Výsledky vyhledávání - Modarresi, Farzaneh

A Novel RNA Transcript with Antiapoptotic Function Is Silenced in Fragile X Syndrome Autor Khalil, Ahmad M., Faghihi, Mohammad Ali, Modarresi, Farzaneh, Brothers, Shaun P., Wahlestedt, Claes

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Screening for Small-Molecule Modulators of Long Noncoding RNA-Protein Interactions Using AlphaScreen Autor Pedram Fatemi, Roya, Salah-Uddin, Sultan, Modarresi, Farzaneh, Khoury, Nathalie, Wahlestedt, Claes, Faghihi, Mohammad Ali

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Knockdown of BACE1-AS Nonprotein-Coding Transcript Modulates Beta-Amyloid-Related Hippocampal Neurogenesis Autor Modarresi, Farzaneh, Faghihi, Mohammad Ali, Patel, Nikunj S., Sahagan, Barbara G., Wahlestedt, Claes, Lopez-Toledano, Miguel A.

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A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis Autor Bordbar, Mohammad Reza, Modarresi, Farzaneh, Farazi Fard, Mohammad Ali, Dastsooz, Hassan, Shakib Azad, Nader, Faghihi, Mohammad Ali

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Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report Autor Maghami, Fatemeh, Tabei, Seyed Mohammad Bagher, Moravej, Hossein, Dastsooz, Hassan, Modarresi, Farzaneh, Silawi, Mohammad, Faghihi, Mohammad Ali

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Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene Autor Karimzadeh, Parvaneh, Naderi, Samaneh, Modarresi, Farzaneh, Dastsooz, Hassan, Nemati, Hamid, Farokhashtiani, Tayebeh, Shamsian, Bibi Shahin, Inaloo, Soroor, Faghihi, Mohammad Ali

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RNAi Screen Indicates Widespread Biological Function for Human Natural Antisense Transcripts Autor Faghihi, Mohammad Ali, Kocerha, Jannet, Modarresi, Farzaneh, Engström, Pär G., Chalk, Alistair M., Brothers, Shaun P., Koesema, Eric, St. Laurent, Georges, Wahlestedt, Claes

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Natural Antisense Inhibition Results in Transcriptional De-Repression and Gene Upregulation Autor Modarresi, Farzaneh, Faghihi, Mohammad Ali, Lopez-Toledano, Miguel A., Fatemi, Roya Pedram, Magistri, Marco, Brothers, Shaun P., van der Brug, Marcel P., Wahlestedt, Claes

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A novel knockout mouse model of the noncoding antisense Brain-Derived Neurotrophic Factor (Bdnf) gene displays increased endogenous Bdnf protein and improved memory function follow... Autor Modarresi, Farzaneh, Pedram Fatemi, Roya, Razavipour, Seyedeh Fatemeh, Ricciardi, Natalie, Makhmutova, Madina, Khoury, Nathalie, Magistri, Marco, Volmar, Claude-Henry, Wahlestedt, Claes, Faghihi, Mohammad Ali

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Evidence for natural antisense transcript-mediated inhibition of microRNA function Autor Faghihi, Mohammad Ali, Zhang, Ming, Huang, Jia, Modarresi, Farzaneh, Van der Brug, Marcel P, Nalls, Michael A, Cookson, Mark R, St-Laurent, Georges, Wahlestedt, Claes

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Expression of a noncoding RNA is elevated in Alzheimer’s disease and drives rapid feed-forward regulation of β-secretase expression Autor Faghihi, Mohammad Ali, Modarresi, Farzaneh, Khalil, Ahmad M, Wood, Douglas E., Sahagan, Barbara G, Morgan, Todd E, Finch, Caleb E, Laurent, Georges St., Kenny, Paul J, Wahlestedt, Claes

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Role of IgG against N-protein of SARS-CoV2 in COVID19 clinical outcomes Autor Batra, Mayank, Tian, Runxia, Zhang, Chongxu, Clarence, Emile, Sacher, Camila Sofia, Miranda, Justin Nestor, De La Fuente, Justin Rafa O., Mathew, Megan, Green, Desmond, Patel, Sayari, Bastidas, Maria Virginia Perez, Haddadi, Sara, Murthi, Mukunthan, Gonzalez, Miguel Santiago, Kambali, Shweta, Santos, Kayo H. M., Asif, Huda, Modarresi, Farzaneh, Faghihi, Mohammad, Mirsaeidi, Mehdi

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia Autor Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt, Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia Autor Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt C., Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Tournev, Ivailo, Chamova, Teodora, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali

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