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Plos One|August 5, 2020
Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agentsNidaa A Ababneh, Dema Ali, Ban Al-Kurdi, et al.Stem Cell Research|September 11, 2020
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 geneNidaa A Ababneh, Dema Ali, Raghda Barham, et al.Molecular Therapy Oncolytics|February 12, 2021
Anti-oncogenic activities exhibited by paracrine factors of MSCs can be mediated by modulation of KITLG and DKK1 genes in glioma SCs in vitroNazneen Aslam, Elham Abusharieh, Duaa Abuarqoub, et al.Biology Open|December 3, 2024
Effect of cigarette smoke on the proliferation, viability, gene expression, and cellular functions of adipose-derived mesenchymal stem cells from smoking and non-smoking donorsBareqa Salah, Diana Shahin, Momen Sarhan, et al.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.International Ophthalmology|July 7, 2018
Platelet lysate promotes re-epithelialization of persistent epithelial defects: a pilot studyMohammed A Abu-Ameerh, Hanan D Jafar, Maram H Hasan, 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.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.World Journal of Stem Cells|January 2, 2026
Impact of differentiation protocols on the functionality of mesenchymal stem cells derived from induced pluripotent stem cellsNidaa A Ababneh, Enas Alwohoush, Razan AlDiqs, et al.Pageof 2