about
Flexible and versatile as a chameleon-sophisticated functions of microRNA-199aMolecular mechanisms of regulation and action of microRNA-199a in testicular germ cell tumor and glioblastomas.Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.Mechanisms for Complex Chromosomal Insertions.Hutterite-type cataract maps to chromosome 6p21.32-p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac deathMechanisms for the Generation of Two Quadruplications Associated with Split-Hand MalformationIdentification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics.Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.microRNA-199a-3p, DNMT3A, and aberrant DNA methylation in testicular cancer.Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathy.A miR-199a/miR-214 self-regulatory network via PSMD10, TP53 and DNMT1 in testicular germ cell tumor.Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis.Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.Nanoparticle delivery of stable miR-199a-5p agomir improves the osteogenesis of human mesenchymal stem cells via the HIF1a pathway.Comparison of multi-lineage differentiation of hiPSCs reveals novel miRNAs that regulate lineage specification.Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome casesPredicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangementsChromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletionsGenetic architecture of laterality defects revealed by whole exome sequencingTruncating variants in UBAP1 associated with childhood-onset nonsyndromic hereditary spastic paraplegia[Recommendation for standardized certification of the directors of genetic diagnostics laboratories][Standards and regulations for reporting clinical genetic testing results in the United States]The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance
P50
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P50
description
investigador
@es
researcher
@en
name
Shen Gu
@en
type
label
Shen Gu
@en
prefLabel
Shen Gu
@en
P31
P496
0000-0003-3107-1218