Cox GA - 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: cox ml, cox ga. 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

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. Among authors: cox ga. Cancer Genet. 2012 May;205(5):232-41. doi: 10.1016/j.cancergen.2012.03.005. Cancer Genet. 2012. PMID: 22682622 Free PMC article.

3

Dysferlin deficiency and the development of cardiomyopathy in a mouse model of limb-girdle muscular dystrophy 2B.

Chase TH, Cox GA, Burzenski L, Foreman O, Shultz LD. Chase TH, et al. Among authors: cox ga. Am J Pathol. 2009 Dec;175(6):2299-308. doi: 10.2353/ajpath.2009.080930. Epub 2009 Oct 29. Am J Pathol. 2009. PMID: 19875504 Free PMC article.

4

Expression of terminal differentiation proteins defines stages of mouse mammary gland development.

Mikaelian I, Hovick M, Silva KA, Burzenski LM, Shultz LD, Ackert-Bicknell CL, Cox GA, Sundberg JP. Mikaelian I, et al. Among authors: cox ga. Vet Pathol. 2006 Jan;43(1):36-49. doi: 10.1354/vp.43-1-36. Vet Pathol. 2006. PMID: 16407485

5

Spontaneous mutations in the mouse Sharpin gene result in multiorgan inflammation, immune system dysregulation and dermatitis.

Seymour RE, Hasham MG, Cox GA, Shultz LD, Hogenesch H, Roopenian DC, Sundberg JP. Seymour RE, et al. Among authors: cox ga. Genes Immun. 2007 Jul;8(5):416-21. doi: 10.1038/sj.gene.6364403. Epub 2007 May 31. Genes Immun. 2007. PMID: 17538631

6

Rhabdomyosarcomas in aging A/J mice.

Sher RB, Cox GA, Mills KD, Sundberg JP. Sher RB, et al. Among authors: cox ga. PLoS One. 2011;6(8):e23498. doi: 10.1371/journal.pone.0023498. Epub 2011 Aug 10. PLoS One. 2011. PMID: 21853140 Free PMC article.

7

Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease.

Heiman-Patterson TD, Blankenhorn EP, Sher RB, Jiang J, Welsh P, Dixon MC, Jeffrey JI, Wong P, Cox GA, Alexander GM. Heiman-Patterson TD, et al. Among authors: cox ga. PLoS One. 2015 Mar 12;10(3):e0117848. doi: 10.1371/journal.pone.0117848. eCollection 2015. PLoS One. 2015. PMID: 25763819 Free PMC article.

8

Complex seizure disorder caused by Brunol4 deficiency in mice.

Yang Y, Mahaffey CL, Bérubé N, Maddatu TP, Cox GA, Frankel WN. Yang Y, et al. Among authors: cox ga. PLoS Genet. 2007 Jul;3(7):e124. doi: 10.1371/journal.pgen.0030124. PLoS Genet. 2007. PMID: 17677002 Free PMC article.

9

Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease.

Alexander GM, Heiman-Patterson TD, Bearoff F, Sher RB, Hennessy L, Terek S, Caccavo N, Cox GA, Philip VM, Blankenhorn EA. Alexander GM, et al. Among authors: cox ga. PLoS One. 2022 Sep 15;17(9):e0274615. doi: 10.1371/journal.pone.0274615. eCollection 2022. PLoS One. 2022. PMID: 36107978 Free PMC article.

10

Major locus on mouse chromosome 17 and minor locus on chromosome 9 are linked with alopecia areata in C3H/HeJ mice.

Sundberg JP, Boggess D, Silva KA, McElwee KJ, King LE, Li R, Churchill G, Cox GA. Sundberg JP, et al. Among authors: cox ga. J Invest Dermatol. 2003 May;120(5):771-5. doi: 10.1046/j.1523-1747.2003.12135.x. J Invest Dermatol. 2003. PMID: 12713579 Free article.

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