Expression of apoptosis inhibitor protein Mcl1 linked to neuroprotection in CNS neurons von Mori, M, Burgess, D L, Gefrides, L A, Foreman, P J, Opferman, J T, Korsmeyer, S J, Cavalheiro, E A, Naffah-Mazzacoratti, Md G, Noebels, J L

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Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10 von Ashizawa, Tetsuo, Matsuura, Tohru, Yamagata, Takanori, Burgess, Daniel L, Rasmussen, Astrid, Grewal, Raji P, Watase, Kei, Khajavi, Mehrdad, McCall, Alanna E, Davis, Caleb F, Zu, Lan, Achari, Madhureeta, Pulst, Stefan M, Alonso, Elisa, Noebels, Jeffrey L, Nelson, David L, Zoghbi, Huda Y

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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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Calcium Channel Defects in Models of Inherited Generalized Epilepsy von Burgess, Daniel L., Noebels, Jeffrey L.

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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse von Burgess, D L, Jones, J M, Meisler, M H, Noebels, J L

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Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions von Meisler, Miriam H, Plummer, Nicholas W, Burgess, Daniel L, Buchner, David A, Sprunger, Leslie K

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Genetic Localization of the Ca2+ Channel Gene CACNG2 Near SCA10 on Chromosome 22q13 von Burgess, Daniel L., Matsuura, Tohru, Ashizawa, Tetsuo, Noebels, Jeffrey L.

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Insertional Mutation on Mouse Chromosome 18 With Vestibular and Craniofacial Abnormalities von Ting, C. N, Kohrman, D, Burgess, D. L, Boyle, A, Altschuler, R. A, Gholizadeh, G, Samuelson, L. C, Jang, W, Meisler, M. H

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Voltage-Dependent Calcium Channel Mutations in Neurological Disease von BURGESS, DANIEL L., NOEBELS, JEFFREY L.

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Listen Carefully: Positional Cloning of an Audiogenic Seizure Mutation May Yield Frings Benefits von Burgess, Daniel L.

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β Subunit Reshuffling Modifies N- and P/Q-Type Ca2+Channel Subunit Compositions in Lethargic Mouse Brain von Burgess, Daniel L., Biddlecome, Gloria H., McDonough, Stefan I., Diaz, Maria E., Zilinski, Carolyn A., Bean, Bruce P., Campbell, Kevin P., Noebels, Jeffrey L.

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Isolation of DNA markers from a region between incontinentia pigmenti 1 (IP1) X-chromosomal translocation breakpoints by a comparative PCR analysis of a radiation hybrid subclone m... von Gorski, Jerome L., Burright, Eric N., Reyner, Eric L., Goodfellow, Peter N., Burgess, Daniel L.

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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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Identification of Three Novel Ca 2+ Channel γ Subunit Genes Reveals Molecular Diversification by Tandem and Chromosome Duplication von Burgess, Daniel L., Davis, Caleb F., Gefrides, Lisa A., Noebels, Jeffrey L.

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A Cluster of Three Novel Ca Channel gamma Subunit Genes on Chromosome 19q13.4: Evolution and Expression Profile of the gamma Subunit Gene Family von Burgess, D L, Gefrides, LA, eman, P J, Noebels, J L

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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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Neonatal Epilepsy Syndromes and GEFS+: Mechanistic Considerations von Burgess, Daniel L.

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Nature in the development of epilepsy von NOEBELS, J. L, BURGESS, D. L, QIAN, J

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Risk of late-preterm stillbirth and neonatal morbidity for monochorionic and dichorionic twins von Burgess, Jennifer L., MD, Unal, Elizabeth R., MD, MSCR, Nietert, Paul J., PhD, Newman, Roger B., MD

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Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication von Burgess, D L, Davis, C F, Gefrides, L A, Noebels, J L

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