Biblio
The new mechanism of Ghrelin/GHSR-1a on autophagy regulation. Peptides. 2020:170264.
. miR-100-3p inhibits the adipogenic differentiation of hMSCs by targeting PIK3R1 via the PI3K/AKT signaling pathway. Aging (Albany NY). 2020;12.
. Migration deficits of the neural crest caused by CXADR triplication in a human Down syndrome stem cell model. Cell Death Dis. 2022;13(12):1018.
ITGA5 inhibition in pancreatic stellate cells re-educates the in vitro tumor-stromal crosstalk. Med Oncol. 2022;40(1):39.
. Investigation of donor KIR content and matching in children undergoing hematopoietic cell transplantation for acute leukemia. Blood Adv. 2020;4(7):1350-1356.
. Injectable nanofiber microspheres modified with metal phenolic networks for effective osteoarthritis treatment. Acta Biomater. 2022.
Improvements in gut microbiota dysbiosis in aged mice transplanted with adipose-derived stem cells. Stem Cells Dev. 2023.
. Identification of a permissible HLA mismatch in hematopoietic stem cell transplantation. Blood. 2014.
Hypoxic pretreatment of adipose-derived stem cell exosomes improved cognition by delivery of circ-Epc1 and shifting microglial M1/M2 polarization in an Alzheimer's disease mice model. Aging (Albany NY). 2022;14(undefined).
. Hypoxic condition induced H3K27me3 modification of the LncRNA Tmem235 promoter thus supporting apoptosis of BMSCs. Apoptosis. 2022.
High-throughput profiling of histone post-translational modifications and chromatin modifying proteins by reverse phase protein array. J Proteomics. 2022:104596.
Haploidentical versus matched unrelated donor transplants using post-transplant cyclophosphamide for lymphomas. Transplant Cell Ther. 2022.
Haploidentical haematopoietic stem cell transplantation for the treatment of severe aplastic anaemia patients with high-risk factors who lack an HLA-matched sibling donor. Transfus Clin Biol. 2021.
. Genetics of HLA peptide presentation, and impact on outcomes in HLA-matched allo-HCT. Transplant Cell Ther. 2021.
Generation of iPSC from peripheral blood mononuclear cells obtained from a patient with TSC2-PKD1 contiguous gene deletion syndrome. Stem Cell Res. 2021;51:102181.
. Generation of induced pluripotent stem cells (iPSCs) from a Chinese infant (XACHi015-A) with type 2 Long QT syndrome carrying the heterozygous mutation c.1814C>T(p.P605L) in KCNH2. Stem Cell Res. 2021;56:102509.
. Generation of induced pluripotent stem cell line (FMCPGHi001-A) from a 25-year-old Chinese Han healthy male donor. Stem Cell Res. 2022;60:102735.
. Generation of induced pluripotent stem cell line derived from FNAIT patient with CD36 deficiency mutations. Stem Cell Res. 2022;61:102749.
. Generation of an induced pluripotent stem cell line (SYSUSCi001-A) from a congenital cataract patient carrying heterozygous mutations in BFSP1 and RHO. Stem Cell Res. 2021;59:102644.
. Generation of a MSX1 knockout human embryonic stem cell line using CRISPR/Cas9 technology. Stem Cell Res. 2022;60:102729.
. GAPDH is critical for superior efficacy of female bone marrow-derived mesenchymal stem cells on pulmonary hypertension. Cardiovasc Res. 2013.
. Factors affecting the CD34(+) cell yields from the second donations of healthy donors: The steady-state lymphocyte count is a good predictive factor. Transfus Apher Sci. 2016.
. Exosomes derived from human umbilical cord mesenchymal stem cells reduce tendon injuries via the miR-27b-3p/ARHGAP5/RhoA signaling pathway. Acta Biochim Biophys Sin (Shanghai). 2022;54(2):1-11.
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