Výsledky vyhledávání - Jamie L. Marshall
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Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice Autor Jamie L. Marshall, Eric Chou, Jennifer Oh, Allan M. F. Kwok, Dean J. Burkin, Rachelle H. Crosbie‐Watson
Vydáno 2012Artigo -
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Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy–Associated Cardiomyopathy Autor Michelle S. Parvatiyar, Jamie L. Marshall, Reginald T Nguyen, Maria C. Jordan, Vanitra A Richardson, Kenneth P. Roos, Rachelle H. Crosbie‐Watson
Vydáno 2015Artigo -
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The effect of background noise and its removal on the analysis of single-cell expression data Autor Philipp Janssen, Zane Kliesmete, Beate Vieth, Xian Adiconis, Sean Simmons, Jamie L. Marshall, Cristin McCabe, Holger Heyn, Joshua Z. Levin, Wolfgang Enard, Ines Hellmann
Vydáno 2023Artigo -
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Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype Autor Natássia M. Vieira, Ingegerd Elvers, Matthew S. Alexander, Yuri B. Moreira, Alal Eran, Juliana Gomes, Jamie L. Marshall, Elinor K. Karlsson, Sérgio Verjovski-Almeida, Kerstin Lindblad‐Toh, Louis M. Kunkel, Mayana Zatz
Vydáno 2015Artigo -
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Disease-associated astrocytes in Alzheimer’s disease and aging Autor Naomi Habib, Cristin McCabe, Sedi Medina, Miri Varshavsky, Daniel Kitsberg, Raz Dvir-Szternfeld, Gilad Green, Danielle Dionne, Lan Nguyễn, Jamie L. Marshall, Fei Chen, Feng Zhang, Tommy Kaplan, Aviv Regev, Michal Schwartz
Vydáno 2020Artigo -
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Single cell census of human kidney organoids shows reproducibility and diminished off-target cells after transplantation Autor Ayshwarya Subramanian, Eriene-Heidi Sidhom, Maheswarareddy Emani, Katherine A. Vernon, Nareh Sahakian, Yiming Zhou, Maria Kost‐Alimova, Michal Slyper, Julia Waldman, Danielle Dionne, Lan Nguyễn, Astrid Weins, Jamie L. Marshall, Orit Rosenblatt-Rosen, Aviv Regev, Anna Greka
Vydáno 2019Artigo -
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MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms Autor Matthew S. Alexander, Juan Carlos Casar, Norio Motohashi, Natássia M. Vieira, Iris Eisenberg, Jamie L. Marshall, Molly Gasperini, Angela Lek, Jennifer A. Myers, Elicia Estrella, Peter B. Kang, Frederic Shapiro, Fedik Rahimov, Genri Kawahara, Jeffrey J. Widrick, Louis M. Kunkel
Vydáno 2014Artigo -
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High-resolution Slide-seqV2 spatial transcriptomics enables discovery of disease-specific cell neighborhoods and pathways Autor Jamie L. Marshall, Teia Noel, Qingbo Wang, Haiqi Chen, Evan Murray, Ayshwarya Subramanian, Katherine A. Vernon, Silvana Bazúa‐Valenti, Katie Liguori, Keith Keller, Robert R. Stickels, Breanna McBean, Rowan M. Heneghan, Astrid Weins, Evan Z. Macosko, Fei Chen, Anna Greka
Vydáno 2022Artigo -
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Landscape of X chromosome inactivation across human tissues Autor Taru Tukiainen, Alexandra‐Chloé Villani, Angela Yen, Manuel A. Rivas, Jamie L. Marshall, Rahul Satija, Matthew Aguirre, Laura D. Gauthier, Mark Fleharty, Andrew Kirby, Beryl B. Cummings, Stephane E. Castel, Konrad J. Karczewski, François Aguet, Andrea Byrnes, Tuuli Lappalainen, Aviv Regev, Kristin Ardlie, Nir Hacohen, Daniel G. MacArthur
Vydáno 2017Artigo -
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Landscape of X chromosome inactivation across human tissues Autor Taru Tukiainen, Alexandra‐Chloé Villani, Angela Yen, Manuel A. Rivas, Jamie L. Marshall, Rahul Satija, Matthew Aguirre, Laura D. Gauthier, Mark Fleharty, Andrew Kirby, Beryl B. Cummings, Stephane E. Castel, Konrad J. Karczewski, François Aguet, Andrea Byrnes, Tuuli Lappalainen, Aviv Regev, Kristin Ardlie, Nir Hacohen, Daniel G. MacArthur
Vydáno 2016Pré-impressão -
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Targeting a Braf/Mapk pathway rescues podocyte lipid peroxidation in CoQ-deficiency kidney disease Autor Eriene-Heidi Sidhom, Choah Kim, Maria Kost‐Alimova, May Theng Ting, Keith Keller, Julián Ávila-Pacheco, Andrew Watts, Katherine A. Vernon, Jamie L. Marshall, Estefanía Reyes-Bricio, Matthew Racette, Nicolas Wieder, Giulio Kleiner, Elizabeth Grinkevich, Fei Chen, Astrid Weins, Clary B. Clish, Jillian L. Shaw, Catarina M. Quinzii, Anna Greka
Vydáno 2021Artigo -
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Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function Autor Gökçen Eraslan, Eugene Drokhlyansky, Shankara Anand, Evgenij Fiškin, Ayshwarya Subramanian, Michal Slyper, Jiali Wang, Nicholas Van Wittenberghe, John M. Rouhana, Julia Waldman, Orr Ashenberg, Monkol Lek, Danielle Dionne, Thet Su Win, Michael S. Cuoco, Olena Kuksenko, Alexander M. Tsankov, Philip A. Branton, Jamie L. Marshall, Anna Greka, Gad Getz, Ayellet V. Segrè, François Aguet, Orit Rozenblatt–Rosen, Kristin Ardlie, Aviv Regev
Vydáno 2022Artigo -
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A recurrent COL6A1 pseudoexon insertion causes muscular dystrophy and is effectively targeted by splice-correction therapies Autor Véronique Bolduc, A. Reghan Foley, Herimela Solomon-Degefa, Apurva Sarathy, Sandra Donkervoort, Ying Hu, Grace S. Chen, Katherine Sizov, Matthew Nalls, Haiyan Zhou, Sara Aguti, Beryl B. Cummings, Monkol Lek, Taru Tukiainen, Jamie L. Marshall, Oded Regev, Dina Marek‐Yagel, Anna Sárközy, Russell J. Butterfield, Cristina Jou, C. Jimenez‐Mallebrera, Yan Li, Corine Gartioux, Kamel Mamchaoui, Valérie Allamand, Francesca Gualandi, Alessandra Ferlini, Eric Hanssen, Steve D. Wilton, Shireen R. Lamandé, Daniel G. MacArthur, Raimund Wagener, Francesco Muntoni, Carsten G. Bönnemann
Vydáno 2019Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Computational biology
Medicine
Gene expression
Internal medicine
Transcriptome
Bioinformatics
Cell biology
Endocrinology
Cell
Disease
Dystrophin
Muscular dystrophy
Duchenne muscular dystrophy
Kidney
Myocyte
Pathology
Phenotype
Computer science
ITGA7
Mutation
Population
Sarcolemma
Skeletal muscle
Utrophin
Environmental health
Artificial intelligence
Biochemistry