about
Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosomeHuman Asf1 and CAF-1 interact and synergize in a repair-coupled nucleosome assembly pathwayThe Polo kinase Plk4 functions in centriole duplicationQuantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosisNovel asymmetrically localizing components of human centrosomes identified by complementary proteomics methodsCep164, a novel centriole appendage protein required for primary cilium formationStructure of a Survivin-Borealin-INCENP core complex reveals how chromosomal passengers travel togetherHuman Tousled like kinases are targeted by an ATM- and Chk1-dependent DNA damage checkpointChoice of Plk1 docking partners during mitosis and cytokinesis is controlled by the activation state of Cdk1Proteomic characterization of the human centrosome by protein correlation profilingCentrosome-associated Chk1 prevents premature activation of cyclin-B-Cdk1 kinaseCep68 and Cep215 (Cdk5rap2) are required for centrosome cohesionKIF14 and citron kinase act together to promote efficient cytokinesisCell cycle-dependent expression of Nek2, a novel human protein kinase related to the NIMA mitotic regulator of Aspergillus nidulansIdentification of human cyclin-dependent kinase 8, a putative protein kinase partner for cyclin CTimely anaphase onset requires a novel spindle and kinetochore complex comprising Ska1 and Ska2The spindle protein CHICA mediates localization of the chromokinesin Kid to the mitotic spindleMitotic control of kinetochore-associated dynein and spindle orientation by human SpindlyStable kinetochore-microtubule interactions depend on the Ska complex and its new component Ska3/C13Orf3.Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivoProbing the in vivo function of Mad1:C-Mad2 in the spindle assembly checkpointProteome analysis of the human mitotic spindlePhosphorylation of mitotic kinesin-like protein 2 by polo-like kinase 1 is required for cytokinesisPlk1 regulates mitotic Aurora A function through betaTrCP-dependent degradation of hBoraA centrosomal function for the human Nek2 protein kinase, a member of the NIMA family of cell cycle regulators.Molecular basis of tubulin transport within the cilium by IFT74 and IFT81.Plk4-induced centriole biogenesis in human cellsThe centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4Structure of the N-terminal domain of the FOP (FGFR1OP) protein and implications for its dimerization and centrosomal localizationRootletin forms centriole-associated filaments and functions in centrosome cohesionActive cyclin B1-Cdk1 first appears on centrosomes in prophaseAurora-A overexpression reveals tetraploidization as a major route to centrosome amplification in p53-/- cellsHuman Mps1 kinase is required for the spindle assembly checkpoint but not for centrosome duplicationSgt1 is required for human kinetochore assemblyA complex of two centrosomal proteins, CAP350 and FOP, cooperates with EB1 in microtubule anchoring.Phosphoproteome analysis of the human mitotic spindleCentromere targeting of the chromosomal passenger complex requires a ternary subcomplex of Borealin, Survivin, and the N-terminal domain of INCENPThe forkhead-associated domain protein Cep170 interacts with Polo-like kinase 1 and serves as a marker for mature centriolesMAT1, cdk7 and cyclin H form a kinase complex which is UV light-sensitive upon association with TFIIHThe crystal structure of the human polo-like kinase-1 polo box domain and its phospho-peptide complex
P50
Q24290949-C903455B-6806-4FC1-AFF4-D0A7104C5596Q24292479-6D2BAB48-E3CE-4B4F-8A44-BA646EF4249AQ24292705-750D2AAD-FE51-4E17-A111-C8C5FE104705Q24294864-D033F5AE-242A-4C23-9A25-AF1D1BAD8B94Q24296940-FCF2D06E-D56B-4E3E-A26D-B87290224852Q24298367-897E59FA-F679-4212-96E2-26C57DA75F04Q24298466-B4A860AF-75C4-4DD1-BF79-51F0BD044905Q24298560-F93D73FA-0254-4AFC-8DA9-40824A4214C5Q24299765-44434021-2618-43C3-8C17-03C561723F57Q24301045-657FAA8D-A60A-4AB3-B99A-9D68EF3D5677Q24301325-5FAB5C55-B4E9-4491-9196-F9595C0935F7Q24301594-D761E5C4-AC42-419F-8164-43206BAC6FFAQ24301784-0957E224-53FA-4172-B88B-28E65A4AD69BQ24306123-87C00D13-9584-4AF2-8C8A-512BBF7600BFQ24311956-268C9BE1-0042-4050-AA7C-D9BDD67A1B35Q24313155-BFBB3105-D364-4C84-9F99-EF5D4F13E3F2Q24313375-E4F69E33-0EB2-4A8D-A1D8-5169EA17D16DQ24314268-5879F00C-2B90-4207-B1CA-5D75821AC267Q24314703-CD7D00DC-20F6-4233-8111-039E6B0D9A7CQ24315026-374D0F15-D6F6-48B8-9081-5857173F02B6Q24315748-E1634080-F669-4308-B3A1-098D0311F200Q24316321-63AD3356-4B07-4EC4-9DFC-065DB93EC66EQ24317964-146AB34E-62A6-44EE-B557-9E991EEBCA1FQ24318919-1DCA6D6D-7168-4602-B83F-549DB7E83349Q24320294-2B782EFA-662D-4455-B524-31A0F9AE1BC7Q24320475-B41FCF28-811A-41AD-B267-D2AF39A1A2A2Q24336451-0447D712-301F-45F6-B71D-BB297BA7CA20Q24336477-9684255F-F618-4BD6-A375-FE44117E5CE4Q24337012-4F72C24B-BC4F-4D5B-BBB3-FE8C77E56486Q24337615-FC2116C2-DEEE-41AE-AB90-EDA4EC939524Q24338617-BC680BFB-DAA7-4AFA-8836-D9054E960648Q24536196-B2990B94-67A9-407A-BF4F-AAD88A553612Q24536263-159B8014-2DFC-44D0-97B8-EDDEDA318115Q24537151-F1BD529A-9545-43FD-B298-9C60BCABBA48Q24540212-D78D6DCD-EE9B-46E9-A9EE-0EE2B5D9FD6CQ24547339-F2CB7152-8FFD-48FF-82AB-989C03821745Q24547361-FD5527FE-9929-4407-A2A4-821979DFB32DQ24556578-F08DB456-85C8-4EBE-B500-8CC25AC2A114Q24563127-95ED6581-3F68-49AE-800A-D6DD65B052AFQ24644910-0E37057D-6565-497B-84FF-07C85061D0AE
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Erich A Nigg
@ast
Erich A Nigg
@en
Erich A Nigg
@es
Erich A Nigg
@nl
type
label
Erich A Nigg
@ast
Erich A Nigg
@en
Erich A Nigg
@es
Erich A Nigg
@nl
prefLabel
Erich A Nigg
@ast
Erich A Nigg
@en
Erich A Nigg
@es
Erich A Nigg
@nl
P106
P214
3250155044911772520009
P31
P496
0000-0003-4835-5719
P734
P735
P7859
viaf-3250155044911772520009