Distribution of an Invasive Aquatic Pathogen (Viral Hemorrhagic Septicemia Virus) in the Great Lakes and Its Relationship to Shipping

por Bain, Mark B., Cornwell, Emily R., Hope, Kristine M., Eckerlin, Geofrey E., Casey, Rufina N., Groocock, Geoffrey H., Getchell, Rodman G., Bowser, Paul R., Winton, James R., Batts, William N., Cangelosi, Allegra, Casey, James W.
Publicado 2010

Economic Evaluation Design within the HEAL Prevention Cooperative

por Dunlap, Laura J., Kuklinski, Margaret R., Cowell, Alexander, McCollister, Kathryn E., Bowser, Diana M., Campbell, Mark, Fernandes, Claudia-Santi F., Kemburu, Pranav, Livingston, Bethany J., Prosser, Lisa A., Rao, Vinod, Smart, Rosanna, Yilmazer, Tansel
Publicado 2022

Blood-spinal cord barrier leakage is independent of motor neuron pathology in ALS

por Waters, Sarah, Swanson, Molly E. V., Dieriks, Birger V., Zhang, Yibin B., Grimsey, Natasha L., Murray, Helen C., Turner, Clinton, Waldvogel, Henry J., Faull, Richard L. M., An, Jiyan, Bowser, Robert, Curtis, Maurice A., Dragunow, Mike, Scotter, Emma
Publicado 2021

Visual and circadian regulation of Drosophila BDBT and BDBT effects on DBT and PER localization

por Nolan, Richard Brent, Bontrager, Colleen, Bowser, Abigail, Corley, Alyssa, Fiedler, Hana, Flathers, Connor, Francis, Lauren, Le, Angel, Mahmoudjafari, Seyyed, Nim, Tinh, Muolo, Connor E., Shores, Brianna, Viermann, Christopher, Waldren, Adam, Zatezalo, Carmen, Fan, Jin-Yuan, Price, Jeffrey L.
Publicado 2023

Glycolysis upregulation is neuroprotective as a compensatory mechanism in ALS

por Manzo, Ernesto, Lorenzini, Ileana, Barrameda, Dianne, O'Conner, Abigail G, Barrows, Jordan M, Starr, Alexander, Kovalik, Tina, Rabichow, Benjamin E, Lehmkuhl, Erik M, Shreiner, Dakotah D, Joardar, Archi, Liévens, Jean-Charles, Bowser, Robert, Sattler, Rita, Zarnescu, Daniela C
Publicado 2019

Longitudinal biomarkers in amyotrophic lateral sclerosis

por Huang, Fen, Zhu, Yuda, Hsiao‐Nakamoto, Jennifer, Tang, Xinyan, Dugas, Jason C., Moscovitch‐Lopatin, Miriam, Glass, Jonathan D., Brown, Robert H., Ladha, Shafeeq S., Lacomis, David, Harris, Jeffrey M., Scearce‐Levie, Kimberly, Ho, Carole, Bowser, Robert, Berry, James D.
Publicado 2020

The PERSonalized Glucose Optimization Through Nutritional Intervention (PERSON) Study: Rationale, Design and Preliminary Screening Results

por Gijbels, Anouk, Trouwborst, Inez, Jardon, Kelly M., Hul, Gabby B., Siebelink, Els, Bowser, Suzanne M., Yildiz, Dilemin, Wanders, Lisa, Erdos, Balázs, Thijssen, Dick H. J., Feskens, Edith J. M., Goossens, Gijs H., Afman, Lydia A., Blaak, Ellen E.
Publicado 2021

Corrigendum: The PERSonalized Glucose Optimization Through Nutritional Intervention (PERSON) Study: Rationale, Design and Preliminary Screening Results

por Gijbels, Anouk, Trouwborst, Inez, Jardon, Kelly M., Hul, Gabby B., Siebelink, Els, Bowser, Suzanne M., Yildiz, Dilemin, Wanders, Lisa, Erdos, Balázs, Thijssen, Dick H. J., Feskens, Edith J. M., Goossens, Gijs H., Afman, Lydia A., Blaak, Ellen E.
Publicado 2022

Bringing Value-Based Perspectives to Care: Including Patient and Family Members in Decision-Making Processes

por Kohler, Graeme, Sampalli, Tara, Ryer, Ashley, Porter, Judy, Wood, Les, Bedford, Lisa, Higgins-Bowser, Irene, Edwards, Lynn, Christian, Erin, Dunn, Susan, Gibson, Rick, Ryan Carson, Shannon, Vallis, Michael, Zed, Joanna, Tugwell, Barna, Van Zoost, Colin, Canfield, Carolyn, Rivoire, Eleanor
Publicado 2017

Aged G Protein-Coupled Receptor Kinase 3 (Grk3)-Deficient Mice Exhibit Enhanced Osteoclastogenesis and Develop Bone Lesions Analogous to Human Paget’s Disease of Bone

por Rabjohns, Emily M., Rampersad, Rishi R., Ghosh, Arin, Hurst, Katlyn, Eudy, Amanda M., Brozowski, Jaime M., Lee, Hyun Ho, Ren, Yinshi, Mirando, Anthony, Gladman, Justin, Bowser, Jessica L., Berg, Kathryn, Wani, Sachin, Ralston, Stuart H., Hilton, Matthew J., Tarrant, Teresa K.
Publicado 2023

TDP-43 proteinopathy alters the ribosome association of multiple mRNAs including the glypican Dally-like protein (Dlp)/GPC6

por Lehmkuhl, Erik M., Loganathan, Suvithanandhini, Alsop, Eric, Blythe, Alexander D., Kovalik, Tina, Mortimore, Nicholas P., Barrameda, Dianne, Kueth, Chuol, Eck, Randall J., Siddegowda, Bhavani B., Joardar, Archi, Ball, Hannah, Macias, Maria E., Bowser, Robert, Van Keuren-Jensen, Kendall, Zarnescu, Daniela C.
Publicado 2021

WiTNNess: An international natural history study of infantile‐onset TNNT1 myopathy

por Strauss, Kevin A., Carson, Vincent J., Bolettieri, Emilienne, Everett, Mariah, Bollinger, Ashton, Bowser, Lauren E., Beiler, Keturah, Young, Millie, Edvardson, Simon, Fraenkel, Nitay, D'Amico, Adele, Bertini, Enrico, Lingappa, Lokesh, Chowdhury, Devyani, Lowes, Linda P., Iammarino, Megan, Alfano, Lindsay N., Brigatti, Karlla W.
Publicado 2023

A model for rigorously applying the Exploration, Preparation, Implementation, Sustainment (EPIS) framework in the design and measurement of a large scale collaborative multi-site s...

por Becan, Jennifer E., Bartkowski, John P., Knight, Danica K., Wiley, Tisha R. A., DiClemente, Ralph, Ducharme, Lori, Welsh, Wayne N., Bowser, Diana, McCollister, Kathryn, Hiller, Matthew, Spaulding, Anne C., Flynn, Patrick M., Swartzendruber, Andrea, Dickson, Megan F., Fisher, Jacqueline Horan, Aarons, Gregory A.
Publicado 2018

Poly(GR) and poly(GA) in cerebrospinal fluid as potential biomarkers for C9ORF72-ALS/FTD

por Krishnan, Gopinath, Raitcheva, Denitza, Bartlett, Daniel, Prudencio, Mercedes, McKenna-Yasek, Diane M., Douthwright, Catherine, Oskarsson, Björn E., Ladha, Shafeeq, King, Oliver D., Barmada, Sami J., Miller, Timothy M., Bowser, Robert, Watts, Jonathan K., Petrucelli, Leonard, Brown, Robert H., Kankel, Mark W., Gao, Fen-Biao
Publicado 2022

CRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individual

por Yun, Yeomin, Hong, Sung-Ah, Kim, Ka-Kyung, Baek, Daye, Lee, Dongsu, Londhe, Ashwini M., Lee, Minhyung, Yu, Jihyeon, McEachin, Zachary T., Bassell, Gary J., Bowser, Robert, Hales, Chadwick M., Cho, Sung-Rae, Kim, Janghwan, Pae, Ae Nim, Cheong, Eunji, Kim, Sangwoo, Boulis, Nicholas M., Bae, Sangsu, Ha, Yoon
Publicado 2020

The M1311V variant of ATP7A is associated with impaired trafficking and copper homeostasis in models of motor neuron disease

por Bakkar, Nadine, Starr, Alexander, Rabichow, Benjamin E., Lorenzini, Ileana, McEachin, Zachary T., Kraft, Robert, Chaung, Matthew, Macklin-Isquierdo, Sam, Wingfield, Taylor, Carhart, Briggs, Zahler, Nathan, Chang, Wen-Hsuan, Bassell, Gary J., Betourne, Alexandre, Boulis, Nicholas, Alworth, Samuel V., Ichida, Justin K., August, Paul R., Zarnescu, Daniela C., Sattler, Rita, Bowser, Robert
Publicado 2021

ADAM8 signaling drives neutrophil migration and ARDS severity

por Conrad, Catharina, Yildiz, Daniela, Cleary, Simon J., Margraf, Andreas, Cook, Lena, Schlomann, Uwe, Panaretou, Barry, Bowser, Jessica L., Karmouty-Quintana, Harry, Li, Jiwen, Berg, Nathaniel K., Martin, Samuel C., Aljohmani, Ahmad, Moussavi-Harami, S. Farshid, Wang, Kristin M., Tian, Jennifer J., Magnen, Mélia, Valet, Colin, Qiu, Longhui, Singer, Jonathan P., Eltzschig, Holger K., Bertrams, Wilhelm, Herold, Susanne, Suttorp, Norbert, Schmeck, Bernd, Ball, Zachary T., Zarbock, Alexander, Looney, Mark R., Bartsch, Jörg W.
Publicado 2022

Moderate intrinsic phenotypic alterations in C9orf72 ALS/FTD iPSC-microglia despite the presence of C9orf72 pathological features

por Lorenzini, Ileana, Alsop, Eric, Levy, Jennifer, Gittings, Lauren M., Lall, Deepti, Rabichow, Benjamin E., Moore, Stephen, Pevey, Ryan, Bustos, Lynette M., Burciu, Camelia, Bhatia, Divya, Singer, Mo, Saul, Justin, McQuade, Amanda, Tzioras, Makis, Mota, Thomas A., Logemann, Amber, Rose, Jamie, Almeida, Sandra, Gao, Fen-Biao, Marks, Michael, Donnelly, Christopher J., Hutchins, Elizabeth, Hung, Shu-Ting, Ichida, Justin, Bowser, Robert, Spires-Jones, Tara, Blurton-Jones, Mathew, Gendron, Tania F., Baloh, Robert H., Van Keuren-Jensen, Kendall, Sattler, Rita
Publicado 2023

CBOL Protist Working Group: Barcoding Eukaryotic Richness beyond the Animal, Plant, and Fungal Kingdoms

por Pawlowski, Jan, Audic, Stéphane, Adl, Sina, Bass, David, Belbahri, Lassaâd, Berney, Cédric, Bowser, Samuel S., Cepicka, Ivan, Decelle, Johan, Dunthorn, Micah, Fiore-Donno, Anna Maria, Gile, Gillian H., Holzmann, Maria, Jahn, Regine, Jirků, Miloslav, Keeling, Patrick J., Kostka, Martin, Kudryavtsev, Alexander, Lara, Enrique, Lukeš, Julius, Mann, David G., Mitchell, Edward A. D., Nitsche, Frank, Romeralo, Maria, Saunders, Gary W., Simpson, Alastair G. B., Smirnov, Alexey V., Spouge, John L., Stern, Rowena F., Stoeck, Thorsten, Zimmermann, Jonas, Schindel, David, de Vargas, Colomban
Publicado 2012

Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers

por Finch, NiCole A., Wang, Xue, Baker, Matthew C., Heckman, Michael G., Gendron, Tania F., Bieniek, Kevin F., Wuu, Joanne, DeJesus-Hernandez, Mariely, Brown, Patricia H., Chew, Jeannie, Jansen-West, Karen R., Daughrity, Lillian M., Nicholson, Alexandra M., Murray, Melissa E., Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Petrucelli, Leonard, Boeve, Bradley F., Graff-Radford, Neill R., Asmann, Yan W., Dickson, Dennis W., Benatar, Michael, Bowser, Robert, Boylan, Kevin B., Rademakers, Rosa, van Blitterswijk, Marka
Publicado 2017