Yoon Dan D - OmicsDI

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Mass spectrometry imaging as an emerging tool for studying metabolism in human brain organoids

Human brain organoids are emerging models to study human brain development and pathology as they recapitulate the development and characteristics of major neural cell types, and enable manipulation through an in vitro system. Over the past decade, with the advent of spatial technologies,...

2023-05-23 | MTBLS7565 | MetaboLights

High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations.

Not available

S-EPMC7002524 | biostudies-literature

Transcriptional perturbations caused by SV40 large T antigen and its fragments

The small genome of polyomaviruses encodes a limited number of proteins that are highly dependent on interactions with host cell proteins for efficient viral replication. The SV40 large T antigen (LT) contains several discrete functional domains that contribute to the viral life cycle, including the...

ORGANISM(S): Homo sapiens

2012-10-26 | E-GEOD-40567 | biostudies-arrayexpress

Mass Spectrometry-Based Proteomics Reveals Potential Roles of NEK9 and MAP2K4 in Resistance to PI3K Inhibition in Triple-Negative Breast Cancers.

Not available

S-EPMC5955814 | biostudies-literature

Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes.

Not available

S-EPMC5065660 | biostudies-literature

Parallel evolution of transcriptome structure during genome reorganization

Genome reorganization by large scale indels, gene displacements, and horizontal gene transfers allow an organism to re-organize genes into operons (“operonization”) and explore novel strategies for adapting to its changing environment. We have characterized the process of operonization by mapping an...

ORGANISM(S): Methanococcus maripaludis S2

2011-06-27 | E-GEOD-26782 | biostudies-arrayexpress

Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy.

Not available

S-EPMC6377633 | biostudies-literature

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation.

Not available

S-EPMC7118694 | biostudies-literature

Longitudinal single-cell transcriptional dynamics throughout neurodegeneration in SCA1.

Not available

S-EPMC10922326 | biostudies-literature

De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.