(Q34699435)

4 August 2017

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title

Smooth, rough and upside-down neocortical development (English)

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4 August 2017

Eric C Olson

1

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4 August 2017

Christopher A Walsh

series ordinal

2

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4 August 2017

publication date

1 June 2002

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Current Opinion in Genetics & Development

4 August 2017

published in

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4 August 2017

volume

12

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4 August 2017

issue

3

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4 August 2017

page(s)

320-327

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Lissencephaly and other malformations of cortical development: 1995 update

4 August 2017

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A classification scheme for malformations of cortical development

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7 January 2021

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

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7 January 2021

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

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7 January 2021

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

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7 January 2021

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

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7 January 2021

Interaction between LIS1 and doublecortin, two lissencephaly gene products

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7 January 2021

Doublecortin, a stabilizer of microtubules

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7 January 2021

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons

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7 January 2021

Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons

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7 January 2021

Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]

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7 January 2021

Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit.

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7 January 2021

NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration

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7 January 2021

Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE

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7 January 2021

LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome

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7 January 2021

NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein

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7 January 2021

A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system

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7 January 2021

NudC associates with Lis1 and the dynein motor at the leading pole of neurons

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7 January 2021

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7 January 2021

Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1

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7 January 2021

A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function

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7 January 2021

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

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7 January 2021

Drosophila Lis1 is required for neuroblast proliferation, dendritic elaboration and axonal transport.

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7 January 2021

The fukutin protein family--predicted enzymes modifying cell-surface molecules

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7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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7 January 2021

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

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7 January 2021

Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin

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7 January 2021

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan

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7 January 2021

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy

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7 January 2021

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease

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7 January 2021

Essential role of alpha 6 integrins in cortical and retinal lamination

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7 January 2021

Perlecan maintains the integrity of cartilage and some basement membranes

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7 January 2021

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

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7 January 2021

A Sibship with a Neuronal Migration Defect, Cerebellar Hypoplasia and Congenital Lymphedema

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7 January 2021

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7 January 2021

The reeler gene encodes a protein with an EGF–like motif expressed by pioneer neurons

1 reference

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7 January 2021

Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

1 reference

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7 January 2021

Distinct functions of alpha3 and alpha(v) integrin receptors in neuronal migration and laminar organization of the cerebral cortex

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7 January 2021

Beta1-class integrins regulate the development of laminae and folia in the cerebral and cerebellar cortex

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7 January 2021

Reelin molecules assemble together to form a large protein complex, which is inhibited by the function-blocking CR-50 antibody

1 reference

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7 January 2021

The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons.

1 reference

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7 January 2021

Reelin is a serine protease of the extracellular matrix

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Reelin, the extracellular matrix protein deficient in reeler mutant mice, is processed by a metalloproteinase.

1 reference

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7 January 2021

Reelin is a ligand for lipoprotein receptors

1 reference

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7 January 2021

Direct binding of Reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Proteins of the CNR family are multiple receptors for Reelin

1 reference

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7 January 2021

Reelin-induced tyrosine [corrected] phosphorylation of disabled 1 during neuronal positioning

1 reference

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7 January 2021

Neuronal position in the developing brain is regulated by mouse disabled-1

1 reference

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7 January 2021

Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Aberrant Splicing of a Mouse disabled Homolog, mdab1, in the scrambler Mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Mouse disabled (mDab1): a Src binding protein implicated in neuronal development

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Dab1 tyrosine phosphorylation sites relay positional signals during mouse brain development.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Diversity revealed by a novel family of cadherins expressed in neurons at a synaptic complex

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

The reelin receptor ApoER2 recruits JNK-interacting proteins-1 and -2

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Cargo of kinesin identified as JIP scaffolding proteins and associated signaling molecules

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Cyclin-dependent kinase 5-deficient mice demonstrate novel developmental arrest in cerebral cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Synergistic contributions of cyclin-dependant kinase 5/p35 and Reelin/Dab1 to the positioning of cortical neurons in the developing mouse brain

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

Rescue of ataxia and preplate splitting by ectopic expression of Reelin in reeler mice

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2802%2900305-2

7 January 2021

10.1016/S0959-437X(02)00305-2

Identifiers

DOI

1 reference

4 August 2017

1 reference