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Stem Cell Research|August 10, 2020
Generation and characterization of induced pluripotent stem cell (iPSC) line (JUCTCi002-A) from a patient with ataxia with oculomotor apraxia type 1 (AOA1) harboring a homozygous mutation in the APTX geneNidaa A Ababneh, Ban Al-Kurdi, Dema Ali, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|March 11, 2019
Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophiesBelal Azab, Raghda Barham, Dema Ali, et al.Genes|April 30, 2021
Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal DystrophiesBilal Azab, Zain Dardas, Dunia Aburizeg, et al.RSC Advances|May 9, 2022
Encapsulation of echinomycin in cyclodextrin inclusion complexes into liposomes: <i>in vitro</i> anti-proliferative and anti-invasive activity in glioblastomaWalhan Alshaer, Manar Zraikat, Amer Amer, et al.World Journal of Stem Cells|December 8, 2025
Cancer cell-dependent increase in senescence-like populations following exosome treatment from bone marrow and induced pluripotent stem cell-derived mesenchymal stem cellsNidaa A Ababneh, Sura Nashwan, Razan AlDiqs, et al.CNS Neuroscience & Therapeutics|September 30, 2017
Mesenchymal stem cells and conditioned media in the treatment of multiple sclerosis patients: Clinical, ophthalmological and radiological assessments of safety and efficacySaid Dahbour, Fatima Jamali, Dana Alhattab, et al.Stem Cell Research|April 25, 2022
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 geneNidaa A Ababneh, Raghda Barham, Ban Al-Kurdi, et al.Journal of Orthopaedic Surgery and Research|December 14, 2017
Intra-articular injection of expanded autologous bone marrow mesenchymal cells in moderate and severe knee osteoarthritis is safe: a phase I/II studyMahasen Al-Najar, Hiba Khalil, Jihad Al-Ajlouni, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|October 8, 2021
The utility of whole-exome sequencing in accurate diagnosis of neuromuscular disorders in consanguineous families in JordanNidaa A Ababneh, Dema Ali, Ban Al-Kurdi, et al.Stem Cell Research|June 4, 2021
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 geneNidaa A Ababneh, Raghda Barham, Ban Al-Kurdi, et al.Pageof 11