🧫
Mouse Cdk5, p35, and p39 mutations in neuronal migration
active
experiment
Created: 2026-04-06T12:34:08
By: etl-v1-backfill
Quality:
50%
✓ SciDEX
ID: exp-eaf169e6-564f-4431-8060-d8f56667a994
🧫 Experiment Protocol
Validationneuronal migration defectsCdk5, p35, p39miceproposed
Experimental study using mouse models with mutations in Cdk5 or its activators p35 and p39 to investigate their roles in neuronal migration. The research examined how these mutations result in migration phenotypes compatible with defective nucleokinesis, while also potentially affecting leading edge formation. This mouse model system provided controlled experimental conditions to study the molecular mechanisms of neuronal migration defects and validate findings from human genetic studies.
PRIMARY OUTCOME
neuronal migration phenotype
EXPECTED OUTCOMES
mutations would cause defective nucleokinesis and potentially leading edge formation defects
SUCCESS CRITERIA
demonstration of migration phenotype consistent with defective nucleokinesis
PROTOCOL
generation and phenotypic analysis of mice with mutations in Cdk5, p35, or p39
Source: PMID 11429281 ↗
🧫 Experiment Extras
PATHWAY
Cdk5 signaling/nucleokinesis/leading edge formation
MARKET PRICE
$0.50
STATUS
proposed
▸Metadataorigin_type: v1_polymorphic_backfill
| origin_type | v1_polymorphic_backfill |
| source_table | experiments |
| _schema_version | 1 |
📊 Evidence Profile
Evidence Balance
+0%
Certainty
0%
Debates
0
Incoming
0
Outgoing
0
0 supporting
0 contradicting
0 neutral
Public annotations (0)Annotate on Hypothes.is →
No public annotations yet.