Clancy KP - Search Results

1

The c-fos gene and early-onset familial Alzheimer's disease.

Bonnycastle LL, Yu CE, Wijsman EM, Orr HT, Patterson D, Clancy KP, Goddard KA, Alonso ME, Nemens E, White JA, et al. Bonnycastle LL, et al. Among authors: clancy kp. Neurosci Lett. 1993 Sep 17;160(1):33-6. doi: 10.1016/0304-3940(93)90910-d. Neurosci Lett. 1993. PMID: 8247328

2

Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2).

Bonnycastle LL, Yu CE, Hunt CR, Trask BJ, Clancy KP, Weber JL, Patterson D, Schellenberg GD. Bonnycastle LL, et al. Among authors: clancy kp. Genomics. 1994 Sep 1;23(1):85-93. doi: 10.1006/geno.1994.1462. Genomics. 1994. PMID: 7829106

3

An expression map from human chromosome 14q24.3.

Sharma V, Poorkaj P, Hisama F, Bonnycastle L, Yu CE, Massa H, Trask B, Clancy KP, Patterson D, Weissman SM, Schellenberg GD. Sharma V, et al. Among authors: clancy kp. Genomics. 1998 Jan 15;47(2):314-8. doi: 10.1006/geno.1997.5106. Genomics. 1998. PMID: 9479506 Free article.

4

Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis.

Berger R, Mezey E, Clancy KP, Harta G, Wright RM, Repine JE, Brown RH, Brownstein M, Patterson D. Berger R, et al. Among authors: clancy kp. Somat Cell Mol Genet. 1995 Mar;21(2):121-31. doi: 10.1007/BF02255787. Somat Cell Mol Genet. 1995. PMID: 7570184

5

Localization of the L-glutamine synthetase gene to chromosome 1q23.

Clancy KP, Berger R, Cox M, Bleskan J, Walton KA, Hart I, Patterson D. Clancy KP, et al. Genomics. 1996 Dec 15;38(3):418-20. doi: 10.1006/geno.1996.0645. Genomics. 1996. PMID: 8975719

6

Human steroidogenic acute regulatory protein: functional activity in COS-1 cells, tissue-specific expression, and mapping of the structural gene to 8p11.2 and a pseudogene to chromosome 13.

Sugawara T, Holt JA, Driscoll D, Strauss JF 3rd, Lin D, Miller WL, Patterson D, Clancy KP, Hart IM, Clark BJ, et al. Sugawara T, et al. Among authors: clancy kp. Proc Natl Acad Sci U S A. 1995 May 23;92(11):4778-82. doi: 10.1073/pnas.92.11.4778. Proc Natl Acad Sci U S A. 1995. PMID: 7761400 Free PMC article.

7

Criteria for gene identification and features of genome organization: analysis of 6.5 Mb of DNA sequence from human chromosome 21.

Slavov D, Hattori M, Sakaki Y, Rosenthal A, Shimizu N, Minoshima S, Kudoh J, Yaspo ML, Ramser J, Reinhardt R, Reimer C, Clancy K, Rynditch A, Gardiner K. Slavov D, et al. Gene. 2000 Apr 18;247(1-2):215-32. doi: 10.1016/s0378-1119(00)00089-5. Gene. 2000. PMID: 10773462

8

A new locus for autosomal dominant cataract on chromosome 12q13.

Bateman JB, Johannes M, Flodman P, Geyer DD, Clancy KP, Heinzmann C, Kojis T, Berry R, Sparkes RS, Spence MA. Bateman JB, et al. Among authors: clancy kp. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2665-70. Invest Ophthalmol Vis Sci. 2000. PMID: 10937580

9

Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.

Geyer DD, Spence MA, Johannes M, Flodman P, Clancy KP, Berry R, Sparkes RS, Jonsen MD, Isenberg SJ, Bateman JB. Geyer DD, et al. Among authors: clancy kp. Am J Ophthalmol. 2006 Apr;141(4):761-3. doi: 10.1016/j.ajo.2005.11.008. Am J Ophthalmol. 2006. PMID: 16564824 Free PMC article.

10

Analysis of pufferfish homologues of the AT-rich human APP gene.

Villard L, Tassone F, Crnogorac-Jurcević T, Clancy K, Gardiner K. Villard L, et al. Gene. 1998 Mar 27;210(1):17-24. doi: 10.1016/s0378-1119(98)00032-8. Gene. 1998. PMID: 9599080

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