PiRNAs interacting proteins, candidate molecular marker for evaluation of idiopathic male infertility von Poursadegh Zonouzi, A., Poursadegh Zonouzi, A. A., Ghorbian, S.

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Methodology to Understand How Perforin Assembles on Membranes von Ghorbian, S., Abkar, M., Poursadegh Zonouzi, A.

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Methylenetetrahydrofolate Reductase C677T and A1298C Mutations in Women with Recurrent Spontaneous Abortions in the Northwest of Iran von Poursadegh Zonouzi, Ahmad, Chaparzadeh, Nader, Asghari Estiar, Mehrdad, Mehrzad Sadaghiani, Mahzad, Farzadi, Laya, Ghasemzadeh, Alieh, Sakhinia, Masoud, Sakhinia, Ebrahim

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Upregulation of the double-stranded RNA binding protein DGCR8 in invasive ductal breast carcinoma von Fardmanesh, Hedieh, Shekari, Mohammad, Movafagh, Abolfazl, Alizadeh Shargh, Shohreh, Poursadegh Zonouzi, Ali Akbar, Shakerizadeh, Samira, Poursadegh Zonouzi, Ahmad, Hosseinzadeh, Asghar

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Mitochondrial complex I gene variations; as a potential genetic risk factor in pathogenesis of multiple sclerosis von Poursadegh Zonouzi, Ahmad, Ghorbian, Saeid, Abkar, Morteza, Poursadegh Zonouzi, Ali Akbar, Azadi, Ali

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Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndrom... von Laleh, Masoud, Naseri, Marzieh, Zonouzi, Ali, Zonouzi, Ahmad, Masoudi, Marjan, Ahangari, Najmeh, Shams, Leila, Nejatizadeh, Azim

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Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations von Naseri, Marzieh, Akbarzadehlaleh, Masoud, Masoudi, Marjan, Ahangari, Najmeh, Poursadegh Zonouzi, Ali Akbar, Poursadegh Zonouzi, Ahmad, Shams, Leila, Nejatizadeh, Azim

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Dysregulated expression of Dicer in invasive ductal breast carcinoma von Poursadegh Zonouzi, Ali Akbar, Nejatizadeh, Azim, Rahmati-Yamchi, Mohammad, Fardmanesh, Hedieh, Shakerizadeh, Samira, Poursadegh Zonouzi, Ahmad, Nejati-Koshki, Kazem, Shekari, Mohammad

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Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss von Masoudi, Marjan, Ahangari, Najmeh, Poursadegh Zonouzi, Ali Akbar, Poursadegh Zonouzi, Ahmad, Nejatizadeh, Azim

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Circulating miR-150, miR-192, miR-200b, and miR-423-3p as Non-invasive Biomarkers of Chronic Allograft Dysfunction von Zununi Vahed, Sepideh, Poursadegh Zonouzi, Ahmad, Mahmoodpoor, Fariba, Samadi, Nasser, Ardalan, Mohammadreza, Omidi, Yadollah

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Differential expression of circulating miR-21, miR-142-3p and miR-155 in renal transplant recipients with impaired graft function von Zununi Vahed, Sepideh, Poursadegh Zonouzi, Ahmad, Ghanbarian, Hossein, Ghojazadeh, Morteza, Samadi, Nasser, Omidi, Yadollah, Ardalan, Mohammadreza

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The expression of Drosha, DGCR8, Dicer and Ago-2 genes are upregulated in human umbilical vein endothelial cells under hyperglycemic condition von Soufi, Farhad Ghadiri, Zonouzi, Ali Akbar Poursadegh, Eftekhar, Ebrahim, Kamali, Kamila, Chegeni, Sara Aghakhani, Zonouzi, Ahmad Poursadegh

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Cell-free fetal DNA: new perspective and clinical implication in diagnosis of polycystic kidney diseases von Poursadegh Zonouzi, Ali Akbar, Poursadegh Zonouzi, Ahmad, Ghorbian, Saeid

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Protocol for the collection and analysis of the different immune cell subsets in the murine intestinal lamina propria von Shanmugavadivu, Arthi, Carter, Katlynn, Zonouzi, Aysan Poursadegh, Waisman, Ari, Regen, Tommy

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Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haploty... von Azani, Alireza, Hosseinzadeh, Asghar, Azadkhah, Roya, Zonouzi, Ali Akbar Poursadegh, Zonouzi, Ahmad Poursadegh, Aftabi, Younes, Khani, Hourieh, Heidary, Leida, Danaii, Shahla, Bargahi, Nasrin, Pouladi, Nasser, Hosseini, Sayed Mostafa

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Apolipoprotein E genotyping in women with recurrent pregnancy loss: An in silico and experimental hybrid study von Poursadegh Zonouzi, Ahmad, Farajzadeh, Davoud, Bargahi, Nasrin, Farajzadeh, Malak

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Congenital heart defects among Down syndrome patients: a clinical profiling von Poursadegh Zonouzi, Ali Akbar, Ahangari, Najmeh, Rajai, Shahrokh, Poursadegh Zonouzi, Ahmad, Akbarzadeh Laleh, Masoud, Nejatizadeh, Azim

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The association between thrombophilic gene mutations and recurrent pregnancy loss von Poursadegh Zonouzi, Ahmad, Chaparzadeh, Nader, Ghorbian, Saeid, Sadaghiani, Mahzad Mehrzad, Farzadi, Laya, Ghasemzadeh, Alieh, Kafshdooz, Taiebeh, Sakhinia, Masoud, Sakhinia, Ebrahim

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Genetic susceptibility to deep venous thromboembolism: the roles of inherited thrombophilia polymorphisms von Bargahi, Nasrin, Ghorbian, Saeid, Zonouzi, Ali Akbar Poursadegh, Zonouzi, Ahmad Poursadegh

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OS-103 Antibiotic-mediated microbiota depletion limits IgA-related fibrogenesis in metabolic dysfunction-associated steatohepatitis von Schuehle, Svenja, Kotsiliti, Eleni, Cohen, Yotam, Deng, Sisi, Omer, Hélčne, Han, Feng, Qiu, Mengjie, Zonouzi, Aysan Poursadegh, Schmidt, Sabine, Avila, Jose Efren Barragan, Vaquero, Mirian Fernández, Focaccia, Enrico, Prokosch, Sandra, Rothermel, Ulrike, Müller, Florian, Hetzer, Jenny, Heide, Danijela, Mager, Lukas, Bucci, Daniele, Waisman, Ari, Trautwein, Christoph, Haller, Dirk, Elinav, Eran, Heikenwälder, Mathias

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