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A new report of autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) with a homozygous pattern from Iran.
Immunol Lett. 2020 May;221:27-32. doi: 10.1016/j.imlet.2020.01.008. Epub 2020 Feb 1.
Immunol Lett. 2020.
PMID: 32014489
Evaluation of microsatellite instability in tumor and tumor marginal samples of sporadic colorectal cancer using mononucleotide markers.
Nouri Nojadeh J, Hashemzadeh S, Samadi Kafil H, Behrouz Sharif S, Eftekharsadat A, Ghasemnejad T, Ghojazadeh M, Sakhinia E.
Nouri Nojadeh J, et al.
EXCLI J. 2018 Sep 24;17:945-951. doi: 10.17179/excli2018-1455. eCollection 2018.
EXCLI J. 2018.
PMID: 30564073
Free PMC article.
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Homozygous mutation in CSF1R causes brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS).
Daghagh H, Rahbar Kafshboran H, Daneshmandpour Y, Nasiri Aghdam M, Talebian S, Nouri Nojadeh J, Hamzeiy H, Biskup S, Sakhinia E.
Daghagh H, et al. Among authors: nouri nojadeh j.
Bioimpacts. 2023;13(3):183-190. doi: 10.34172/bi.2022.23528. Epub 2022 Nov 26.
Bioimpacts. 2023.
PMID: 37431483
Free PMC article.
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A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case.
Ghasemnejad T, Shekari Khaniani M, Nouri Nojadeh J, Mansoori Derakhshan S.
Ghasemnejad T, et al. Among authors: nouri nojadeh j.
BMC Med Genomics. 2022 Feb 1;15(1):18. doi: 10.1186/s12920-022-01165-4.
BMC Med Genomics. 2022.
PMID: 35101039
Free PMC article.
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CRISPR/Cas9 genome editing for neurodegenerative diseases.
Nouri Nojadeh J, Bildiren Eryilmaz NS, Ergüder BI.
Nouri Nojadeh J, et al.
EXCLI J. 2023 Jul 3;22:567-582. doi: 10.17179/excli2023-6155. eCollection 2023.
EXCLI J. 2023.
PMID: 37636024
Free PMC article.
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