Murphy TL - Search Results

1

Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse.

Vulpe CD, Kuo YM, Murphy TL, Cowley L, Askwith C, Libina N, Gitschier J, Anderson GJ. Vulpe CD, et al. Among authors: murphy tl. Nat Genet. 1999 Feb;21(2):195-9. doi: 10.1038/5979. Nat Genet. 1999. PMID: 9988272

2

Mapping the gene for sex-linked anemia: an inherited defect of intestinal iron absorption in the mouse.

Anderson GJ, Murphy TL, Cowley L, Evans BA, Halliday JW, McLaren GD. Anderson GJ, et al. Among authors: murphy tl. Genomics. 1998 Feb 15;48(1):34-9. doi: 10.1006/geno.1997.5138. Genomics. 1998. PMID: 9503013

3

A rapid decrease in the expression of DMT1 and Dcytb but not Ireg1 or hephaestin explains the mucosal block phenomenon of iron absorption.

Frazer DM, Wilkins SJ, Becker EM, Murphy TL, Vulpe CD, McKie AT, Anderson GJ. Frazer DM, et al. Among authors: murphy tl. Gut. 2003 Mar;52(3):340-6. doi: 10.1136/gut.52.3.340. Gut. 2003. PMID: 12584213 Free PMC article.

4

Relationship between intestinal iron-transporter expression, hepatic hepcidin levels and the control of iron absorption.

Anderson GJ, Frazer DM, Wilkins SJ, Becker EM, Millard KN, Murphy TL, McKie AT, Vulpe CD. Anderson GJ, et al. Among authors: murphy tl. Biochem Soc Trans. 2002 Aug;30(4):724-6. doi: 10.1042/bst0300724. Biochem Soc Trans. 2002. PMID: 12196177

5

Hepcidin is down-regulated in alcoholic liver injury: implications for the pathogenesis of alcoholic liver disease.

Bridle K, Cheung TK, Murphy T, Walters M, Anderson G, Crawford DG, Fletcher LM. Bridle K, et al. Alcohol Clin Exp Res. 2006 Jan;30(1):106-12. doi: 10.1111/j.1530-0277.2006.00002.x. Alcohol Clin Exp Res. 2006. PMID: 16433737

6

Transcription factor C/EBPα is required for the development of Ly6C^hi monocytes but not Ly6C^lo monocytes.

Kim S, Chen J, Ou F, Liu TT, Jo S, Gillanders WE, Murphy TL, Murphy KM. Kim S, et al. Among authors: murphy tl. Proc Natl Acad Sci U S A. 2024 Apr 9;121(15):e2315659121. doi: 10.1073/pnas.2315659121. Epub 2024 Apr 2. Proc Natl Acad Sci U S A. 2024. PMID: 38564635

7

Atopic dermatitis is associated with an increased risk of central sensitivity disorders: a retrospective cohort analysis.

Garate D, Murphy TL, Ravanassa S, Golovko G, Hansen A, Wilkerson MG. Garate D, et al. Among authors: murphy tl. Arch Dermatol Res. 2023 Dec 20;316(1):56. doi: 10.1007/s00403-023-02795-z. Arch Dermatol Res. 2023. PMID: 38117346 No abstract available.

8

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD.

Wang S, Wang B, Drury V, Drake S, Sun N, Alkhairo H, Arbelaez J, Duhn C; Tourette International Collaborative Genetics (TIC Genetics); Bal VH, Langley K, Martin J, Hoekstra PJ, Dietrich A, Xing J, Heiman GA, Tischfield JA, Fernandez TV, Owen MJ, O'Donovan MC, Thapar A, State MW, Willsey AJ. Wang S, et al. Nat Commun. 2023 Dec 6;14(1):8077. doi: 10.1038/s41467-023-43776-0. Nat Commun. 2023. PMID: 38057346 Free PMC article.

9

Bcl6, Irf2, and Notch2 promote nonclassical monocyte development.

O'Connor KW, Liu T, Kim S, Briseño CG, Georgopoulos K, Murphy TL, Murphy KM. O'Connor KW, et al. Among authors: murphy tl. Proc Natl Acad Sci U S A. 2023 Aug 29;120(35):e2220853120. doi: 10.1073/pnas.2220853120. Epub 2023 Aug 22. Proc Natl Acad Sci U S A. 2023. PMID: 37607223 Free PMC article.

10

IL-6 selectively suppresses cDC1 specification via C/EBPβ.

Kim S, Chen J, Jo S, Ou F, Ferris ST, Liu TT, Ohara RA, Anderson DA, Wu R, Chen MY, Gillanders WE, Gillanders WE, Murphy TL, Murphy KM. Kim S, et al. Among authors: murphy tl. J Exp Med. 2023 Oct 2;220(10):e20221757. doi: 10.1084/jem.20221757. Epub 2023 Jul 11. J Exp Med. 2023. PMID: 37432392 Free PMC article.

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