scholarly article | Q13442814 |
P50 | author | Anthony Wynshaw-Boris | Q28607004 |
Gabriella D'Arcangelo | Q42333919 | ||
P2093 | author name string | Joachim Herz | |
Amir H Assadi | |||
Gary D Clark | |||
Guangcheng Zhang | |||
Uwe Beffert | |||
Robert S McNeil | |||
P2860 | cites work | Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2 | Q22010158 |
Reelin is a ligand for lipoprotein receptors | Q22010835 | ||
Direct binding of Reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation | Q22010836 | ||
Interactions of the low density lipoprotein receptor gene family with cytosolic adaptor and scaffold proteins suggest diverse biological functions in cellular communication and signal transduction | Q22254170 | ||
A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function | Q24290458 | ||
Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected] | Q24313605 | ||
Regulation of actin cytoskeleton by mDab1 through N-WASP and ubiquitination of mDab1 | Q24528128 | ||
Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification | Q24534023 | ||
Brain acetylhydrolase that inactivates platelet-activating factor is a G-protein-like trimer | Q27734277 | ||
Binding of purified Reelin to ApoER2 and VLDLR mediates tyrosine phosphorylation of Disabled-1 | Q28188030 | ||
Reelin and brain development | Q28207865 | ||
Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain | Q28210231 | ||
Interaction of reelin signaling and Lis1 in brain development | Q28212561 | ||
Role of the reelin signaling pathway in central nervous system development | Q28214353 | ||
Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse | Q28248620 | ||
Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice | Q28251984 | ||
Neuronal position in the developing brain is regulated by mouse disabled-1 | Q28251995 | ||
Activation of a Dab1/CrkL/C3G/Rap1 pathway in Reelin-stimulated neurons | Q28254404 | ||
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats | Q28261729 | ||
Absence of Fyn and Src causes a reeler-like phenotype | Q28272263 | ||
Reelin promotes hippocampal dendrite development through the VLDLR/ApoER2-Dab1 pathway | Q28508565 | ||
Platelet-activating factor acetylhydrolase expression and activity suggest a link between neuronal migration and platelet-activating factor | Q28509886 | ||
The reelin receptor ApoER2 recruits JNK-interacting proteins-1 and -2 | Q28511338 | ||
Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1 | Q28565028 | ||
Modulation of synaptic plasticity and memory by Reelin involves differential splicing of the lipoprotein receptor Apoer2 | Q28566778 | ||
Phosphatidylinositol 3-kinase interacts with the adaptor protein Dab1 in response to Reelin signaling and is required for normal cortical lamination | Q28572324 | ||
LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages | Q28574389 | ||
Targeted disruption of intracellular type I platelet activating factor-acetylhydrolase catalytic subunits causes severe impairment in spermatogenesis | Q28588411 | ||
Multiple dose-dependent effects of Lis1 on cerebral cortical development | Q28589891 | ||
Alternative splicing in the ligand binding domain of mouse ApoE receptor-2 produces receptor variants binding reelin but not alpha 2-macroglobulin | Q28591112 | ||
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality | Q28592982 | ||
Tyrosine phosphorylated Disabled 1 recruits Crk family adapter proteins | Q33202355 | ||
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations | Q33845128 | ||
Reelin-mediated signaling locally regulates protein kinase B/Akt and glycogen synthase kinase 3beta | Q34154141 | ||
LIS1 and dynein motor function in neuronal migration and development | Q34198470 | ||
Previously uncharacterized roles of platelet-activating factor acetylhydrolase 1b complex in mouse spermatogenesis | Q35163299 | ||
Reelin-induced tyrosine [corrected] phosphorylation of disabled 1 during neuronal positioning | Q35192054 | ||
The reeler mouse: anatomy of a mutant. | Q36411557 | ||
Nckβ Interacts with Tyrosine-Phosphorylated Disabled 1 and Redistributes in Reelin-Stimulated Neurons | Q36549477 | ||
Identification of reelin-induced sites of tyrosyl phosphorylation on disabled 1. | Q43560391 | ||
Essential role of the apolipoprotein E receptor-2 in sperm development. | Q44403694 | ||
Tyrosine phosphorylation of Disabled-1 is essential for Reelin-stimulated activation of Akt and Src family kinases | Q44617813 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 | Q15319474 |
Low density lipoprotein receptor-related protein 8, apolipoprotein e receptor | Q21980330 | ||
P304 | page(s) | e252 | |
P577 | publication date | 2007-01-01 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | The Pafah1b complex interacts with the reelin receptor VLDLR | |
P478 | volume | 2 |
Q37963183 | A PLA1-2 punch regulates the Golgi complex |
Q33968060 | A novel function of apolipoprotein E: upregulation of ATP-binding cassette transporter A1 expression |
Q64056496 | Aberrant expression of PAFAH1B3 associates with poor prognosis and affects proliferation and aggressiveness in hypopharyngeal squamous cell carcinoma |
Q24607165 | Apolipoprotein E receptors in the nervous system |
Q57806939 | Ataxia telangiectasia alters the ApoB and reelin pathway |
Q26738423 | Canonical and Non-canonical Reelin Signaling |
Q28273868 | Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor gene |
Q48556279 | Developmental dynamics of PAFAH1B subunits during mouse brain development |
Q43140471 | Differential interaction of the Pafah1b alpha subunits with the Reelin transducer Dab1. |
Q42637718 | Dynamic changes in the gene expression of zebrafish Reelin receptors during embryogenesis and hatching period |
Q39180867 | Functional Roles of the Interaction of APP and Lipoprotein Receptors. |
Q36998695 | Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly |
Q33506556 | Genetics and biology of microcephaly and lissencephaly |
Q37785418 | Go or Stop? Divergent Roles of Reelin in Radial Neuronal Migration |
Q39164827 | How does Reelin signaling regulate the neuronal cytoskeleton during migration? |
Q30494517 | Leading process branch instability in Lis1+/- nonradially migrating interneurons |
Q36486210 | Lipoprotein receptors – an evolutionarily ancient multifunctional receptor family |
Q33835930 | Lis1 reduction causes tangential migratory errors in mouse spinal cord |
Q51843744 | Loss of PAFAH1B2 reduces amyloid-β generation by promoting the degradation of amyloid precursor protein C-terminal fragments. |
Q27024970 | Neuronal migration and its disorders affecting the CA3 region |
Q26744747 | New Insights into Reelin-Mediated Signaling Pathways |
Q39050928 | PAFAH Ib phospholipase A2 subunits have distinct roles in maintaining Golgi structure and function |
Q37186834 | Pafah1b2 mutations suppress the development of hydrocephalus in compound Pafah1b1; Reln and Pafah1b1; Dab1 mutant mice |
Q59047757 | Reelin in the Years: Controlling Neuronal Migration and Maturation in the Mammalian Brain |
Q46836089 | Reelin promotes microtubule dynamics in processes of developing neurons |
Q21202834 | Similarities and differences in structure, expression, and functions of VLDLR and ApoER2 |
Q91726833 | The Reeler Mouse: A Translational Model of Human Neurological Conditions, or Simply a Good Tool for Better Understanding Neurodevelopment? |
Q57289111 | The Reelin Receptors Apolipoprotein E receptor 2 (ApoER2) and VLDL Receptor |
Q60933253 | The Role of APOE and TREM2 in Alzheimer's Disease-Current Understanding and Perspectives |
Q24632484 | The involvement of Reelin in neurodevelopmental disorders |
Q34057992 | Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes |
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