NS28722/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1993	1
1994	2
1995	2
1996	3
1997	4
2024	0

1

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. Am J Med Genet. 1995 Jun 5;57(2):327-32. doi: 10.1002/ajmg.1320570245. Am J Med Genet. 1995. PMID: 7668357 Review.

2

Spectrum of mutations in the Batten disease gene, CLN3.

Munroe PB, Mitchison HM, O'Rawe AM, Anderson JW, Boustany RM, Lerner TJ, Taschner PE, de Vos N, Breuning MH, Gardiner RM, Mole SE. Munroe PB, et al. Am J Hum Genet. 1997 Aug;61(2):310-6. doi: 10.1086/514846. Am J Hum Genet. 1997. PMID: 9311735 Free PMC article.

3

Prenatal diagnosis of Batten's disease.

Munroe PB, Rapola J, Mitchison HM, Mustonen A, Mole SE, Gardiner RM, Jarvela I. Munroe PB, et al. Lancet. 1996 Apr 13;347(9007):1014-5. doi: 10.1016/s0140-6736(96)90148-8. Lancet. 1996. PMID: 8606564

4

GABAA receptor subtypes: ligand binding heterogeneity demonstrated by photoaffinity labeling and autoradiography.

Bureau MH, Olsen RW. Bureau MH, et al. J Neurochem. 1993 Oct;61(4):1479-91. doi: 10.1111/j.1471-4159.1993.tb13643.x. J Neurochem. 1993. PMID: 8397295

5

Modulation of GABAA receptor binding in human brain by neuroactive steroids: species and brain regional differences.

Nguyen Q, Sapp DW, Van Ness PC, Olsen RW. Nguyen Q, et al. Synapse. 1995 Feb;19(2):77-87. doi: 10.1002/syn.890190203. Synapse. 1995. PMID: 7725245

6

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. Genomics. 1997 Mar 1;40(2):346-50. doi: 10.1006/geno.1996.4576. Genomics. 1997. PMID: 9119403

7

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. Neuropediatrics. 1997 Feb;28(1):12-4. doi: 10.1055/s-2007-973656. Neuropediatrics. 1997. PMID: 9151311

8

Rapid diagnostic test for the major mutation underlying Batten disease.

Järvelä I, Mitchison HM, Munroe PB, O'Rawe AM, Mole SE, Syvänen AC. Järvelä I, et al. J Med Genet. 1996 Dec;33(12):1041-2. doi: 10.1136/jmg.33.12.1041. J Med Genet. 1996. PMID: 9004140 Free PMC article.

9

Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic association.

Mitchison HM, Taschner PE, O'Rawe AM, de Vos N, Phillips HA, Thompson AD, Kozman HM, Haines JL, Schlumpf K, D'Arigo K, et al. Mitchison HM, et al. Genomics. 1994 Jul 15;22(2):465-8. doi: 10.1006/geno.1994.1412. Genomics. 1994. PMID: 7806237

10

A model for Batten disease protein CLN3: functional implications from homology and mutations.

Janes RW, Munroe PB, Mitchison HM, Gardiner RM, Mole SE, Wallace BA. Janes RW, et al. FEBS Lett. 1996 Dec 9;399(1-2):75-7. doi: 10.1016/s0014-5793(96)01290-2. FEBS Lett. 1996. PMID: 8980123 Free article.

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