檢索結果 - Modarresi, Farzaneh

A Novel RNA Transcript with Antiapoptotic Function Is Silenced in Fragile X Syndrome 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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... 由 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 由 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 由 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 由 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 由 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 由 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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