Mole SE - Search Results

1

Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes.

Mitchison HM, O'Rawe AM, Taschner PE, Sandkuijl LA, Santavuori P, de Vos N, Breuning MH, Mole SE, Gardiner RM, Järvelä IE. Mitchison HM, et al. Among authors: mole se. Am J Hum Genet. 1995 Mar;56(3):654-62. Am J Hum Genet. 1995. PMID: 7887419 Free PMC article.

2

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: mole se. Am J Med Genet. 1995 Jun 5;57(2):316-9. doi: 10.1002/ajmg.1320570242. Am J Med Genet. 1995. PMID: 7668354

3

Analysis of Batten disease candidate genes STP and STM.

Munroe PB, Mitchison HM, Dooley TP, Gardiner RM, Mole SE. Munroe PB, et al. Among authors: mole se. Am J Med Genet. 1995 Jun 5;57(2):324-6. doi: 10.1002/ajmg.1320570244. Am J Med Genet. 1995. PMID: 7668356

4

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

5

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. Among authors: mole se. Am J Hum Genet. 1995 Mar;56(3):663-8. Am J Hum Genet. 1995. PMID: 7887420 Free PMC article.

6

Prenatal diagnosis of Batten's disease.

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

7

Recent advances in the molecular genetics of the neuronal ceroid lipofuscinoses.

Mole SE. Mole SE. J Inherit Metab Dis. 1996;19(3):269-74. doi: 10.1007/BF01799253. J Inherit Metab Dis. 1996. PMID: 8803767

8

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. Among authors: mole se. 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.

9

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. Among authors: mole se. 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.

10

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

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