Comprehensive in silico identification of impacts of ACE2 SNPs on COVID-19 susceptibility in different populations von Paniri, Alireza, Hosseini, Mohammad Mahdi, Moballegh-Eslam, Mojtaba, Akhavan-Niaki, Haleh

Volltext

Emerging role of IL-6 and NLRP3 inflammasome as potential therapeutic targets to combat COVID-19: Role of lncRNAs in cytokine storm modulation von Paniri, Alireza, Akhavan-Niaki, Haleh

Volltext

A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations von Paniri, Alireza, Fattahi, Sadegh, Rasoulinejad, Ahmad, Akhavan-Niaki, Haleh

Volltext

Alzheimer’s Disease-Related Epigenetic Changes: Novel Therapeutic Targets von Paniri, Alireza, Hosseini, Mohammad Mahdi, Akhavan-Niaki, Haleh

Volltext

Molecular effects and retinopathy induced by hydroxychloroquine during SARS-CoV-2 therapy: Role of CYP450 isoforms and epigenetic modulations von Paniri, Alireza, Hosseini, Mohammad Mahdi, Rasoulinejad, Ahmad, Akhavan-Niaki, Haleh

Volltext

Insights into the Links between MYC and 3D Chromatin Structure and Epigenetics Regulation: Implications for Cancer Therapy von Amjadi-Moheb, Fatemeh, Paniri, Alireza, Akhavan-Niaki, Haleh

Volltext

The epigenetics orchestra of Notch signaling: a symphony for cancer therapy von Paniri, Alireza, Hosseini, Mohammad Mahdi, Amjadi-Moheb, Fatemeh, Tabaripour, Reza, Soleimani, Elnaz, Langroudi, Maryam Pilehchian, Zafari, Parisa, Akhavan-Niaki, Haleh

Volltext

Impact of new UK (B.1.1.7) SARS-Cov-2 variant on interacting with ACE2 and host immune response von Paniri, Alireza, Hosseini, Mohammad Mahdi, Akhavan-Niaki, Haleh

Volltext

Genetic variations in IKZF3, LET7‐a2, and CDKN2B‐AS1: Exploring associations with metabolic syndrome susceptibility and clinical manifestations von Paniri, Alireza, Hosseini, Mohammad Mahdi, Fattahi, Sadegh, Amiribozorgi, Galia, Asouri, Mohsen, Maadi, Mansooreh, Motamed, Nima, Zamani, Farhad, Akhavan‐Niaki, Haleh

Volltext

The association of MMUT mutation with wide spectrum clinical manifestations in a child affected with methylmalonic academia von Pasha, Yadollah Zahed, Paniri, Alireza, Ahmadpour-Kacho, Mousa, Fattahi, Sadegh, Yazarlou, Nafiseh, Akhavan-Niaki, Haleh

Volltext

The association of MMUT mutation (NM_000255.4: C.976a>g) with wide spectrum clinical manifestations in a child affected with methylmalonic acidaemia von Yadollah Zahed Pasha, Alireza Paniri, Mousa Ahmadpour-Kacho, Sadegh Fattahi, Nafiseh Yazarlou, Haleh Akhavan-Niaki

Volltext

A broad spectrum manifestation in a case affected by 3q29 microdeletion syndrome: a literature review and in silico analysis von Esmaeilnejad-Ganji, Seyed Mokhtar, Paniri, Alireza, Golpour, Monireh, Tabaripour, Reza, Akhavan-Niaki, Haleh

Volltext

The association of MMUT mutation (NM_000255.4:c.976A>G) with wide spectrum clinical manifestations in a child affected with methylmalonic acidemia von Pasha, Yadollah Zahed, Paniri, Alireza, Ahmadpour-Kacho, Mousa, Fattahi, Sadegh, Yazarlou, Nahseh, Akhavan-Niaki, Haleh

Volltext

Genotype-phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening von Tamaddoni, Ahmad, Nesheli, Hassan, Paniri, Alireza, Azizi, Mandana, Banihashemi, Ali, Kamangari, Reza, Akhavan-Niaki, Haleh

Volltext

The epigenetics orchestra of Notch signaling: a symphony for cancer therapy von Paniri, Alireza, Hosseini, Mohammad Mahdi, Amjadi-Moheb, Fatemeh, Tabaripour, Reza, Soleimani, Elnaz, Langroudi, Maryam Pilehchian, Zafari, Parisa, Akhavan-Niaki, Haleh

Volltext bestellen