(Q35197811)

7 August 2017

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title

Developmental genetic malformations of the cerebral cortex (English)

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7 August 2017

Volney L Sheen

1

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7 August 2017

Christopher A Walsh

series ordinal

2

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7 August 2017

publication date

1 September 2003

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Current Neurology and Neuroscience Reports

7 August 2017

published in

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7 August 2017

volume

3

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7 August 2017

issue

5

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7 August 2017

page(s)

433-441

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The BRCA1 C-terminal domain: structure and function.

7 August 2017

cites work

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https://api.crossref.org/works/10.1007%2FS11910-003-0027-8

Periventricular heterotopia associated with chromosome 5p anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-003-0027-8

Autosomal recessive form of periventricular heterotopia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-003-0027-8

Interaction between LIS1 and doublecortin, two lissencephaly gene products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-003-0027-8

Familial schizencephaly associated with EMX2 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-003-0027-8

Filamin A-interacting protein (FILIP) regulates cortical cell migration out of the ventricular zone

21 January 2018

1 reference

12 December 2020

Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

1 reference

12 December 2020

The TSC1 tumour suppressor hamartin regulates cell adhesion through ERM proteins and the GTPase Rho

1 reference

12 December 2020

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

1 reference

12 December 2020

Purification and cloning of a brefeldin A-inhibited guanine nucleotide-exchange protein for ADP-ribosylation factors

1 reference

12 December 2020

ASPM is a major determinant of cerebral cortical size

1 reference

12 December 2020

Molecular genetics of human microcephaly

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12 December 2020

Migfilin and Mig-2 link focal adhesions to filamin and the actin cytoskeleton and function in cell shape modulation

1 reference

12 December 2020

BIG1 and BIG2: brefeldin A-inhibited guanine nucleotide-exchange proteins for ADP-ribosylation factors

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.

1 reference

12 December 2020

A number of schizencephaly patients including 2 brothers are heterozygous for germline mutations in the homeobox gene EMX2.

1 reference

12 December 2020

Differential origins of neocortical projection and local circuit neurons: role of Dlx genes in neocortical interneuronogenesis

1 reference

12 December 2020

Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

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12 December 2020

Microcephaly: general considerations and aids to nosology

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12 December 2020

Deficiency of alpha-dystroglycan in muscle-eye-brain disease.

1 reference

12 December 2020

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

1 reference

12 December 2020

Identification of microcephalin, a protein implicated in determining the size of the human brain

1 reference

12 December 2020

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

12 December 2020

Inhibition of axonal growth by brefeldin A in hippocampal neurons in culture

1 reference

12 December 2020

Positional cloning of the gene for Nijmegen breakage syndrome

1 reference

12 December 2020

Abnormal spindle protein, Asp, and the integrity of mitotic centrosomal microtubule organizing centers

1 reference

12 December 2020

Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings

1 reference

12 December 2020

Human endothelial actin-binding protein (ABP-280, nonmuscle filamin): a molecular leaf spring

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

1 reference

12 December 2020

Inactivation of the cyclin-dependent kinase inhibitor p27 upon loss of the tuberous sclerosis complex gene-2

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Role of moving growth cone-like "wave" structures in the outgrowth of cultured hippocampal axons and dendrites

1 reference

12 December 2020

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findings

1 reference

12 December 2020

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact

1 reference

12 December 2020

Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions

1 reference

12 December 2020

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

1 reference

12 December 2020

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

1 reference

12 December 2020

Nested expression domains of four homeobox genes in developing rostral brain

1 reference

12 December 2020

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

1 reference

12 December 2020

ATM phosphorylation of Nijmegen breakage syndrome protein is required in a DNA damage response

1 reference

12 December 2020

Specification of cerebral cortical areas

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12 December 2020

Mutant deoxynucleotide carrier is associated with congenital microcephaly

1 reference

12 December 2020

Syndromes of bilateral symmetrical polymicrogyria

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12 December 2020

The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response

1 reference

12 December 2020

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

1 reference

12 December 2020

Diagnostic criteria for Walker-Warburg syndrome

1 reference

12 December 2020

On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders

1 reference

12 December 2020

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

1 reference

12 December 2020

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21

1 reference

12 December 2020

10.1007/S11910-003-0027-8

Identifiers

DOI

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7 August 2017

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