PDF) RNA-Seq analysis of Gtf2ird1 knockout epidermal tissue
Por um escritor misterioso
Last updated 22 dezembro 2024
Streamlined computational pipeline for genetic background characterization of genetically engineered mice based on next generation sequencing data, BMC Genomics
The role of GTF2IRD1 in the auditory pathology of Williams–Beuren Syndrome
Frontiers RNA sequencing profiling of mRNAs, long noncoding RNAs, and circular RNAs in Trigeminal Ganglion following Temporomandibular Joint inflammation
Frontiers Single-Cell Sequencing Reveals Differential Cell Types in Skin Tissues of Liaoning Cashmere Goats and Key Genes Related Potentially to the Fineness of Cashmere Fiber
Gtf2i and Gtf2ird1 mutation are not sufficient to reproduce mouse phenotypes caused by the Williams Syndrome critical region
Single-nuclear transcriptomics reveals diversity of proximal tubule cell states in a dynamic response to acute kidney injury
Frontiers RNA sequencing profiling of mRNAs, long noncoding RNAs, and circular RNAs in Trigeminal Ganglion following Temporomandibular Joint inflammation
Repression of Adipose Tissue Fibrosis through a PRDM16-GTF2IRD1 Complex Improves Systemic Glucose Homeostasis - ScienceDirect
Whole-genome resequencing of wild and domestic sheep identifies genes associated with morphological and agronomic traits
The role of GTF2IRD1 in the auditory pathology of Williams–Beuren Syndrome
PDF) A transcriptomic study of Williams-Beuren syndrome associated genes in mouse embryonic stem cells
The novel driver gene ASAP2 is a potential druggable target in pancreatic cancer - Fujii - 2021 - Cancer Science - Wiley Online Library
A transcriptomic study of Williams-Beuren syndrome associated genes in mouse embryonic stem cells
Genome annotation for clinical genomic diagnostics: strengths and weaknesses, Genome Medicine
Frontiers Molecular Subtypes Based on Cell Differentiation Trajectories in Head and Neck Squamous Cell Carcinoma: Differential Prognosis and Immunotherapeutic Responses
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