Haines JL - Search Results

1

Isolation of genes from the Batten candidate region using exon amplification. Batten Disease Consortium.

Lerner TJ, D'Arigo KL, Haines JL, Doggett NA, Taschner PE, de Vos N, Buckler AJ. Lerner TJ, et al. Among authors: haines jl. Am J Med Genet. 1995 Jun 5;57(2):320-3. doi: 10.1002/ajmg.1320570243. Am J Med Genet. 1995. PMID: 7668355

2

Genome-wide search for CLN2, the gene causing late-infantile neuronal ceroid-lipofuscinosis (LNCL).

Haines JL, Boustany RM, Worster T, Ter-Minassian M, Jondro P, Lerner TJ. Haines JL, et al. Am J Med Genet. 1995 Jun 5;57(2):344-7. doi: 10.1002/ajmg.1320570248. Am J Med Genet. 1995. PMID: 7668360

3

Microsatellite repeat polymorphism at the D16S366 locus.

Schultz EA, Callen DF, Doggett NA, Haines JL, Lerner TJ. Schultz EA, et al. Among authors: haines jl. Hum Mol Genet. 1994 Sep;3(9):1713. doi: 10.1093/hmg/3.9.1713-a. Hum Mol Genet. 1994. PMID: 7833946 No abstract available.

4

Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1.

Lerner TJ, Boustany RM, MacCormack K, Gleitsman J, Schlumpf K, Breakefield XO, Gusella JF, Haines JL. Lerner TJ, et al. Among authors: haines jl. Am J Hum Genet. 1994 Jan;54(1):88-94. Am J Hum Genet. 1994. PMID: 8279474 Free PMC article.

5

Sequence analysis and mapping of a novel human mitochondrial ATP synthase subunit 9 cDNA (ATP5G3).

Yan WL, Lerner TJ, Haines JL, Gusella JF. Yan WL, et al. Among authors: haines jl. Genomics. 1994 Nov 15;24(2):375-7. doi: 10.1006/geno.1994.1631. Genomics. 1994. PMID: 7698763

6

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. Among authors: haines jl. Genomics. 1994 Jul 15;22(2):465-8. doi: 10.1006/geno.1994.1412. Genomics. 1994. PMID: 7806237

7

Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16.

Yan W, Boustany RM, Konradi C, Ozelius L, Lerner T, Trofatter JA, Julier C, Breakefield XO, Gusella JF, Haines JL. Yan W, et al. Among authors: haines jl. Am J Hum Genet. 1993 Jan;52(1):89-95. Am J Hum Genet. 1993. PMID: 8434611 Free PMC article.

8

Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis.

Haines JL, Boustany RM, Alroy J, Auger KJ, Shook KS, Terwedow H, Lerner TJ. Haines JL, et al. Neurogenetics. 1998 Mar;1(3):217-22. doi: 10.1007/s100480050032. Neurogenetics. 1998. PMID: 10737126

9

Peripherin gene is linked to keratin 18 gene on human chromosome 12.

Blumenfeld A, Lucente DE, Trofatter JA, Lerner T, Slaugenhaupt SA, Liebert CB, Monahan M, Haines JL, Gusella JF, Breakefield XO, Parysek LM. Blumenfeld A, et al. Among authors: haines jl. Somat Cell Mol Genet. 1995 Jan;21(1):83-8. doi: 10.1007/BF02255825. Somat Cell Mol Genet. 1995. PMID: 7541564

10

Linkage analysis in juvenile neuronal ceroid lipofuscinosis.

Haines JL, Yan WL, Boustany RM, Jewell A, Julier C, Breakefield XO, Gusella JF. Haines JL, et al. Am J Med Genet. 1992 Feb 15;42(4):542-5. doi: 10.1002/ajmg.1320420424. Am J Med Genet. 1992. PMID: 1609835

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