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Whole-Exome Sequencing Identified a Novel Variant (C.405_422+39del) in DSP Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy.
Eshaghkhani Y, Mohamadifar A, Asadollahi M, Taghizadeh M, Karamzade A, Saberi M, Nourmohammadi P, Golchehre Z, Amin A, Keramatipour M. Eshaghkhani Y, et al. Among authors: saberi m. Rep Biochem Mol Biol. 2021 Jul;10(2):280-287. doi: 10.52547/rbmb.10.2.280. Rep Biochem Mol Biol. 2021. PMID: 34604417 Free PMC article.
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families.
Akbaroghli S, Kooshavar D, Golchehre Z, Karamzade A, Saberi M, Alaei MR, Abbasi Sadegh M, Asadollahi M, Keramatipour M. Akbaroghli S, et al. Among authors: saberi m. Iran J Child Neurol. 2022 Winter;16(1):123-133. doi: 10.22037/ijcn.v16i1.31650. Epub 2022 Jan 1. Iran J Child Neurol. 2022. PMID: 35222663 Free PMC article.
TRAIL gene expression analysis in multiple sclerosis patients.
Taheri M, Nemati S, Movafagh A, Saberi M, Mirfakhraie R, Eftekharian MM, Arsang-Jang S, Rezagholizadeh A, Sayad A. Taheri M, et al. Among authors: saberi m. Hum Antibodies. 2016 May 20;24(1-2):33-8. doi: 10.3233/HAB-160291. Hum Antibodies. 2016. PMID: 27472871
196 results