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Differential Expression and Phosphorylation of BTK Protein Domain in X-linked Agammaglobulinemia
Mahsa Sohani, Samaneh Delavari, Amir Hassan Zarnani, Leila Parvaneh, Shima Rasouli, Sepideh Shahkarami, Sepideh Babaie, Fatemeh Kiaee
Published: 2019-06-01
Correlation Analysis of Mutation Severity and BTK-expression by Clinical Manifestations in Patients with X-linked Agammaglobulinemia
Fatemeh Kiaee, Saeed Nasseri, Mahsa Sohani, Samaneh Delavari, Sima Habibi, Sepideh Shahkarami
Published: 2018-09-01
A Novel Homozygous RAB27A Mutation is Associated with Griscelli Syndrom type II and Less Severe Presentations
Mostafa Kamali, Sepideh Shahkarami, Elham Rayzan, Iraj Mohammazadeh, Meino Rohlfs, Christoph Klein, Nima Rezaei
Published: 2024-06-22
De novo CXCR4 Mutation in WHIM Syndrome: Report of a 4-Year-Old Case without Wart and Myelokathexis
Shayan Roshdi, Sepideh Shahkarami, Samaneh Zoghi, Elham Rayzan, Rasol Molatefi, Meino Rohlfs, Christoph Klein, Nima Rezaei
Published: 2025-03-12
Associations of TNF-Α -308 and -238 Polymorphisms with Inflammatory Bowel Disease: A Case-Control Study and Meta-Analysis of Published Data
Shirin Moosavi, Aaron Shanker, Maryam Sadr, Samaneh Soltani, Sepideh Shahkarami, Elham Farhadi, Nasser Ebrahimi Daryani, Behnoud Baradaran Noveiry, Farnaz Najmi Varzaneh, Mohammad Bashashati, Nima Rezaei
Published: 2025-03-04
HMGB1 Polymorphisms in Acute Lymphoblastic Leukemia
Elham Rayzan, Saeed Farajzadeh Valilou, Sara Hemmati, Amin Sadeghi, Hamid Farajifard, Sepideh Shahkarami, Nima Rezaei
Published: 2025-02-24
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