Doggett NA - Search Results

1

Mapping of two phenol sulphotransferase genes, STP and STM, to 16p: candidate genes for Batten disease.

Dooley TP, Mitchison HM, Munroe PB, Probst P, Neal M, Siciliano MJ, Deng Z, Doggett NA, Callen DF, Gardiner RM, et al. Dooley TP, et al. Among authors: doggett na. Biochem Biophys Res Commun. 1994 Nov 30;205(1):482-9. doi: 10.1006/bbrc.1994.2691. Biochem Biophys Res Commun. 1994. PMID: 7999068

2

Phenol sulfotransferases: candidate genes for Batten disease.

Dooley TP, Probst P, Obermoeller RD, Siciliano MJ, Doggett NA, Callen DF, Mitchison HM, Mole SE. Dooley TP, et al. Among authors: doggett na. Am J Med Genet. 1995 Jun 5;57(2):327-32. doi: 10.1002/ajmg.1320570245. Am J Med Genet. 1995. PMID: 7668357 Review.

3

Genomic organization and DNA sequence of the human catecholamine-sulfating phenol sulfotransferase gene (STM).

Dooley TP, Probst P, Munroe PB, Mole SE, Liu Z, Doggett NA. Dooley TP, et al. Among authors: doggett na. Biochem Biophys Res Commun. 1994 Dec 15;205(2):1325-32. doi: 10.1006/bbrc.1994.2810. Biochem Biophys Res Commun. 1994. PMID: 7802665

4

Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease).

Taschner PE, de Vos N, Thompson AD, Callen DF, Doggett N, Mole SE, Dooley TP, Barth PG, Breuning MH. Taschner PE, et al. Am J Hum Genet. 1995 Mar;56(3):663-8. Am J Hum Genet. 1995. PMID: 7887420 Free PMC article.

5

Physical map of the region containing the gene for Batten disease (CLN3).

Järvelä IE, Mitchison HM, Callen DF, Lerner TJ, Doggett NA, Taschner PE, Gardiner RM, Mole SE. Järvelä IE, et al. Among authors: doggett na. Am J Med Genet. 1995 Jun 5;57(2):316-9. doi: 10.1002/ajmg.1320570242. Am J Med Genet. 1995. PMID: 7668354

6

Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci.

Mitchison HM, Thompson AD, Mulley JC, Kozman HM, Richards RI, Callen DF, Stallings RL, Doggett NA, Attwood J, McKay TR, et al. Mitchison HM, et al. Among authors: doggett na. Genomics. 1993 May;16(2):455-60. doi: 10.1006/geno.1993.1210. Genomics. 1993. PMID: 8314582

7

Refined physical mapping of chromosome 16-specific low-abundance repetitive DNA sequences.

Stallings RL, Whitmore SA, Doggett NA, Callen DF. Stallings RL, et al. Among authors: doggett na. Cytogenet Cell Genet. 1993;63(2):97-101. doi: 10.1159/000133509. Cytogenet Cell Genet. 1993. PMID: 8467715

8

Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3.

Mitchison HM, Munroe PB, O'Rawe AM, Taschner PE, de Vos N, Kremmidiotis G, Lensink I, Munk AC, D'Arigo KL, Anderson JW, Lerner TJ, Moyzis RK, Callen DF, Breuning MH, Doggett NA, Gardiner RM, Mole SE. Mitchison HM, et al. Among authors: doggett na. Genomics. 1997 Mar 1;40(2):346-50. doi: 10.1006/geno.1996.4576. Genomics. 1997. PMID: 9119403

9

Report and abstracts of the third international workshop on human chromosome 16 mapping 1994. Pittsburgh, Pennsylvania, May 7-9, 1994.

Doggett NA, Callen DF. Doggett NA, et al. Cytogenet Cell Genet. 1995;68(3-4):165-84. doi: 10.1159/000133909. Cytogenet Cell Genet. 1995. PMID: 7842732 No abstract available.

10

Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein.

Mitchison HM, Taschner PE, Kremmidiotis G, Callen DF, Doggett NA, Lerner TJ, Janes RB, Wallace BA, Munroe PB, O'Rawe AM, Gardiner RM, Mole SE. Mitchison HM, et al. Among authors: doggett na. Neuropediatrics. 1997 Feb;28(1):12-4. doi: 10.1055/s-2007-973656. Neuropediatrics. 1997. PMID: 9151311

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