Biblio
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021;385(20):1868-1880.
Electrospun Magnetic Composite Poly-3-hydroxybutyrate/Magnetite Scaffolds for Biomedical Applications: Composition, Structure, Magnetic Properties, and Biological Performance. ACS Appl Bio Mater. 2022.
NOTCH3 Is a Prognostic Factor That Promotes Glioma Cell Proliferation, Migration and Invasion via Activation of CCND1 and EGFR. PLoS One. 2013;8(10):e77299.
. Demonstration of the Presence of the "Deleted" MIR122 Gene in HepG2 Cells. PLoS One. 2015;10(3):e0122471.
. Control of Hyperglycemia Using Differentiated and Undifferentiated Mesenchymal Stem Cells in Rats with Type 1 Diabetes. Cells Tissues Organs. 2020:1-13.
. In silico drug repurposing for the treatment of heart diseases using gene expression data and molecular docking techniques. Biochem Biophys Res Commun. 2021;572:138-144.
. Hair-follicle mesenchymal stem-cell activity during homeostasis and wound healing. J Invest Dermatol. 2021.
. Evaluation of bone marrow microenvironment could change how myelodysplastic syndromes are diagnosed and treated. Cytometry A. 2018.
. Systematic identification of gene family regulators in mouse and human embryonic stem cells. Nucleic Acids Res. 2016.
. Formation and functionalization of Ge-nanoparticles in ZnO. Nanotechnology. 2021.
. Generation and characterization of a control and patient-derived human iPSC line containing the Hermansky Pudlak type 2 (HPS2) associated heterozygous compound mutation in AP3B1. Stem Cell Res. 2021;54:102444.
Generation and characterization of a human iPSC line SANi008-A from a Chédiak-Higashi Syndrome patient. Stem Cell Res. 2021;55:102442.
. Generation and characterization of a human iPSC line SANi007-A from a patient with a heterozygous dominant mutation in ELANE. Stem Cell Res. 2021;55:102440.
. Generation and characterization of a human iPSC line SANi006-A from a Gray Platelet Syndrome patient. Stem Cell Res. 2021;55:102443.
. The role of osteoblast cells in the pathogenesis of unicameral bone cysts. J Child Orthop. 2012;6(4):339-46.
. New Drug Discovery Paradigms for Retinal Diseases: A Focus on Retinal Organoids. J Ocul Pharmacol Ther. 2019.
. Advances in management of type 1 diabetes mellitus. World J Diabetes. 2014;5(5):689-96.
. Establishment of (JUCTCi007-A) iPSC line from a patient with congenital myasthenic syndrome (CMS) carrying a homozygous mutation p.Arg331Trp (c.991C > T) in the CHRNE gene. Stem Cell Res. 2020;47:101906.
. Establishment of a human induced pluripotent stem cell line, JUCTCi012-A, from multiple symmetric lipomatosis (MSL) patient carrying a homozygous Arg707Trp (c.2119C > T) mutation in the MFN2 gene. Stem Cell Res. 2020;48:101967.
. Derivation of three human induced pluripotent stem cell lines (JUCTCi014-A, JUCTCi015-A, JUCTCi016-A) from mesenchymal stem cells (MSCs) derived from bone marrow, adipose tissue and Wharton's jelly samples. Stem Cell Res. 2020;49:102000.
. Generation of an induced pluripotent stem cell (iPSC) line (JUCTCi017-A) from a patient with limb-girdle muscular dystrophy (LGMD) due to a homozygous p.Lue287Ser fs14* mutation in the SGCB gene. Stem Cell Res. 2021;54:102358.
Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi019-A) from a patient with Charcot-Marie-Tooth disease type 2A2 (CMT2A2) due to a heterozygous missense substitution c.2119C > T (p.Arg707Trp) in MFN2 gene. Stem Cell Res. 2022;62:102786.
Assessing the Role of Radiotherapy in Patients with Refractory or Relapsed High-Grade B-Cell Lymphomas Treated with CAR T-Cell Therapy. Radiother Oncol. 2022.
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