Meisler MH - Search Results

1

Prominent role of forebrain excitatory neurons in SCN8A encephalopathy.

Bunton-Stasyshyn RKA, Wagnon JL, Wengert ER, Barker BS, Faulkner A, Wagley PK, Bhatia K, Jones JM, Maniaci MR, Parent JM, Goodkin HP, Patel MK, Meisler MH. Bunton-Stasyshyn RKA, et al. Among authors: meisler mh. Brain. 2019 Feb 1;142(2):362-375. doi: 10.1093/brain/awy324. Brain. 2019. PMID: 30601941 Free PMC article.

2

Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7.

Jones JM, Meisler MH, Seldin MF, Lee BK, Eicher EM. Jones JM, et al. Among authors: meisler mh. Genomics. 1992 Sep;14(1):197-9. doi: 10.1016/s0888-7543(05)80308-8. Genomics. 1992. PMID: 1358794 Free article.

3

A salivary amylase transgene is efficiently expressed in liver but not in parotid gland of transgenic mice.

Jones JM, Keller SA, Samuelson LC, Osborn L, Rosenberg MP, Meisler MH. Jones JM, et al. Among authors: meisler mh. Nucleic Acids Res. 1989 Aug 25;17(16):6613-23. doi: 10.1093/nar/17.16.6613. Nucleic Acids Res. 1989. PMID: 2476716 Free PMC article.

4

Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15.

Kohrman DC, Plummer NW, Schuster T, Jones JM, Jang W, Burgess DL, Galt J, Spear BT, Meisler MH. Kohrman DC, et al. Among authors: meisler mh. Genomics. 1995 Mar 20;26(2):171-7. doi: 10.1016/0888-7543(95)80198-u. Genomics. 1995. PMID: 7601440

5

Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'.

Burgess DL, Kohrman DC, Galt J, Plummer NW, Jones JM, Spear B, Meisler MH. Burgess DL, et al. Among authors: meisler mh. Nat Genet. 1995 Aug;10(4):461-5. doi: 10.1038/ng0895-461. Nat Genet. 1995. PMID: 7670495

6

Synaptotagmin genes on mouse chromosomes 1, 7, and 10 and human chromosome 19.

Jones JM, Popma SJ, Mizuta M, Seino S, Meisler MH. Jones JM, et al. Among authors: meisler mh. Mamm Genome. 1995 Mar;6(3):212-3. doi: 10.1007/BF00293017. Mamm Genome. 1995. PMID: 7749232 Free article. No abstract available.

7

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.

Keller SA, Jones JM, Boyle A, Barrow LL, Killen PD, Green DG, Kapousta NV, Hitchcock PF, Swank RT, Meisler MH. Keller SA, et al. Among authors: meisler mh. Genomics. 1994 Sep 15;23(2):309-20. doi: 10.1006/geno.1994.1506. Genomics. 1994. PMID: 7835879 Free article.

8

Conserved linkage of early growth response 4, annexin 4, and transforming growth factor alpha on mouse chromosome 6.

Barrow LL, Simin K, Jones JM, Lee DC, Meisler MH. Barrow LL, et al. Among authors: meisler mh. Genomics. 1994 Jan 15;19(2):388-90. doi: 10.1006/geno.1994.1078. Genomics. 1994. PMID: 8188273 Free article.

9

Insertional mutation of the hairless locus on mouse chromosome 14.

Jones JM, Elder JT, Simin K, Keller SA, Meisler MH. Jones JM, et al. Among authors: meisler mh. Mamm Genome. 1993 Nov;4(11):639-43. doi: 10.1007/BF00360900. Mamm Genome. 1993. PMID: 8281013 Free article.

10

mnd2: a new mouse model of inherited motor neuron disease.

Jones JM, Albin RL, Feldman EL, Simin K, Schuster TG, Dunnick WA, Collins JT, Chrisp CE, Taylor BA, Meisler MH. Jones JM, et al. Among authors: meisler mh. Genomics. 1993 Jun;16(3):669-77. doi: 10.1006/geno.1993.1246. Genomics. 1993. PMID: 8325640 Free article.

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