Conditional deletion ofL1CAMin human neurons impairs both axonal and dendritic arborization and action potential generation

L1CAMwhole gene deletion in a child with L1 syndrome

(2014) Brandalyn A. Chidsey et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Axon initial segments: diverse and dynamic neuronal compartments

(2014) Takeshi Yoshimura et al.   CURRENT OPINION IN NEUROBIOLOGY

Ankyrin-G Directly Binds to Kinesin-1 to Transport Voltage-Gated Na+ Channels into Axons

(2014) Joshua Barry et al.   DEVELOPMENTAL CELL

Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases

(2013) Homa Adle-Biassette et al.   ACTA NEUROPATHOLOGICA

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders

(2013) Z. Iqbal et al.   HUMAN MOLECULAR GENETICS

Rapid Single-Step Induction of Functional Neurons from Human Pluripotent Stem Cells

(2013) Yingsha Zhang et al.   NEURON

Role of L1CAM for axon sprouting and branching

(2012) Michael K. E. Schäfer et al.   CELL AND TISSUE RESEARCH

Signal Processing in the Axon Initial Segment

(2012) Maarten H.P. Kole et al.   NEURON

L1CAM

(2012) Helena Kiefel et al.   Cell Adhesion & Migration

Cdk-mediated phosphorylation of the Kvβ2 auxiliary subunit regulates Kv1 channel axonal targeting

(2011) Hélène Vacher et al.   JOURNAL OF CELL BIOLOGY

A Critical Role for Neurofascin in Regulating Action Potential Initiation through Maintenance of the Axon Initial Segment

(2011) Barbara Zonta et al.   NEURON

L1CAM malfunction in the nervous system and human carcinomas

(2010) Michael K. E. Schäfer et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Homophilic Adhesion Mechanism of Neurofascin, a Member of the L1 Family of Neural Cell Adhesion Molecules

(2010) Heli Liu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

L1 syndrome mutations impair neuronal L1 function at different levels by divergent mechanisms

(2010) Michael K.E. Schäfer et al.   NEUROBIOLOGY OF DISEASE

An updated and upgradedL1CAMmutation database

(2009) Yvonne J. Vos et al.   HUMAN MUTATION

Role of the cytoplasmic domain of the L1 cell adhesion molecule in brain development

(2009) Yukiko Nakamura et al.   JOURNAL OF COMPARATIVE NEUROLOGY

Genotype-phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysis

(2009) Y. J. Vos et al.   JOURNAL OF MEDICAL GENETICS

Cryo-Electron Tomography of Homophilic Adhesion Mediated by the Neural Cell Adhesion Molecule L1

(2009) Yongning He et al.   STRUCTURE

The genetic landscape of intellectual disability arising from chromosome X

(2009) Jozef Gécz et al.   TRENDS IN GENETICS

AnkyrinG is required for maintenance of the axon initial segment and neuronal polarity

(2008) Kristian L. Hedstrom et al.   JOURNAL OF CELL BIOLOGY

L1 Interaction with Ankyrin Regulates Mediolateral Topography in the Retinocollicular Projection

(2008) M. Buhusi et al.   JOURNAL OF NEUROSCIENCE

Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

(2008) T G Schulze et al.   MOLECULAR PSYCHIATRY

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

(2008) Manuel A R Ferreira et al.   NATURE GENETICS