Lyons BL - Search Results

1

The mouse mutation "thrombocytopenia and cardiomyopathy" (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia.

Chase TH, Lyons BL, Bronson RT, Foreman O, Donahue LR, Burzenski LM, Gott B, Lane P, Harris B, Ceglarek U, Thiery J, Wittenburg H, Thon JN, Italiano JE Jr, Johnson KR, Shultz LD. Chase TH, et al. Among authors: lyons bl. Blood. 2010 Feb 11;115(6):1267-76. doi: 10.1182/blood-2009-05-219808. Epub 2009 Oct 21. Blood. 2010. PMID: 19846887 Free PMC article.

2

NOD/LtSz-Rag1nullPfpnull mice: a new model system with increased levels of human peripheral leukocyte and hematopoietic stem-cell engraftment.

Shultz LD, Banuelos S, Lyons B, Samuels R, Burzenski L, Gott B, Lang P, Leif J, Appel M, Rossini A, Greiner DL. Shultz LD, et al. Transplantation. 2003 Oct 15;76(7):1036-42. doi: 10.1097/01.TP.0000083041.44829.2C. Transplantation. 2003. PMID: 14557749

3

Inflammatory dilated cardiomyopathy in Abcg5-deficient mice.

Wilson DW, Oslund KL, Lyons B, Foreman O, Burzenski L, Svenson KL, Chase TH, Shultz LD. Wilson DW, et al. Toxicol Pathol. 2013 Aug;41(6):880-92. doi: 10.1177/0192623312466191. Epub 2012 Nov 5. Toxicol Pathol. 2013. PMID: 23129576 Free PMC article.

4

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. Among authors: lyons bl. Hum Mol Genet. 2003 Jan 1;12(1):61-9. doi: 10.1093/hmg/ddg003. Hum Mol Genet. 2003. PMID: 12490533

5

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: lyons bl. Genomics. 2003 Jan;81(1):6-14. doi: 10.1016/s0888-7543(02)00013-7. Genomics. 2003. PMID: 12573256

6

Dystrophin and dysferlin double mutant mice: a novel model for rhabdomyosarcoma.

Hosur V, Kavirayani A, Riefler J, Carney LM, Lyons B, Gott B, Cox GA, Shultz LD. Hosur V, et al. Cancer Genet. 2012 May;205(5):232-41. doi: 10.1016/j.cancergen.2012.03.005. Cancer Genet. 2012. PMID: 22682622 Free PMC article.

7

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: lyons bl. In Vivo. 2002 Jul-Aug;16(4):223-8. In Vivo. 2002. PMID: 12224130

8

Accelerated wound healing of alkali-burned corneas in MRL mice is associated with a reduced inflammatory signature.

Ueno M, Lyons BL, Burzenski LM, Gott B, Shaffer DJ, Roopenian DC, Shultz LD. Ueno M, et al. Among authors: lyons bl. Invest Ophthalmol Vis Sci. 2005 Nov;46(11):4097-106. doi: 10.1167/iovs.05-0548. Invest Ophthalmol Vis Sci. 2005. PMID: 16249486

9

Deficiency of SHP-1 protein-tyrosine phosphatase in "viable motheaten" mice results in retinal degeneration.

Lyons BL, Smith RS, Hurd RE, Hawes NL, Burzenski LM, Nusinowitz S, Hasham MG, Chang B, Shultz LD. Lyons BL, et al. Invest Ophthalmol Vis Sci. 2006 Mar;47(3):1201-9. doi: 10.1167/iovs.05-1161. Invest Ophthalmol Vis Sci. 2006. PMID: 16505059

10

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: lyons bl. PLoS One. 2013;8(1):e53426. doi: 10.1371/journal.pone.0053426. Epub 2013 Jan 2. PLoS One. 2013. PMID: 23301070 Free PMC article.

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