نتائج البحث - Michael S. Hildebrand
- يعرض 1 - 20 نتائج من 61
- اذهب إلى الاصفحة التالية
-
1
Clinical aspects of hereditary hearing loss حسب Amit Kochhar, Michael S. Hildebrand, Richard J. Smith
منشور في 2007Revisão -
2
-
3
-
4
Deafness in the genomics era حسب A. Eliot Shearer, Michael S. Hildebrand, Christina M. Sloan, Richard J. Smith
منشور في 2011Revisão -
5
-
6
-
7
-
8
-
9
-
10
-
11
-
12
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing حسب A. Eliot Shearer, Adam P. DeLuca, Michael S. Hildebrand, Kyle R. Taylor, José Gurrola, Stephen W. Scherer, Todd E. Scheetz, Richard J. Smith
منشور في 2010Artigo -
13
A Mutation in the Srrm4 Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse حسب Yoko Nakano, Israt Jahan, Gregory Bonde, Xingshen Sun, Michael S. Hildebrand, John F. Engelhardt, Richard J. Smith, Robert A. Cornell, Bernd Fritzsch, Botond Bánfi
منشور في 2012Artigo -
14
Speech, Language and Non‐verbal Communication in <scp>CLN2</scp> and <scp>CLN3</scp> Batten Disease حسب 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
منشور في 2025Artigo -
15
Genetic male infertility and mutation of CATSPER ion channels حسب 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
منشور في 2010Revisão -
16
Loss of STEP61 couples disinhibition to N-methyl-d-aspartate receptor potentiation in rodent and human spinal pain processing حسب 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
منشور في 2019Artigo -
17
Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children حسب 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
منشور في 2010Artigo -
18
Advances in Molecular and Cellular Therapies for Hearing Loss حسب 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
منشور في 2008Revisão -
19
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 حسب 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
منشور في 2009Artigo -
20
Sexual dimorphism in a neuronal mechanism of spinal hyperexcitability across rodent and human models of pathological pain حسب 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
منشور في 2021Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Medicine
Genetics
Gene
Neuroscience
Mutation
Internal medicine
Epilepsy
Cell biology
Audiology
Phenotype
Psychology
Hearing loss
Psychiatry
Chemistry
Missense mutation
Pathology
Receptor
Biochemistry
Exome sequencing
Calcium
Voltage-dependent calcium channel
Disease
Epilepsy syndromes
Exome
Inner ear
NMDA receptor
T-type calcium channel
Cochlea
Computational biology