Eyre HJ - Search Results

1

Mapping of the trichohyalin gene: co-localization with the profilaggrin, involucrin, and loricrin genes.

Fietz MJ, Rogers GE, Eyre HJ, Baker E, Callen DF, Sutherland GR. Fietz MJ, et al. Among authors: eyre hj. J Invest Dermatol. 1992 Nov;99(5):542-4. doi: 10.1111/1523-1747.ep12667301. J Invest Dermatol. 1992. PMID: 1431214 Free article.

2

Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.

Kremmidiotis G, Baker E, Crawford J, Eyre HJ, Nahmias J, Callen DF. Kremmidiotis G, et al. Among authors: eyre hj. Genomics. 1998 May 1;49(3):467-71. doi: 10.1006/geno.1998.5281. Genomics. 1998. PMID: 9615235

3

An expanded mouse-human hybrid cell panel for mapping human chromosome 16.

Callen DF, Baker E, Eyre HJ, Lane SA. Callen DF, et al. Among authors: eyre hj. Ann Genet. 1990;33(4):190-5. Ann Genet. 1990. PMID: 2095701

4

Chromosomal localization of the human alpha-L-iduronidase gene (IDUA) to 4p16.3.

Scott HS, Ashton LJ, Eyre HJ, Baker E, Brooks DA, Callen DF, Sutherland GR, Morris CP, Hopwood JJ. Scott HS, et al. Among authors: eyre hj. Am J Hum Genet. 1990 Nov;47(5):802-7. Am J Hum Genet. 1990. PMID: 2220820 Free PMC article.

5

A new DNA marker tightly linked to the fragile X locus (FRAXA).

Suthers GK, Callen DF, Hyland VJ, Kozman HM, Baker E, Eyre H, Harper PS, Roberts SH, Hors-Cayla MC, Davies KE, et al. Suthers GK, et al. Science. 1989 Dec 8;246(4935):1298-300. doi: 10.1126/science.2573953. Science. 1989. PMID: 2573953

6

Assignment of the human skeletal muscle alpha-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization.

Eyre H, Akkari PA, Wilton SD, Callen DC, Baker E, Laing NG. Eyre H, et al. Cytogenet Cell Genet. 1995;69(1-2):15-7. doi: 10.1159/000133928. Cytogenet Cell Genet. 1995. PMID: 7835079

7

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.

Nancarrow JK, Kremer E, Holman K, Eyre H, Doggett NA, Le Paslier D, Callen DF, Sutherland GR, Richards RI. Nancarrow JK, et al. Science. 1994 Jun 24;264(5167):1938-41. doi: 10.1126/science.8009225. Science. 1994. PMID: 8009225

8

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.

Callen DF, Eyre H, Lane S, Shen Y, Hansmann I, Spinner N, Zackai E, McDonald-McGinn D, Schuffenhauer S, Wauters J, et al. Callen DF, et al. J Med Genet. 1993 Oct;30(10):828-32. doi: 10.1136/jmg.30.10.828. J Med Genet. 1993. PMID: 8230159 Free PMC article.

9

Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer.

Whitmore SA, Crawford J, Apostolou S, Eyre H, Baker E, Lower KM, Settasatian C, Goldup S, Seshadri R, Gibson RA, Mathew CG, Cleton-Jansen AM, Savoia A, Pronk JC, Auerbach AD, Doggett NA, Sutherland GR, Callen DF. Whitmore SA, et al. Genomics. 1998 May 15;50(1):1-8. doi: 10.1006/geno.1998.5316. Genomics. 1998. PMID: 9628816

10

ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, and is shown to be expressed in primitive hematopoietic precursors.

Kuss BJ, O'Neill GM, Eyre H, Doggett NA, Callen DF, Davey RA. Kuss BJ, et al. Genomics. 1998 Aug 1;51(3):455-8. doi: 10.1006/geno.1998.5349. Genomics. 1998. PMID: 9721217

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