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Journal of Medical Microbiology|April 17, 2019
Synthesis of conjugated PIA-rSesC and immunological evaluation against biofilm-forming Staphylococcus epidermidisBahman Mirzaei, Seyed Fazlollah Mousavi, Reyhane Babaei, et al.
Infection and Immunity|July 18, 2012
Vaccination with SesC decreases Staphylococcus epidermidis biofilm formationMohammad Shahrooei, Vishal Hira, Laleh Khodaparast, et al.
Pediatric Rheumatology Online Journal|October 18, 2024
Three cases of autoinflammatory disease with novel NLRC4 mutations, and the first mutation reported in the CARD domain of NLRC4 associated with autoinflammatory infantile enterocolitis (AIFEC)Kosar Asna Ashari, Nima Parvaneh, Kayvan Mirnia, et al.
Annals of Human Genetics|October 2, 2019
A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasiaMohammad Miryounesi, Ali Nikfar, Majid Changi-Ashtiani, et al.
Plos One|January 23, 2016
The Possible Role of Staphylococcus epidermidis LPxTG Surface Protein SesC in Biofilm FormationLaleh Khodaparast, Ladan Khodaparast, Mohammad Shahrooei, et al.
Archives of Dermatological Research|April 8, 2025
A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature reviewLeyla Norouzi-Barough, Nasrin Alipour Olyaei, Raphael Carapito, et al.
Biorxiv : the Preprint Server for Biology|November 1, 2024
Syntaxin11 Deficiency Inhibits CRAC Channel Priming To Suppress Cytotoxicity And Gene Expression In FHLH4 Patient T LymphocytesSritama Datta, Abhikarsh Gupta, Kunal Mukesh Jagetiya, et al.
Pediatric Rheumatology Online Journal|June 13, 2023
A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in IranKosar Asna Ashari, Nahid Aslani, Nima Parvaneh, et al.
Iranian Journal of Allergy, Asthma, and Immunology|May 7, 2020
Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE SyndromeAli Aghebati-Maleki, Tina Shahani, Tooba Momen, et al.
Journal of Clinical Immunology|October 11, 2017
Functional Evaluation of an IKBKG Variant Suspected to Cause Immunodeficiency Without Ectodermal DysplasiaGlynis Frans, Jutte van der Werff Ten Bosch, Leen Moens, et al.
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