O'Sullivan TN - Search Results

1

Absence epilepsy in tottering mutant mice is associated with calcium channel defects.

Fletcher CF, Lutz CM, O'Sullivan TN, Shaughnessy JD Jr, Hawkes R, Frankel WN, Copeland NG, Jenkins NA. Fletcher CF, et al. Cell. 1996 Nov 15;87(4):607-17. doi: 10.1016/s0092-8674(00)81381-1. Cell. 1996. PMID: 8929530 Free article.

2

Deletion and interallelic complementation analysis of Steel mutant mice.

Bedell MA, Cleveland LS, O'Sullivan TN, Copeland NG, Jenkins NA. Bedell MA, et al. Genetics. 1996 Mar;142(3):935-44. doi: 10.1093/genetics/142.3.935. Genetics. 1996. PMID: 8849899 Free PMC article.

3

The itchy locus encodes a novel ubiquitin protein ligase that is disrupted in a18H mice.

Perry WL, Hustad CM, Swing DA, O'Sullivan TN, Jenkins NA, Copeland NG. Perry WL, et al. Nat Genet. 1998 Feb;18(2):143-6. doi: 10.1038/ng0298-143. Nat Genet. 1998. PMID: 9462742

4

A mutation in Rab27a causes the vesicle transport defects observed in ashen mice.

Wilson SM, Yip R, Swing DA, O'Sullivan TN, Zhang Y, Novak EK, Swank RT, Russell LB, Copeland NG, Jenkins NA. Wilson SM, et al. Proc Natl Acad Sci U S A. 2000 Jul 5;97(14):7933-8. doi: 10.1073/pnas.140212797. Proc Natl Acad Sci U S A. 2000. PMID: 10859366 Free PMC article.

5

Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice.

Matesic LE, Yip R, Reuss AE, Swing DA, O'Sullivan TN, Fletcher CF, Copeland NG, Jenkins NA. Matesic LE, et al. Proc Natl Acad Sci U S A. 2001 Aug 28;98(18):10238-43. doi: 10.1073/pnas.181336698. Epub 2001 Aug 14. Proc Natl Acad Sci U S A. 2001. PMID: 11504925 Free PMC article.

6

dsu functions in a MYO5A-independent pathway to suppress the coat color of dilute mice.

O'Sullivan TN, Wu XS, Rachel RA, Huang JD, Swing DA, Matesic LE, Hammer JA 3rd, Copeland NG, Jenkins NA. O'Sullivan TN, et al. Proc Natl Acad Sci U S A. 2004 Nov 30;101(48):16831-6. doi: 10.1073/pnas.0407339101. Epub 2004 Nov 18. Proc Natl Acad Sci U S A. 2004. PMID: 15550542 Free PMC article.

7

Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6.

Zhang Q, Zhao B, Li W, Oiso N, Novak EK, Rusiniak ME, Gautam R, Chintala S, O'Brien EP, Zhang Y, Roe BA, Elliott RW, Eicher EM, Liang P, Kratz C, Legius E, Spritz RA, O'Sullivan TN, Copeland NG, Jenkins NA, Swank RT. Zhang Q, et al. Among authors: o sullivan tn. Nat Genet. 2003 Feb;33(2):145-53. doi: 10.1038/ng1087. Epub 2003 Jan 27. Nat Genet. 2003. PMID: 12548288

8

The role of MITF phosphorylation sites during coat color and eye development in mice analyzed by bacterial artificial chromosome transgene rescue.

Bauer GL, Praetorius C, Bergsteinsdóttir K, Hallsson JH, Gísladóttir BK, Schepsky A, Swing DA, O'Sullivan TN, Arnheiter H, Bismuth K, Debbache J, Fletcher C, Warming S, Copeland NG, Jenkins NA, Steingrímsson E. Bauer GL, et al. Among authors: o sullivan tn. Genetics. 2009 Oct;183(2):581-94. doi: 10.1534/genetics.109.103945. Epub 2009 Jul 27. Genetics. 2009. PMID: 19635938 Free PMC article.

9

Melanoregulin, product of the dsu locus, links the BLOC-pathway and OA1 in organelle biogenesis.

Rachel RA, Nagashima K, O'Sullivan TN, Frost LS, Stefano FP, Marigo V, Boesze-Battaglia K. Rachel RA, et al. Among authors: o sullivan tn. PLoS One. 2012;7(9):e42446. doi: 10.1371/journal.pone.0042446. Epub 2012 Sep 11. PLoS One. 2012. PMID: 22984402 Free PMC article.

10

Evolutionary etiology of high-grade astrocytomas.

Song Y, Zhang Q, Kutlu B, Difilippantonio S, Bash R, Gilbert D, Yin C, O'Sullivan TN, Yang C, Kozlov S, Bullitt E, McCarthy KD, Kafri T, Louis DN, Miller CR, Hood L, Van Dyke T. Song Y, et al. Among authors: o sullivan tn. Proc Natl Acad Sci U S A. 2013 Oct 29;110(44):17933-8. doi: 10.1073/pnas.1317026110. Epub 2013 Oct 10. Proc Natl Acad Sci U S A. 2013. PMID: 24114272 Free PMC article.

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