Hasil Pencarian - Steven S. Scherer

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  1. 1
    Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling

    Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling oleh Sameh K. Wasseff, Steven S. Scherer

    Diterbitkan 2011-06-01
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  2. 2
    Activated immune response in an inherited leukodystrophy disease caused by the loss of oligodendrocyte gap junctions

    Activated immune response in an inherited leukodystrophy disease caused by the loss of oligodendrocyte gap junctions oleh Sameh K. Wasseff, Steven S. Scherer

    Diterbitkan 2015-10-01
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  3. 3
    Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30

    Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30 oleh Sabrina W. Yum, Junxian Zhang, Steven S. Scherer

    Diterbitkan 2010-05-01
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  4. 4
    Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom

    Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom oleh Philipp Berger, Erich E. Sirkowski, Steven S. Scherer, Ueli Suter

    Diterbitkan 2004-11-01
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  5. 5
    Diverse Trafficking Abnormalities of Connexin32 Mutants Causing CMTX

    Diverse Trafficking Abnormalities of Connexin32 Mutants Causing CMTX oleh Sabrina W. Yum, Kleopas A. Kleopa, Susan Shumas, Steven S. Scherer

    Diterbitkan 2002-10-01
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  6. 6
    Connexin32 and X-linked Charcot–Marie–Tooth Disease

    Connexin32 and X-linked Charcot–Marie–Tooth Disease oleh Linda Jo Bone, Suzanne M. Deschênes, Rita J. Balice-Gordon, Kenneth H. Fischbeck, Steven S. Scherer

    Diterbitkan 1997-01-01
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  7. 7
    Human oligodendrocytes express Cx31.3: Function and interactions with Cx32 mutants

    Human oligodendrocytes express Cx31.3: Function and interactions with Cx32 mutants oleh Irene Sargiannidou, Meejin Ahn, Alan D. Enriquez, Alejandro Peinado, Richard Reynolds, Charles Abrams, Steven S. Scherer, Kleopas A. Kleopa

    Diterbitkan 2008-05-01
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  8. 8
    A recessive Trim2 mutation causes an axonal neuropathy in mice

    A recessive Trim2 mutation causes an axonal neuropathy in mice oleh Jian J. Li, Nicolas Sarute, Eunjoo Lancaster, Guliz Otkiran-Clare, Bani Medegan Fagla, Susan R. Ross, Steven S. Scherer

    Diterbitkan 2020-07-01
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  9. 9
    The Importance of Offering Exome or Genome Sequencing in Adult Neuromuscular Clinics

    The Importance of Offering Exome or Genome Sequencing in Adult Neuromuscular Clinics oleh Laynie Dratch, Tanya M. Bardakjian, Kelsey Johnson, Nareen Babaian, Pedro Gonzalez-Alegre, Lauren Elman, Colin Quinn, Michael H. Guo, Steven S. Scherer, Defne A. Amado

    Diterbitkan 2024-02-01
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  10. 10
    Inducible knockout of Clec16a in mice results in sensory neurodegeneration

    Inducible knockout of Clec16a in mice results in sensory neurodegeneration oleh Heather S. Hain, Rahul Pandey, Marina Bakay, Bryan P. Strenkowski, Danielle Harrington, Micah Romer, William W. Motley, Jian Li, Eunjoo Lancaster, Lindsay Roth, Judith B. Grinspan, Steven S. Scherer, Hakon Hakonarson

    Diterbitkan 2021-04-01
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  11. 11
    Accelerate Clinical Trials in Charcot-Marie-Tooth Disease (ACT-CMT): A Protocol to Address Clinical Trial Readiness in CMT1A

    Accelerate Clinical Trials in Charcot-Marie-Tooth Disease (ACT-CMT): A Protocol to Address Clinical Trial Readiness in CMT1A oleh Katy Eichinger, Janet E. Sowden, Joshua Burns, Michael P. McDermott, Michael P. McDermott, Jeffrey Krischer, John Thornton, Davide Pareyson, Steven S. Scherer, Michael E. Shy, Mary M. Reilly, David N. Herrmann

    Diterbitkan 2022-06-01
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  12. 12
    Differentially expressed gene transcripts using RNA sequencing from the blood of immunosuppressed kidney allograft recipients.

    Differentially expressed gene transcripts using RNA sequencing from the blood of immunosuppressed kidney allograft recipients. oleh Casey Dorr, Baolin Wu, Weihua Guan, Amutha Muthusamy, Kinjal Sanghavi, David P Schladt, Jonathan S Maltzman, Steven E Scherer, Marcia J Brott, Arthur J Matas, Pamala A Jacobson, William S Oetting, Ajay K Israni

    Diterbitkan 2015-01-01
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  13. 13
    Deep sequencing of candidate genes identified 14 variants associated with smoking abstinence in an ethnically diverse sample

    Deep sequencing of candidate genes identified 14 variants associated with smoking abstinence in an ethnically diverse sample oleh Paul M. Cinciripini, David W. Wetter, Jian Wang, Robert Yu, George Kypriotakis, Tapsi Kumar, Jason D. Robinson, Yong Cui, Charles E. Green, Andrew W. Bergen, Thomas R. Kosten, Steven E. Scherer, Sanjay Shete

    Diterbitkan 2024-03-01
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  14. 14
    HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling

    HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling oleh Matilde Malcorps, Silvia Amor-Barris, Birute Burnyte, Ramune Vilimiene, Camila Armirola-Ricaurte, Kristina Grigalioniene, Alexandra Ekshteyn, Ausra Morkuniene, Arunas Vaitkevicius, Els De Vriendt, Jonathan Baets, Steven S. Scherer, Laima Ambrozaityte, Algirdas Utkus, Albena Jordanova, Kristien Peeters

    Diterbitkan 2022-10-01
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  15. 15
    Breast cancer chemoprevention pharmacogenomics: Deep sequencing and functional genomics of the ZNF423 and CTSO genes

    Breast cancer chemoprevention pharmacogenomics: Deep sequencing and functional genomics of the ZNF423 and CTSO genes oleh Duan Liu, Ming-Fen Ho, Daniel J. Schaid, Steven E. Scherer, Krishna Kalari, Mohan Liu, Joanna Biernacka, Vivien Yee, Jared Evans, Erin Carlson, Matthew P. Goetz, Michiaki Kubo, D. Lawrence Wickerham, Liewei Wang, James N. Ingle, Richard M. Weinshilboum

    Diterbitkan 2017-08-01
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  16. 16
    TUBB4A mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model

    TUBB4A mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model oleh Sunetra Sase, Akshata A Almad, C Alexander Boecker, Pedro Guedes-Dias, Jian J Li, Asako Takanohashi, Akshilkumar Patel, Tara McCaffrey, Heta Patel, Divya Sirdeshpande, Julian Curiel, Judy Shih-Hwa Liu, Quasar Padiath, Erika LF Holzbaur, Steven S Scherer, Adeline Vanderver

    Diterbitkan 2020-05-01
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  17. 17
    Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies

    Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies oleh Ana Caroline C. Sá, Amy Webb, Yan Gong, Caitrin W. McDonough, Mohamed H. Shahin, Somnath Datta, Taimour Y. Langaee, Stephen T. Turner, Amber L. Beitelshees, Arlene B. Chapman, Eric Boerwinkle, John G. Gums, Steven E. Scherer, Rhonda M. Cooper-DeHoff, Wolfgang Sadee, Julie A. Johnson

    Diterbitkan 2018-06-01
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  18. 18
    Whole-Organ Genomic Characterization of Mucosal Field Effects Initiating Bladder Carcinogenesis

    Whole-Organ Genomic Characterization of Mucosal Field Effects Initiating Bladder Carcinogenesis oleh Tadeusz Majewski, Hui Yao, Jolanta Bondaruk, Woonbok Chung, Sangkyou Lee, June Goo Lee, Shizhen Zhang, David Cogdell, Guoliang Yang, Woonyoung Choi, Colin Dinney, H. Barton Grossman, Christopher Logothetis, Steven E. Scherer, Charles C. Guo, Li Zhang, Peng Wei, John N. Weinstein, Jean-Pierre Issa, Keith Baggerly, David J. McConkey, Bogdan Czerniak

    Diterbitkan 2019-02-01
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  19. 19
    Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks

    Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks oleh Melanie Meister-Broekema, Rebecca Freilich, Chandhuru Jagadeesan, Jennifer N. Rauch, Rocio Bengoechea, William W. Motley, E. F. Elsiena Kuiper, Melania Minoia, Gabriel V. Furtado, Maria A. W. H. van Waarde, Shawn J. Bird, Adriana Rebelo, Stephan Zuchner, Peter Pytel, Steven S. Scherer, Federica F. Morelli, Serena Carra, Conrad C. Weihl, Steven Bergink, Jason E. Gestwicki, Harm H. Kampinga

    Diterbitkan 2018-12-01
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  20. 20
    Genomic analysis of two phlebotomine sand fly vectors of Leishmania from the New and Old World.

    Genomic analysis of two phlebotomine sand fly vectors of Leishmania from the New and Old World. oleh Frédéric Labbé, Maha Abdeladhim, Jenica Abrudan, Alejandra Saori Araki, Ricardo N Araujo, Peter Arensburger, Joshua B Benoit, Reginaldo Pecanha Brazil, Rafaela V Bruno, Gustavo Bueno da Silva Rivas, Vinicius Carvalho de Abreu, Jason Charamis, Iliano V Coutinho-Abreu, Samara G da Costa-Latgé, Alistair Darby, Viv M Dillon, Scott J Emrich, Daniela Fernandez-Medina, Nelder Figueiredo Gontijo, Catherine M Flanley, Derek Gatherer, Fernando A Genta, Sandra Gesing, Gloria I Giraldo-Calderón, Bruno Gomes, Eric Roberto Guimaraes Rocha Aguiar, James G C Hamilton, Omar Hamarsheh, Mallory Hawksworth, Jacob M Hendershot, Paul V Hickner, Jean-Luc Imler, Panagiotis Ioannidis, Emily C Jennings, Shaden Kamhawi, Charikleia Karageorgiou, Ryan C Kennedy, Andreas Krueger, José M Latorre-Estivalis, Petros Ligoxygakis, Antonio Carlos A Meireles-Filho, Patrick Minx, Jose Carlos Miranda, Michael J Montague, Ronald J Nowling, Fabiano Oliveira, João Ortigão-Farias, Marcio G Pavan, Marcos Horacio Pereira, Andre Nobrega Pitaluga, Roenick Proveti Olmo, Marcelo Ramalho-Ortigao, José M C Ribeiro, Andrew J Rosendale, Mauricio R V Sant'Anna, Steven E Scherer, Nágila F C Secundino, Douglas A Shoue, Caroline da Silva Moraes, João Silveira Moledo Gesto, Nataly Araujo Souza, Zainulabueddin Syed, Samuel Tadros, Rayane Teles-de-Freitas, Erich L Telleria, Chad Tomlinson, Yara M Traub-Csekö, João Trindade Marques, Zhijian Tu, Maria F Unger, Jesus Valenzuela, Flávia V Ferreira, Karla P V de Oliveira, Felipe M Vigoder, John Vontas, Lihui Wang, Gareth D Weedall, Elyes Zhioua, Stephen Richards, Wesley C Warren, Robert M Waterhouse, Rod J Dillon, Mary Ann McDowell

    Diterbitkan 2023-04-01
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