Hagemann TL - Search Results

1

Wiskott-Aldrich syndrome protein-deficient mice reveal a role for WASP in T but not B cell activation.

Snapper SB, Rosen FS, Mizoguchi E, Cohen P, Khan W, Liu CH, Hagemann TL, Kwan SP, Ferrini R, Davidson L, Bhan AK, Alt FW. Snapper SB, et al. Among authors: hagemann tl. Immunity. 1998 Jul;9(1):81-91. doi: 10.1016/s1074-7613(00)80590-7. Immunity. 1998. PMID: 9697838 Free article.

2

Variable expression of WASP in B cell lines of Wiskott-Aldrich syndrome patients.

Remold-O'Donnell E, Cooley J, Shcherbina A, Hagemann TL, Kwan SP, Kenney DM, Rosen FS. Remold-O'Donnell E, et al. Among authors: hagemann tl. J Immunol. 1997 May 1;158(9):4021-5. J Immunol. 1997. PMID: 9126958

3

The identification and characterization of two promoters and the complete genomic sequence for the Wiskott-Aldrich syndrome gene.

Hagemann TL, Kwan SP. Hagemann TL, et al. Biochem Biophys Res Commun. 1999 Mar 5;256(1):104-9. doi: 10.1006/bbrc.1999.0292. Biochem Biophys Res Commun. 1999. PMID: 10066431

4

Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene.

Kwan SP, Hagemann TL, Radtke BE, Blaese RM, Rosen FS. Kwan SP, et al. Among authors: hagemann tl. Proc Natl Acad Sci U S A. 1995 May 9;92(10):4706-10. doi: 10.1073/pnas.92.10.4706. Proc Natl Acad Sci U S A. 1995. PMID: 7753869 Free PMC article.

5

Gene regulation of Wiskott-Aldrich syndrome protein and the human homolog of the Drosophila Su(var)3-9: WASP and SUV39H1, two adjacent genes at Xp11.23.

Hagemann TL, Mares D, Kwan S. Hagemann TL, et al. Biochim Biophys Acta. 2000 Oct 2;1493(3):368-72. doi: 10.1016/s0167-4781(00)00199-8. Biochim Biophys Acta. 2000. PMID: 11018264

6

Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3.

Kwan SP, Lehner T, Hagemann T, Lu B, Blaese M, Ochs H, Wedgwood R, Ott J, Craig IW, Rosen FS. Kwan SP, et al. Genomics. 1991 May;10(1):29-33. doi: 10.1016/0888-7543(91)90480-3. Genomics. 1991. PMID: 1675197

7

Scanning of the Wiskott-Aldrich syndrome (WAS) gene: identification of 18 novel alterations including a possible mutation hotspot at Arg86 resulting in thrombocytopenia, a mild WAS phenotype.

Kwan SP, Hagemann TL, Blaese RM, Knutsen A, Rosen FS. Kwan SP, et al. Among authors: hagemann tl. Hum Mol Genet. 1995 Oct;4(10):1995-8. doi: 10.1093/hmg/4.10.1995. Hum Mol Genet. 1995. PMID: 8595430 No abstract available.

8

A high-resolution map of genes, microsatellite markers, and new dinucleotide repeats from UBE1 to the GATA locus in the region Xp11.23.

Kwan SP, Hagemann TL, Blaese RM, Rosen FS. Kwan SP, et al. Among authors: hagemann tl. Genomics. 1995 Sep 1;29(1):247-52. doi: 10.1006/geno.1995.1238. Genomics. 1995. PMID: 8530079

9

Characterization of germline mutations of the gene encoding Bruton's tyrosine kinase in families with X-linked agammaglobulinemia.

Hagemann TL, Rosen FS, Kwan SP. Hagemann TL, et al. Hum Mutat. 1995;5(4):296-302. doi: 10.1002/humu.1380050405. Hum Mutat. 1995. PMID: 7627183

10

ABI sequencing analysis. Manipulation of sequence data from the ABI DNA sequencer.

Hagemann TL, Kwan SP. Hagemann TL, et al. Mol Biotechnol. 1999 Dec 1;13(2):137-52. doi: 10.1385/MB:13:2:137. Mol Biotechnol. 1999. PMID: 10934528 Review.

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