Age-related changes in auditory nerve–inner hair cell connections, hair cell numbers, auditory brain stem response and gap detection in UM-HET4 mice von Altschuler, R.A, Dolan, D.F, Halsey, K, Kanicki, A, Deng, N, Martin, C, Eberle, J, Kohrman, D.C, Miller, R.A, Schacht, J

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Rapamycin but not acarbose decreases age-related loss of outer hair cells in the mouse Cochlea von Altschuler, R.A., Kanicki, A., Martin, C., Kohrman, D.C., Miller, R.A.

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Gene therapy for deafness von Kohrman, D C, Raphael, Y

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Mutation of a new sodium channel gene, Scn8a , in the mouse mutant 'motor endplate disease' von Burgess, Daniel L, Kohrman, David C, Galt, James, Plummer, Nicholas W, Jones, Julie M, Spear, Brett, Meisler, Miriam H

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Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A von PLUMMER, N. W, GALT, J, JONES, J. M, BURGESS, D. L, SPRUNGER, L. K, KOHRMAN, D. C, MEISLER, M. H

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Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus von Naz, Sadaf, Giguere, Chantal M., Kohrman, David C., Mitchem, Kristina L., Riazuddin, Saima, Morell, Robert J., Ramesh, Arabandi, Srisailpathy, Srikumari, Deshmukh, Dilip, Riazuddin, Sheikh, Griffith, Andrew J., Friedman, Thomas B., Smith, Richard J.H., Wilcox, Edward R.

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Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6 von Mitchem, Kristina L., Hibbard, Ellen, Beyer, Lisa A., Bosom, Ken, Dootz, Gary A., Dolan, David F., Johnson, Kenneth R., Raphael, Yehoash, Kohrman, David C.

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Simian virus 40 large T antigen stably complexes with a 185-kilodalton host protein von KOHRMAN, DC, IMPERIALE, MJ

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A Missense Mutation in the Sodium Channel Scn8a Is Responsible for Cerebellar Ataxia in the Mouse Mutant jolting von Kohrman, David C, Smith, Marianne R, Goldin, Alan L, Harris, John, Meisler, Miriam H

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Location of the 9257 and ataxia mutations on mouse chromosome 18 von Griffith, A J, Radice, G L, Burgess, D L, Kohrman, D C, Hansen, G M, Justice, M J, Johnson, K R, Davisson, M T, Meisler, M H

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Insertional mutation of the motor endplate disease ( med) locus on mouse chromosome 15 von Kohrman, David C., Plummer, Nicholas W., Schuster, Timothy, Jones, Julie M., Jang, Wonhee, Burgess, Daniel L., Galt, James, Spear, Brett T., Meisler, Miriam H.

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An SV40 transformation revertant due to a host mutation: Isolation and complementation analysis von Silverstein, Gary H., Kohrman, David C., Christensen, Joan B., Brockman, William W., Imperiale, Michael J.

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Localization of the Homolog of a Mouse Craniofacial Mutant to Human Chromosome 18q11 and Evaluation of Linkage to Human CLP and CPO von Griffith, Andrew J., Burgess, Daniel L., Kohrman, David C., Yu, Jennifer, Blaschak, Jillian, Blanton, Susan H., Boehnke, Michael, Hecht, Jacqueline T., Overhauser, Joan, Meisler, Miriam H.

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A novel mouse kinesin of the UNC-104/KIF1 subfamily encoded by the Kif1b gene von Gong, Tzy-Wen L., Winnicki, Robert S., Kohrman, David C., Lomax, Margaret I.

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Characterization of Two Transgene Insertional Mutations at Pirouette, a Mouse Deafness Locus von Odeh, Hana, Hagiwara, Nobuko, Skynner, Michael, Mitchem, Kristina L., Beyer, Lisa A., Allen, Nicholas D., Brilliant, Murray H., Lebart, M.C., Dolan, David F., Raphael, Yehoash, Kohrman, David C.

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Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron von Kohrman, D C, Harris, J B, Meisler, M H

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Mutation detection in the med and med super(J) alleles of the sodium channel Scn8a: Unusual splicing due to a minor class AT-AC intron von Kohrman, D C, Harris, J B, Meisler, M H

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Localization of the homolog of a mouse cranofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO von GRIFFITH, A. J, BURGESS, D. L, KOHRMAN, D. C, YU, J, BLASCHAK, J, BLANTON, S. H, BOEHNKE, M, HECHT, J. T, OVERHAUSER, J, MEISLER, M. H

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Safety and efficacy of ALD403, an antibody to calcitonin gene-related peptide, for the prevention of frequent episodic migraine: a randomised, double-blind, placebo-controlled, exp... von Dodick, David W, Prof, Goadsby, Peter J, Prof, Silberstein, Stephen D, Prof, Lipton, Richard B, Prof, Olesen, Jes, Prof, Ashina, Messoud, Prof, Wilks, Kerri, MD, Kudrow, David, MD, Kroll, Robin, MD, Kohrman, Bruce, MD, Bargar, Robert, MD, Hirman, Joe, PhD, Smith, Jeff, MD

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Cochlear Neurotrophin‐3 overexpression at mid‐life prevents age‐related inner hair cell synaptopathy and slows age‐related hearing loss von Cassinotti, Luis R., Ji, Lingchao, Borges, Beatriz C., Cass, Nathan D., Desai, Aditi S., Kohrman, David C., Liberman, M. Charles, Corfas, Gabriel

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