Annotation inferences using phylogenetic trees
Mitotic control of kinetochore-associated dynein and spindle orientation by human Spindly.
Cenp-F links kinetochores to Ndel1/Nde1/Lis1/dynein microtubule motor complexes.
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
p78/MCRS1 forms a complex with centrosomal protein Nde1 and is essential for cell viability.
Centrosomal proteins Nde1 and Su48 form a complex regulated by phosphorylation.
The mitosis and neurodevelopment proteins NDE1 and NDEL1 form dimers, tetramers, and polymers with a folded back structure in solution.
Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.
Endogenous Cell Type-Specific Disrupted in Schizophrenia 1 Interactomes Reveal Protein Networks Associated With Neurodevelopmental Disorders.
HENA, heterogeneous network-based data set for Alzheimer's disease.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Multimodal cell maps as a foundation for structural and functional genomics.
Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods.
The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.
Combined Automated Annotation using Multiple IEA Methods
MAD2 converted to an inhibitory state via interaction with Mad1
MAD2 associates with the Mad1 kinetochore complex
Release of activated MAD2 from kinetochores
Phosphorylation of cohesin by PLK1 at centromeres
PP2A-B56 dephosphorylates centromeric cohesin
ESPL1 (Separase) cleaves centromeric cohesin
Separation of sister chromatids
CDK1 phosphorylates CDCA5 (Sororin) at centromeres
AJUBA facilitates AURKA autophosphorylation
AJUBA binds centrosome-associated AURKA
AURKA phosphorylates PLK1
BORA binds PLK1 and AURKA
Kinetochore capture of astral microtubules
Plk1-mediated phosphorylation of Nlp
Recruitment of additional gamma tubulin/ gamma TuRC to the centrosome
Loss of C-Nap-1 from centrosomes
Dissociation of Phospho-Nlp from the centrosome
Recruitment of Plk1 to centrosomes
Association of NuMA with microtubules
Recruitment of CDK11p58 to the centrosomes
Translocation of NuMA to the centrosomes
RAB3IP stimulates nucleotide exchange on RAB8A
C2CD3 binds the mother centriole
C2CD3 and OFD1 recruit 5 distal appendage proteins to the centriole
CP110 and CEP97 dissociate from the centriole
The distal appendage proteins recruit TTBK2
Recruitment of transition zone proteins
MARK4 binds ODF2 in the centriole
CEP164 recruits RAB3IP-carrying Golgi-derived vesicles to the basal body
CDC42:GTP recruits DIAPH2-2 to kinetochores
AURKB phosphorylates DIAPH2-2 at kinetochores
Kinetochore capture of astral microtubules is positively regulated by CDC42:GTP:p-S196-DIAPH2-2
TPX2 binds AURKA at centrosomes
TPX2 promotes AURKA autophosphorylation
EML4 recruits NUDC to mitotic spindle
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Defining the membrane proteome of NK cells.
Nde1 is a Rab9 effector for loading late endosomes to cytoplasmic dynein motor complex.
NudE and NudEL are required for mitotic progression and are involved in dynein recruitment to kinetochores.
Severe NDE1-mediated microcephaly results from neural progenitor cell cycle arrests at multiple specific stages.
A Nup133-dependent NPC-anchored network tethers centrosomes to the nuclear envelope in prophase.
The scaffold protein Nde1 safeguards the brain genome during S phase of early neural progenitor differentiation.
Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry.
Nde1 and Ndel1: Outstanding Mysteries in Dynein-Mediated Transport.
Mitotic spindle regulation by Nde1 controls cerebral cortical size.
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].
Nde1 promotes Lis1-mediated activation of dynein.
LIS1 and NudE induce a persistent dynein force-producing state.
The Role of Nde1 phosphorylation in interkinetic nuclear migration and neural migration during cortical development.