Cox DR - Search Results

1

Human GAP-43: its deduced amino acid sequence and chromosomal localization in mouse and human.

Kosik KS, Orecchio LD, Bruns GA, Benowitz LI, MacDonald GP, Cox DR, Neve RL. Kosik KS, et al. Among authors: cox dr. Neuron. 1988 Apr;1(2):127-32. doi: 10.1016/0896-6273(88)90196-1. Neuron. 1988. PMID: 3272162

2

Fine structure physical mapping of the region of mouse chromosome 10 homologous to human chromosome 21.

MacDonald G, Chu ML, Cox DR. MacDonald G, et al. Among authors: cox dr. Genomics. 1991 Oct;11(2):317-23. doi: 10.1016/0888-7543(91)90138-5. Genomics. 1991. PMID: 1837533

3

Recent evolution of DNA sequence homology in the pericentromeric regions of human acrocentric chromosomes.

Kurnit DM, Neve RL, Morton CC, Bruns GA, Ma NS, Cox DR, Klinger HP. Kurnit DM, et al. Among authors: cox dr. Cytogenet Cell Genet. 1984;38(2):99-105. doi: 10.1159/000132039. Cytogenet Cell Genet. 1984. PMID: 6205826

4

The mouse homolog of the human amyloid beta protein (AD-AP) gene is located on the distal end of mouse chromosome 16: further extension of the homology between human chromosome 21 and mouse chromosome 16.

Lovett M, Goldgaber D, Ashley P, Cox DR, Gajdusek DC, Epstein CJ. Lovett M, et al. Among authors: cox dr. Biochem Biophys Res Commun. 1987 Apr 29;144(2):1069-75. doi: 10.1016/s0006-291x(87)80073-6. Biochem Biophys Res Commun. 1987. PMID: 3555492

5

The development of sequence-tagged sites for human chromosome 4.

Goold RD, diSibio GL, Xu H, Lang DB, Dadgar J, Magrane GG, Dugaiczyk A, Smith KA, Cox DR, Masters SB, et al. Goold RD, et al. Among authors: cox dr. Hum Mol Genet. 1993 Aug;2(8):1271-88. doi: 10.1093/hmg/2.8.1271. Hum Mol Genet. 1993. PMID: 8401509

6

Fine mapping in 94 inbred mouse strains using a high-density haplotype resource.

Kirby A, Kang HM, Wade CM, Cotsapas C, Kostem E, Han B, Furlotte N, Kang EY, Rivas M, Bogue MA, Frazer KA, Johnson FM, Beilharz EJ, Cox DR, Eskin E, Daly MJ. Kirby A, et al. Among authors: cox dr. Genetics. 2010 Jul;185(3):1081-95. doi: 10.1534/genetics.110.115014. Epub 2010 May 3. Genetics. 2010. PMID: 20439770 Free PMC article.

7

The chromosomal location of mouse interferon alpha genes.

Lovett M, Cox DR, Yee D, Boll W, Weissmann C, Epstein CJ, Epstein LB. Lovett M, et al. Among authors: cox dr. EMBO J. 1984 Jul;3(7):1643-6. doi: 10.1002/j.1460-2075.1984.tb02023.x. EMBO J. 1984. PMID: 6745245 Free PMC article.

8

Functional effects of the mouse weaver mutation on G protein-gated inwardly rectifying K+ channels.

Slesinger PA, Patil N, Liao YJ, Jan YN, Jan LY, Cox DR. Slesinger PA, et al. Among authors: cox dr. Neuron. 1996 Feb;16(2):321-31. doi: 10.1016/s0896-6273(00)80050-1. Neuron. 1996. PMID: 8789947 Free article.

9

Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7.

O'Donnell JJ, Vannas-Sulonen K, Shows TB, Cox DR. O'Donnell JJ, et al. Among authors: cox dr. Am J Hum Genet. 1988 Dec;43(6):922-8. Am J Hum Genet. 1988. PMID: 3195589 Free PMC article.

10

Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome.

Allore R, O'Hanlon D, Price R, Neilson K, Willard HF, Cox DR, Marks A, Dunn RJ. Allore R, et al. Among authors: cox dr. Science. 1988 Mar 11;239(4845):1311-3. doi: 10.1126/science.2964086. Science. 1988. PMID: 2964086

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