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Nucleic Acid Therapeutics|November 1, 2013
In vitro selection of modified RNA aptamers against CD44 cancer stem cell markerNidaa Ababneh, Walhan Alshaer, Omar Allozi, et al.
European Journal of Medical Genetics|April 22, 2006
Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype-genotype correlationHanadi Mattit, Muhidin Joma, Salwa Al-Cheikh, et al.
International Journal of Environmental Research and Public Health|July 27, 2022
Osteoporosis among Postmenopausal Women in Jordan: A National Cross-Sectional StudyRami Saadeh, Duaa Jumaa, Lina Elsalem, et al.
Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|December 18, 2025
A case-control study of promoter and 5'UTR VEGF polymorphisms in diabetic retinopathyDiala Walid Abu-Hassan, Muawyah D Al-Bdour, Huda Tahir, et al.
Journal of the Endocrine Society|August 18, 2020
A Novel Syndrome With Short Stature, Mandibular Hypoplasia, and Osteoporosis May Be Associated With a <i>PRRT3</i> VariantAbhimanyu Garg, Hatem El-Shanti, Chao Xing, et al.
Annals of Medicine and Surgery (2012)|April 3, 2023
Control of diabetes, hypertension, and dyslipidemia in Jordan: a cross-sectional studyDana Hyassat, Nancy Abu Noor, Qais AlAjlouni, et al.
Neuro Endocrinology Letters|November 7, 2007
Prevalence of factor V G1691A (Leiden) and prothrombin G20210A polymorphisms among apparently healthy JordaniansMohamad K Nusier, Abdelrahman M Radaideh, Nida'a A Ababneh, et al.
Cell Transplantation|November 6, 2014
Transplantation of purified autologous leukapheresis-derived CD34+ and CD133+ stem cells for patients with chronic spinal cord injuries: long-term evaluation of safety and efficacyAdeeb Al-Zoubi, Emad Jafar, Mohammad Jamous, 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.
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