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Arch Iran Med. 2020;23(10): 688-696. doi: 10.34172/aim.2020.87

Original Article

Functional Analysis of RELN S2486G Mutation and its Contribution to Pathogenesis of Ankylosing Spondylitis

Elika Esmaeilzadeh-Gharehdaghi 1 ORCID, Ehsan Razmara 2 ORCID, Amirreza Bitaraf 3, Ahmadreza Jamshidi 4, Mahdi Mahmoudi 4,5, Masoud Garshasbi 1 * ORCID

Cited by CrossRef: 1

1- Priyadarshi S, Hansdah K, Singh N, Bouzid A, Ray C, Panda K, Biswal N, Desai A, Choudhury J, Tekari A, Masmoudi S, Ramchander P, Boon-Peng H. The risks of RELN polymorphisms and its expression in the development of otosclerosis. PLoS ONE. 2022;17(6):e0269558 [Crossref]
2- Alexander A, Herz J, Calvier L. Reelin through the years: From brain development to inflammation. Cell Reports. 2023;42(6):112669 [Crossref]
3- Mathew A, Bhagavaldas M, Biswas R, Biswas L. Genetic risk factors in ankylosing spondylitis: Insights into etiology and disease pathogenesis. Int J of Rheum Dis. 2024;27(1) [Crossref]

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A Monthly Peer-Reviewed Medical Journal Published by the Academy of Medical Sciences of the I.R. Iran; Indexed in PubMed/MEDLINE, ISI Web of Science, EMBASE, SCOPUS, CINHAL, PASCAL, CSA, SID, ISSN: Print 1029-2977, Online 1735-3947.The impact factor of Archives of Iranian Medicine according to Journal Citation Reports® (JCR®) 2016 is 1.20.