Scherer SW - Search Results

1

Analysis of the monomeric alphoid sequences in the pericentromeric region of human chromosome 7.

de la Puente A, Velasco E, Pérez Jurado LA, Hernández-Chico C, van de Rijke FM, Scherer SW, Raap AK, Cruces J. de la Puente A, et al. Among authors: scherer sw. Cytogenet Cell Genet. 1998;83(3-4):176-81. doi: 10.1159/000015175. Cytogenet Cell Genet. 1998. PMID: 10072574

2

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.

Brooks-Wilson A, Marcil M, Clee SM, Zhang LH, Roomp K, van Dam M, Yu L, Brewer C, Collins JA, Molhuizen HO, Loubser O, Ouelette BF, Fichter K, Ashbourne-Excoffon KJ, Sensen CW, Scherer S, Mott S, Denis M, Martindale D, Frohlich J, Morgan K, Koop B, Pimstone S, Kastelein JJ, Genest J Jr, Hayden MR. Brooks-Wilson A, et al. Nat Genet. 1999 Aug;22(4):336-45. doi: 10.1038/11905. Nat Genet. 1999. PMID: 10431236

3

Identification of an amplified gene cluster in glioma including two novel amplified genes isolated by exon trapping.

Mueller HW, Michel A, Heckel D, Fischer U, Tönnes M, Tsui LC, Scherer S, Zang KD, Meese E. Mueller HW, et al. Hum Genet. 1997 Dec;101(2):190-7. doi: 10.1007/s004390050612. Hum Genet. 1997. PMID: 9402967

4

Localization of the human SP3 gene to chromosome 7p14-p15.2. The lack of expression in multiple sclerosis does not reflect abnormal gene organization.

Grekova MC, Scherer SW, Trabb J, Richert JR. Grekova MC, et al. Among authors: scherer sw. J Neuroimmunol. 2000 Jul 1;106(1-2):214-9. doi: 10.1016/s0165-5728(99)00264-7. J Neuroimmunol. 2000. PMID: 10814800 Free article.

5

Delineation of multiple deleted regions in 7q in myeloid disorders.

Tosi S, Scherer SW, Giudici G, Czepulkowski B, Biondi A, Kearney L. Tosi S, et al. Among authors: scherer sw. Genes Chromosomes Cancer. 1999 Aug;25(4):384-92. doi: 10.1002/(sici)1098-2264(199908)25:4<384::aid-gcc11>3.0.co;2-d. Genes Chromosomes Cancer. 1999. PMID: 10398433

6

Structural organization and chromosomal localization of the human Na,K-ATPase beta 3 subunit gene and pseudogene.

Malik N, Canfield V, Sanchez-Watts G, Watts AG, Scherer S, Beatty BG, Gros P, Levenson R. Malik N, et al. Mamm Genome. 1998 Feb;9(2):136-43. doi: 10.1007/s003359900704. Mamm Genome. 1998. PMID: 9457675

7

Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.

Tosi S, Giudici G, Rambaldi A, Scherer SW, Bray-Ward P, Dirscherl L, Biondi A, Kearney L. Tosi S, et al. Among authors: scherer sw. Genes Chromosomes Cancer. 1999 Mar;24(3):213-21. Genes Chromosomes Cancer. 1999. PMID: 10451701

8

Large-scale sequencing of two regions in human chromosome 7q22: analysis of 650 kb of genomic sequence around the EPO and CUTL1 loci reveals 17 genes.

Glöckner G, Scherer S, Schattevoy R, Boright A, Weber J, Tsui LC, Rosenthal A. Glöckner G, et al. Genome Res. 1998 Oct;8(10):1060-73. doi: 10.1101/gr.8.10.1060. Genome Res. 1998. PMID: 9799793 Free PMC article.

9

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.

Ross AJ, Ruiz-Perez V, Wang Y, Hagan DM, Scherer S, Lynch SA, Lindsay S, Custard E, Belloni E, Wilson DI, Wadey R, Goodman F, Orstavik KH, Monclair T, Robson S, Reardon W, Burn J, Scambler P, Strachan T. Ross AJ, et al. Nat Genet. 1998 Dec;20(4):358-61. doi: 10.1038/3828. Nat Genet. 1998. PMID: 9843207

10

Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.

Tosi S, Hughes J, Scherer SW, Nakabayashi K, Harbott J, Haas OA, Cazzaniga G, Biondi A, Kempski H, Kearney L. Tosi S, et al. Among authors: scherer sw. Genes Chromosomes Cancer. 2003 Oct;38(2):191-200. doi: 10.1002/gcc.10258. Genes Chromosomes Cancer. 2003. PMID: 12939747

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