Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

Karine Poirier, Nicolas Lebrun, Loïc Broix, +32

Nature Genetics

Developmental AnomalyDevelopmental BiologyBrain DevelopmentDevelopmental GeneticsGenetics +7

Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

David A. Keays, Guoling Tian, Karine Poirier, +16

Cell

Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria

Xavier H. Jaglin, Karine Poirier, Yoann Saillour, +21

Nature Genetics

BiologyNatural SciencesGeneticsMolecular BiologyAsymmetrical Polymicrogyria +3

Mutations in <i>TUBB8</i> and Human Oocyte Meiotic Arrest

Ruizhi Feng, Qing Sang, Yanping Kuang, +30

New England Journal of Medicine

SpermatogenesisOocyteGeneticsHuman Oocyte MaturationMolecular Genetics +19

Pathway Leading to Correctly Folded β-Tubulin

Guoling Tian, Yi Huang, Heidi Rommelaere, +3

Cell

Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities

Martin W. Breuss, Julian Ik‐Tsen Heng, Karine Poirier, +20

Cell Reports

Brain DevelopmentCytoskeletonStructural Brain AbnormalitiesCellular NeurobiologyMammalian Cortex +17

Tubulin Subunits Exist in an Activated Conformational State Generated and Maintained by Protein Cofactors

Guoling Tian, Sally A. Lewis, Becket Feierbach, +4

The Journal of Cell Biology

The α- and β-tubulin folding pathways

Sally A. Lewis, Guoling Tian, Nicholas J. Cowan

Trends in Cell Biology

Mutations in <i>TUBB8</i> cause a multiplicity of phenotypes in human oocytes and early embryos

Ruizhi Feng, Zheng Yan, Bin Li, +13

Journal of Medical Genetics

Specificity in chaperonin-mediated protein folding

Guoling Tian, Irina E. Vainberg, William D. Tap, +2

Nature

Protein ChemistryChaperonin-mediated Protein FoldingProtein AssemblyBiochemistryProtein Folding +4