Cerebellar gene expression changes in Pdgfc and Pdgfra mutant

Expression data from CCL2 overexpression in MCF7 breast cancer cell line and CCL2 knockdown in MB231 breast cancer cell line.

Gene expression profiling of BMMC derived-MMCs and BMMC-derived CTMCs.

Gene expression of cardiomyocytes exposed to L-lactate

Single-cell sequencing data for circulating CAR T cells in lymphoma patients

Dysfunction of histone demethylase IBM1 in Arabidopsis causes autoimmunity and reshapes the root microbiome

Parathyroid Hormone Treatment Effect on Gene Expression in Primary Calvarial Osteoblasts

Single-cell analysis of Kaposi’s sarcoma-associated herpesvirus infection in three-dimensional air-liquid interface culture model

Single cell transcriptome of regional human embryonic stem cell-derived ventral cultures from the spinal cord

Single cell transcriptome of regional human embryonic stem cell-derived dorsal and ventral neurons from the hindbrain and spinal cord

Single cell transcriptome of human embryonic stem cell-derived neurons spanning the rostrocaudal and dorsoventral axes

RNAseq analysis of skeletal muscle transcriptomes from wild-type, LONP1 skeletal muscle specific knockout (LONP1 mKO) and LONP1ATF4 skeletal muscle double-knockout (LONP1ATF4 DmKO) mice.

RNAseq analysis of skeletal muscle transcriptomes from non-transgenic (NTG) and skeletal muscle specific overexpression a deletion mutant form of ornithine transcarbamylase (MCK-ΔOTC) mice.

Identifying DAP5 mRNA translation and direct-binding targets in human embryonic stem cells (hESCs) using Ribo-seq and CLIP-seq.

Multimodal single cell sequencing of human diabetic kidney disease implicates chromatin accessibility and genetic background in disease progression [cut-and-run and bulk ATAC-seq to support single cell data]

Multimodal single cell sequencing implicates chromatin accessibility and genetic background in diabetic kidney disease progression

DDX17 modulates expression and alternative splicing of genes involved in cell apoptosis in lung adenocarcinoma cells

Antibody from Single Human VH-rearranging Mouse Potently Neutralizes All SARS-CoV-2 Variants Through BA.5 by Inhibiting Membrane Fusion

A novel somatic mutation in GNAQ in Sturge-Weber Syndrome provides insight into disease pathogenesis

Super-enhancer-associated core regulatory circuits mediate susceptibility to retinoic acid in neuroblastoma cells [RNA-seq]