Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mostafa Saghi"'
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-16 (2022)
Abstract Background Intellectual disability (ID) is a clinically important disease and a most prevalent neurodevelopmental disorder. The etiology and pathogenesis of ID are poorly recognized. Exome sequencing revealed a homozygous missense mutation i
Externí odkaz:
https://doaj.org/article/dd3ba46317904183b38fff42f15a0508
Autor:
Sara Azhdari, Mostafa Saghi, Behrang Alani, Maryam Zare Rafie, Taiebe Kenarangi, Mehrdad Nasrollahzadeh Sabet, Bahram Pakzad, Tahereh Ghorashi, Milad Gholami, Mohsen Soosanabadi
Publikováno v:
Lupus. 31(8)
Objective Over the past decades, TNIP1 has been identified as a strong risk locus in multiple genome-wide association studies (GWAS), spanning multiple populations and various autoimmune diseases. TNIP1 is a polyubiquitin-binding protein that works a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a371484f84de57bcd634af64c9c2f278
https://pubmed.ncbi.nlm.nih.gov/35475371
https://pubmed.ncbi.nlm.nih.gov/35475371
Autor:
Naeim Ehtesham, Meysam Mosallaei, Shima Rahimirad, Sharifeh Khosravi, Nasim Vatandoost, Mostafa Saghi
Publikováno v:
Archives of Physiology and Biochemistry. 128:1081-1087
There are various types of molecular biomarkers that are derived from distinct starting materials. Although many indirect biomarkers are found in blood, their detection remains a challenging issue because of the high degree of fragmentation, minute q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbbdcef5aa6047063c6928d69fbfdf4c
https://doi.org/10.1080/13813455.2020.1752257
https://doi.org/10.1080/13813455.2020.1752257
Autor:
Sepideh Ghobakhloo, Emran Esmaeilzadeh, Saeideh Davar, Mehdi Hassani, Mostafa Saghi, Sharifeh Khosravi, Behrang Alani, Bahram Pakzad, Mehrdad Sabet
Publikováno v:
Clinical rheumatology. 40(11)
Systemic lupus erythematosus (SLE) is a multifactorial systemic autoimmune disease, in which genetic susceptibility plays a pivotal role. The nucleotide oligomerization domain 2 (NOD2) gene is one of the main regulators of chronic inflammatory condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbe5752c8c0a1d6a8152b54e123eccef
https://pubmed.ncbi.nlm.nih.gov/34173079
https://pubmed.ncbi.nlm.nih.gov/34173079