Chromosome 3q26 Gain Is an Early Event Driving Coordinated Overexpression of the PRKCI, SOX2, and ECT2 Oncogenes in Lung Squamous Cell Carcinoma.Cell Rep30, 771-782.e6.(2020).
Cold-inducible RNA-binding protein modulates atrial fibrillation onset by targeting multiple ion channels.Heart Rhythm.(2020).
Enhanced tenogenic differentiation and tendon-like tissue formation by Scleraxis overexpression in human amniotic mesenchymal stem cells.J Mol Histol.(2020).
Generation of a Human iPSC line (SDQLCHi021-A) from a patient with methylmalonic acidemia cblC type carrying compound heterozygous mutations in MMAHC gene.Stem Cell Res43, 101709.(2020).
Generation of patient-specific pluripotent induced stem cell line SDUBMSI002-A from a patient with X-linked mental retardation syndrome.Stem Cell Res43, 101724.(2020).
Human Amniotic Mesenchymal Stem Cell Sheets Encapsulating Cartilage Particles Facilitate Repair of Rabbit Osteochondral Defects.Am J Sports Med363546519897912.(2020).
An integration-free iPSC line SDQLCHi025-A from a girl with multiminicore disease carrying compound heterozygote mutations in RYR1 gene.Stem Cell Res45, 101775.(2020).
A 17 gene panel for non-small cell lung cancer prognosis identified through integrative epigenomic-transcriptomic analyses of hypoxia-induced epithelial-mesenchymal transition.Mol Oncol.(2019).
3D printed HUVECs/MSCs cocultures impact cellular interactions and angiogenesis depending on cell-cell distance.Biomaterials222, 119423.(2019).
Cross-lineage protection by human antibodies binding the influenza B hemagglutinin.Nat Commun10, 324.(2019).
Down-regulation of long non-coding RNA MEG3 suppresses osteogenic differentiation of periodontal ligament stem cells (PDLSCs) through miR-27a-3p/IGF1 axis in periodontitis.Aging (Albany Ny)11.(2019).
Establishment of a human induced pluripotent stem cell line (SDQLCHi005-A) from a patient with mastocytosis carrying heterozygous mutation in KIT gene.Stem Cell Res40, 101565.(2019).
Generation of an induced pluripotent stem cell line (SDQLCHi003-a) from a patient with short rib-thoracic dysplasia syndrome type III carrying compound heterozygous mutations in DYNC2H1.Stem Cell Res39, 101505.(2019).
Generation of an induced pluripotent stem cell line (SDQLCHi008-A) from a patient with ASD and DD carrying an 830 kb de novo deletion at chr7q11.22 including the exon 1 of AUTS2 gene.Stem Cell Res40, 101557.(2019).
Generation of two induced pluripotent stem cell lines from patients with unbalanced translocation (3;22).Stem Cell Res40, 101545.(2019).
Identification of tumor stem-like cells in admanatimomatous craniopharyngioma and determination of these cells' pathological significance.J Neurosurg1-11.(2019).
An induced pluripotent stem cell line (SDQLCHi006-A) derived from a patient with maple syrup urine disease type Ib carrying compound heterozygous mutations of p.R168C and p.T322I in BCKDHB gene.Stem Cell Res40, 101579.(2019).
An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303 kb de novo deletion at chr3p26.1 implicating GRM7 gene.Stem Cell Res41, 101635.(2019).
An integration-free iPSC line (SDQLCHi013-A) derived from a patient with maple syrup urine disease carrying compound heterozygote mutations in BCKDHA gene.Stem Cell Res41, 101585.(2019).
Mesenchymal stem cells enhance microglia M2 polarization and attenuate neuroinflammation through TSG-6.Brain Res146422.(2019).
A novel transgenic murine model with persistently brittle bones simulating osteogenesis imperfecta type I.Bone.(2019).
Reprogramming of human Peripheral Blood Mononuclear Cell (PBMC) from a Chinese patient suffering Duchenne muscular dystrophy to iPSC line (SDQLCHi007-A) carrying deletion of 49-50 exons in the DMD gene.Stem Cell Res42, 101666.(2019).