Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 174

1.

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. 2014 Nov 11. doi: 10.1002/humu.22728. [Epub ahead of print]

PMID:
25385316
[PubMed - as supplied by publisher]
2.

A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome.

Vancampenhout K, Caljon B, Spits C, Stouffs K, Jonckheere A, De Meirleir L, Lissens W, Vanlander A, Smet J, De Paepe B, Van Coster R, Seneca S.

PLoS One. 2014 Nov 10;9(11):e112950. doi: 10.1371/journal.pone.0112950. eCollection 2014.

PMID:
25383547
[PubMed - in process]
Free PMC Article
3.

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-Kozicz E, Sperl W, Zeman J, Honzik T.

J Inherit Metab Dis. 2014 Oct 18. [Epub ahead of print]

PMID:
25326274
[PubMed - as supplied by publisher]
4.

Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q.

Vanlander AV, Okun JG, de Jaeger A, Smet J, De Latter E, De Paepe B, Dacremont G, Wuyts B, Vanheel B, De Paepe P, Jorens PG, Regenmortel Van N, Coster Van R.

Anesthesiology. 2014 Oct 7. [Epub ahead of print]

PMID:
25296107
[PubMed - as supplied by publisher]
5.

Genomic standards consortium projects.

Field D, Sterk P, Kottmann R, De Smet JW, Amaral-Zettler L, Cochrane G, Cole JR, Davies N, Dawyndt P, Garrity GM, Gilbert JA, Glöckner FO, Hirschman L, Klenk HP, Knight R, Kyrpides N, Meyer F, Karsch-Mizrachi I, Morrison N, Robbins R, San Gil I, Sansone S, Schriml L, Tatusova T, Ussery D, Yilmaz P, White O, Wooley J, Caporaso G.

Stand Genomic Sci. 2014 Feb 15;9(3):599-601. doi: 10.4056/sigs.5559680. eCollection 2014 Jun 15.

PMID:
25197446
[PubMed]
Free PMC Article
6.

Systematic identification of hypothetical bacteriophage proteins targeting key protein complexes of pseudomonas aeruginosa.

Van den Bossche A, Ceyssens PJ, De Smet J, Hendrix H, Bellon H, Leimer N, Wagemans J, Delattre AS, Cenens W, Aertsen A, Landuyt B, Minakhin L, Severinov K, Noben JP, Lavigne R.

J Proteome Res. 2014 Oct 3;13(10):4446-56. doi: 10.1021/pr500796n. Epub 2014 Sep 15.

PMID:
25185497
[PubMed - in process]
7.

Signatures for Wigner crystal formation in the chemical potential of a two-dimensional electron system.

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

Phys Rev Lett. 2014 Aug 15;113(7):076804. Epub 2014 Aug 14.

PMID:
25170727
[PubMed - in process]
8.

Probing the microscopic structure of the stripe phase at filling factor 5/2.

Friess B, Umansky V, Tiemann L, von Klitzing K, Smet JH.

Phys Rev Lett. 2014 Aug 15;113(7):076803. Epub 2014 Aug 13.

PMID:
25170726
[PubMed - in process]
9.

Functional elucidation of antibacterial phage ORFans targeting Pseudomonas aeruginosa.

Wagemans J, Blasdel BG, Van den Bossche A, Uytterhoeven B, De Smet J, Paeshuyse J, Cenens W, Aertsen A, Uetz P, Delattre AS, Ceyssens PJ, Lavigne R.

Cell Microbiol. 2014 Dec;16(12):1822-35. doi: 10.1111/cmi.12330. Epub 2014 Aug 26.

PMID:
25059764
[PubMed - in process]
10.

Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisions.

De Praeter C, Vanlander A, Vanhaesebrouck P, Smet J, Seneca S, De Sutter P, Van Coster R.

Eur J Pediatr. 2014 Jul 10. [Epub ahead of print]

PMID:
25009317
[PubMed - as supplied by publisher]
11.

Development of giant bacteriophage ϕKZ is independent of the host transcription apparatus.

Ceyssens PJ, Minakhin L, Van den Bossche A, Yakunina M, Klimuk E, Blasdel B, De Smet J, Noben JP, Bläsi U, Severinov K, Lavigne R.

J Virol. 2014 Sep;88(18):10501-10. doi: 10.1128/JVI.01347-14. Epub 2014 Jun 25.

PMID:
24965474
[PubMed - in process]
12.

Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene.

Debray FG, Seneca S, Gonce M, Vancampenhaut K, Bianchi E, Boemer F, Weekers L, Smet J, Van Coster R.

Mitochondrion. 2014 Jul;17:101-5. doi: 10.1016/j.mito.2014.06.003. Epub 2014 Jun 20.

PMID:
24956508
[PubMed - in process]
13.

Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

Seneca S, Vancampenhout K, Van Coster R, Smet J, Lissens W, Vanlander A, De Paepe B, Jonckheere A, Stouffs K, De Meirleir L.

Eur J Hum Genet. 2014 Mar 26. doi: 10.1038/ejhg.2014.49. [Epub ahead of print]

PMID:
24667782
[PubMed - as supplied by publisher]
14.

Pneumococcal aetiology and serotype distribution in paediatric community-acquired pneumonia.

De Schutter I, Vergison A, Tuerlinckx D, Raes M, Smet J, Smeesters PR, Verhaegen J, Mascart F, Surmont F, Malfroot A.

PLoS One. 2014 Feb 18;9(2):e89013. doi: 10.1371/journal.pone.0089013. eCollection 2014.

PMID:
24558464
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Defects in bilayer silica and graphene: common trends in diverse hexagonal two-dimensional systems.

Björkman T, Kurasch S, Lehtinen O, Kotakoski J, Yazyev OV, Srivastava A, Skakalova V, Smet JH, Kaiser U, Krasheninnikov AV.

Sci Rep. 2013 Dec 16;3:3482. doi: 10.1038/srep03482.

PMID:
24336488
[PubMed - in process]
Free PMC Article
16.

Different T cell memory in preadolescents after whole-cell or acellular pertussis vaccination.

Smits K, Pottier G, Smet J, Dirix V, Vermeulen F, De Schutter I, Carollo M, Locht C, Ausiello CM, Mascart F.

Vaccine. 2013 Dec 17;32(1):111-8. doi: 10.1016/j.vaccine.2013.10.056. Epub 2013 Oct 29.

PMID:
24176499
[PubMed - indexed for MEDLINE]
Free Article
17.

Forearm muscle oxygenation responses during and following arterial occlusion in patients with mitochondrial myopathy.

Boone J, Celie B, Dumortier J, Barstow TJ, De Bleecker J, Smet J, Van Lander A, Van Coster R, Bourgois J.

Respir Physiol Neurobiol. 2014 Jan 1;190:70-5. doi: 10.1016/j.resp.2013.09.007. Epub 2013 Sep 23.

PMID:
24070894
[PubMed - indexed for MEDLINE]
18.

A new mutation in MT-ND1 m.3928G>C p.V208L causes Leigh disease with infantile spasms.

Wray CD, Friederich MW, du Sart D, Pantaleo S, Smet J, Kucera C, Fenton L, Scharer G, Van Coster R, Van Hove JL.

Mitochondrion. 2013 Nov;13(6):656-61. doi: 10.1016/j.mito.2013.09.004. Epub 2013 Sep 22.

PMID:
24063851
[PubMed - indexed for MEDLINE]
19.

Fractional quantum Hall phase transitions and four-flux states in graphene.

Feldman BE, Levin AJ, Krauss B, Abanin DA, Halperin BI, Smet JH, Yacoby A.

Phys Rev Lett. 2013 Aug 16;111(7):076802. Epub 2013 Aug 16.

PMID:
23992076
[PubMed]
20.

Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2).

Scalais E, Chafai R, Van Coster R, Bindl L, Nuttin C, Panagiotaraki C, Seneca S, Lissens W, Ribes A, Geers C, Smet J, De Meirleir L.

Eur J Paediatr Neurol. 2013 Nov;17(6):625-30. doi: 10.1016/j.ejpn.2013.05.013. Epub 2013 Jun 28.

PMID:
23816342
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk