Author pages are created from data sourced from our academic publisher partnerships and public sources.
- Publications
- Influence
The microtubule binding domain of microtubule-associated protein MAP1B contains a repeated sequence motif unrelated to that of MAP2 and tau
We report the complete sequence of the microtubule-associated protein MAP1B, deduced from a series of overlapping genomic and cDNA clones. The encoded protein has a predicted molecular mass of… Expand
Prefoldin, a Chaperone that Delivers Unfolded Proteins to Cytosolic Chaperonin
- I. E. Vainberg, S. Lewis, +4 authors N. Cowan
- Biology, Medicine
- Cell
- 29 May 1998
We describe the discovery of a heterohexameric chaperone protein, prefoldin, based on its ability to capture unfolded actin. Prefoldin binds specifically to cytosolic chaperonin (c-cpn) and transfers… Expand
Number and evolutionary conservation of α- and β-tubulin and cytoplasmic β- and γ-actin genes using specific cloned cDNA probes
- D. Cleveland, M. A. Lopata, Raymond J MacDonald, N. Cowan, M. Kirschner
- Biology
- Cell
- 1 May 1980
Abstract Bacterial clones containing inserted DNA sequences specific for α-tubulin, β-tubulin, β-actin and γ-actin have been constructed from mRNA of embryonic chick brain. Plasmids containing… Expand
Projection domains of MAP2 and tau determine spacings between microtubules in dendrites and axons
- J. Chen, Y. Kanai, N. Cowan, N. Hirokawa
- Biology, Medicine
- Nature
- 17 December 1992
NEURONS develop a highly polarized morphology consisting of dendrites and a long axon. Both axons and dendrites contain microtubules and microtubule-associated proteins (MAPs) with characteristic… Expand
Tubulin Subunits Exist in an Activated Conformational State Generated and Maintained by Protein Cofactors
The production of native α/β tubulin heterodimer in vitro depends on the action of cytosolic chaperonin and several protein cofactors. We previously showed that four such cofactors (termed A, C, D,… Expand
Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans
Summary The development of the mammalian brain is dependent on extensive neuronal migration. Mutations in mice and humans that affect neuronal migration result in abnormal lamination of brain… Expand
Adp Ribosylation Factor-like Protein 2 (Arl2) Regulates the Interaction of Tubulin-Folding Cofactor D with Native Tubulin
- A. Bhamidipati, S. Lewis, N. Cowan
- Biology, Medicine
- The Journal of cell biology
- 29 May 2000
The ADP ribosylation factor-like proteins (Arls) are a family of small monomeric G proteins of unknown function. Here, we show that Arl2 interacts with the tubulin-specific chaperone protein known as… Expand
GFAP Is Necessary for the Integrity of CNS White Matter Architecture and Long-Term Maintenance of Myelination
- W. Liedtke, W. Edelmann, +4 authors C. Raine
- Biology, Medicine
- Neuron
- 1 October 1996
To investigate the structural role of glial fibrillary acidic protein (GFAP) in vivo, mice carrying a null mutation in GFAP were generated. In 7/14 mutant animals older than 18 months of age,… Expand
Increased microtubule stability and alpha tubulin acetylation in cells transfected with microtubule-associated proteins MAP1B, MAP2 or tau.
- R. Takemura, S. Okabe, T. Umeyama, Y. Kanai, N. Cowan, N. Hirokawa
- Biology, Medicine
- Journal of cell science
- 1 December 1992
We previously transfected MAP2, tau and MAP1B cDNA into fibroblasts and have studied the effect of expression of these microtubule-associated proteins on microtubule organization. In this study, we… Expand
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
- K. Poirier, N. Lebrun, +32 authors J. Chelly
- Biology, Medicine
- Nature Genetics
- 1 June 2013
The genetic causes of malformations of cortical development (MCD) remain largely unknown. Here we report the discovery of multiple pathogenic missense mutations in TUBG1, DYNC1H1 and KIF2A, as well… Expand