NudE-L, a novel Lis1-interacting protein, belongs to a family of vertebrate coiled-coil proteins (Q28590012)

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English	NudE-L, a novel Lis1-interacting protein, belongs to a family of vertebrate coiled-coil proteins	scientific journal article

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scholarly article

1 reference

PubMed publication ID

31 January 2017

NudE-L, a novel Lis1-interacting protein, belongs to a family of vertebrate coiled-coil proteins (English)

1 reference

PubMed publication ID

31 January 2017

Protein with homology to Neurospora crassa RO11

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Platelet-activating factor acetylhydrolase, isoform 1b, subunit 1

1 reference

GOA release 2020-03-11

NudE neurodevelopment protein 1 like 1

1 reference

GOA release 2020-03-11

Platelet-activating factor acetylhydrolase, isoform 1b, subunit 3

1 reference

GOA release 2020-03-11

author name string

K. J. Sweeney

1

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PubMed publication ID

31 January 2017

A. Prokscha

2

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PubMed publication ID

31 January 2017

G. Eichele

3

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PubMed publication ID

31 January 2017

publication date

1 March 2001

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PubMed publication ID

31 January 2017

Mechanisms of Development

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PubMed publication ID

31 January 2017

101

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PubMed publication ID

31 January 2017

1-2

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PubMed publication ID

31 January 2017

21–33

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PubMed publication ID

31 January 2017

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

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

1 reference

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

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

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Platelet-activating factor produces neuronal growth cone collapse

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

1 reference

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The LIS1-related NUDF protein of Aspergillus nidulans interacts with the coiled-coil domain of the NUDE/RO11 protein

1 reference

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Endo-oligopeptidase A, a putative enkephalin-generating enzyme, in the vertebrate retina

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Secretion of a neuropeptide-metabolizing enzyme similar to endopeptidase 22.19 by glioma C6 cells

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

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

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

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

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

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Molecular and immunochemical evidences demonstrate that endooligopeptidase A is the predominant cytosolic oligopeptidase of rabbit brain

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

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

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

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

1 reference

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The 2.0 A crystal structure of a heterotrimeric G protein

1 reference

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

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Predicting coiled coils from protein sequences

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

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Neurospora crassa ro-10 and ro-11 genes encode novel proteins required for nuclear distribution

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

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The ancient regulatory-protein family of WD-repeat proteins

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

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

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

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

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

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

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

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Matrix metalloproteinase degradation of extracellular matrix: biological consequences

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

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Systematic identification of mitotic phosphoproteins

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Potential mechanisms of mutations that affect neuronal migration in man and mouse

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

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

1 reference

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Characterization and localization of the cytoplasmic dynein heavy chain in Aspergillus nidulans

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Identifiers

10.1016/S0925-4773(00)00543-8

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PubMed publication ID

1 reference

PubMed publication ID

31 January 2017

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