Brain development and the genetics of brain development (Q30773677)

26 June 2017

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title

Brain development and the genetics of brain development (English)

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26 June 2017

Gary D Clark

1

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26 June 2017

publication date

1 November 2002

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26 June 2017

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26 June 2017

volume

20

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26 June 2017

issue

4

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26 June 2017

page(s)

917-939

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Developmental biology. Reading the retinoid signals.

26 June 2017

cites work

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7 January 2021

Transcription factors in early development of the central nervous system

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7 January 2021

Isolation of 3,4-didehydroretinoic acid, a novel morphogenetic signal in the chick wing bud.

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7 January 2021

Closure of the neural tube in the cephalic region of the mouse embryo

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7 January 2021

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

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7 January 2021

Familial schizencephaly

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7 January 2021

Disorders of neuronal migration

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7 January 2021

Epilepsy and anomalies of neuronal migration: MRI and clinical aspects

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Magnetic resonance imaging in developmental disorders of the cerebral cortex

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7 January 2021

The syndrome of absence of the septum pellucidum with porencephalies and other developmental defects

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Midline telencephalic dysgenesis: report of three cases

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7 January 2021

Hedgehog, the floor plate, and the zone of polarizing activity

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7 January 2021

Sonic hedgehogParticipates in Craniofacial Morphogenesis and Is Down-regulated by Teratogenic Doses of Retinoic Acid

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7 January 2021

Human homolog of patched, a candidate gene for the basal cell nevus syndrome

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

The tumour-suppressor gene patched encodes a candidate receptor for Sonic hedgehog

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7 January 2021

Retinoic acid and pattern formation in vertebrates

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7 January 2021

Retinoic acid embryopathy

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7 January 2021

An anatomic comparison of cebocephaly and ethmocephaly

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7 January 2021

Letter: Hypothalamo-pituitary dysfunction in siblings of patients with holoprosencephaly

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Holoprosencephaly in infants of diabetic mothers

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7 January 2021

Syndromes with cephaloceles

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7 January 2021

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

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7 January 2021

Extreme variability of expression of a Sonic Hedgehog mutation: attention difficulties and holoprosencephaly

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

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7 January 2021

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly

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7 January 2021

Mutations in holoprosencephaly

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7 January 2021

Optic nerve hypoplasia: a review

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Optic nerve hypoplasia with hypopituitarism. Septo-optic dysplasia with hypopituitarism

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Proliferative events in the cerebral ventricular zone

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Cell division and the nervous system: regulating the cycle from neural differentiation to death

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7 January 2021

D-type cyclin-dependent kinase activity in mammalian cells

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Identification of G1 kinase activity for cdk6, a novel cyclin D partner

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

G1 events and regulation of cell proliferation

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

G1 phase progression: cycling on cue

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7 January 2021

Developmental cell death: morphological diversity and multiple mechanisms

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7 January 2021

Do all programmed cell deaths occur via apoptosis?

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Autosomal dominant microcephaly

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Perinatal loss and neurological abnormalities among children of the atomic bomb. Nagasaki and Hiroshima revisited, 1949 to 1989.

1 reference

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7 January 2021

Neuropathologic findings in surgically treated hemimegalencephaly: immunohistochemical, morphometric, and ultrastructural study

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Unusual magnetic resonance and neuropathological findings in hemimegalencephaly: report of a case following hemispherectomy.

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Hemimegalencephaly: evaluation with positron emission tomography

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Megalencephaly in children: Clinical syndromes, genetic patterns, and differential diagnosis from other causes of megalocephaly

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7 January 2021

Megalencephaly: types, clinical syndromes, and management

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7 January 2021

Linear nevus sebaceous syndrome: megalencephaly and heterotopic gray matter

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures, and facial hemihypertrophy

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7 January 2021

Hypomelanosis of Ito ("incontinentia pigmenti achromians"). Report of three cases and review of the literature

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Neuronal migration, with special reference to developing human brain: a review

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

The place of neuronal migration abnormalities in child neurology.

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Detection of the reelin breakpoint in reeler mice.

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

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/S0733-8619(02)50024-5

7 January 2021

Miller-Dieker syndrome with ring chromosome 17

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Miller-Dieker syndrome: lissencephaly and monosomy 17p.

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

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

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https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Genetic and neuroradiological heterogeneity of double cortex syndrome

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

A Golgi study of the cerebral cortex in Fukuyama-type congenital muscular dystrophy, Walker-type "lissencephaly," and classical lissencephaly.

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

22q11 deletion and polymicrogyria--cause or coincidence?

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patie

1 reference

https://api.crossref.org/works/10.1016/S0733-8619(02)50024-5

7 January 2021

10.1016/S0733-8619(02)00024-5

Identifiers

DOI

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26 June 2017

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