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Items: 1 to 20 of 193

1.

Charge Inversion and Topological Phase Transition at a Twist Angle Induced van Hove Singularity of Bilayer Graphene.

Kim Y, Herlinger P, Moon P, Koshino M, Taniguchi T, Watanabe K, Smet JH.

Nano Lett. 2016 Jul 11. [Epub ahead of print]

PMID:
27387484
2.

Next-Generation "-omics" Approaches Reveal a Massive Alteration of Host RNA Metabolism during Bacteriophage Infection of Pseudomonas aeruginosa.

Chevallereau A, Blasdel BG, De Smet J, Monot M, Zimmermann M, Kogadeeva M, Sauer U, Jorth P, Whiteley M, Debarbieux L, Lavigne R.

PLoS Genet. 2016 Jul 5;12(7):e1006134. doi: 10.1371/journal.pgen.1006134. eCollection 2016 Jul.

3.

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype.

Alston CL, Compton AG, Formosa LE, Strecker V, Oláhová M, Haack TB, Smet J, Stouffs K, Diakumis P, Ciara E, Cassiman D, Romain N, Yarham JW, He L, De Paepe B, Vanlander AV, Seneca S, Feichtinger RG, Płoski R, Rokicki D, Pronicka E, Haller RG, Van Hove JL, Bahlo M, Mayr JA, Van Coster R, Prokisch H, Wittig I, Ryan MT, Thorburn DR, Taylor RW.

Am J Hum Genet. 2016 Jul 7;99(1):217-27. doi: 10.1016/j.ajhg.2016.05.021. Epub 2016 Jun 30.

4.

MgZnO/ZnO heterostructures with electron mobility exceeding 1 × 10(6) cm(2)/Vs.

Falson J, Kozuka Y, Uchida M, Smet JH, Arima TH, Tsukazaki A, Kawasaki M.

Sci Rep. 2016 May 27;6:26598. doi: 10.1038/srep26598.

5.

Erratum: Signatures for Wigner Crystal Formation in the Chemical Potential of a Two-Dimensional Electron System [Phys. Rev. Lett. 113, 076804 (2014)].

Zhang D, Huang X, Dietsche W, von Klitzing K, Smet JH.

Phys Rev Lett. 2016 May 6;116(18):189902. Epub 2016 May 2.

PMID:
27203351
6.

High coverage metabolomics analysis reveals phage-specific alterations to Pseudomonas aeruginosa physiology during infection.

De Smet J, Zimmermann M, Kogadeeva M, Ceyssens PJ, Vermaelen W, Blasdel B, Bin Jang H, Sauer U, Lavigne R.

ISME J. 2016 Feb 16. doi: 10.1038/ismej.2016.3. [Epub ahead of print]

PMID:
26882266
7.

Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses.

Vanlander AV, Muiño Mosquera L, Panzer J, Deconinck T, Smet J, Seneca S, Van Dorpe J, Ferdinande L, Ceuterick-de Groote C, De Jonghe P, Van Coster R, Baets J.

Mitochondrion. 2016 Mar;27:32-8. doi: 10.1016/j.mito.2016.02.001. Epub 2016 Feb 23.

PMID:
26855408
8.

Disulfiram inhibition of cyanide formation after acetonitrile poisoning.

De Paepe P, Colin P, Depuydt P, Decavele AS, De Smet J, Boussery K, Stove C, Benoit D, Verstraete A, Van Bocxlaer J, Buylaert W.

Clin Toxicol (Phila). 2016;54(1):56-60. doi: 10.3109/15563650.2015.1101770. Epub 2015 Dec 1.

PMID:
26623950
9.

Antibacterial phage ORFans of Pseudomonas aeruginosa phage LUZ24 reveal a novel MvaT inhibiting protein.

Wagemans J, Delattre AS, Uytterhoeven B, De Smet J, Cenens W, Aertsen A, Ceyssens PJ, Lavigne R.

Front Microbiol. 2015 Nov 6;6:1242. doi: 10.3389/fmicb.2015.01242. eCollection 2015.

10.

Fractional Quantum Hall States in Bilayer Graphene Probed by Transconductance Fluctuations.

Kim Y, Lee DS, Jung S, Skákalová V, Taniguchi T, Watanabe K, Kim JS, Smet JH.

Nano Lett. 2015 Nov 11;15(11):7445-51. doi: 10.1021/acs.nanolett.5b02876. Epub 2015 Oct 22.

PMID:
26479836
11.

Random flips of electric field in microwave-induced states with spontaneously broken symmetry.

Dorozhkin SI, Umansky V, Pfeiffer LN, West KW, Baldwin K, von Klitzing K, Smet JH.

Phys Rev Lett. 2015 May 1;114(17):176808. Epub 2015 May 1.

PMID:
25978254
12.

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy.

Debray FG, Stümpfig C, Vanlander AV, Dideberg V, Josse C, Caberg JH, Boemer F, Bours V, Stevens R, Seneca S, Smet J, Lill R, van Coster R.

J Inherit Metab Dis. 2015 Nov;38(6):1147-53. doi: 10.1007/s10545-015-9857-1. Epub 2015 May 14.

PMID:
25971455
13.

Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency.

Ahting U, Mayr JA, Vanlander AV, Hardy SA, Santra S, Makowski C, Alston CL, Zimmermann FA, Abela L, Plecko B, Rohrbach M, Spranger S, Seneca S, Rolinski B, Hagendorff A, Hempel M, Sperl W, Meitinger T, Smet J, Taylor RW, Van Coster R, Freisinger P, Prokisch H, Haack TB.

Front Genet. 2015 Apr 13;6:123. doi: 10.3389/fgene.2015.00123. eCollection 2015.

14.

Erratum to: TMEM70 deficiency: long-term outcome of 48 patients.

Magner M, Dvorakova V, Tesarova M, Mazurova S, Hansikova H, Zahorec M, Brennerova K, Bzduch V, Spiegel R, Horovitz Y, Mandel H, Eminoğlu FT, Mayr JA, Koch J, Martinelli D, Bertini E, Konstantopoulou V, Smet J, Rahman S, Broomfield A, Stojanović V, Dionisi-Vici C, van Coster R, Morava E, Sperl W, Zeman J, Honzik T.

J Inherit Metab Dis. 2015 May;38(3):583-4. doi: 10.1007/s10545-015-9833-9. No abstract available.

PMID:
25778942
15.

Health-related physical fitness in patients with bipolar disorder vs. healthy controls: an exploratory study.

Vancampfort D, Sienaert P, Wyckaert S, De Hert M, Stubbs B, Soundy A, De Smet J, Probst M.

J Affect Disord. 2015 May 15;177:22-7. doi: 10.1016/j.jad.2014.12.058. Epub 2015 Feb 7.

PMID:
25745831
16.

A protocol to assess insect resistance to heat waves, applied to bumblebees (Bombus Latreille, 1802).

Martinet B, Lecocq T, Smet J, Rasmont P.

PLoS One. 2015 Mar 4;10(3):e0118591. doi: 10.1371/journal.pone.0118591. eCollection 2015.

17.

Forearm deoxyhemoglobin and deoxymyoglobin (deoxy[Hb + Mb]) measured by near-infrared spectroscopy (NIRS) using a handgrip test in mitochondrial myopathy.

Celie BM, Boone J, Smet JE, Vanlander AV, De Bleecker JL, Van Coster RN, Bourgois JG.

Appl Spectrosc. 2015 Mar;69(3):342-7. doi: 10.1366/14-07604. Epub 2015 Feb 1.

PMID:
25665184
18.

Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation.

Peeters A, Shinde AB, Dirkx R, Smet J, De Bock K, Espeel M, Vanhorebeek I, Vanlander A, Van Coster R, Carmeliet P, Fransen M, Van Veldhoven PP, Baes M.

Biochim Biophys Acta. 2015 Feb;1853(2):285-98. doi: 10.1016/j.bbamcr.2014.11.017. Epub 2014 Nov 20.

19.

Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.

Kopajtich R, Nicholls TJ, Rorbach J, Metodiev MD, Freisinger P, Mandel H, Vanlander A, Ghezzi D, Carrozzo R, Taylor RW, Marquard K, Murayama K, Wieland T, Schwarzmayr T, Mayr JA, Pearce SF, Powell CA, Saada A, Ohtake A, Invernizzi F, Lamantea E, Sommerville EW, Pyle A, Chinnery PF, Crushell E, Okazaki Y, Kohda M, Kishita Y, Tokuzawa Y, Assouline Z, Rio M, Feillet F, Mousson de Camaret B, Chretien D, Munnich A, Menten B, Sante T, Smet J, Régal L, Lorber A, Khoury A, Zeviani M, Strom TM, Meitinger T, Bertini ES, Van Coster R, Klopstock T, Rötig A, Haack TB, Minczuk M, Prokisch H.

Am J Hum Genet. 2014 Dec 4;95(6):708-20. doi: 10.1016/j.ajhg.2014.10.017. Epub 2014 Nov 26.

20.

Two siblings with homozygous pathogenic splice-site variant in mitochondrial asparaginyl-tRNA synthetase (NARS2).

Vanlander AV, Menten B, Smet J, De Meirleir L, Sante T, De Paepe B, Seneca S, Pearce SF, Powell CA, Vergult S, Michotte A, De Latter E, Vantomme L, Minczuk M, Van Coster R.

Hum Mutat. 2015 Feb;36(2):222-31. doi: 10.1002/humu.22728.

PMID:
25385316
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