Burgess DL - Search Results

1

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. Among authors: burgess dl. Genetics. 1994 Jan;136(1):247-54. doi: 10.1093/genetics/136.1.247. Genetics. 1994. PMID: 7511123 Free PMC article.

2

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: burgess dl. Mamm Genome. 1996 Jun;7(6):417-9. doi: 10.1007/s003359900124. Mamm Genome. 1996. PMID: 8662222 Free article.

3

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: burgess dl. Genomics. 1996 Jun 15;34(3):299-303. doi: 10.1006/geno.1996.0290. Genomics. 1996. PMID: 8786128

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

6

Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20.

Ting CN, Burgess DL, Chamberlain JS, Keith TP, Falls K, Meisler MH. Ting CN, et al. Among authors: burgess dl. Genomics. 1993 Jun;16(3):698-706. doi: 10.1006/geno.1993.1250. Genomics. 1993. PMID: 8325643 Free article.

7

Dlgh1, a mouse homolog of the drosophila discs-large gene, is located on chromosome 16.

Burgess DL, Rafael JA, Meisler MH, Chamberlain JS. Burgess DL, et al. Mamm Genome. 1996 Aug;7(8):623-4. doi: 10.1007/s003359900187. Mamm Genome. 1996. PMID: 8678991 No abstract available.

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: burgess dl. Genomics. 1998 Dec 1;54(2):287-96. doi: 10.1006/geno.1998.5550. Genomics. 1998. PMID: 9828131

9

Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions.

Meisler MH, Plummer NW, Burgess DL, Buchner DA, Sprunger LK. Meisler MH, et al. Among authors: burgess dl. Genetica. 2004 Sep;122(1):37-45. doi: 10.1007/s10709-004-1441-9. Genetica. 2004. PMID: 15619959 Free article. Review.

10

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. Cell. 1997 Feb 7;88(3):385-92. doi: 10.1016/s0092-8674(00)81877-2. Cell. 1997. PMID: 9039265 Free article.

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