(Q28139341)

2

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A Prokscha

3

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W B Dobyns

4

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G Eichele

Mechanisms of Development

5

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language of work or name

English

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publication date

April 2000

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published in

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volume

92

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issue

2

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page(s)

263-71

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cites work

PAF analogues capable of inhibiting PAF acetylhydrolase activity suppress migration of isolated rat cerebellar granule cells.

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7 January 2021

Platelet-activating factor acetylhydrolase expression and activity suggest a link between neuronal migration and platelet-activating factor

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7 January 2021

Platelet-activating factor receptor stimulation disrupts neuronal migration In vitro.

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7 January 2021

Time of origin or corresponding cell classes in the cerebral cortex of normal and reeler mutant mice: an autoradiographic analysis.

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7 January 2021

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

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7 January 2021

Platelet-activating factor produces neuronal growth cone collapse

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7 January 2021

Reelin is a ligand for lipoprotein receptors

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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

Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.

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7 January 2021

Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly

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7 January 2021

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

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7 January 2021

Folding of proteins with WD-repeats: comparison of six members of the WD-repeat superfamily to the G protein beta subunit

1 reference

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7 January 2021

Crystal structure at 2.4 angstroms resolution of the complex of transducin betagamma and its regulator, phosducin

1 reference

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7 January 2021

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

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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

1 reference

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7 January 2021

Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype.

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7 January 2021

Ubiquitin-dependent degradation of IkappaBalpha is mediated by a ubiquitin ligase Skp1/Cul 1/F-box protein FWD1.

1 reference

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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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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Brain acetylhydrolase that inactivates platelet-activating factor is a G-protein-like trimer

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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

An F-box protein, FWD1, mediates ubiquitin-dependent proteolysis of beta-catenin

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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

The 2.0 A crystal structure of a heterotrimeric G protein

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Switching of platelet-activating factor acetylhydrolase catalytic subunits in developing rat brain

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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Biochemical characterization of various catalytic complexes of the brain platelet-activating factor acetylhydrolase

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https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Neuronal cytoskeletal alterations evoked by a platelet-activating factor (PAF) analogue

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

The lissencephaly gene product Lis1, a protein involved in neuronal migration, interacts with a nuclear movement protein, NudC

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

The ancient regulatory-protein family of WD-repeat proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

New directions for neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Lissencephaly-1 is one of the most conserved proteins between mouse and human: a single amino-acid difference in 410 residues

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Cloning and characterization of cDNAs and the gene encoding the mouse platelet-activating factor acetylhydrolase Ib alpha subunit/lissencephaly-1 protein

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

LIS1 is a microtubule-associated phosphoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

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%2FS0925-4773%2800%2900242-2

7 January 2021

A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

The WD repeat: a common architecture for diverse functions

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Crystal structure of a G-protein beta gamma dimer at 2.1A resolution

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

The structure of the G protein heterotrimer Gi alpha 1 beta 1 gamma 2

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Binding of pleckstrin homology domains to WD40/beta-transducin repeat containing segments of the protein product of the Lis-1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021

Genetic identification of residues involved in association of alpha and beta G-protein subunits

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2800%2900242-2

7 January 2021