Lutz CM - Search Results

1

Decreased (45)Ca(2)(+) uptake in P/Q-type calcium channels in homozygous lethargic (Cacnb4lh) mice is associated with increased beta3 and decreased beta4 calcium channel subunit mRNA expression.

Lin F, Barun S, Lutz CM, Wang Y, Hosford DA. Lin F, et al. Among authors: lutz cm. Brain Res Mol Brain Res. 1999 Jul 23;71(1):1-10. doi: 10.1016/s0169-328x(99)00141-2. Brain Res Mol Brain Res. 1999. PMID: 10407181

2

Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.

Miki T, Zwingman TA, Wakamori M, Lutz CM, Cook SA, Hosford DA, Herrup K, Fletcher CF, Mori Y, Frankel WN, Letts VA. Miki T, et al. Among authors: lutz cm. Neuroscience. 2008 Jul 31;155(1):31-44. doi: 10.1016/j.neuroscience.2008.05.028. Epub 2008 Jul 1. Neuroscience. 2008. PMID: 18597946 Free PMC article.

3

Absence epilepsy in tottering mutant mice is associated with calcium channel defects.

Fletcher CF, Lutz CM, O'Sullivan TN, Shaughnessy JD Jr, Hawkes R, Frankel WN, Copeland NG, Jenkins NA. Fletcher CF, et al. Among authors: lutz cm. Cell. 1996 Nov 15;87(4):607-17. doi: 10.1016/s0092-8674(00)81381-1. Cell. 1996. PMID: 8929530 Free article.

4

Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner.

Lorenzon NM, Lutz CM, Frankel WN, Beam KG. Lorenzon NM, et al. Among authors: lutz cm. J Neurosci. 1998 Jun 15;18(12):4482-9. doi: 10.1523/JNEUROSCI.18-12-04482.1998. J Neurosci. 1998. PMID: 9614225 Free PMC article.

5

Congenic strains reveal effects of the epilepsy quantitative trait locus, El2, separate from other El loci.

Frankel WN, Johnson EW, Lutz CM. Frankel WN, et al. Among authors: lutz cm. Mamm Genome. 1995 Dec;6(12):839-43. doi: 10.1007/BF00292432. Mamm Genome. 1995. PMID: 8747921

6

Neuropeptide Y receptor genes on human chromosome 4q31-q32 map to conserved linkage groups on mouse chromosomes 3 and 8.

Lutz CM, Frankel WN, Richards JE, Thompson DA. Lutz CM, et al. Genomics. 1997 May 1;41(3):498-500. doi: 10.1006/geno.1997.4698. Genomics. 1997. PMID: 9169155

7

Genetic epilepsy model derived from common inbred mouse strains.

Frankel WN, Taylor BA, Noebels JL, Lutz CM. Frankel WN, et al. Among authors: lutz cm. Genetics. 1994 Oct;138(2):481-9. doi: 10.1093/genetics/138.2.481. Genetics. 1994. PMID: 7828829 Free PMC article.

8

Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.

Cox GA, Lutz CM, Yang CL, Biemesderfer D, Bronson RT, Fu A, Aronson PS, Noebels JL, Frankel WN. Cox GA, et al. Among authors: lutz cm. Cell. 1997 Oct 3;91(1):139-48. doi: 10.1016/s0092-8674(01)80016-7. Cell. 1997. PMID: 9335342 Free article.

9

Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YY.

Lutz CM, Richards JE, Scott KL, Sinha S, Yang-Feng TL, Frankel WN, Thompson DA. Lutz CM, et al. Genomics. 1997 Dec 1;46(2):287-90. doi: 10.1006/geno.1997.5024. Genomics. 1997. PMID: 9417917 Free article.

10

Modelling and treating GRIN2A developmental and epileptic encephalopathy in mice.

Amador A, Bostick CD, Olson H, Peters J, Camp CR, Krizay D, Chen W, Han W, Tang W, Kanber A, Kim S, Teoh J, Sah M, Petri S, Paek H, Kim A, Lutz CM, Yang M, Myers SJ, Bhattacharya S, Yuan H, Goldstein DB, Poduri A, Boland MJ, Traynelis SF, Frankel WN. Amador A, et al. Among authors: lutz cm. Brain. 2020 Jul 1;143(7):2039-2057. doi: 10.1093/brain/awaa147. Brain. 2020. PMID: 32577763 Free PMC article.

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