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Items: 1 to 50 of 86

1.

Roles of prefrontal cortex and mediodorsal thalamus in task engagement and behavioral flexibility.

Marton T, Seifikar H, Luongo FJ, Lee AT, Sohal VS.

J Neurosci. 2018 Feb 7. pii: 1728-17. doi: 10.1523/JNEUROSCI.1728-17.2018. [Epub ahead of print]

PMID:
29437889
2.

The first antenatal diagnosis of KBG syndrome: a microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD11 associated with the disorder.

Hodgetts Morton V, Quinlan-Jones E, Butts N, Williams D, Hamilton S, Marton T, Morris K.

Clin Case Rep. 2017 Dec 11;6(1):189-191. doi: 10.1002/ccr3.1285. eCollection 2018 Jan.

3.

High intraspecific genome diversity in the model arbuscular mycorrhizal symbiont Rhizophagus irregularis.

Chen ECH, Morin E, Beaudet D, Noel J, Yildirir G, Ndikumana S, Charron P, St-Onge C, Giorgi J, Krüger M, Marton T, Ropars J, Grigoriev IV, Hainaut M, Henrissat B, Roux C, Martin F, Corradi N.

New Phytol. 2018 Jan 22. doi: 10.1111/nph.14989. [Epub ahead of print]

PMID:
29355972
4.

Parallel palaeogenomic transects reveal complex genetic history of early European farmers.

Lipson M, Szécsényi-Nagy A, Mallick S, Pósa A, Stégmár B, Keerl V, Rohland N, Stewardson K, Ferry M, Michel M, Oppenheimer J, Broomandkhoshbacht N, Harney E, Nordenfelt S, Llamas B, Gusztáv Mende B, Köhler K, Oross K, Bondár M, Marton T, Osztás A, Jakucs J, Paluch T, Horváth F, Csengeri P, Koós J, Sebők K, Anders A, Raczky P, Regenye J, Barna JP, Fábián S, Serlegi G, Toldi Z, Gyöngyvér Nagy E, Dani J, Molnár E, Pálfi G, Márk L, Melegh B, Bánfai Z, Domboróczki L, Fernández-Eraso J, Antonio Mujika-Alustiza J, Alonso Fernández C, Jiménez Echevarría J, Bollongino R, Orschiedt J, Schierhold K, Meller H, Cooper A, Burger J, Bánffy E, Alt KW, Lalueza-Fox C, Haak W, Reich D.

Nature. 2017 Nov 16;551(7680):368-372. doi: 10.1038/nature24476. Epub 2017 Nov 8.

PMID:
29144465
5.

Possible cases of leprosy from the Late Copper Age (3780-3650 cal BC) in Hungary.

Köhler K, Marcsik A, Zádori P, Biro G, Szeniczey T, Fábián S, Serlegi G, Marton T, Donoghue HD, Hajdu T.

PLoS One. 2017 Oct 12;12(10):e0185966. doi: 10.1371/journal.pone.0185966. eCollection 2017.

6.

Re: Stillbirth collection by Man et al.

Cox P, Marton T, Hargitai B, Coetzee A, Bowen C, Penman D, Evans M, Gannon C, French P, Cohen M, Holden S, Allotey J, Evans C, Murphy A, Turner K, Cullinane C, Stahlschmidt J, Kokai G, Al Adnani M, Marnerides A, Vadgama B, McPartland J.

Ultrasound Obstet Gynecol. 2017 Feb;49(2):281-282. doi: 10.1002/uog.17380. No abstract available.

7.

Limited Tumor Tissue Drug Penetration Contributes to Primary Resistance against Angiogenesis Inhibitors.

Torok S, Rezeli M, Kelemen O, Vegvari A, Watanabe K, Sugihara Y, Tisza A, Marton T, Kovacs I, Tovari J, Laszlo V, Helbich TH, Hegedus B, Klikovits T, Hoda MA, Klepetko W, Paku S, Marko-Varga G, Dome B.

Theranostics. 2017 Jan 1;7(2):400-412. doi: 10.7150/thno.16767. eCollection 2017.

8.

Evidence for the sexual origin of heterokaryosis in arbuscular mycorrhizal fungi.

Ropars J, Toro KS, Noel J, Pelin A, Charron P, Farinelli L, Marton T, Krüger M, Fuchs J, Brachmann A, Corradi N.

Nat Microbiol. 2016 Mar 21;1(6):16033. doi: 10.1038/nmicrobiol.2016.33.

PMID:
27572831
9.

Homer 1a and mGluR5 phosphorylation in reward-sensitive metaplasticity: A hypothesis of neuronal selection and bidirectional synaptic plasticity.

Marton TM, Hussain Shuler MG, Worley PF.

Brain Res. 2015 Dec 2;1628(Pt A):17-28. doi: 10.1016/j.brainres.2015.06.037. Epub 2015 Jul 14. Review.

PMID:
26187757
10.

Of Mice, Men, and Microbial Opsins: How Optogenetics Can Help Hone Mouse Models of Mental Illness.

Marton TF, Sohal VS.

Biol Psychiatry. 2016 Jan 1;79(1):47-52. doi: 10.1016/j.biopsych.2015.04.012. Epub 2015 Apr 23. Review.

11.

Tracing the genetic origin of Europe's first farmers reveals insights into their social organization.

Szécsényi-Nagy A, Brandt G, Haak W, Keerl V, Jakucs J, Möller-Rieker S, Köhler K, Mende BG, Oross K, Marton T, Osztás A, Kiss V, Fecher M, Pálfi G, Molnár E, Sebők K, Czene A, Paluch T, Šlaus M, Novak M, Pećina-Šlaus N, Ősz B, Voicsek V, Somogyi K, Tóth G, Kromer B, Bánffy E, Alt KW.

Proc Biol Sci. 2015 Apr 22;282(1805). pii: 20150339. doi: 10.1098/rspb.2015.0339.

12.

Murine pheromone proteins constitute a context-dependent combinatorial code governing multiple social behaviors.

Kaur AW, Ackels T, Kuo TH, Cichy A, Dey S, Hays C, Kateri M, Logan DW, Marton TF, Spehr M, Stowers L.

Cell. 2014 Apr 24;157(3):676-88. doi: 10.1016/j.cell.2014.02.025.

13.

A general theory of intertemporal decision-making and the perception of time.

Namboodiri VM, Mihalas S, Marton TM, Hussain Shuler MG.

Front Behav Neurosci. 2014 Feb 28;8:61. doi: 10.3389/fnbeh.2014.00061. eCollection 2014.

14.

[Status epilepticus and its treatment--update 2013].

Csilla G, Vera J, Réka H, Beáta B, Márton T, András F, Sámuel K, József J.

Ideggyogy Sz. 2013 Nov 30;66(11-12):372-82. Review. Hungarian.

PMID:
24555236
15.

Placenta chorioangioma: a rare case and systematic review of literature.

Al Wattar BH, Hillman SC, Marton T, Foster K, Kilby MD.

J Matern Fetal Neonatal Med. 2014 Jul;27(10):1055-63. doi: 10.3109/14767058.2013.847424. Epub 2013 Oct 17. Review.

PMID:
24460422
16.

Elevated brain weight/liver weight ratio in normal body weight centile term perinatal deaths: an indicator of terminal intrauterine malnourishment.

Marton T, Hargitai B, Bowen C, Cox PM.

Pediatr Dev Pathol. 2013 Jul-Aug;16(4):267-71. doi: 10.2350/12-11-1278-OA.1. Epub 2013 Apr 9.

PMID:
23570414
17.

Implementation and experience of an alternative QF-PCR and MLPA diagnostic strategy to detect chromosomal abnormalities in fetal and neonatal pathology samples.

McClelland LS, Allen SK, Larkins SA, Hamilton SJ, Marton T, Cox PM, Hargitai B, Johnston EH, Morgan C, Hardy G.

Pediatr Dev Pathol. 2011 Nov-Dec;14(6):460-8. doi: 10.2350/11-01-0971-OA.1. Epub 2011 Aug 29.

PMID:
21875355
18.

Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome).

Meyer E, Ricketts C, Morgan NV, Morris MR, Pasha S, Tee LJ, Rahman F, Bazin A, Bessières B, Déchelotte P, Yacoubi MT, Al-Adnani M, Marton T, Tannahill D, Trembath RC, Fallet-Bianco C, Cox P, Williams D, Maher ER.

Am J Hum Genet. 2010 Mar 12;86(3):471-8. doi: 10.1016/j.ajhg.2010.02.004. Epub 2010 Mar 4.

19.

Fowler syndrome-a clinical, radiological, and pathological study of 14 cases.

Williams D, Patel C, Fallet-Bianco C, Kalyanasundaram K, Yacoubi M, Déchelotte P, Scott R, Bazin A, Bessières B, Marton T, Cox P.

Am J Med Genet A. 2010 Jan;152A(1):153-60. doi: 10.1002/ajmg.a.33094.

PMID:
20014121
20.

Pathological assessment of intrauterine growth restriction.

Cox P, Marton T.

Best Pract Res Clin Obstet Gynaecol. 2009 Dec;23(6):751-64. doi: 10.1016/j.bpobgyn.2009.06.006. Epub 2009 Oct 23. Review.

PMID:
19854107
21.

Germline mutation in DOK7 associated with fetal akinesia deformation sequence.

Vogt J, Morgan NV, Marton T, Maxwell S, Harrison BJ, Beeson D, Maher ER.

J Med Genet. 2009 May;46(5):338-40. doi: 10.1136/jmg.2008.065425. Epub 2009 Mar 3.

PMID:
19261599
22.

Species specificity in major urinary proteins by parallel evolution.

Logan DW, Marton TF, Stowers L.

PLoS One. 2008 Sep 25;3(9):e3280. doi: 10.1371/journal.pone.0003280.

23.

Cranial vault defects: the description of three cases that illustrate a spectrum of anomalies.

Evans C, Marton T, Rutter S, Anumba DO, Whitby EH, Cohen MC.

Pediatr Dev Pathol. 2009 Mar-Apr;12(2):96-102. doi: 10.2350/08-02-0415.1. Epub 2008 Apr 28.

PMID:
18442303
24.

Identification of protein pheromones that promote aggressive behaviour.

Chamero P, Marton TF, Logan DW, Flanagan K, Cruz JR, Saghatelian A, Cravatt BF, Stowers L.

Nature. 2007 Dec 6;450(7171):899-902.

PMID:
18064011
25.

Prenatal diagnosis of abnormal course of umbilical vein and absent ductus venosus--report of three cases.

Hajdú J, Marton T, Kozsurek M, Pete B, Csapó Z, Beke A, Papp Z.

Fetal Diagn Ther. 2008;23(2):136-9. Epub 2007 Nov 26. Review.

PMID:
18046072
27.

Ultrasound and magnetic resonance imaging in the assessment of a fetal intracardiac mass.

Ong S, Usher-Somers M, Philip S, Miller P, Foster K, Marton T, Martin W, Kilby M.

Ultrasound Obstet Gynecol. 2007 May;29(5):600-1. No abstract available.

28.

[Congenital absence of the ductus venosus associated with severe congenital heart malformation--case report and review of the literature].

Hajdú J, Csapó Z, Rigó J Jr, Marton T, Pete B, Papp Z.

Orv Hetil. 2006 Oct 1;147(39):1901-3. Review. Hungarian.

PMID:
17117510
29.

Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome.

Morgan NV, Brueton LA, Cox P, Greally MT, Tolmie J, Pasha S, Aligianis IA, van Bokhoven H, Marton T, Al-Gazali L, Morton JE, Oley C, Johnson CA, Trembath RC, Brunner HG, Maher ER.

Am J Hum Genet. 2006 Aug;79(2):390-5. Epub 2006 Jun 20.

30.

Congenital heart diseases in twin pregnancies.

Hajdu J, Beke A, Marton T, Hruby E, Pete B, Papp Z.

Fetal Diagn Ther. 2006;21(2):198-203.

PMID:
16491003
31.

Hydrops fetalis and neonatal death from human parvovirus B19: an unusual complication.

Marton T, Martin WL, Whittle MJ.

Prenat Diagn. 2005 Jul;25(7):543-5.

PMID:
16034838
32.

What is a pheromone? Mammalian pheromones reconsidered.

Stowers L, Marton TF.

Neuron. 2005 Jun 2;46(5):699-702. Review.

33.

[Congenital heart malformations is twin pregnancies].

Hajdú J, Beke A, Marton T, Hruby E, Pete B, Papp Z.

Orv Hetil. 2005 Feb 20;146(8):355-60. Hungarian.

PMID:
15803886
34.

Birmingham women's health care.

Marton T, Hajdú J.

Prenat Diagn. 2004 Sep;24(9):754. No abstract available.

PMID:
15386457
35.

Best practice no 178. Examination of the human placenta.

Hargitai B, Marton T, Cox PM.

J Clin Pathol. 2004 Aug;57(8):785-92.

36.

[Fetal examination of first trimester abortions].

Marton T, Hargitai B, Böze T, Tankó A, Csapó Z, Szende B, Papp Z.

Orv Hetil. 2003 Jun 15;144(24):1185-98. Hungarian.

PMID:
12866148
37.

[Pathophysiology and therapeutic possibilities in twin-to-twin transfusion syndrome].

Marton T, Hruby E, Hajdú J, Papp Z.

Orv Hetil. 2002 May 19;143(20):1145-51. Hungarian.

PMID:
12073662
38.
39.

[Heterotaxy syndrome, analysis of 13 cases and review of the literature].

Marton T, Cesko I, Hajdú J, Hargitai B, Papp Z.

Orv Hetil. 2002 Feb 10;143(6):299-301. Review. Hungarian.

PMID:
11915190
40.

Diagnosis of an unusual form of iniencephaly in the first trimester of pregnancy.

Marton T, Tankó A, Mezei G, Papp Z.

Ultrasound Obstet Gynecol. 2001 Nov;18(5):549-51. No abstract available.

41.
42.

Pulmonary stenosis and reactive right ventricular hypertrophy in the recipient fetus as a consequence of twin-to-twin transfusion.

Marton T, Hajdú J, Papp C, Patkós P, Hruby E, Papp Z.

Prenat Diagn. 2001 Jun;21(6):452-6.

PMID:
11438948
43.

[Confirmation of a prenatal diagnosis of trisomy 13 with comparative genomic hybridization (CGH)].

Marton T, Thein A, Bán Z, Soothill P, Oroszné NJ, Papp Z.

Orv Hetil. 2001 May 13;142(19):997-1000. Review. Hungarian.

PMID:
11419300
44.

A rare case of non-immune hydrops fetalis: double-chambered right ventricle. A case report.

Marton T, Hajdú J, Papp Z.

Fetal Diagn Ther. 2001 Jul-Aug;16(4):251-3.

PMID:
11399891
45.

Hypercapnia stimulates prostaglandin E(2) but not prostaglandin I(2) release in endothelial cells cultured from microvessels of human fetal brain.

Kövecs K, Komjáti K, Marton T, Skopál J, Sándor P, Nagy Z.

Brain Res Bull. 2001 Mar 1;54(4):387-90.

PMID:
11306189
46.

Polysplenia and situs inversus in siblings. Case reports.

Cesko I, Hajdú J, Marton T, Tarnai L, Papp Z.

Fetal Diagn Ther. 2001 Jan-Feb;16(1):1-3.

PMID:
11125242
47.

["Maternal floor infarct", simultaneous manifestation of intrauterine fetal retardation and high maternal AFP level].

Görbe E, Rigó J Jr, Marton T, Köhalmi B, Csabay L, Csapó Z.

Z Geburtshilfe Neonatol. 1999 Sep-Oct;203(5):218-20. German.

PMID:
10596416
48.
49.

[Practice of fetal pathological examination].

Marton T, Hargitai B, Patkós P, Csapó Z, Szende B, Papp Z.

Orv Hetil. 1999 Jun 20;140(25):1411-6. Hungarian.

PMID:
10489769
50.

Familial association of congenital left heart abnormalities and sustained fetal arrhythmia.

Hajdú J, Marton T, Tóth-Pál E, Papp Z.

Pediatr Cardiol. 1999 Sep-Oct;20(5):368-70.

PMID:
10441694

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