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Results: 1 to 20 of 159

1.

Economic Disruption and Childhood Obesity: Distraction, Disconnection, Displacement of Children's Health, and a Need for Social Change.

Balog JE.

Health Educ Behav. 2015 Apr;42(1 Suppl):67S-75S. doi: 10.1177/1090198114566802.

PMID:
25829120
2.

Efficient meltwater drainage through supraglacial streams and rivers on the southwest Greenland ice sheet.

Smith LC, Chu VW, Yang K, Gleason CJ, Pitcher LH, Rennermalm AK, Legleiter CJ, Behar AE, Overstreet BT, Moustafa SE, Tedesco M, Forster RR, LeWinter AL, Finnegan DC, Sheng Y, Balog J.

Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):1001-6. doi: 10.1073/pnas.1413024112. Epub 2015 Jan 12.

3.

XMS: cross-platform normalization method for multimodal mass spectrometric tissue profiling.

Golf O, Muirhead LJ, Speller A, Balog J, Abbassi-Ghadi N, Kumar S, Mróz A, Veselkov K, Takáts Z.

J Am Soc Mass Spectrom. 2015 Jan;26(1):44-54. doi: 10.1007/s13361-014-0997-6. Epub 2014 Nov 8.

PMID:
25380777
4.

Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.

Lemmers RJ, Goeman JJ, van der Vliet PJ, van Nieuwenhuizen MP, Balog J, Vos-Versteeg M, Camano P, Ramos Arroyo MA, Jerico I, Rogers MT, Miller DG, Upadhyaya M, Verschuuren JJ, Lopez de Munain Arregui A, van Engelen BG, Padberg GW, Sacconi S, Tawil R, Tapscott SJ, Bakker B, van der Maarel SM.

Hum Mol Genet. 2015 Feb 1;24(3):659-69. doi: 10.1093/hmg/ddu486. Epub 2014 Sep 25.

PMID:
25256356
5.

Social experience modulates ocular dominance plasticity differentially in adult male and female mice.

Balog J, Matthies U, Naumann L, Voget M, Winter C, Lehmann K.

Neuroimage. 2014 Dec;103:454-61. doi: 10.1016/j.neuroimage.2014.08.040. Epub 2014 Aug 28.

PMID:
25173416
6.

Characterization and identification of clinically relevant microorganisms using rapid evaporative ionization mass spectrometry.

Strittmatter N, Rebec M, Jones EA, Golf O, Abdolrasouli A, Balog J, Behrends V, Veselkov KA, Takats Z.

Anal Chem. 2014 Jul 1;86(13):6555-62. doi: 10.1021/ac501075f. Epub 2014 Jun 19.

PMID:
24896667
7.

DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscle.

Yao Z, Snider L, Balog J, Lemmers RJ, Van Der Maarel SM, Tawil R, Tapscott SJ.

Hum Mol Genet. 2014 Oct 15;23(20):5342-52. doi: 10.1093/hmg/ddu251. Epub 2014 May 26.

PMID:
24861551
8.

Genetic and epigenetic characteristics of FSHD-associated 4q and 10q D4Z4 that are distinct from non-4q/10q D4Z4 homologs.

Zeng W, Chen YY, Newkirk DA, Wu B, Balog J, Kong X, Ball AR Jr, Zanotti S, Tawil R, Hashimoto N, Mortazavi A, van der Maarel SM, Yokomori K.

Hum Mutat. 2014 Aug;35(8):998-1010. doi: 10.1002/humu.22593. Epub 2014 Jun 24.

PMID:
24838473
9.

DUX4 promotes transcription of FRG2 by directly activating its promoter in facioscapulohumeral muscular dystrophy.

Thijssen PE, Balog J, Yao Z, Pham TP, Tawil R, Tapscott SJ, Van der Maarel SM.

Skelet Muscle. 2014 Oct 24;4:19. doi: 10.1186/2044-5040-4-19. eCollection 2014.

10.

Managed ventricular pacing facilitating atrioventricular nodal reentrant tachycardia.

Frisch DR, Kenia AS, Walinsky P, Balog J.

Pacing Clin Electrophysiol. 2014 Nov;37(11):1568-71. doi: 10.1111/pace.12318. Epub 2013 Dec 3. No abstract available.

PMID:
24354537
11.

DUX4 binding to retroelements creates promoters that are active in FSHD muscle and testis.

Young JM, Whiddon JL, Yao Z, Kasinathan B, Snider L, Geng LN, Balog J, Tawil R, van der Maarel SM, Tapscott SJ.

PLoS Genet. 2013 Nov;9(11):e1003947. doi: 10.1371/journal.pgen.1003947. Epub 2013 Nov 21.

12.

The FSHD2 gene SMCHD1 is a modifier of disease severity in families affected by FSHD1.

Sacconi S, Lemmers RJ, Balog J, van der Vliet PJ, Lahaut P, van Nieuwenhuizen MP, Straasheijm KR, Debipersad RD, Vos-Versteeg M, Salviati L, Casarin A, Pegoraro E, Tawil R, Bakker E, Tapscott SJ, Desnuelle C, van der Maarel SM.

Am J Hum Genet. 2013 Oct 3;93(4):744-51. doi: 10.1016/j.ajhg.2013.08.004. Epub 2013 Sep 26.

13.

Temporally coherent visual stimuli boost ocular dominance plasticity.

Matthies U, Balog J, Lehmann K.

J Neurosci. 2013 Jul 17;33(29):11774-8. doi: 10.1523/JNEUROSCI.4262-12.2013.

14.

Intraoperative tissue identification using rapid evaporative ionization mass spectrometry.

Balog J, Sasi-Szabó L, Kinross J, Lewis MR, Muirhead LJ, Veselkov K, Mirnezami R, Dezső B, Damjanovich L, Darzi A, Nicholson JK, Takáts Z.

Sci Transl Med. 2013 Jul 17;5(194):194ra93. doi: 10.1126/scitranslmed.3005623.

15.

Chromatin remodeling of human subtelomeres and TERRA promoters upon cellular senescence: commonalities and differences between chromosomes.

Thijssen PE, Tobi EW, Balog J, Schouten SG, Kremer D, El Bouazzaoui F, Henneman P, Putter H, Eline Slagboom P, Heijmans BT, van der Maarel SM.

Epigenetics. 2013 May;8(5):512-21. doi: 10.4161/epi.24450. Epub 2013 Apr 17.

16.

Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD.

Krom YD, Thijssen PE, Young JM, den Hamer B, Balog J, Yao Z, Maves L, Snider L, Knopp P, Zammit PS, Rijkers T, van Engelen BG, Padberg GW, Frants RR, Tawil R, Tapscott SJ, van der Maarel SM.

PLoS Genet. 2013 Apr;9(4):e1003415. doi: 10.1371/journal.pgen.1003415. Epub 2013 Apr 4.

17.

DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics.

Simeonov DR, Wang X, Wang C, Sergeev Y, Dolinska M, Bower M, Fischer R, Winer D, Dubrovsky G, Balog JZ, Huizing M, Hart R, Zein WM, Gahl WA, Brooks BP, Adams DR.

Hum Mutat. 2013 Jun;34(6):827-35. doi: 10.1002/humu.22315. Epub 2013 Apr 30. Review.

18.

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2.

Lemmers RJ, Tawil R, Petek LM, Balog J, Block GJ, Santen GW, Amell AM, van der Vliet PJ, Almomani R, Straasheijm KR, Krom YD, Klooster R, Sun Y, den Dunnen JT, Helmer Q, Donlin-Smith CM, Padberg GW, van Engelen BG, de Greef JC, Aartsma-Rus AM, Frants RR, de Visser M, Desnuelle C, Sacconi S, Filippova GN, Bakker B, Bamshad MJ, Tapscott SJ, Miller DG, van der Maarel SM.

Nat Genet. 2012 Dec;44(12):1370-4. doi: 10.1038/ng.2454. Epub 2012 Nov 11.

19.

A genome-wide signature of glucocorticoid receptor binding in neuronal PC12 cells.

Polman JA, Welten JE, Bosch DS, de Jonge RT, Balog J, van der Maarel SM, de Kloet ER, Datson NA.

BMC Neurosci. 2012 Oct 3;13:118. doi: 10.1186/1471-2202-13-118.

20.

Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog.

Solomon BD, Bear KA, Wyllie A, Keaton AA, Dubourg C, David V, Mercier S, Odent S, Hehr U, Paulussen A, Clegg NJ, Delgado MR, Bale SJ, Lacbawan F, Ardinger HH, Aylsworth AS, Bhengu NL, Braddock S, Brookhyser K, Burton B, Gaspar H, Grix A, Horovitz D, Kanetzke E, Kayserili H, Lev D, Nikkel SM, Norton M, Roberts R, Saal H, Schaefer GB, Schneider A, Smith EK, Sowry E, Spence MA, Shalev SA, Steiner CE, Thompson EM, Winder TL, Balog JZ, Hadley DW, Zhou N, Pineda-Alvarez DE, Roessler E, Muenke M.

J Med Genet. 2012 Jul;49(7):473-9. doi: 10.1136/jmedgenet-2012-101008.

PMID:
22791840
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