Scherer SW - Search Results

1

Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene.

Leclerc D, Odièvre M, Wu Q, Wilson A, Huizenga JJ, Rozen R, Scherer SW, Gravel RA. Leclerc D, et al. Among authors: scherer sw. Gene. 1999 Nov 15;240(1):75-88. doi: 10.1016/s0378-1119(99)00431-x. Gene. 1999. PMID: 10564814

2

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.

Osborne LR, Martindale D, Scherer SW, Shi XM, Huizenga J, Heng HH, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui LC. Osborne LR, et al. Among authors: scherer sw. Genomics. 1996 Sep 1;36(2):328-36. doi: 10.1006/geno.1996.0469. Genomics. 1996. PMID: 8812460 Free article.

3

Physical mapping of the chromosome 7 breakpoint region in an SLOS patient with t(7;20) (q32.1;q13.2).

Alley TL, Scherer SW, Huizenga JJ, Tsui LC, Wallace MR. Alley TL, et al. Among authors: scherer sw. Am J Med Genet. 1997 Jan 31;68(3):279-81. Am J Med Genet. 1997. PMID: 9024559

4

Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human chromosome band 5q14.

Crackower MA, Scherer SW, Heng HH, Tsui LC. Crackower MA, et al. Among authors: scherer sw. Mamm Genome. 1997 Feb;8(2):159-60. Mamm Genome. 1997. PMID: 9060422 No abstract available.

5

Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas.

Zeng WR, Scherer SW, Koutsilieris M, Huizenga JJ, Filteau F, Tsui LC, Nepveu A. Zeng WR, et al. Among authors: scherer sw. Oncogene. 1997 May 15;14(19):2355-65. doi: 10.1038/sj.onc.1201076. Oncogene. 1997. PMID: 9178912

6

The human metabotropic glutamate receptor 8 (GRM8) gene: a disproportionately large gene located at 7q31.3-q32.1.

Scherer SW, Soder S, Duvoisin RM, Huizenga JJ, Tsui LC. Scherer SW, et al. Genomics. 1997 Sep 1;44(2):232-6. doi: 10.1006/geno.1997.4842. Genomics. 1997. PMID: 9299241 Free article.

7

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria.

Leclerc D, Wilson A, Dumas R, Gafuik C, Song D, Watkins D, Heng HH, Rommens JM, Scherer SW, Rosenblatt DS, Gravel RA. Leclerc D, et al. Among authors: scherer sw. Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):3059-64. doi: 10.1073/pnas.95.6.3059. Proc Natl Acad Sci U S A. 1998. PMID: 9501215 Free PMC article.

8

Human PON2 gene at 7q21.3: cloning, multiple mRNA forms, and missense polymorphisms in the coding sequence.

Mochizuki H, Scherer SW, Xi T, Nickle DC, Majer M, Huizenga JJ, Tsui LC, Prochazka M. Mochizuki H, et al. Among authors: scherer sw. Gene. 1998 Jun 15;213(1-2):149-57. doi: 10.1016/s0378-1119(98)00193-0. Gene. 1998. PMID: 9714608

9

Genomic structure of the human congenital chloride diarrhea (CLD) gene.

Haila S, Höglund P, Scherer SW, Lee JR, Kristo P, Coyle B, Trembath R, Holmberg C, de la Chapelle A, Kere J. Haila S, et al. Among authors: scherer sw. Gene. 1998 Jul 3;214(1-2):87-93. doi: 10.1016/s0378-1119(98)00261-3. Gene. 1998. PMID: 9729124

10

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy.

Minassian BA, Lee JR, Herbrick JA, Huizenga J, Soder S, Mungall AJ, Dunham I, Gardner R, Fong CY, Carpenter S, Jardim L, Satishchandra P, Andermann E, Snead OC 3rd, Lopes-Cendes I, Tsui LC, Delgado-Escueta AV, Rouleau GA, Scherer SW. Minassian BA, et al. Among authors: scherer sw. Nat Genet. 1998 Oct;20(2):171-4. doi: 10.1038/2470. Nat Genet. 1998. PMID: 9771710

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