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Items: 1 to 50 of 89

1.

Signals from the brain and olfactory epithelium control shaping of the mammalian nasal capsule cartilage.

Kaucka M, Petersen J, Tesarova M, Szarowska B, Kastriti ME, Xie M, Kicheva A, Annusver K, Kasper M, Symmons O, Pan L, Spitz F, Kaiser J, Hovorakova M, Zikmund T, Sunadome K, Matise MP, Wang H, Marklund U, Abdo H, Ernfors P, Maire P, Wurmser M, Chagin AS, Fried K, Adameyko I.

Elife. 2018 Jun 13;7. pii: e34465. doi: 10.7554/eLife.34465.

2.

Revisiting mitochondrial diagnostic criteria in the new era of genomics.

Witters P, Saada A, Honzik T, Tesarova M, Kleinle S, Horvath R, Goldstein A, Morava E.

Genet Med. 2018 Apr;20(4):444-451. doi: 10.1038/gim.2017.125. Epub 2017 Oct 26.

PMID:
29261183
3.

Changes in transcription pattern lead to a marked decrease in COX, CS and SQR activity after the developmental point of the 22(nd) gestational week.

Kolarova H, Krizova J, Hulkova M, Hansikova H, Hulkova H, Smid V, Zeman J, Honzik T, Tesarova M.

Physiol Res. 2018 Mar 16;67(1):79-91. Epub 2017 Nov 10.

4.

Extensive flagellar remodeling during the complex life cycle of Paratrypanosoma, an early-branching trypanosomatid.

Skalický T, Dobáková E, Wheeler RJ, Tesařová M, Flegontov P, Jirsová D, Votýpka J, Yurchenko V, Ayala FJ, Lukeš J.

Proc Natl Acad Sci U S A. 2017 Oct 31;114(44):11757-11762. doi: 10.1073/pnas.1712311114. Epub 2017 Oct 16.

5.

Hereditary Multiple Exostoses: Clinical, Molecular and Radiologic Survey in 9 Families.

Medek K, Zeman J, Honzík T, Hansíková H, Švecová Š, Beránková K, Kučerová Vidrová V, Kuklík M, Chomiak J, Tesařová M.

Prague Med Rep. 2017;118(2-3):87-94. doi: 10.14712/23362936.2017.8.

6.

Revealing 3D Ultrastructure and Morphology of Stem Cell Spheroids by Electron Microscopy.

Jaros J, Petrov M, Tesarova M, Hampl A.

Methods Mol Biol. 2017;1612:417-431. doi: 10.1007/978-1-4939-7021-6_30.

PMID:
28634960
7.

Oriented clonal cell dynamics enables accurate growth and shaping of vertebrate cartilage.

Kaucka M, Zikmund T, Tesarova M, Gyllborg D, Hellander A, Jaros J, Kaiser J, Petersen J, Szarowska B, Newton PT, Dyachuk V, Li L, Qian H, Johansson AS, Mishina Y, Currie JD, Tanaka EM, Erickson A, Dudley A, Brismar H, Southam P, Coen E, Chen M, Weinstein LS, Hampl A, Arenas E, Chagin AS, Fried K, Adameyko I.

Elife. 2017 Apr 17;6. pii: e25902. doi: 10.7554/eLife.25902.

8.

Molecular mechanisms of thermal resistance of the insect trypanosomatid Crithidia thermophila.

Ishemgulova A, Butenko A, Kortišová L, Boucinha C, Grybchuk-Ieremenko A, Morelli KA, Tesařová M, Kraeva N, Grybchuk D, Pánek T, Flegontov P, Lukeš J, Votýpka J, Pavan MG, Opperdoes FR, Spodareva V, d'Avila-Levy CM, Kostygov AY, Yurchenko V.

PLoS One. 2017 Mar 22;12(3):e0174165. doi: 10.1371/journal.pone.0174165. eCollection 2017.

9.

OPA1 analysis in an international series of probands with bilateral optic atrophy.

Liskova P, Tesarova M, Dudakova L, Svecova S, Kolarova H, Honzik T, Seto S, Votruba M.

Acta Ophthalmol. 2017 Jun;95(4):363-369. doi: 10.1111/aos.13285. Epub 2016 Nov 17.

10.

Thymidine kinase 2 and alanyl-tRNA synthetase 2 deficiencies cause lethal mitochondrial cardiomyopathy: case reports and review of the literature.

Mazurova S, Magner M, Kucerova-Vidrova V, Vondrackova A, Stranecky V, Pristoupilova A, Zamecnik J, Hansikova H, Zeman J, Tesarova M, Honzik T.

Cardiol Young. 2017 Jul;27(5):936-944. doi: 10.1017/S1047951116001876. Epub 2016 Nov 14. Review.

PMID:
27839525
11.

Unique presentation of LHON/MELAS overlap syndrome caused by m.13046T>C in MTND5.

Kolarova H, Liskova P, Tesarova M, Kucerova Vidrova V, Forgac M, Zamecnik J, Hansikova H, Honzik T.

Ophthalmic Genet. 2016 Dec;37(4):419-423. Epub 2016 Feb 19.

PMID:
26894521
12.

Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency.

Sarajlija A, Magner M, Djordjevic M, Kecman B, Grujic B, Tesarova M, Minic P.

Congenit Anom (Kyoto). 2017 Mar;57(2):64-65. doi: 10.1111/cga.12194. No abstract available.

PMID:
27649480
13.

Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing.

Hrčková G, Jankó V, Kytnarová J, Čižmárová M, Tesařová M, Košťálová Ľ, Virgová D, Dallos T, Hána V, Lebl J, Zeman J, Kovács L.

Eur J Pediatr. 2016 Sep;175(9):1199-1207. doi: 10.1007/s00431-016-2759-x. Epub 2016 Aug 18.

PMID:
27539621
14.

Analysis of neural crest-derived clones reveals novel aspects of facial development.

Kaucka M, Ivashkin E, Gyllborg D, Zikmund T, Tesarova M, Kaiser J, Xie M, Petersen J, Pachnis V, Nicolis SK, Yu T, Sharpe P, Arenas E, Brismar H, Blom H, Clevers H, Suter U, Chagin AS, Fried K, Hellander A, Adameyko I.

Sci Adv. 2016 Aug 3;2(8):e1600060. doi: 10.1126/sciadv.1600060. eCollection 2016 Aug.

15.

The phenotypic spectrum of fifty Czech m.3243A>G carriers.

Dvorakova V, Kolarova H, Magner M, Tesarova M, Hansikova H, Zeman J, Honzik T.

Mol Genet Metab. 2016 Aug;118(4):288-95. doi: 10.1016/j.ymgme.2016.06.003. Epub 2016 Jun 6.

PMID:
27296531
16.

Mechanism of formation of 3-chloropropan-1,2-diol (3-MCPD) esters under conditions of the vegetable oil refining.

Šmidrkal J, Tesařová M, Hrádková I, Berčíková M, Adamčíková A, Filip V.

Food Chem. 2016 Nov 15;211:124-9. doi: 10.1016/j.foodchem.2016.05.039. Epub 2016 May 6.

PMID:
27283615
17.

Phase I study of orally administered S-1 in combination with epirubicin and oxaliplatin in patients with advanced solid tumors and chemotherapy-naïve advanced or metastatic esophagogastric cancer.

Moehler M, Mahlberg R, Heinemann V, Obermannová R, Kubala E, Melichar B, Weinmann A, Scigalla P, Tesařová M, Janda P, Hédouin-Biville F, Mansoor W.

Gastric Cancer. 2017 Mar;20(2):358-367. doi: 10.1007/s10120-016-0618-0. Epub 2016 Jun 2.

PMID:
27255289
18.

Analysis of expression profiles of genes involved in F(o)F(1)-ATP synthase biogenesis during perinatal development in rat liver and skeletal muscle.

Spáčilová J, Hůlková M, Hruštincová A, Čapek V, Tesařová M, Hansíková H, Zeman J.

Physiol Res. 2016 Nov 8;65(4):597-608. Epub 2016 Mar 15.

19.

SDS-PAGE and Gel IEF: Tool for Differentiation of Methicillin-Resistant and Methicillin-Sensitive Strains of Staphylococcus aureus.

Tesařová M, Horká M, Moravcová D, Svojanovská L, Mlynarikova K, Růžička F.

Curr Microbiol. 2016 Mar;72(3):315-20. doi: 10.1007/s00284-015-0939-y. Epub 2015 Dec 21.

PMID:
26687464
20.

Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry.

Pecina P, Houšťková H, Mráček T, Pecinová A, Nůsková H, Tesařová M, Hansíková H, Janota J, Zeman J, Houštěk J.

BBA Clin. 2014 Oct 1;2:62-71. doi: 10.1016/j.bbacli.2014.09.003. eCollection 2014 Dec.

21.

Characterization of Dickeya and Pectobacterium species by capillary electrophoretic techniques and MALDI-TOF MS.

Šalplachta J, Kubesová A, Horký J, Matoušková H, Tesařová M, Horká M.

Anal Bioanal Chem. 2015 Oct;407(25):7625-35. doi: 10.1007/s00216-015-8920-y. Epub 2015 Jul 31.

PMID:
26229029
22.

Analysis of Mitochondrial Network Morphology in Cultured Myoblasts from Patients with Mitochondrial Disorders.

Sládková J, Spáčilová J, Čapek M, Tesařová M, Hansíková H, Honzík T, Martínek J, Zámečník J, Kostková O, Zeman J.

Ultrastruct Pathol. 2015;39(5):340-50. doi: 10.3109/01913123.2015.1054013. Epub 2015 Jul 27.

PMID:
26214044
23.

Determination of methicillin-resistant and methicillin-susceptible Staphylococcus aureus bacteria in blood by capillary zone electrophoresis.

Horká M, Tesařová M, Karásek P, Růžička F, Holá V, Sittová M, Roth M.

Anal Chim Acta. 2015 Apr 8;868:67-72. doi: 10.1016/j.aca.2015.02.001. Epub 2015 Feb 4.

PMID:
25813236
24.

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
25.

[Psychiatric disturbances in five patients with MELAS syndrome].

Magner M, Honzik T, Tesarova M, Dvorakova V, Hansiková H, Raboch J, Zeman J.

Psychiatr Pol. 2014 Sep-Oct;48(5):1035-45. Polish.

PMID:
25639022
26.

High-resolution melting analysis for identifying sequence variations in nuclear genes for assembly factors and structural subunits of cytochrome c oxidase.

Vondráčková A, Veselá K, Zeman J, Tesařová M.

Methods Mol Biol. 2015;1264:351-67. doi: 10.1007/978-1-4939-2257-4_31.

PMID:
25631028
27.

Non-invasive screening of cytochrome c oxidase deficiency in children using a dipstick immunocapture assay.

Rodinová M, Trefilová E, Honzík T, Tesařová M, Zeman J, Hansíková H.

Folia Biol (Praha). 2014;60(6):268-74.

28.

Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model.

Martins C, Hůlková H, Dridi L, Dormoy-Raclet V, Grigoryeva L, Choi Y, Langford-Smith A, Wilkinson FL, Ohmi K, DiCristo G, Hamel E, Ausseil J, Cheillan D, Moreau A, Svobodová E, Hájková Z, Tesařová M, Hansíková H, Bigger BW, Hrebícek M, Pshezhetsky AV.

Brain. 2015 Feb;138(Pt 2):336-55. doi: 10.1093/brain/awu355. Epub 2015 Jan 6. Erratum in: Brain. 2015 Jul;138(Pt 7):e366.

29.

Kentomonas gen. n., a new genus of endosymbiont-containing trypanosomatids of Strigomonadinae subfam. n.

Votýpka J, Kostygov AY, Kraeva N, Grybchuk-Ieremenko A, Tesařová M, Grybchuk D, Lukeš J, Yurchenko V.

Protist. 2014 Dec;165(6):825-38. doi: 10.1016/j.protis.2014.09.002. Epub 2014 Oct 7.

PMID:
25460233
30.

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):417-26. doi: 10.1007/s10545-014-9774-8. Epub 2014 Oct 18. Erratum in: J Inherit Metab Dis. 2015 May;38(3):583-4. Morava-Kozicz, Eva [corrected to Morava, Eva].

PMID:
25326274
31.

Glycogen storage disease-like phenotype with central nervous system involvement in a PGM1-CDG patient.

Ondruskova N, Honzik T, Vondrackova A, Tesarova M, Zeman J, Hansikova H.

Neuro Endocrinol Lett. 2014;35(2):137-41.

PMID:
24878975
32.

Ultrastructure and molecular phylogeny of four new species of monoxenous trypanosomatids from flies (Diptera: Brachycera) with redefinition of the genus Wallaceina.

Yurchenko V, Votýpka J, Tesarová M, Klepetková H, Kraeva N, Jirků M, Lukes J.

Folia Parasitol (Praha). 2014 Apr;61(2):97-112.

33.

Mitochondrial membrane assembly of TMEM70 protein.

Kratochvílová H, Hejzlarová K, Vrbacký M, Mráček T, Karbanová V, Tesařová M, Gombitová A, Cmarko D, Wittig I, Zeman J, Houštěk J.

Mitochondrion. 2014 Mar;15:1-9. doi: 10.1016/j.mito.2014.02.010. Epub 2014 Feb 25.

PMID:
24576557
34.

Lipoprotein lipase deficiency: clinical, biochemical and molecular characteristics in three patients with novel mutations in the LPL gene.

Kolářová H, Tesařová M, Švecová Š, Stránecký V, Přistoupilová A, Zima T, Uhrová J, Volgina SY, Zeman J, Honzík T.

Folia Biol (Praha). 2014;60(5):235-43.

35.

Cluster of patients with Familial Mediterranean fever and heterozygous carriers of mutations in MEFV gene in the Czech Republic.

Sedivá A, Horváth R, Maňásek V, Gregorová A, Plevová P, Horáčková M, Tesařová M, Toplak N, Debeljak M.

Clin Genet. 2014 Dec;86(6):564-9. doi: 10.1111/cge.12323. Epub 2013 Dec 20.

PMID:
24251727
36.

Novel mutations in the TAZ gene in patients with Barth syndrome.

Mazurová S, Tesařová M, Magner M, Houšťková H, Hansíková H, Augustínová J, Tomek V, Vondráčková A, Zeman J, Honzík T.

Prague Med Rep. 2013;114(3):139-53.

PMID:
24093814
37.

Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders.

Vondráčková A, Veselá K, Kratochvílová H, Kučerová Vidrová V, Vinšová K, Stránecký V, Honzík T, Hansíková H, Zeman J, Tesařová M.

Eur J Hum Genet. 2014 Mar;22(3):431-4. doi: 10.1038/ejhg.2013.148. Epub 2013 Jul 10.

38.

Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.

Liskova P, Ulmanova O, Tesina P, Melsova H, Diblik P, Hansikova H, Tesarova M, Votruba M.

Acta Ophthalmol. 2013 May;91(3):e225-31. doi: 10.1111/aos.12038. Epub 2013 Feb 7.

39.

Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C>T diagnosed in an adult male.

Palecek T, Tesarova M, Kuchynka P, Dytrych V, Elleder M, Hulkova H, Hansikova H, Honzik T, Zeman J, Linhart A.

Int Heart J. 2012;53(6):383-7.

40.

Different laboratory and muscle biopsy findings in a family with an m.8851T>C mutation in the mitochondrial MTATP6 gene.

Honzik T, Tesarova M, Vinsova K, Hansikova H, Magner M, Kratochvilova H, Zamecnik J, Zeman J, Jesina P.

Mol Genet Metab. 2013 Jan;108(1):102-5. doi: 10.1016/j.ymgme.2012.11.002. Epub 2012 Nov 13.

PMID:
23206802
41.

[Hereditary leiomyomatosis and renal cell cancer - HLRCC/multiple cutaneous and uterine leimomyomatosis - MCUL].

Plevová P, Hladíková A, Tesařová M.

Klin Onkol. 2012;25 Suppl:S55-8. Czech.

PMID:
22920208
42.

Fumarate hydratase gene mutation in two young patients with sporadic uterine fibroids.

Kubinova K, Tesarova M, Hansikova H, Vesela K, Kuzel D, Mara M.

J Obstet Gynaecol Res. 2013 Jan;39(1):410-4. doi: 10.1111/j.1447-0756.2012.01939.x. Epub 2012 Jul 6.

PMID:
22764886
43.

Novel mutations in the tyrosine hydroxylase gene in the first Czech patient with tyrosine hydroxylase deficiency.

Szentiványi K, Hansíková H, Krijt J, Vinšová K, Tesařová M, Rozsypalová E, Klement P, Zeman J, Honzík T.

Prague Med Rep. 2012;113(2):136-46.

PMID:
22691284
44.

Ultrastructure of hydathode trichomes of hemiparasitic Rhinanthus alectorolophus and Odontites vernus: how important is their role in physiology and evolution of parasitism in Orobanchaceae?

Těšitel J, Tesařová M.

Plant Biol (Stuttg). 2013 Jan;15(1):119-25. doi: 10.1111/j.1438-8677.2012.00610.x. Epub 2012 Jun 8.

PMID:
22676139
45.

High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency.

Vondrackova A, Vesela K, Hansikova H, Docekalova DZ, Rozsypalova E, Zeman J, Tesarova M.

J Hum Genet. 2012 Jul;57(7):442-8. doi: 10.1038/jhg.2012.49. Epub 2012 May 17.

PMID:
22592081
46.

Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.

Haack TB, Haberberger B, Frisch EM, Wieland T, Iuso A, Gorza M, Strecker V, Graf E, Mayr JA, Herberg U, Hennermann JB, Klopstock T, Kuhn KA, Ahting U, Sperl W, Wilichowski E, Hoffmann GF, Tesarova M, Hansikova H, Zeman J, Plecko B, Zeviani M, Wittig I, Strom TM, Schuelke M, Freisinger P, Meitinger T, Prokisch H.

J Med Genet. 2012 Apr;49(4):277-83. doi: 10.1136/jmedgenet-2012-100846.

PMID:
22499348
47.

Core/shell nanofibers with embedded liposomes as a drug delivery system.

Mickova A, Buzgo M, Benada O, Rampichova M, Fisar Z, Filova E, Tesarova M, Lukas D, Amler E.

Biomacromolecules. 2012 Apr 9;13(4):952-62. doi: 10.1021/bm2018118. Epub 2012 Mar 26.

PMID:
22401557
48.

[Corneal ulceration complicating surgical correction of ptosis in patient with Kearns-Sayre syndrome--a case report].

Cesneková T, Jurecka T, Skorkovská K, Tesarová M, Hanisková H, Wenchich L, Zámecník J, Zeman J.

Cesk Slov Oftalmol. 2011 Oct;67(4):133-5. Czech.

PMID:
22299522
49.

Neonatal onset of mitochondrial disorders in 129 patients: clinical and laboratory characteristics and a new approach to diagnosis.

Honzik T, Tesarova M, Magner M, Mayr J, Jesina P, Vesela K, Wenchich L, Szentivanyi K, Hansikova H, Sperl W, Zeman J.

J Inherit Metab Dis. 2012 Sep;35(5):749-59. doi: 10.1007/s10545-011-9440-3. Epub 2012 Jan 10.

PMID:
22231385
50.

Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9.

Haack TB, Madignier F, Herzer M, Lamantea E, Danhauser K, Invernizzi F, Koch J, Freitag M, Drost R, Hillier I, Haberberger B, Mayr JA, Ahting U, Tiranti V, Rötig A, Iuso A, Horvath R, Tesarova M, Baric I, Uziel G, Rolinski B, Sperl W, Meitinger T, Zeviani M, Freisinger P, Prokisch H.

J Med Genet. 2012 Feb;49(2):83-9. doi: 10.1136/jmedgenet-2011-100577. Epub 2011 Dec 26.

PMID:
22200994

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