Shultz LD - Search Results

1

Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) mice.

Hosur V, Cox ML, Burzenski LM, Riding RL, Alley L, Lyons BL, Kavirayani A, Martin KA, Cox GA, Johnson KR, Shultz LD. Hosur V, et al. Among authors: shultz ld. PLoS One. 2013;8(1):e53426. doi: 10.1371/journal.pone.0053426. Epub 2013 Jan 2. PLoS One. 2013. PMID: 23301070 Free PMC article.

2

Hairpatches, a single gene mutation characterized by progressive renal disease and alopecia in the mouse. A potential model for a newly described heritable human disorder.

Shultz LD, Lane PW, Coman DR, Taylor S, Hall E, Lyons B, Wood BG, Schlager G. Shultz LD, et al. Lab Invest. 1991 Nov;65(5):588-600. Lab Invest. 1991. PMID: 1836514

3

The interleukin-12 beta subunit (p40) maps to mouse chromosome 11.

Noben-Trauth N, Schweitzer PA, Johnson KR, Wolf SF, Knowles BB, Shultz LD. Noben-Trauth N, et al. Among authors: shultz ld. Mamm Genome. 1996 May;7(5):392. doi: 10.1007/s003359900113. Mamm Genome. 1996. PMID: 8661733 No abstract available.

4

Genetic mapping of the IL-12 alpha chain gene (Il12a) on mouse chromosome 3.

Schweitzer PA, Noben-Trauth N, Pelsue SC, Johnson KR, Wolf SF, Shultz LD. Schweitzer PA, et al. Among authors: shultz ld. Mamm Genome. 1996 May;7(5):394-5. doi: 10.1007/s003359900115. Mamm Genome. 1996. PMID: 8661735 No abstract available.

5

NOD/LtSz-Rag1null mice: an immunodeficient and radioresistant model for engraftment of human hematolymphoid cells, HIV infection, and adoptive transfer of NOD mouse diabetogenic T cells.

Shultz LD, Lang PA, Christianson SW, Gott B, Lyons B, Umeda S, Leiter E, Hesselton R, Wagar EJ, Leif JH, Kollet O, Lapidot T, Greiner DL. Shultz LD, et al. J Immunol. 2000 Mar 1;164(5):2496-507. doi: 10.4049/jimmunol.164.5.2496. J Immunol. 2000. PMID: 10679087

6

Absence of CD5 dramatically reduces progression of pulmonary inflammatory lesions in SHP-1 protein-tyrosine phosphatase-deficient 'viable motheaten' mice.

Joliat MJ, Lang PA, Lyons BL, Burzenski L, Lynes MA, Yi T, Sundberg JP, Shultz LD. Joliat MJ, et al. Among authors: shultz ld. J Autoimmun. 2002 Mar;18(2):105-17. doi: 10.1006/jaut.2001.0570. J Autoimmun. 2002. PMID: 11908943

7

T cell developmental defects in 'viable motheaten' mice deficient in SHP-1 protein-tyrosine phosphatase. Developmental defects are corrected in vitro in the presence of normal hematopoietic-origin stromal cells and in vivo by exogenous IL-7.

Christianson SW, Greiner DL, Deluca D, Leif J, Phillips NE, Hayes SM, Hayashi S, Joliat MJ, Lyons BL, Shultz LD. Christianson SW, et al. Among authors: shultz ld. J Autoimmun. 2002 Mar;18(2):119-30. doi: 10.1006/jaut.2001.0571. J Autoimmun. 2002. PMID: 11908944

8

Establishment and characterization of a new osteogenic cell line (MOS-J) from a spontaneous C57BL/6J mouse osteosarcoma.

Joliat MJ, Umeda S, Lyons BL, Lynes MA, Shultz LD. Joliat MJ, et al. Among authors: shultz ld. In Vivo. 2002 Jul-Aug;16(4):223-8. In Vivo. 2002. PMID: 12224130

9

Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly.

Shultz LD, Lyons BL, Burzenski LM, Gott B, Samuels R, Schweitzer PA, Dreger C, Herrmann H, Kalscheuer V, Olins AL, Olins DE, Sperling K, Hoffmann K. Shultz LD, et al. Hum Mol Genet. 2003 Jan 1;12(1):61-9. doi: 10.1093/hmg/ddg003. Hum Mol Genet. 2003. PMID: 12490533

10

Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.

Johnson KR, Lane PW, Cook SA, Harris BS, Ward-Bailey PF, Bronson RT, Lyons BL, Shultz LD, Davisson MT. Johnson KR, et al. Among authors: shultz ld. Genomics. 2003 Jan;81(1):6-14. doi: 10.1016/s0888-7543(02)00013-7. Genomics. 2003. PMID: 12573256

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