The unusual suspects: Regulation of retinal calcium channels by somatostatin

Por Hildebrand, Michael E, Snutch, Terrance P
Publicado no Channels (Austin) (2015)

Contributions of T-Type Voltage-Gated Calcium Channels to Postsynaptic Calcium Signaling within Purkinje Neurons

Por Isope, Philippe, Hildebrand, Michael E., Snutch, Terrance P.
Publicado em 2010

Solution-based targeted genomic enrichment for precious DNA samples

Por Shearer, Aiden Eliot, Hildebrand, Michael S, Smith, Richard JH
Publicado em 2012

Deafness in the Genomics Era

Por Shearer, A. Eliot, Hildebrand, Michael S., Sloan, Christina M., Smith, Richard J.H.
Publicado em 2011

Autoimmune Disease in a DFNA6/14/38 Family carrying a Novel Missense Mutation in WFS1

Por Hildebrand, Michael S., Sorensen, Jessica L., Jensen, Maren, Kimberling, William J., Smith, Richard J.H.
Publicado em 2008

Identification of sodium channel isoforms that mediate action potential firing in lamina I/II spinal cord neurons

Por Hildebrand, Michael E, Mezeyova, Janette, Smith, Paula L, Salter, Michael W, Tringham, Elizabeth, Snutch, Terrance P
Publicado em 2011

GluN2B and GluN2D NMDARs dominate synaptic responses in the adult spinal cord

Por Hildebrand, Michael E., Pitcher, Graham M., Harding, Erika K., Li, Hongbin, Beggs, Simon, Salter, Michael W.
Publicado em 2014

Synaptic Zn(2) (+) and febrile seizure susceptibility

Por Reid, Christopher A, Hildebrand, Michael S, Mullen, Saul A, Hildebrand, Joanne M, Berkovic, Samuel F, Petrou, Steven
Publicado no Br J Pharmacol (2016)

Is a microRNA‐328 binding site in PAX6 associated with Rolandic epilepsy?

Por McGlade, Amelia, Myers, Kenneth A., Berkovic, Samuel F., Scheffer, Ingrid E., Petrovski, Slavé, Hildebrand, Michael S.
Publicado no Ann Clin Transl Neurol (2017)

Survival of Partially Differentiated Mouse Embryonic Stem Cells in the Scala Media of the Guinea Pig Cochlea

Por Hildebrand, Michael S., Dahl, Hans-Henrik M., Hardman, Jennifer, Coleman, Bryony, Shepherd, Robert K., de Silva, Michelle G.
Publicado em 2005

miRNA Mutations are Not a Common Cause of Deafness

Por Hildebrand, Michael S., Witmer, P. Dane, Xu, Shunbin, Newton, Stephen S., Kahrizi, Kimia, Najmabadi, Hossein, Valle, David, Smith, Richard J.H.
Publicado em 2010

Early neuroimaging markers of FOXP2 intragenic deletion

Por Liégeois, Frédérique J., Hildebrand, Michael S., Bonthrone, Alexandra, Turner, Samantha J., Scheffer, Ingrid E., Bahlo, Melanie, Connelly, Alan, Morgan, Angela T.
Publicado no Sci Rep (2016)

KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhood

Por Myers, Kenneth A., McGlade, Amelia, Neubauer, Bernd A., Lal, Dennis, Berkovic, Samuel F., Scheffer, Ingrid E., Hildebrand, Michael S.
Publicado no PLoS One (2018)

Viral vector tropism for supporting cells in the developing murine cochlea

Por Sheffield, Abraham M., Gubbels, Samuel P., Hildebrand, Michael S., Newton, Stephen S., Chiorini, John A., Di Pasquale, Giovanni, Smith, Richard J. H.
Publicado em 2011

Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein

Por Avenarius, Matthew R., Hildebrand, Michael S., Zhang, Yuzhou, Meyer, Nicole C., Smith, Luke L.H., Kahrizi, Kimia, Najmabadi, Hossein, Smith, Richard J.H.
Publicado em 2009

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing

Por Shearer, A. Eliot, DeLuca, Adam P., Hildebrand, Michael S., Taylor, Kyle R., Gurrola, José, Scherer, Steve, Scheetz, Todd E., Smith, Richard J. H.
Publicado em 2010

Pre-capture multiplexing improves efficiency and cost-effectiveness of targeted genomic enrichment

Por Shearer, A Eliot, Hildebrand, Michael S, Ravi, Harini, Joshi, Swati, Guiffre, Angelica C, Novak, Barbara, Happe, Scott, LeProust, Emily M, Smith, Richard JH
Publicado em 2012

Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus

Por Hildebrand, Michael S., Tack, Dylan, McMordie, Sarah J., DeLuca, Adam, Hur, In Ae, Nishimura, Carla, Huygen, Patrick, Casavant, Thomas L., Smith, Richard J.H.
Publicado em 2008

A Mutation in the Srrm4 Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse

Por Nakano, Yoko, Jahan, Israt, Bonde, Gregory, Sun, Xingshen, Hildebrand, Michael S., Engelhardt, John F., Smith, Richard J. H., Cornell, Robert A., Fritzsch, Bernd, Bánfi, Botond
Publicado em 2012

Genetic male infertility and mutation of CATSPER ion channels

Por Hildebrand, Michael S, Avenarius, Matthew R, Fellous, Marc, Zhang, Yuzhou, Meyer, Nicole C, Auer, Jana, Serres, Catherine, Kahrizi, Kimia, Najmabadi, Hossein, Beckmann, Jacques S, Smith, Richard J H
Publicado em 2010