Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Raghda, Barham"'
Autor:
Enas Alwohoush, Mohammad A. Ismail, Ban Al-Kurdi, Raghda Barham, Sabal Al Hadidi, Abdalla Awidi, Nidaa A. Ababneh
Publikováno v:
Heliyon, Vol 10, Iss 19, Pp e38857- (2024)
Although mesenchymal stem cells (MSCs) are extensively applied in the regenerative field, the majority of MSCs die after a few weeks of transplantation. Therefore, hypoxia pre-conditioning is a crucial step in increasing the MSCs' tolerance to physio
Externí odkaz:
https://doaj.org/article/3110ec5d531240e78ace96cf30311641
Autor:
Nidaa A. Ababneh, Raghda Barham, Ban Al-Kurdi, Dema Ali, Sabal Al Hadidi, Mohammad A. Ismail, Ahmed S.H. Muamar, Ahmed A. Abdulelah, Adan Madadha, Malik Sallam, Yazan Hassona, Amira Masri, Abdalla Awidi
Publikováno v:
Stem Cell Research, Vol 62, Iss , Pp 102786- (2022)
Charcot-Marie-Tooth disease (CMT) is an inherited neurological disorder characterized by the progressive damage of the peripheral nerves. We generated a human induced pluripotent stem cell (iPSC) line JUCTCi019-A using dermal fibroblasts-derived from
Externí odkaz:
https://doaj.org/article/cf81349604614a798db1a462231c1374
Autor:
Nidaa A. Ababneh, Raghda Barham, Ban Al-Kurdi, Dema Ali, Nour Sharar, Sabal Al Hadidi, Renata M. Alatoom, Suzan Zalloum, Mohammad H. Gharandouq, Leen Makahleh, Leena N. Alnsour, Hebah Alshahwan, Mohammed El-Khateeb, Abdalla Awidi
Publikováno v:
Stem Cell Research, Vol 54, Iss , Pp 102358- (2021)
Limb-girdle muscular dystrophies (LGMDs) are a large group of heterogenous genetic diseases characterized by muscle weakness. In this study, an induced pluripotent stem cell (iPSC) line was generated from LGMD patient’s skin dermal fibroblasts, car
Externí odkaz:
https://doaj.org/article/e4748b2aaa1d4606b0fc01fe56462392
Autor:
Nidaa A. Ababneh, Ban Al-Kurdi, Raghda Barham, Dema Ali, Nour Sharar, Duaa Abuarqoub, Hanan Jafar, Bareqa Salah, Abdalla Awidi
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102000- (2020)
Mesenchymal stem cells (MSCs) are recognized as a valuable source of cells in clinical treatment and tissue engineering applications. In this study, we created human induced pluripotent stem cells (hiPSCs) from different MSC sources to evaluate the c
Externí odkaz:
https://doaj.org/article/4d89cd66c11e4b5cbd1013fd85b2da89
Autor:
Nidaa A. Ababneh, Ban Al-Kurdi, Dema Ali, Raghda Barham, Nour Sharar, Mairvat M. Mrahleh, Bareqa Salah, Abdalla Awidi
Publikováno v:
Stem Cell Research, Vol 48, Iss , Pp 101923- (2020)
Human induced pluripotent stem cell line (JUCTCi011-A) was generated from skin fibroblasts obtained from a 34-year-old healthy male subject from Jordan. The generated iPSCs showed typical embryonic-like characteristics. They retained their normal kar
Externí odkaz:
https://doaj.org/article/0dfa26273f2046f8913ac8515247cd1f
Autor:
Nidaa A. Ababneh, Ban Al-Kurdi, Dema Ali, Duaa Abuarqoub, Raghda Barham, Abdulla M. Alzibdeh, Asim N. Khanfar, Ahmad M. Altantawi, Abdee T. Ryalat, Basil Sharrack, Abdalla Awidi
Publikováno v:
Stem Cell Research, Vol 48, Iss , Pp 101925- (2020)
Ataxia with Oculomotor Apraxia Type 1 (AOA1) is an autosomal-recessive cerebellar ataxia characterized by early-onset cerebellar atrophy and axonal sensorimotor polyneuropathy. AOA1 is related to mutations in the aprataxin (APTX) gene encoding for th
Externí odkaz:
https://doaj.org/article/bfc3ae2d8d714726916977c791906e65
Autor:
Nidaa A. Ababneh, Dema Ali, Raghda Barham, Ban Al-Kurdi, Nour Sharar, Sabal Al Hadidi, Omar Qanno', Abdee T. Ryalat, Bareqa Salah, Abdalla Awidi
Publikováno v:
Stem Cell Research, Vol 48, Iss , Pp 101967- (2020)
Induced pluripotent stem cells (iPSCs) were generated from skin fibroblasts collected from a 39-year-old multiple symmetric lipomatosis (MLS) female patient carrying a point mutation in MFN2 gene (c.2119C > T). The resulting iPSCs showed typical embr
Externí odkaz:
https://doaj.org/article/5579fa858eb94996ac4d33fd16265909
Autor:
Nidaa A. Ababneh, Ban Al-Kurdi, Dema Ali, Duaa Abuarqoub, Raghda Barham, Abdee T. Ryalat, Abdalla Awidi
Publikováno v:
Stem Cell Research, Vol 47, Iss , Pp 101906- (2020)
Induced pluripotent stem cells (iPSCs) were generated from skin fibroblasts obtained from a 24-year-old female diagnosed with hereditary congenital myasthenic syndrome (CMS), caused by p.Arg331Trp (c.991C > T) homozygous mutation in the gene coding f
Externí odkaz:
https://doaj.org/article/65cf534afd20402686b783e4b25e483a
Autor:
Nidaa A. Ababneh, Ban Al-Kurdi, Dema Ali, Duaa Abuarqoub, Raghda Barham, Bareqa Salah, Abdalla Awidi
Publikováno v:
Stem Cell Research, Vol 47, Iss , Pp 101891- (2020)
Human integration-free induced pluripotent pluripotent stem cells (hiPSCs) were generated from skin fibroblasts obtained from a 27-year-old healthy Jordanian female. The resulting iPSCs expressed the most common pluripotency stem cell markers, they r
Externí odkaz:
https://doaj.org/article/40ff3fb52ee14ccfb14f7c866d429e03
Autor:
Mohammed Abu‐Ameerh, Hashim Mohammad, Zain Dardas, Raghda Barham, Dema Ali, Maysa Bijawi, Mohamed Tawalbeh, Sami Amr, Ma'mon M. Hatmal, Muawyah Al‐Bdour, Abdalla Awidi, Belal Azab
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Inherited retinal dystrophies (IRDs) are characterized by extreme genetic and clinical heterogeneity. There are many genes that are known to cause IRD which makes the identification of the underlying genetic causes quite challengi
Externí odkaz:
https://doaj.org/article/52aa1d76770348c28ddef0fcb4d7fab1