Kohrman DC - Search Results

1

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. Genomics. 1995 Mar 20;26(2):171-7. doi: 10.1016/0888-7543(95)80198-u. Genomics. 1995. PMID: 7601440

2

Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalities.

Ting CN, Kohrman D, Burgess DL, Boyle A, Altschuler RA, Gholizadeh G, Samuelson LC, Jang W, Meisler MH. Ting CN, et al. Genetics. 1994 Jan;136(1):247-54. doi: 10.1093/genetics/136.1.247. Genetics. 1994. PMID: 7511123 Free PMC article.

3

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: kohrman dc. Nat Genet. 1995 Aug;10(4):461-5. doi: 10.1038/ng0895-461. Nat Genet. 1995. PMID: 7670495

4

Location of the 9257 and ataxia mutations on mouse chromosome 18.

Griffith AJ, Radice GL, Burgess DL, Kohrman DC, Hansen GM, Justice MJ, Johnson KR, Davisson MT, Meisler MH. Griffith AJ, et al. Among authors: kohrman dc. Mamm Genome. 1996 Jun;7(6):417-9. doi: 10.1007/s003359900124. Mamm Genome. 1996. PMID: 8662222 Free article.

5

Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron.

Kohrman DC, Harris JB, Meisler MH. Kohrman DC, et al. J Biol Chem. 1996 Jul 19;271(29):17576-81. doi: 10.1074/jbc.271.29.17576. J Biol Chem. 1996. PMID: 8663325 Free article.

6

Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.

Griffith AJ, Burgess DL, Kohrman DC, Yu J, Blaschak J, Blanton SH, Boehnke M, Hecht JT, Overhauser J, Meisler MH. Griffith AJ, et al. Among authors: kohrman dc. Genomics. 1996 Jun 15;34(3):299-303. doi: 10.1006/geno.1996.0290. Genomics. 1996. PMID: 8786128

7

A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting.

Kohrman DC, Smith MR, Goldin AL, Harris J, Meisler MH. Kohrman DC, et al. J Neurosci. 1996 Oct 1;16(19):5993-9. doi: 10.1523/JNEUROSCI.16-19-05993.1996. J Neurosci. 1996. PMID: 8815882 Free PMC article.

8

Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A.

Plummer NW, Galt J, Jones JM, Burgess DL, Sprunger LK, Kohrman DC, Meisler MH. Plummer NW, et al. Among authors: kohrman dc. Genomics. 1998 Dec 1;54(2):287-96. doi: 10.1006/geno.1998.5550. Genomics. 1998. PMID: 9828131

9

Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus.

Odeh H, Hagiwara N, Skynner M, Mitchem KL, Beyer LA, Allen ND, Brilliant MH, Lebart MC, Dolan DF, Raphael Y, Kohrman DC. Odeh H, et al. Among authors: kohrman dc. Audiol Neurootol. 2004 Sep-Oct;9(5):303-14. doi: 10.1159/000080701. Epub 2004 Sep 3. Audiol Neurootol. 2004. PMID: 15347914

10

A novel mouse kinesin of the UNC-104/KIF1 subfamily encoded by the Kif1b gene.

Gong TW, Winnicki RS, Kohrman DC, Lomax MI. Gong TW, et al. Among authors: kohrman dc. Gene. 1999 Oct 18;239(1):117-27. doi: 10.1016/s0378-1119(99)00370-4. Gene. 1999. PMID: 10571041

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