Intron retention induced by microsatellite expansions as a disease biomarker von Sznajder, Łukasz J., Thomas, James D., Carrell, Ellie M., Reid, Tammy, McFarland, Karen N., Cleary, John D., Oliveira, Ruan, Nutter, Curtis A., Bhatt, Kirti, Sobczak, Krzysztof, Ashizawa, Tetsuo, Thornton, Charles A., Ranum, Laura P. W., Swanson, Maurice S.

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Autoregulation of MBNL1 function by exon 1 exclusion from MBNL1 transcript von Konieczny, Patryk, Stepniak-Konieczna, Ewa, Taylor, Katarzyna, Sznajder, Lukasz J, Sobczak, Krzysztof

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MBNL splicing activity depends on RNA binding site structural context von Taylor, Katarzyna, Sznajder, Łukasz J, Cywoniuk, Piotr, Thomas, James D, Swanson, Maurice S, Sobczak, Krzysztof

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Short antisense-locked nucleic acids (all-LNAs) correct alternative splicing abnormalities in myotonic dystrophy von Wojtkowiak-Szlachcic, Agnieszka, Taylor, Katarzyna, Stepniak-Konieczna, Ewa, Sznajder, Lukasz J, Mykowska, Agnieszka, Sroka, Joanna, Thornton, Charles A, Sobczak, Krzysztof

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Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy von Sznajder, Łukasz J, Swanson, Maurice S

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Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy von Thomas, James D, Sznajder, Łukasz J, Bardhi, Olgert, Aslam, Faaiq N, Anastasiadis, Zacharias P, Scotti, Marina M, Nishino, Ichizo, Nakamori, Masayuki, Wang, Eric T, Swanson, Maurice S

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MBNL splicing factors regulate the microtranscriptome of skeletal muscles von Piasecka, Agnieszka, Szcześniak, Michał W, Sekrecki, Michał, Kajdasz, Arkadiusz, Sznajder, Łukasz J, Baud, Anna, Sobczak, Krzysztof

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Mechanistic determinants of MBNL activity von Sznajder, Łukasz J, Michalak, Michał, Taylor, Katarzyna, Cywoniuk, Piotr, Kabza, Michał, Wojtkowiak-Szlachcic, Agnieszka, Matłoka, Magdalena, Konieczny, Patryk, Sobczak, Krzysztof

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Hybrid splicing minigene and antisense oligonucleotides as efficient tools to determine functional protein/RNA interactions von Cywoniuk, Piotr, Taylor, Katarzyna, Sznajder, Łukasz J., Sobczak, Krzysztof

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Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood von Sznajder, Łukasz J., Scotti, Marina M., Shin, Jihae, Taylor, Katarzyna, Ivankovic, Franjo, Nutter, Curtis A., Aslam, Faaiq N., Subramony, S. H., Ranum, Laura P. W., Swanson, Maurice S.

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Modulatory role of RNA helicases in MBNL-dependent alternative splicing regulation von Taylor, Katarzyna, Piasecka, Agnieszka, Kajdasz, Arkadiusz, Brzęk, Aleksandra, Polay Espinoza, Micaela, Bourgeois, Cyril F., Jankowski, Artur, Borowiak, Małgorzata, Raczyńska, Katarzyna D., Sznajder, Łukasz J., Sobczak, Krzysztof

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Chemical Correction of Pre-mRNA Splicing Defects Associated with Sequestration of Muscleblind-like 1 Protein by Expanded r(CAG)-Containing Transcripts von Kumar, Amit, Parkesh, Raman, Sznajder, Lukasz J, Childs-Disney, Jessica L, Sobczak, Krzysztof, Disney, Matthew D

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Choroid plexus mis-splicing and altered cerebrospinal fluid composition in myotonic dystrophy type 1 von Nutter, Curtis A, Kidd, Benjamin M, Carter, Helmut A, Hamel, Johanna I, Mackie, Philip M, Kumbkarni, Nayha, Davenport, Mackenzie L, Tuyn, Dana M, Gopinath, Adithya, Creigh, Peter D, Sznajder, Łukasz J, Wang, Eric T, Ranum, Laura P W, Khoshbouei, Habibeh, Day, John W, Sampson, Jacinda B, Prokop, Stefan, Swanson, Maurice S

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Northern blotting analysis of microRNAs, their precursors and RNA interference triggers von Koscianska, Edyta, Starega-Roslan, Julia, Sznajder, Lukasz J, Olejniczak, Marta, Galka-Marciniak, Paulina, Krzyzosiak, Wlodzimierz J

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Cell-type-specific dysregulation of RNA alternative splicing in short tandem repeat mouse knockin models of myotonic dystrophy von Nutter, Curtis A, Bubenik, Jodi L, Oliveira, Ruan, Ivankovic, Franjo, Sznajder, Łukasz J, Kidd, Benjamin M, Pinto, Belinda S, Otero, Brittney A, Carter, Helmut A, Vitriol, Eric A, Wang, Eric T, Swanson, Maurice S

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The sustained expression of Cas9 targeting toxic RNAs reverses disease phenotypes in mouse models of myotonic dystrophy type 1 von Batra, Ranjan, Nelles, David A., Roth, Daniela M., Krach, Florian, Nutter, Curtis A., Tadokoro, Takahiro, Thomas, James D., Sznajder, Łukasz J., Blue, Steven M., Gutierrez, Haydee L., Liu, Patrick, Aigner, Stefan, Platoshyn, Oleksandr, Miyanohara, Atsushi, Marsala, Martin, Swanson, Maurice S., Yeo, Gene W.

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C9orf72 repeat expansion creates the unstable folate-sensitive fragile site FRA9A von Mirceta, Mila, Schmidt, Monika H M, Shum, Natalie, Prasolava, Tanya K, Meikle, Bryanna, Lanni, Stella, Mohiuddin, Mohiuddin, McKeever, Paul M, Zhang, Ming, Liang, Minggao, van der Werf, Ilse, Scheers, Stefaan, Dion, Patrick A, Wang, Peixiang, Wilson, Michael D, Abell, Theresa, Philips, Elliot A, Sznajder, Łukasz J, Swanson, Maurice S, Mehkary, Mustafa, Khan, Mahreen, Yokoi, Katsuyuki, Jung, Christine, de Jong, Pieter J, Freudenreich, Catherine H, McGoldrick, Philip, Yuen, Ryan K C, Abrahão, Agessandro, Keith, Julia, Zinman, Lorne, Robertson, Janice, Rogaeva, Ekaterina, Rouleau, Guy A, Kooy, R Frank, Pearson, Christopher E

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Chemical correction of pre-mRNA splicing defects associated with sequestration of muscleblind-like 1 protein by expanded r(CAG) transcripts von Kumar, Amit, Parkesh, Raman, Sznajder, Lukasz J., Childs-Disney, Jessica, Sobczak, Krzysztof, Disney, Matthew D.

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Do we differ in terms of indications and demographics in cardiac resynchronisation recipients in Poland? Insights from the European CRT Survey II Registry von Łasocha, Damian, Sterliński, Maciej, Tajstra, Mateusz, Josiak, Krystian, Zając, Dariusz, Tłuczek, Sławomir, Sokal, Adam, Januszkiewicz, Łukasz J., Galar, Bogdan, Sznajder, Rafał, Kaźmierczak, Jarosław, Szumowski, Łukasz, Normand, Camilla, Linde, Cecilia, Dickstein, Kenneth

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