LTBP2 mutations cause Weill–Marchesani and Weill–Marchesani‐like syndrome and affect disruptions in the extracellular matrix R Haji‐Seyed‐Javadi, S Jelodari‐Mamaghani, SH Paylakhi, S Yazdani, ... Human mutation 33 (8), 1182-1187, 2012 | 128 | 2012 |
Contribution of the latent transforming growth factor-beta binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome S Jelodari-Mamaghani, R Haji-Seyed-Javadi, F Suri, N Nilforushan, ... Molecular vision 19, 333, 2013 | 57 | 2013 |
New insights into cartilage tissue engineering: improvement of tissue‐scaffold integration to enhance cartilage regeneration S Jelodari, A Ebrahimi Sadrabadi, F Zarei, S Jahangir, M Azami, ... BioMed Research International 2022 (1), 7638245, 2022 | 28 | 2022 |
Decellularization of small intestinal submucosa S Jelodari, E Sadroddiny Decellularization Methods of Tissue and Whole Organ in Tissue Engineering, 71-84, 2021 | 7 | 2021 |
Assessment of the efficacy of an LL-37-encapsulated keratin hydrogel for the treatment of full-thickness wounds S Jelodari, H Daemi, P Mohammadi, J Verdi, M J Al-Awady, J Ai, M Azami ACS Applied Bio Materials 6 (6), 2122-2136, 2023 | 5 | 2023 |
Familial Prion Disease Cases Without Mutation in PRNPGene S Jelodari-Mamaghani, GA Shahidi, M Roohani, F Sina Progress in Biological Sciences 2 (2), 98-103, 2013 | | 2013 |