Hakutulokset - Michael S. Hildebrand
- Näytetään 1 - 20 yhteensä 60 tuloksesta
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Clinical aspects of hereditary hearing loss Tekijä Amit Kochhar, Michael S. Hildebrand, Richard J. Smith
Julkaistu 2007Revisão -
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Deafness in the genomics era Tekijä A. Eliot Shearer, Michael S. Hildebrand, Christina M. Sloan, Richard J. Smith
Julkaistu 2011Revisão -
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Genetic architecture of childhood speech disorder: a review Tekijä Angela Morgan, David J. Amor, Miya St John, Ingrid E. Scheffer, Michael S. Hildebrand
Julkaistu 2024Revisão -
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A Mutation in the Srrm4 Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse Tekijä Yoko Nakano, Israt Jahan, Gregory Bonde, Xingshen Sun, Michael S. Hildebrand, John F. Engelhardt, Richard J. Smith, Robert A. Cornell, Bernd Fritzsch, Botond Bánfi
Julkaistu 2012Artigo -
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Speech, Language and Non‐verbal Communication in <scp>CLN2</scp> and <scp>CLN3</scp> Batten Disease Tekijä Lottie D. Morison, Ineka T. Whiteman, Adam P. Vogel, Lisa Tilbrook, Michael Fahey, Ruth Braden, Joanna Bredebusch, Michael S. Hildebrand, Ingrid E. Scheffer, Angela Morgan
Julkaistu 2025Artigo -
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Genetic male infertility and mutation of CATSPER ion channels Tekijä Michael S. Hildebrand, Matthew R. Avenarius, Marc Fellous, Yuzhou Zhang, Nicole C. Meyer, Jana Auer, Catherine Serres, Kimia Kahrizi, Hossein Najmabadi, J. Beckmann, Richard J. Smith
Julkaistu 2010Revisão -
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Loss of STEP61 couples disinhibition to N-methyl-d-aspartate receptor potentiation in rodent and human spinal pain processing Tekijä Annemarie Dedek, Jian Xu, Chaya M Kandegedara, Louis‐Etienne Lorenzo, Antoine G. Godin, Yves De Koninck, Paul J. Lombroso, Eve C. Tsai, Michael E. Hildebrand
Julkaistu 2019Artigo -
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Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children Tekijä William J. Kimberling, Michael S. Hildebrand, A. Eliot Shearer, Maren Jensen, Jennifer A. Halder, Karmen M Trzupek, Edward Cohn, Richard G. Weleber, Edwin M. Stone, Richard J. Smith
Julkaistu 2010Artigo -
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Advances in Molecular and Cellular Therapies for Hearing Loss Tekijä Michael S. Hildebrand, Stephen S. Newton, Samuel P. Gubbels, Abraham M. Sheffield, Amit Kochhar, M. De Silva, Hans‐Henrik M. Dahl, Scott D. Rose, Mark A. Behlke, Richard J. Smith
Julkaistu 2008Revisão -
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Functional Coupling between mGluR1 and Ca<sub>v</sub>3.1 T-Type Calcium Channels Contributes to Parallel Fiber-Induced Fast Calcium Signaling within Purkinje Cell Dendritic Spines Tekijä Michael E. Hildebrand, Philippe Isope, Taisuke Miyazaki, Toshitaka Nakaya, Esperanza Garcı́a, Anne Feltz, Toni Schneider, Jürgen Hescheler, Masanobu Kano, Kenji Sakimura, Masahiko Watanabe, Stéphane Dieudonné, Terrance P. Snutch
Julkaistu 2009Artigo -
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Sexual dimorphism in a neuronal mechanism of spinal hyperexcitability across rodent and human models of pathological pain Tekijä Annemarie Dedek, Jian Xu, Louis‐Etienne Lorenzo, Antoine G. Godin, Chaya M Kandegedara, Geneviève Glavina, Jeffrey Landrigan, Paul J. Lombroso, Yves De Koninck, Eve C. Tsai, Michael E. Hildebrand
Julkaistu 2021Artigo
Työkalut:
Liittyvät aiheet
Biology
Medicine
Genetics
Gene
Neuroscience
Mutation
Internal medicine
Epilepsy
Cell biology
Audiology
Phenotype
Psychology
Hearing loss
Psychiatry
Chemistry
Missense mutation
Receptor
Pathology
Biochemistry
Exome sequencing
Calcium
Voltage-dependent calcium channel
Epilepsy syndromes
Exome
Inner ear
NMDA receptor
T-type calcium channel
Cochlea
Computational biology
Disease