Noebels JL - Search Results

1

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T. Matsuura T, et al. Among authors: noebels jl. Nat Genet. 2000 Oct;26(2):191-4. doi: 10.1038/79911. Nat Genet. 2000. PMID: 11017075

2

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.

Burgess DL, Jones JM, Meisler MH, Noebels JL. Burgess DL, et al. Among authors: noebels jl. Cell. 1997 Feb 7;88(3):385-92. doi: 10.1016/s0092-8674(00)81877-2. Cell. 1997. PMID: 9039265 Free article.

3

beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain.

Burgess DL, Biddlecome GH, McDonough SI, Diaz ME, Zilinski CA, Bean BP, Campbell KP, Noebels JL. Burgess DL, et al. Among authors: noebels jl. Mol Cell Neurosci. 1999 Apr;13(4):293-311. doi: 10.1006/mcne.1999.0748. Mol Cell Neurosci. 1999. PMID: 10328888

4

Voltage-dependent calcium channel mutations in neurological disease.

Burgess DL, Noebels JL. Burgess DL, et al. Among authors: noebels jl. Ann N Y Acad Sci. 1999 Apr 30;868:199-212. doi: 10.1111/j.1749-6632.1999.tb11287.x. Ann N Y Acad Sci. 1999. PMID: 10414295 Review.

5

Single gene defects in mice: the role of voltage-dependent calcium channels in absence models.

Burgess DL, Noebels JL. Burgess DL, et al. Among authors: noebels jl. Epilepsy Res. 1999 Sep;36(2-3):111-22. doi: 10.1016/s0920-1211(99)00045-5. Epilepsy Res. 1999. PMID: 10515159 Review.

6

Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication.

Burgess DL, Davis CF, Gefrides LA, Noebels JL. Burgess DL, et al. Among authors: noebels jl. Genome Res. 1999 Dec;9(12):1204-13. doi: 10.1101/gr.9.12.1204. Genome Res. 1999. PMID: 10613843 Free PMC article.

7

Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.

Burgess DL, Matsuura T, Ashizawa T, Noebels JL. Burgess DL, et al. Among authors: noebels jl. Epilepsia. 2000 Jan;41(1):24-7. doi: 10.1111/j.1528-1157.2000.tb01500.x. Epilepsia. 2000. PMID: 10643919 Free article.

8

Calcium channel defects in models of inherited generalized epilepsy.

Burgess DL, Noebels JL. Burgess DL, et al. Among authors: noebels jl. Epilepsia. 2000 Aug;41(8):1074-5. doi: 10.1111/j.1528-1157.2000.tb00305.x. Epilepsia. 2000. PMID: 10961647 Free article. Review. No abstract available.

9

A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.4: evolution and expression profile of the gamma subunit gene family.

Burgess DL, Gefrides LA, Foreman PJ, Noebels JL. Burgess DL, et al. Among authors: noebels jl. Genomics. 2001 Feb 1;71(3):339-50. doi: 10.1006/geno.2000.6440. Genomics. 2001. PMID: 11170751

10

Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome.

Heilstedt HA, Burgess DL, Anderson AE, Chedrawi A, Tharp B, Lee O, Kashork CD, Starkey DE, Wu YQ, Noebels JL, Shaffer LG, Shapira SK. Heilstedt HA, et al. Among authors: noebels jl. Epilepsia. 2001 Sep;42(9):1103-11. doi: 10.1046/j.1528-1157.2001.08801.x. Epilepsia. 2001. PMID: 11580756 Free article.

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