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Brain, ISSN 0006-8950, 2014, Volume 137, Issue 6, pp. 1676 - 1700
Journal Article
Journal Article
CELLS, ISSN 2073-4409, 07/2019, Volume 8, Issue 7, p. 669
Mutations in tubulin genes are responsible for a large spectrum of brain malformations secondary to abnormal neuronal migration, organization, differentiation... 
epilepsy | NEURONAL MIGRATION | GENETIC-BASIS | TUBA1A MUTATION | malformations cortical development | EEG | CLINICAL-FEATURES | MICROTUBULE DYNAMICS | WIDE SPECTRUM | CORTICAL DEVELOPMENT | SEIZURE ACTIVITY | CELL BIOLOGY | tubulin genes | TUBB2B | TUBA1A | MALFORMATIONS | TUBB3
Journal Article
Journal of Developmental Biology, ISSN 2221-3759, 09/2017, Volume 5, Issue 3, p. 8
Microtubules are dynamic cytoskeletal polymers that mediate numerous, essential functions such as axon and dendrite growth and neuron migration throughout... 
Neurodevelopment | Polymicrogyria | TUBA1A | Microtubule | Lissencephaly | Tubulinopathy | microtubule | polymicrogyria | lissencephaly | tubulinopathy | neurodevelopment
Journal Article
Journal Article
GENETICS IN MEDICINE, ISSN 1098-3600, 11/2018, Volume 20, Issue 11, pp. 1354 - 1364
Purpose: To estimate diagnostic yield and genotype-phenotype correlations in a cohort of 811 patients with lissencephaly or subcortical band heterotopia.... 
NEURONAL MIGRATION | TUBA1A MUTATIONS | actinopathy | subcortical band heterotopia | ACTIN-FILAMENTS | WIDE SPECTRUM | INTELLECTUAL DISABILITY | lissencephaly | MALFORMATIONS | tubulinopathy | KIF5C | GENETICS & HEREDITY | LIS1 | PROTEINS | reelinopathy | ASSOCIATION | Mutation
Journal Article
Clinical Genetics, ISSN 0009-9163, 11/2008, Volume 74, Issue 5, pp. 425 - 433
Mutations in the α‐1a Tubulin (TUBA1A) gene have recently been found to cause cortical malformations resemblant of classical lissencephaly but with a specific... 
lissencephaly | TUBA1A | α‐1a Tubulin | mutation analysis | neuronal migration | Neuronal migration | Mutation analysis | Lissencephaly | α-1a Tubulin
Journal Article
CLINICAL GENETICS, ISSN 0009-9163, 01/2010, Volume 77, Issue 1, pp. 35 - 35
Jaglin et al. (2009) Nature Genetics 41: 746-752. 
TUBA1A | GENETICS & HEREDITY | MUTATIONS
Journal Article
Brain and Development, ISSN 0387-7604, 10/2018, Volume 40, Issue 9, pp. 819 - 823
Tubulinopathies include a wide spectrum of disorders ranging from abnormal ocular movement to severe brain malformations, and typically present as diffuse... 
TUBA1A gene | Porencephaly | Tubulinopathy | TUBAk1 A gene | ALPHA | DISORDERS | WIDE SPECTRUM | BRAIN | CLINICAL NEUROLOGY | FEATURES | Genetic research | Medical colleges | Genetic aspects | Tubulins | Neurons | Genes
Journal Article
Journal Article
Journal Article
PLOS GENETICS, ISSN 1553-7404, 08/2019, Volume 15, Issue 8, p. e1008243
Tubulin genes encode a series of homologous proteins used to construct microtubules which are essential for multiple cellular processes. Neural development is... 
BETA-TUBULIN | NEURONAL MIGRATION | TUBB2B | TUBA1A MUTATION | ABNORMALITIES | POLYMICROGYRIA | GENETICS & HEREDITY | ALPHA | WIDE SPECTRUM | CORTICAL DEVELOPMENT | BRAIN | Dysmorphology | Analysis | Microtubules | Physiological aspects | Genetic aspects | Tubulins | Structure | Prosencephalon | CRISPR | Pediatrics | Phenotypes | Developmental biology | Genes | Cortex | Forebrain | Genomes | Medicine | Ethyl nitrosourea | Hospitals | Tubulin | Mutagenesis | Alleles | Genetics | Mutation
Journal Article