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

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

Cited by CrossRef: 3

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]

4- Biglari S, Rezaei H, Asadollahzadeh E, Asl M, Galehdari H, Garshasbi M, Esmaeilzadeh E, Khalesi R, Jamali P, Parvini F, Shariati G, Chamanrou N, Saligheh R, Moghaddam A, Khorshid H, Shohani S, Nafar S, Eslahi A, Lotfi M, Bakhshoodeh B, Hajizadeh F, Abtahi S, Jomehei R, Vahidnezhad H, Toosi M, Heidari M, Mirzadeh H, Mojarrad M, Sarband M, Karimiani E, Saleem S. Zygosity‐Dependent Phenotypic Spectrum of RELN‐Related Disorders: 10 New Patients and Genotype–Phenotype Correlations Across 48 Kindreds. Human Mutation. 2026;2026(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.