Zobrazeno 1 - 10
of 214
pro vyhledávání: '"Turinsky, P."'
Autor:
Henry Quach, Spencer Farrell, Ming Jia Michael Wu, Kayshani Kanagarajah, Joseph Wai-Hin Leung, Xiaoqiao Xu, Prajkta Kallurkar, Andrei L. Turinsky, Christine E. Bear, Felix Ratjen, Brian Kalish, Sidhartha Goyal, Theo J. Moraes, Amy P. Wong
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-24 (2024)
Abstract Studying human fetal lungs can inform how developmental defects and disease states alter the function of the lungs. Here, we sequenced >150,000 single cells from 19 healthy human pseudoglandular fetal lung tissues ranging between gestational
Externí odkaz:
https://doaj.org/article/a4b68a6bade64f2b97f6c7af28a41953
Autor:
Aurore Claude-Taupin, Pierre Isnard, Alessia Bagattin, Nicolas Kuperwasser, Federica Roccio, Biagina Ruscica, Nicolas Goudin, Meriem Garfa-Traoré, Alice Regnier, Lisa Turinsky, Martine Burtin, Marc Foretz, Marco Pontoglio, Etienne Morel, Benoit Viollet, Fabiola Terzi, Patrice Codogno, Nicolas Dupont
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-20 (2023)
Abstract Shear stress generated by urinary fluid flow is an important regulator of renal function. Its dysregulation is observed in various chronic and acute kidney diseases. Previously, we demonstrated that primary cilium-dependent autophagy allows
Externí odkaz:
https://doaj.org/article/e254472962f4442b9d2e6ee13c808669
Akademický článek
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Autor:
Alaina Mahalanabis, Andrei L. Turinsky, Mia Husić, Erik Christensen, Ping Luo, Alaine Naidas, Michael Brudno, Trevor Pugh, Arun K. Ramani, Parisa Shooshtari
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 20, Iss , Pp 6375-6387 (2022)
Tumors are complex biological entities that comprise cell types of different origins, with different mutational profiles and different patterns of transcriptional dysregulation. The exploration of data related to cancer biology requires careful analy
Externí odkaz:
https://doaj.org/article/ff2bc6b24902403e9edd7b45084e3ccf
Autor:
Sarah J. Goodman, Christie L. Burton, Darci T. Butcher, Michelle T. Siu, Mathieu Lemire, Eric Chater-Diehl, Andrei L. Turinsky, Michael Brudno, Noam Soreni, David Rosenberg, Kate D. Fitzgerald, Gregory L. Hanna, Evdokia Anagnostou, Paul D. Arnold, Jennifer Crosbie, Russell Schachar, Rosanna Weksberg
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-15 (2020)
Abstract Background A growing body of research has demonstrated associations between specific neurodevelopmental disorders and variation in DNA methylation (DNAm), implicating this molecular mark as a possible contributor to the molecular etiology of
Externí odkaz:
https://doaj.org/article/e2c63c023729431c9951220028dadec0
Autor:
Alexander Joachim, Felix Dewald, Isabelle Suárez, Michael Zemlin, Isabelle Lang, Regine Stutz, Anna Marthaler, Hans Martin Bosse, Nadine Lübke, Juliane Münch, Marie-Annett Bernard, Kathrin Jeltsch, Burkhard Tönshoff, Niklas Weidner, Hans-Georg Kräusslich, Lena Birzele, Johannes Hübner, Patricia Schmied, Melanie Meyer-Bühn, Gibran Horemheb-Rubio, Oliver A. Cornely, Heinz Haverkamp, Gerhard Wiesmüller, Gerd Fätkenheuer, Barbara Hero, Rolf Kaiser, Jörg Dötsch, Jan Rybniker, Zülfü C. Cosgun, Christoph Hünseler, Jana Schönenkorb, Juliane Wurm, Florian Klein, Eva Heger, Elena Knops, Saleta Sierra-Aragón, Alina Chloé Kretschmer, Rosanne Sprute, Annelene Kossow, Martin Hellmich, Kija Shah-Hosseini, Michael Weiss, Sybelle Goedicke-Fritz, Elisabeth Kaiser, Sascha Meyer, Nastasja Seiwert, Sigrun Smola, Thorsten Pfuhl, Stefan Lohse, Anna-Kathrin Schupp, Jörg Timm, Nehle Gröne, Hellen Lesmann, Renate Bredahl, Lukas Schneble, Martin Turinsky, Christian Patry, Georg F Hoffmann, Barbara Müller, Kathleen Börner, Paul Schnitzler, Anke-Mareil Heuser, Andreas Welker, Ulrich von Both, Anna Kern
Publikováno v:
EClinicalMedicine, Vol 39, Iss , Pp 101082- (2021)
Background: The extent to which children and adolescents contribute to SARS-CoV-2 transmission remains not fully understood. Novel high-capacity testing methods may provide real-time epidemiological data in educational settings helping to establish a
Externí odkaz:
https://doaj.org/article/0637ea85d3d9416fa8369cfffe01ec5c
Akademický článek
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Akademický článek
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Autor:
Eric Chater-Diehl, Resham Ejaz, Cheryl Cytrynbaum, Michelle T. Siu, Andrei Turinsky, Sanaa Choufani, Sarah J. Goodman, Omar Abdul-Rahman, Melanie Bedford, Naghmeh Dorrani, Kendra Engleman, Josue Flores-Daboub, David Genevieve, Roberto Mendoza-Londono, Wendy Meschino, Laurence Perrin, Nicole Safina, Sharron Townshend, Stephen W. Scherer, Evdokia Anagnostou, Amelie Piton, Matthew Deardorff, Michael Brudno, David Chitayat, Rosanna Weksberg
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-14 (2019)
Abstract Background Nicolaides-Baraitser syndrome (NCBRS) is a neurodevelopmental disorder caused by pathogenic sequence variants in SMARCA2 which encodes the catalytic component of the chromatin remodeling BAF complex. Pathogenic variants in genes t
Externí odkaz:
https://doaj.org/article/1e206ed1cc744139884353eb7cb8a537
Publikováno v:
Nuclear Engineering and Technology, Vol 51, Iss 4, Pp 968-976 (2019)
This paper presents a number of verification case studies for a recently developed sensitivity/uncertainty code package. The code package, ROMUSE (Reduced Order Modeling based Uncertainty/Sensitivity Estimator) is an effort to provide an analysis too
Externí odkaz:
https://doaj.org/article/496783dec8d64c84978dc8dc129f51b0