of lissencephaly with Crouzon syndrome heterozygous for FGFR2 mutation
Dear Editor, We are pleased to report a unique case of posterior predominant lissencephaly in a child with Crouzon syndrome… 
2017
2017
Tubulin alpha 8 is expressed in hepatic stellate cells and is induced in transformed hepatocytes
Tubulin alpha 8 (TUBA8) is highly abundant in murine liver tumors suggesting a role in hepatocellular carcinoma (HCC). Non… 
2015
2015
PMG: Polymicrogyria BFPP: Bilateral frontoparietal PMG BPP: Bilateral perisylvian PMG CNV: copy number variants EEG: Electroencephalogram ILS: isolated LIS LIS: Lissencephaly MCD: Malformations of…
The malformations of cortical development (MCD) represent a major cause of developmental disabilities, severe epilepsy and… 
2013
2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria
Polymicrogyria (PMG) is a clinically heterogeneous malformation of cortical development, characterized by a loss of the normal… 
Review
2011
Review
2011
A Novel Sporadic 614-Kb Duplication of the 22q11.2 Chromosome in a Child With Amyoplasia
Arthrogryposis is a rare congenital disorder characterized by multiple fixed joint contractures. Decreased fetal movement… 
2007
2007
Bipolar I Disorder and Schizophrenia : A 440 – Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish
Bipolar, schizophrenia, and schizoaffective disorders are common, highly heritable psychiatric disorders, for which familial… 
2006
2006
Radiation hybrid mapping of 18 positional and physiological candidate genes for arthrogryposis multiplex congenita on porcine chromosome 5.
We report the chromosomal assignment of 18 porcine genes to human homologues using the INRA-Minnesota swine radiation hybrid… 
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