Bilaketaren emaitzak - Brett Collins

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  1. 1
    Empowering Adult Stem Cells for Myocardial Regeneration

    Empowering Adult Stem Cells for Myocardial Regeneration nork Sadia Mohsin, Sailay Siddiqi, Brett Collins, Mark A. Sussman

    Argitaratua 2011
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  2. 2
    Selective effects of CPAP on sleep apnoea‐associated manifestations

    Selective effects of CPAP on sleep apnoea‐associated manifestations nork Alexandros N. Vgontzas, E. Zoumakis, Edward O. Bixler, H‐M. Lin, Brett Collins, Maria Basta, S. Pejovic, George P. Chrousos

    Argitaratua 2008
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  3. 3
    Disease tolerance mediated by microbiome <i>E. coli</i> involves inflammasome and IGF-1 signaling

    Disease tolerance mediated by microbiome <i>E. coli</i> involves inflammasome and IGF-1 signaling nork Alexandria M. Palaferri Schieber, Yujung Michelle Lee, Max W. Chang, Mathias Leblanc, Brett Collins, Michael Downes, Ronald M. Evans, Janelle S. Ayres

    Argitaratua 2015
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  4. 4
    Enhancement of Myocardial Regeneration Through Genetic Engineering of Cardiac Progenitor Cells Expressing Pim-1 Kinase

    Enhancement of Myocardial Regeneration Through Genetic Engineering of Cardiac Progenitor Cells Expressing Pim-1 Kinase nork Kimberlee M. Fischer, Christopher T. Cottage, Weitao Wu, Shabana Din, Natalie Gude, Daniele Avitabile, Pearl Quijada, Brett Collins, Jenna Fransioli, Mark A. Sussman

    Argitaratua 2009
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  5. 5
    Fibronectin contributes to pathological cardiac hypertrophy but not physiological growth

    Fibronectin contributes to pathological cardiac hypertrophy but not physiological growth nork Mathias H. Konstandin, Mirko Völkers, Brett Collins, Pearl Quijada, Mercédès Quintana, Andrea De La Torre, Lucy Ormachea, Shabana Din, Natalie Gude, Haruhiro Toko, Mark A. Sussman

    Argitaratua 2013
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  6. 6
    Cardiac Progenitor Cell Cycling Stimulated by Pim-1 Kinase

    Cardiac Progenitor Cell Cycling Stimulated by Pim-1 Kinase nork Christopher T. Cottage, Brandi Bailey, Kimberlee M. Fischer, Daniele Avitabile, Brett Collins, Savilla Tuck, Pearl Quijada, Natalie Gude, Roberto Baelo Álvarez, John A. Muraski, Mark A. Sussman

    Argitaratua 2010
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  7. 7
    Fibronectin Is Essential for Reparative Cardiac Progenitor Cell Response After Myocardial Infarction

    Fibronectin Is Essential for Reparative Cardiac Progenitor Cell Response After Myocardial Infarction nork Mathias H. Konstandin, Haruhiro Toko, Grady Gastelum, Pearl Quijada, Andrea De La Torre, Mercédès Quintana, Brett Collins, Shabana Din, Daniele Avitabile, Mirko Völkers, Natalie Gude, Reinhard Fässler, Mark A. Sussman

    Argitaratua 2013
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  8. 8
    High-fat diet and FGF21 cooperatively promote aerobic thermogenesis in mtDNA mutator mice

    High-fat diet and FGF21 cooperatively promote aerobic thermogenesis in mtDNA mutator mice nork Christopher E. Wall, Jamie Whyte, Jae Myoung Suh, Weiwei Fan, Brett Collins, Christopher Liddle, Ruth T. Yu, Annette R. Atkins, Jane C. Naviaux, Kefeng Li, Andrew Bright, William A. Alaynick, Michael Downes, Robert K. Naviaux, Ronald M. Evans

    Argitaratua 2015
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  9. 9
    Metabolic Dysfunction Consistent With Premature Aging Results From Deletion of Pim Kinases

    Metabolic Dysfunction Consistent With Premature Aging Results From Deletion of Pim Kinases nork Shabana Din, Mathias H. Konstandin, Bevan Johnson, Jacqueline Emathinger, Mirko Völkers, Haruhiro Toko, Brett Collins, Lucy Ormachea, Kaitlen Samse, Dieter A. Kubli, Andrea De La Torre, Andrew S. Kraft, Åsa B. Gustafsson, Daniel P. Kelly, Mark A. Sussman

    Argitaratua 2014
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  10. 10
    Regulation of Cardiac Hypertrophic Signaling by Prolyl Isomerase Pin1

    Regulation of Cardiac Hypertrophic Signaling by Prolyl Isomerase Pin1 nork Haruhiro Toko, Mathias H. Konstandin, Shirin Doroudgar, Lucia Ormachea, Eri Joyo, Anya Joyo, Shabana Din, Natalie Gude, Brett Collins, Mirko Völkers, Donna J. Thuerauf, Christopher C. Glembotski, Chun-Hau Chen, Kun Ping Lu, Oliver J. Müller, Takafumi Uchida, Mark A. Sussman

    Argitaratua 2013
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  11. 11
    Human Cardiac Progenitor Cells Engineered With Pim-I Kinase Enhance Myocardial Repair

    Human Cardiac Progenitor Cells Engineered With Pim-I Kinase Enhance Myocardial Repair nork Sadia Mohsin, Mohsin Khan, Haruhiro Toko, Brandi Bailey, Christopher T. Cottage, Kathleen Wallach, Divya Nag, Andrew Lee, Sailay Siddiqi, Feng Lan, Kimberlee M. Fischer, Natalie Gude, Pearl Quijada, Daniele Avitabile, Silvia Truffa, Brett Collins, Walter P. Dembitsky, Joseph C. Wu, Mark A. Sussman

    Argitaratua 2012
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  12. 12
    Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease

    Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease nork Jacqueline M. Ward, Colleen A. Stoyas, Paweł M. Świtoński, Farid Ichou, Weiwei Fan, Brett Collins, Christopher E. Wall, Isaac Adanyeguh, Chenchen Niu, Bryce L. Sopher, C. Kinoshita, Richard S. Morrison, Alexandra Dürr, Alysson R. Muotri, Ronald M. Evans, Fanny Mochel, Albert R. La Spada

    Argitaratua 2019
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  13. 13
    FGF1 and insulin control lipolysis by convergent pathways

    FGF1 and insulin control lipolysis by convergent pathways nork Gencer Sancar, Sihao Liu, Emanuel Gasser, Jacqueline G. Alvarez, Christopher P. Moutos, Kyeongkyu Kim, Tim van Zutphen, Yuhao Wang, Timothy F. Huddy, Brittany N. Ross, Yang Dai, David Zepeda, Brett Collins, Emma Tilley, Matthew J. Kolar, Ruth T. Yu, Annette R. Atkins, Theo H. van Dijk, Alan Saghatelian, Johan W. Jonker, Michael Downes, Ronald M. Evans

    Argitaratua 2022
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  14. 14
    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism nork Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Lambertus Klei, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Alfredo Brusco, Brian Hon‐Yin Chung, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina Girard, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Evelise Riberi, Rebecca J. Schmidt, Moyra Smith, Claudia I.C. Souza, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, David J. Cutler, Silvia De Rubeis, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Stephan Sanders, Michael E. Talkowski

    Argitaratua 2021
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  15. 15
    Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

    Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations nork Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, Henry S. Aghanwa, Moin Ahmad Ansari, Aftab Asif, Rubina Aslam, José Luis Ayuso, Tim B. Bigdeli, Stefano Bignotti, Julio Bobes, Bekh Bradley, P.F. Buckley, Murray J. Cairns, Stanley V. Catts, Abdul Rashid Chaudhry, David Cohen, Brett Collins, Angèle Consoli, Javier Costas, Benedicto Crespo‐Facorro, Nikolaos P. Daskalakis, Michael Davidson, Kenneth L. Davis, Faith Dickerson, Imtiaz Ahmad Dogar, Elodie Drapeau, Lourdes Fañanás, Ayman H. Fanous, Warda Fatima, Mar Fatjó‐Vilas, Cheryl Filippich, Joseph I. Friedman, John F. Fullard, Penelope Georgakopoulos, Marianna Giannitelli, Ina Giegling, Melissa J. Green, Olivier Guillin, Blanca Gutiérrez, Herlina Y. Handoko, Stella Kim Hansen, Maryam Haroon, Vahram Haroutunian, Frans Henskens, Fahad Hussain, Assen Jablensky, Jamil Junejo, Brian Kelly, Shams-ud-Din Ahmad Khan, Muhammad Nasar Sayeed Khan, Anisuzzaman Khan, Hamid R. Khawaja, Bakht Khizar, Steven P. Kleopoulos, James A. Knowles, Bettina Konte, Agung Kusumawardhani, Naeemullah Leghari, Xudong Liu, Adriana Lori, Carmel M. Loughland, Khalid Mahmood, Saqib Mahmood, Dolores Malaspina, Danish J. Malik, Amy J. M. McNaughton, Patricia T. Michie, Vasiliki Michopolous, Esther Molina, María Dolores Moltó, Asim Munir, Gerard Muntané, Farooq Naeem, Derek J. Nancarrow, Amina Nasar, Tanvir Nasr, Jude U. Ohaeri, Jürg Ott, Christos Pantelis, Sathish Periyasamy, Ana González‐Pinto, Abigail Powers, Belén Ramos, Nusrat Habib Rana, Mark Hyman Rapaport, Abraham Reichenberg

    Argitaratua 2023
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  16. 16
    Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Rare coding variation provides insight into the genetic architecture and phenotypic context of autism nork Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ángel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montserrat Fernández Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt

    Argitaratua 2022
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