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UnknownPhosphorylation of CEP83 by TTBK2 is necessary for cilia initiation.
Not available
S-EPMC6781440 | biostudies-literature
TranscriptomicsmRNA sequencing of wildtype versus CEP83 knockout hiPSCs at diffirent time points of differentiation to kidney organoids [scRNA-seq]
Centrosomal protein 83 (CEP83) is a component of the distal appendages proteins of centrioles, which is necessary for the assembly of primary cilia. Previous studies have implicated primary cilia in normal development and tissue homeostasis, including kidney development. The kidney develops from hum...
ORGANISM(S): Homo sapiens 
2022-10-12 | GSE205977 | GEO
GenomicsmRNA sequencing of wildtype versus CEP83 knockout hiPSCs at diffirent time points of differentiation to kidney organoids [scRNA-seq]
mRNA sequencing of wildtype versus CEP83 knockout hiPSCs at diffirent time points of differentiation to kidney organoids [scRNA-seq]
PRJNA848753 | ENA
TranscriptomicsmRNA sequencing of wildtype versus CEP83 knockout hiPSCs at diffirent time points of differentiation to kidney organoids [bulk RNA-seq]
Centrosomal protein 83 (CEP83) is a component of the distal appendages proteins of centrioles, which is necessary for the assembly of primary cilia. Previous studies have implicated primary cilia in normal development and tissue homeostasis, including kidney development. The kidney develops from hum...
ORGANISM(S): Homo sapiens 
2022-10-12 | GSE205976 | GEO
GenomicsmRNA sequencing of wildtype versus CEP83 knockout hiPSCs at diffirent time points of differentiation to kidney organoids [bulk RNA-seq]
mRNA sequencing of wildtype versus CEP83 knockout hiPSCs at diffirent time points of differentiation to kidney organoids [bulk RNA-seq]
PRJNA848754 | ENA
UnknownBeyond nephronophthisis: Retinal dystrophy in the absence of kidney dysfunction in childhood expands the clinical spectrum of CEP83 deficiency.
Not available
S-EPMC8252653 | biostudies-literature
UnknownThe centrosomal protein 83 (CEP83) regulates human pluripotent stem cell differentiation toward the kidney lineage.
Not available
S-EPMC9629839 | biostudies-literature
UnknownMutations of CEP83 cause infantile nephronophthisis and intellectual disability.
Not available
S-EPMC4121475 | biostudies-literature
UnknownA ciliopathy combining Joubert syndrome and Oro-Facial-Digital syndrome caused by bi-allelic 5'-UTR loss-of-function CEP83 variant.
Not available
S-EPMC12514222 | biostudies-literature
ProteomicsProteomic profiling of centrosomes isolated from HAP1 cells
Centrosomes are cytoplasmic membraneless organelles that comprise a pair of centrioles, and a pericentriolar material. We developed a new centrosome affinity capture method termed CAPture that achieves high-coverage proteomes from 20-30 million cells. Here we present CAPture-MS data from HAP1 cells ...
ORGANISM(S): Homo sapiens (Human) 
2023-10-17 | PXD043692 | Pride
Centrosome Human Hap1 
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