Glaser TM - Search Results

1

Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor.

Arriza JL, Weinberger C, Cerelli G, Glaser TM, Handelin BL, Housman DE, Evans RM. Arriza JL, et al. Among authors: glaser tm. Science. 1987 Jul 17;237(4812):268-75. doi: 10.1126/science.3037703. Science. 1987. PMID: 3037703

2

A mouse model of the aniridia-Wilms tumor deletion syndrome.

Glaser T, Lane J, Housman D. Glaser T, et al. Science. 1990 Nov 9;250(4982):823-7. doi: 10.1126/science.2173141. Science. 1990. PMID: 2173141

3

Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development.

Buckler AJ, Pelletier J, Haber DA, Glaser T, Housman DE. Buckler AJ, et al. Mol Cell Biol. 1991 Mar;11(3):1707-12. doi: 10.1128/mcb.11.3.1707-1712.1991. Mol Cell Biol. 1991. PMID: 1671709 Free PMC article.

4

Mapping of human chromosome 11: organization of genes within the Wilms' tumor region of the chromosome.

Housman DE, Glaser T, Gerhard DS, Jones C, Bruns GA, Lewis WH. Housman DE, et al. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 2:837-41. doi: 10.1101/sqb.1986.051.01.097. Cold Spring Harb Symp Quant Biol. 1986. PMID: 3034498 No abstract available.

5

Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10.

Brilliant MH, Szabo G, Katarova Z, Kozak CA, Glaser TM, Greenspan RJ, Housman DE. Brilliant MH, et al. Among authors: glaser tm. Genomics. 1990 Jan;6(1):115-22. doi: 10.1016/0888-7543(90)90455-4. Genomics. 1990. PMID: 1968040

6

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor.

Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE. Haber DA, et al. Cell. 1990 Jun 29;61(7):1257-69. doi: 10.1016/0092-8674(90)90690-g. Cell. 1990. PMID: 2163761

7

Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively.

Glaser T, Matthews KE, Hudson JW, Seth P, Housman DE, Crerar MM. Glaser T, et al. Genomics. 1989 Oct;5(3):510-21. doi: 10.1016/0888-7543(89)90017-7. Genomics. 1989. PMID: 2575583

8

A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome.

Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D. Glaser T, et al. Genomics. 1989 Nov;5(4):880-93. doi: 10.1016/0888-7543(89)90130-4. Genomics. 1989. PMID: 2574149

9

A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.

Glaser T, Housman D, Lewis WH, Gerhard D, Jones C. Glaser T, et al. Somat Cell Mol Genet. 1989 Nov;15(6):477-501. doi: 10.1007/BF01534910. Somat Cell Mol Genet. 1989. PMID: 2595451

10

A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex.

Glaser T, Rose E, Morse H, Housman D, Jones C. Glaser T, et al. Genomics. 1990 Jan;6(1):48-64. doi: 10.1016/0888-7543(90)90447-3. Genomics. 1990. PMID: 2154397

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