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ProteomicsFunctional characterization of the human Cdk10/Cyclin Q complex
Cyclin-dependent kinases (CDKs) are key players in cell cycle regulation and transcription. The CDK-family member Cdk10 is important for neural development and can act as a tumor suppressor but the underlying molecular mechanisms are largely unknown. Here, we provide an in depth analysis of Cdk10 su...
ORGANISM(S): Escherichia coli 
2022-03-20 | PXD028792 | Pride
Transcription  cell cycle  cdk10  cyclin q  cyclin m  rna polymerase ii 
ProteomicsIntegrated proteomic and N-glycoproteomic analyses of doxorubicin sensitive and resistant ovarian cancer cells reveal glycoprotein alteration in protein abundance and glycosylation
Ovarian cancer is one of the most common cancer among women in the world, and chemotherapy remains the principal treatment for patients. However, drug resistance is a major obstacle to the effective treatment of ovarian cancers and the underlying mechanism is not clear. An increased understanding of...
ORGANISM(S): Homo sapiens (Human) 
2019-02-15 | PXD012655 | Pride
Multidrug resistance Ovarian cancer N-glycoproteome Silac Global proteome 
ProteomicsBranch point evolution controls species-specific alternative splicing and regulates long term potentiation
Regulation and functionality of species-specific alternative splicing has remained enigmatic for many years. Calcium/calmodulin-dependent protein kinase IIβ (CaMKIIβ) is expressed in several splice variants and plays a key role in learning and memory. Here, we identify and characterize several prima...
ORGANISM(S): Mus musculus (Mouse) 
2022-12-19 | PXD035346 | Pride
Mouse Thiophosphorylation 
TranscriptomicsPRPF8 CLIP seq for iPSC, kidney organoid, retinal organoid, and retinal epithelium derived from c.6926A>C RPE with Retinitis Pigmentosa patients and CRISPR/Cas9 corrected
Retinitis Pigmentosa is a group of inherited eye disorders characterized by progressive degeneration of photoreceptor cells in the retina, leading to vision loss and eventual blindness. One of the known genetic mutations associated with RP is the c.6926A>C mutation in the RPE (retinal pigment epithe...
ORGANISM(S): Homo sapiens 
2024-03-13 | E-MTAB-13171 | biostudies-arrayexpress
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