Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 42

1.

Pillars Article: Isolation of a Novel Gene Mutated in Wiskott-Aldrich Syndrome. Cell. 1994. 78: 635-644.

Derry JMJ, Ochs HD, Francke U.

J Immunol. 2018 Jun 1;200(11):3671-3680. No abstract available.

PMID:
29784763
2.

Sulforaphane reduces hepatic glucose production and improves glucose control in patients with type 2 diabetes.

Axelsson AS, Tubbs E, Mecham B, Chacko S, Nenonen HA, Tang Y, Fahey JW, Derry JMJ, Wollheim CB, Wierup N, Haymond MW, Friend SH, Mulder H, Rosengren AH.

Sci Transl Med. 2017 Jun 14;9(394). pii: eaah4477. doi: 10.1126/scitranslmed.aah4477.

PMID:
28615356
3.

Sox5 regulates beta-cell phenotype and is reduced in type 2 diabetes.

Axelsson AS, Mahdi T, Nenonen HA, Singh T, Hänzelmann S, Wendt A, Bagge A, Reinbothe TM, Millstein J, Yang X, Zhang B, Gusmao EG, Shu L, Szabat M, Tang Y, Wang J, Salö S, Eliasson L, Artner I, Fex M, Johnson JD, Wollheim CB, Derry JMJ, Mecham B, Spégel P, Mulder H, Costa IG, Zhang E, Rosengren AH.

Nat Commun. 2017 Jun 6;8:15652. doi: 10.1038/ncomms15652.

4.

Gene expression elucidates functional impact of polygenic risk for schizophrenia.

Fromer M, Roussos P, Sieberts SK, Johnson JS, Kavanagh DH, Perumal TM, Ruderfer DM, Oh EC, Topol A, Shah HR, Klei LL, Kramer R, Pinto D, Gümüş ZH, Cicek AE, Dang KK, Browne A, Lu C, Xie L, Readhead B, Stahl EA, Xiao J, Parvizi M, Hamamsy T, Fullard JF, Wang YC, Mahajan MC, Derry JM, Dudley JT, Hemby SE, Logsdon BA, Talbot K, Raj T, Bennett DA, De Jager PL, Zhu J, Zhang B, Sullivan PF, Chess A, Purcell SM, Shinobu LA, Mangravite LM, Toyoshiba H, Gur RE, Hahn CG, Lewis DA, Haroutunian V, Peters MA, Lipska BK, Buxbaum JD, Schadt EE, Hirai K, Roeder K, Brennand KJ, Katsanis N, Domenici E, Devlin B, Sklar P.

Nat Neurosci. 2016 Nov;19(11):1442-1453. doi: 10.1038/nn.4399. Epub 2016 Sep 26.

5.

Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge.

Plenge RM, Greenberg JD, Mangravite LM, Derry JM, Stahl EA, Coenen MJ, Barton A, Padyukov L, Klareskog L, Gregersen PK, Mariette X, Moreland LW, Bridges SL Jr, de Vries N, Huizinga TW, Guchelaar HJ; International Rheumatoid Arthritis Consortium (INTERACT), Friend SH, Stolovitzky G.

Nat Genet. 2013 May;45(5):468-9. doi: 10.1038/ng.2623. No abstract available.

6.

Lung eQTLs to help reveal the molecular underpinnings of asthma.

Hao K, Bossé Y, Nickle DC, Paré PD, Postma DS, Laviolette M, Sandford A, Hackett TL, Daley D, Hogg JC, Elliott WM, Couture C, Lamontagne M, Brandsma CA, van den Berge M, Koppelman G, Reicin AS, Nicholson DW, Malkov V, Derry JM, Suver C, Tsou JA, Kulkarni A, Zhang C, Vessey R, Opiteck GJ, Curtis SP, Timens W, Sin DD.

PLoS Genet. 2012;8(11):e1003029. doi: 10.1371/journal.pgen.1003029. Epub 2012 Nov 29. Erratum in: PLoS Genet. 2012 Dec;8(12). doi: 10.1371/annotation/80d53ac6-4f5d-4c34-b92b-3fec00d514ac.

7.

Resolving candidate genes of mouse skeletal muscle QTL via RNA-Seq and expression network analyses.

Lionikas A, Meharg C, Derry JM, Ratkevicius A, Carroll AM, Vandenbergh DJ, Blizard DA.

BMC Genomics. 2012 Nov 5;13:592. doi: 10.1186/1471-2164-13-592.

8.

Developing predictive molecular maps of human disease through community-based modeling.

Derry JM, Mangravite LM, Suver C, Furia MD, Henderson D, Schildwachter X, Bot B, Izant J, Sieberts SK, Kellen MR, Friend SH.

Nat Genet. 2012 Jan 27;44(2):127-30. doi: 10.1038/ng.1089. No abstract available.

9.

Identification of genes and networks driving cardiovascular and metabolic phenotypes in a mouse F2 intercross.

Derry JM, Zhong H, Molony C, MacNeil D, Guhathakurta D, Zhang B, Mudgett J, Small K, El Fertak L, Guimond A, Selloum M, Zhao W, Champy MF, Monassier L, Vogt T, Cully D, Kasarskis A, Schadt EE.

PLoS One. 2010 Dec 14;5(12):e14319. doi: 10.1371/journal.pone.0014319.

10.

Integrative genomics and drug development.

Lum PY, Derry JM, Schadt EE.

Pharmacogenomics. 2009 Feb;10(2):203-12. doi: 10.2217/14622416.10.2.203. Review.

PMID:
19207021
11.

Differentially regulated functional gene clusters identified during ischemia and reperfusion in isolated cardiac myocytes using coverslip hypoxia.

Pitts KR, Derry JM, Kerkof K, Lawrence WA, Toombs CF.

J Pharmacol Toxicol Methods. 2008 Jan-Feb;57(1):42-51. Epub 2007 Sep 19.

PMID:
17928241
12.

A conserved tyrosine in the beta2 subunit M4 segment is a determinant of gamma-aminobutyric acid type A receptor sensitivity to propofol.

Richardson JE, Garcia PS, O'Toole KK, Derry JM, Bell SV, Jenkins A.

Anesthesiology. 2007 Sep;107(3):412-8.

PMID:
17721243
13.

Impaired regulation of NF-kappaB and increased susceptibility to colitis-associated tumorigenesis in CYLD-deficient mice.

Zhang J, Stirling B, Temmerman ST, Ma CA, Fuss IJ, Derry JM, Jain A.

J Clin Invest. 2006 Nov;116(11):3042-9. Epub 2006 Oct 19.

14.

A single point mutation of the GABA(A) receptor alpha5-subunit confers fluoxetine sensitivity.

Derry JM, Paulsen IM, Davies M, Dunn SM.

Neuropharmacology. 2007 Feb;52(2):497-505. Epub 2006 Oct 10.

PMID:
17045313
15.

Impaired dendritic-cell function in ectodermal dysplasia with immune deficiency is linked to defective NEMO ubiquitination.

Temmerman ST, Ma CA, Borges L, Kubin M, Liu S, Derry JM, Jain A.

Blood. 2006 Oct 1;108(7):2324-31. Epub 2006 Jun 22.

16.

Nectin-like protein 2 defines a subset of T-cell zone dendritic cells and is a ligand for class-I-restricted T-cell-associated molecule.

Galibert L, Diemer GS, Liu Z, Johnson RS, Smith JL, Walzer T, Comeau MR, Rauch CT, Wolfson MF, Sorensen RA, Van der Vuurst de Vries AR, Branstetter DG, Koelling RM, Scholler J, Fanslow WC, Baum PR, Derry JM, Yan W.

J Biol Chem. 2005 Jun 10;280(23):21955-64. Epub 2005 Mar 21.

17.

Specific NEMO mutations impair CD40-mediated c-Rel activation and B cell terminal differentiation.

Jain A, Ma CA, Lopez-Granados E, Means G, Brady W, Orange JS, Liu S, Holland S, Derry JM.

J Clin Invest. 2004 Dec;114(11):1593-602.

18.

Osteoclast differentiation is impaired in the absence of inhibitor of kappa B kinase alpha.

Chaisson ML, Branstetter DG, Derry JM, Armstrong AP, Tometsko ME, Takeda K, Akira S, Dougall WC.

J Biol Chem. 2004 Dec 24;279(52):54841-8. Epub 2004 Oct 14.

20.
21.

Transgenic rescue of the tattered phenotype by using a BAC encoding Ebp.

Means GD, Boyd Y, Willis CR, Derry JM.

Mamm Genome. 2001 Apr;12(4):323-5. No abstract available.

PMID:
11309666
22.

Characterization of the interaction of zopiclone with gamma-aminobutyric acid type A receptors.

Davies M, Newell JG, Derry JM, Martin IL, Dunn SM.

Mol Pharmacol. 2000 Oct;58(4):756-62.

23.
24.

Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins.

Huang MM, Tsuboi S, Wong A, Yu XJ, Oh-Eda M, Derry JM, Francke U, Fukuda M, Weinberg KI, Kohn DB.

Gene Ther. 2000 Feb;7(4):314-20.

25.

Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com.

Derry JM, Gormally E, Means GD, Zhao W, Meindl A, Kelley RI, Boyd Y, Herman GE.

Nat Genet. 1999 Jul;22(3):286-90.

PMID:
10391218
26.

Molecular characterization of the human interleukin (IL)-17 receptor.

Yao Z, Spriggs MK, Derry JM, Strockbine L, Park LS, VandenBos T, Zappone JD, Painter SL, Armitage RJ.

Cytokine. 1997 Nov;9(11):794-800.

PMID:
9367539
27.

Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization.

Symons M, Derry JM, Karlak B, Jiang S, Lemahieu V, Mccormick F, Francke U, Abo A.

Cell. 1996 Mar 8;84(5):723-34.

28.

RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain.

Derry JM, Kerns JA, Francke U.

Hum Mol Genet. 1995 Dec;4(12):2307-11.

PMID:
8634703
29.

Cloning and characterization of a novel zinc finger gene in Xp11.2.

Derry JM, Jess U, Francke U.

Genomics. 1995 Nov 20;30(2):361-5.

PMID:
8586441
30.

The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene.

Zhu Q, Zhang M, Blaese RM, Derry JM, Junker A, Francke U, Chen SH, Ochs HD.

Blood. 1995 Nov 15;86(10):3797-804.

31.

The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome.

Derry JM, Wiedemann P, Blair P, Wang Y, Kerns JA, Lemahieu V, Godfrey VL, Wilkinson JE, Francke U.

Genomics. 1995 Sep 20;29(2):471-7.

PMID:
8666397
32.

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

Derry JM, Kerns JA, Weinberg KI, Ochs HD, Volpini V, Estivill X, Walker AP, Francke U.

Hum Mol Genet. 1995 Jul;4(7):1127-35.

PMID:
8528199
33.

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.

Derry JM, Ochs HD, Francke U.

Cell. 1994 Dec 2;79(5):following 922. No abstract available.

PMID:
8001129
34.

Dystroglycan: brain localisation and chromosome mapping in the mouse.

Górecki DC, Derry JM, Barnard EA.

Hum Mol Genet. 1994 Sep;3(9):1589-97.

PMID:
7833916
35.

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.

Derry JM, Ochs HD, Francke U.

Cell. 1994 Aug 26;78(4):635-44. Erratum in: Cell. 1994 Dec 2;79(5):following 922.

PMID:
8069912
36.

Mapping of a liver phosphorylase kinase alpha-subunit gene on the mouse X chromosome.

Geng Y, Derry JM, Hendrickx J, Coucke P, Willems PR, Barnard PJ.

Genomics. 1993 Jan;15(1):191-3.

PMID:
8432533
37.

Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters.

Górecki DC, Monaco AP, Derry JM, Walker AP, Barnard EA, Barnard PJ.

Hum Mol Genet. 1992 Oct;1(7):505-10.

PMID:
1307251
38.
39.
40.

Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome.

Barnard PJ, Derry JM, Ryder-Cook AS, Zander NF, Kilimann MW.

Cytogenet Cell Genet. 1990;53(2-3):91-4.

PMID:
1973380
41.

Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease.

Buckle VJ, Fujita N, Ryder-Cook AS, Derry JM, Barnard PJ, Lebo RV, Schofield PR, Seeburg PH, Bateson AN, Darlison MG, et al.

Neuron. 1989 Nov;3(5):647-54.

PMID:
2561974
42.

Localization of monoamine oxidase A and B genes on the mouse X chromosome.

Derry JM, Lan NC, Shih JC, Barnard EA, Barnard PJ.

Nucleic Acids Res. 1989 Oct 25;17(20):8403. No abstract available.

Supplemental Content

Loading ...
Support Center