Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 207

1.

A cre-inducible DUX4 transgenic mouse model for investigating facioscapulohumeral muscular dystrophy.

Jones T, Jones PL.

PLoS One. 2018 Feb 7;13(2):e0192657. doi: 10.1371/journal.pone.0192657. eCollection 2018.

2.

CRISPR/Cas9 knockouts reveal genetic interaction between strain-transcendent erythrocyte determinants of Plasmodium falciparum invasion.

Kanjee U, Grüring C, Chaand M, Lin KM, Egan E, Manzo J, Jones PL, Yu T, Barker R Jr, Weekes MP, Duraisingh MT.

Proc Natl Acad Sci U S A. 2017 Oct 31;114(44):E9356-E9365. doi: 10.1073/pnas.1711310114. Epub 2017 Oct 19.

PMID:
29078358
3.

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME.

Nat Genet. 2017 May 26;49(6):969. doi: 10.1038/ng0617-969c. No abstract available.

PMID:
28546579
4.

Early Vision for the CTSA Program Trial Innovation Network: A Perspective from the National Center for Advancing Translational Sciences.

Shah MR, Culp MA, Gersing KR, Jones PL, Purucker ME, Urv T, Wilson TM, Kaufmann P.

Clin Transl Sci. 2017 Sep;10(5):311-313. doi: 10.1111/cts.12463. Epub 2017 Apr 6. No abstract available.

5.

Large family cohorts of lymphoblastoid cells provide a new cellular model for investigating facioscapulohumeral muscular dystrophy.

Jones TI, Himeda CL, Perez DP, Jones PL.

Neuromuscul Disord. 2017 Mar;27(3):221-238. doi: 10.1016/j.nmd.2016.12.007. Epub 2016 Dec 23.

6.

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME.

Nat Genet. 2017 Feb;49(2):238-248. doi: 10.1038/ng.3743. Epub 2017 Jan 9. Erratum in: Nat Genet. 2017 May 26;49(6):969.

7.

Consequences of toxic secondary compounds in nectar for mutualist bees and antagonist butterflies.

Jones PL, Agrawal AA.

Ecology. 2016 Oct;97(10):2570-2579. doi: 10.1002/ecy.1483. Epub 2016 Sep 1.

PMID:
27859127
8.

Learning in Insect Pollinators and Herbivores.

Jones PL, Agrawal AA.

Annu Rev Entomol. 2017 Jan 31;62:53-71. doi: 10.1146/annurev-ento-031616-034903. Epub 2016 Oct 28. Review.

PMID:
27813668
9.

Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD).

Jones TI, Parilla M, Jones PL.

PLoS One. 2016 Mar 4;11(3):e0150938. doi: 10.1371/journal.pone.0150938. eCollection 2016.

10.

Scalpel or Straitjacket: CRISPR/Cas9 Approaches for Muscular Dystrophies.

Himeda CL, Jones TI, Jones PL.

Trends Pharmacol Sci. 2016 Apr;37(4):249-51. doi: 10.1016/j.tips.2016.02.001. Epub 2016 Feb 22.

11.

CRISPR/dCas9-mediated Transcriptional Inhibition Ameliorates the Epigenetic Dysregulation at D4Z4 and Represses DUX4-fl in FSH Muscular Dystrophy.

Himeda CL, Jones TI, Jones PL.

Mol Ther. 2016 Mar;24(3):527-35. doi: 10.1038/mt.2015.200. Epub 2015 Nov 3.

12.

Antenatal Magnesium and Cerebral Palsy in Preterm Infants.

Hirtz DG, Weiner SJ, Bulas D, DiPietro M, Seibert J, Rouse DJ, Mercer BM, Varner MW, Reddy UM, Iams JD, Wapner RJ, Sorokin Y, Thorp JM Jr, Ramin SM, Malone FD, Carpenter MW, O'Sullivan MJ, Peaceman AM, Hankins GD, Dudley D, Caritis SN; Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network.

J Pediatr. 2015 Oct;167(4):834-839.e3. doi: 10.1016/j.jpeds.2015.06.067. Epub 2015 Aug 5.

13.

Role played by Prx1-dependent extracellular matrix properties in vascular smooth muscle development in embryonic lungs.

Ihida-Stansbury K, Ames J, Chokshi M, Aiad N, Sanyal S, Kawabata KC, Levental I, Sundararaghavan HG, Burdick JA, Janmey P, Miyazono K, Wells RG, Jones PL.

Pulm Circ. 2015 Jun;5(2):382-97. doi: 10.1086/681272.

14.

Sensory-based niche partitioning in a multiple predator - multiple prey community.

Falk JJ, ter Hofstede HM, Jones PL, Dixon MM, Faure PA, Kalko EK, Page RA.

Proc Biol Sci. 2015 Jun 7;282(1808):20150520. doi: 10.1098/rspb.2015.0520.

15.

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy.

Jones TI, King OD, Himeda CL, Homma S, Chen JC, Beermann ML, Yan C, Emerson CP Jr, Miller JB, Wagner KR, Jones PL.

Clin Epigenetics. 2015 Mar 29;7:37. doi: 10.1186/s13148-015-0072-6. eCollection 2015.

16.

Emerging preclinical animal models for FSHD.

Lek A, Rahimov F, Jones PL, Kunkel LM.

Trends Mol Med. 2015 May;21(5):295-306. doi: 10.1016/j.molmed.2015.02.011. Epub 2015 Mar 20. Review.

17.

Medical device risk management and safety cases.

Jones PL, Taylor A.

Biomed Instrum Technol. 2015 Spring;Suppl:45-53. doi: 10.2345/0899-8205-49.s1.45. No abstract available.

PMID:
25793451
18.

The efflux pump inhibitor timcodar improves the potency of antimycobacterial agents.

Grossman TH, Shoen CM, Jones SM, Jones PL, Cynamon MH, Locher CP.

Antimicrob Agents Chemother. 2015 Mar;59(3):1534-41. doi: 10.1128/AAC.04271-14. Epub 2014 Dec 22.

19.

Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing.

Jones TI, Yan C, Sapp PC, McKenna-Yasek D, Kang PB, Quinn C, Salameh JS, King OD, Jones PL.

Clin Epigenetics. 2014 Oct 29;6(1):23. doi: 10.1186/1868-7083-6-23. eCollection 2014.

20.

Facioscapulohumeral muscular dystrophy as a model for epigenetic regulation and disease.

Himeda CL, Jones TI, Jones PL.

Antioxid Redox Signal. 2015 Jun 1;22(16):1463-82. doi: 10.1089/ars.2014.6090. Epub 2014 Dec 4. Review.

Supplemental Content

Loading ...
Support Center