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Items: 37

1.

Merle phenotypes in dogs - SILV SINE insertions from Mc to Mh.

Langevin M, Synkova H, Jancuskova T, Pekova S.

PLoS One. 2018 Sep 20;13(9):e0198536. doi: 10.1371/journal.pone.0198536. eCollection 2018.

2.

TYRP1:c.555T>G is a recurrent mutation found in Australian Shepherd and Miniature American Shepherd dogs.

Jancuskova T, Langevin M, Pekova S.

Anim Genet. 2018 Oct;49(5):500-501. doi: 10.1111/age.12709. Epub 2018 Aug 14. No abstract available.

PMID:
30109695
3.

Small Supernumerary Marker Chromosome May Provide Information on Dosage-insensitive Pericentric Regions in Human.

Al-Rikabi ABH, Pekova S, Fan X, Jančušková T, Liehr T.

Curr Genomics. 2018 Apr;19(3):192-199. doi: 10.2174/1389202918666170717163830.

4.

Antifungal effects of the biological agent Pythium oligandrum observed in vitro.

Načeradská M, Fridrichová M, Kellnerová D, Peková S, Lány P.

J Feline Med Surg. 2017 Aug;19(8):817-823. doi: 10.1177/1098612X16658690. Epub 2016 Jul 1.

PMID:
27418287
5.

Mantle cell lymphoma-variant Richter syndrome: Detailed molecular-cytogenetic and backtracking analysis reveals slow evolution of a pre-MCL clone in parallel with CLL over several years.

Klener P, Fronkova E, Berkova A, Jaksa R, Lhotska H, Forsterova K, Soukup J, Kulvait V, Vargova J, Fiser K, Prukova D, Alam M, Calvin Lenyeletse Maswabi B, Michalova K, Zemanova Z, Jancuskova T, Pekova S, Trneny M.

Int J Cancer. 2016 Nov 15;139(10):2252-60. doi: 10.1002/ijc.30263. Epub 2016 Aug 2.

6.

Multilocus Sequence Analysis of Clinical "Candidatus Neoehrlichia mikurensis" Strains from Europe.

Grankvist A, Moore ER, Svensson Stadler L, Pekova S, Bogdan C, Geißdörfer W, Grip-Lindén J, Brandström K, Marsal J, Andréasson K, Lewerin C, Welinder-Olsson C, Wennerås C.

J Clin Microbiol. 2015 Oct;53(10):3126-32. doi: 10.1128/JCM.00880-15. Epub 2015 Jul 8.

7.

Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome.

Weise A, Kosyakova N, Voigt M, Aust N, Mrasek K, Löhmer S, Rubtsov N, Karamysheva TV, Trifonov VA, Hardekopf D, Jančušková T, Pekova S, Wilhelm K, Liehr T, Fan X.

Cytogenet Genome Res. 2015;145(1):42-9. doi: 10.1159/000381764. Epub 2015 Apr 24.

8.

Long term follow-up in a patient with a de novo microdeletion of 14q11.2 involving CHD8.

Drabova J, Seemanova E, Hancarova M, Pourova R, Horacek M, Jancuskova T, Pekova S, Novotna D, Sedlacek Z.

Am J Med Genet A. 2015 Apr;167A(4):837-41. doi: 10.1002/ajmg.a.36957. Epub 2015 Mar 3.

PMID:
25735987
9.

Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient.

Jancuskova T, Plachy R, Zemankova L, Hardekopf DW, Stika J, Zejskova L, Praulich I, Kreuzer KA, Rothe A, Othman MA, Kosyakova N, Pekova S.

Mol Cytogenet. 2014 Jul 15;7:47. doi: 10.1186/1755-8166-7-47. eCollection 2014.

10.

Infections with the tick-borne bacterium "Candidatus Neoehrlichia mikurensis" mimic noninfectious conditions in patients with B cell malignancies or autoimmune diseases.

Grankvist A, Andersson PO, Mattsson M, Sender M, Vaht K, Höper L, Sakiniene E, Trysberg E, Stenson M, Fehr J, Pekova S, Bogdan C, Bloemberg G, Wennerås C.

Clin Infect Dis. 2014 Jun;58(12):1716-22. doi: 10.1093/cid/ciu189. Epub 2014 Mar 18.

11.

A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients.

Jancuskova T, Plachy R, Stika J, Zemankova L, Hardekopf DW, Liehr T, Kosyakova N, Cmejla R, Zejskova L, Kozak T, Zak P, Zavrelova A, Havlikova P, Karas M, Junge A, Ramel C, Pekova S.

Leuk Res. 2013 Oct;37(10):1363-73. doi: 10.1016/j.leukres.2013.06.009. Epub 2013 Jul 17.

PMID:
23870092
12.

Pathogenetic role of ETV6 fusion gene in leukemic transformation of myelodysplastic syndrome refractory anemia with excess blasts-1 with a new, rare translocation t(11;19)(q24.3;q13.12) and insertion ins(6;12)(p22.3p13).

Jarošová M, Rohoň P, Živná J, Peková S, Nedomová R, Holzerová M, Mičková P, Reptová S, Papajík T, Indrák K.

Leuk Lymphoma. 2014 Apr;55(4):950-3. doi: 10.3109/10428194.2013.814127. Epub 2013 Jul 29. No abstract available.

PMID:
23772667
13.

Infective endocarditis due to Bartonella quintana: a severe disease and underdiagnosed etiology.

Džupová O, Peková S, Sojková N, Feuereisl R, Beneš J.

Folia Microbiol (Praha). 2013 Nov;58(6):491-4. doi: 10.1007/s12223-013-0235-9. Epub 2013 Mar 2. No abstract available.

PMID:
23456350
14.

DNA released by leukemic cells contributes to the disruption of the bone marrow microenvironment.

Dvořáková M, Karafiát V, Pajer P, Kluzáková E, Jarkovská K, Peková S, Krutílková L, Dvořák M.

Oncogene. 2013 Oct 31;32(44):5201-9. doi: 10.1038/onc.2012.553. Epub 2012 Dec 10.

PMID:
23222712
15.

[Patient with B-CLL with a history of unrelated hematopoietic cells donation--retrospective analysis of CLL development and implication for the recipient].

Jindra P, Žejšková L, Peková S, Navrátilová J, Schutzová M, Vokurka S, Koza V.

Klin Onkol. 2012;25(3):212-5. Czech.

PMID:
22724571
16.

Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report.

Mulatinho MV, de Carvalho Serao CL, Scalco F, Hardekopf D, Pekova S, Mrasek K, Liehr T, Weise A, Rao N, Llerena JC Jr.

Mol Cytogenet. 2012 Jun 11;5(1):30. doi: 10.1186/1755-8166-5-30.

17.

How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe set.

Hamid AB, Kreskowski K, Weise A, Kosayakova N, Mrasek K, Voigt M, Guilherme RS, Wagner R, Hardekopf D, Pekova S, Karamysheva T, Liehr T, Klein E.

J Appl Genet. 2012 Aug;53(3):259-69. doi: 10.1007/s13353-012-0098-9. Epub 2012 Apr 29.

PMID:
22544657
18.

Microdeletion and microduplication syndromes.

Weise A, Mrasek K, Klein E, Mulatinho M, Llerena JC Jr, Hardekopf D, Pekova S, Bhatt S, Kosyakova N, Liehr T.

J Histochem Cytochem. 2012 May;60(5):346-58. doi: 10.1369/0022155412440001. Epub 2012 Mar 6. Review.

19.

The effects of siRNA-mediated RGS4 gene silencing on the whole genome transcription profile: implications for schizophrenia.

Vrajová M, Peková S, Horácek J, Höschl C.

Neuro Endocrinol Lett. 2011;32(3):246-52.

PMID:
21712773
20.

Candidatus Neoehrlichia mikurensis infection identified in 2 hematooncologic patients: benefit of molecular techniques for rare pathogen detection.

Pekova S, Vydra J, Kabickova H, Frankova S, Haugvicova R, Mazal O, Cmejla R, Hardekopf DW, Jancuskova T, Kozak T.

Diagn Microbiol Infect Dis. 2011 Mar;69(3):266-70. doi: 10.1016/j.diagmicrobio.2010.10.004.

PMID:
21353949
21.

A comprehensive study of TP53 mutations in chronic lymphocytic leukemia: Analysis of 1287 diagnostic and 1148 follow-up CLL samples.

Pekova S, Mazal O, Cmejla R, Hardekopf DW, Plachy R, Zejskova L, Haugvicova R, Jancuskova T, Karas M, Koza V, Smolej L, Bezdickova L, Kozak T.

Leuk Res. 2011 Jul;35(7):889-98. doi: 10.1016/j.leukres.2010.12.016. Epub 2011 Jan 13.

PMID:
21232794
22.

Angiopoietin-2 mRNA expression is increased in chronic lymphocytic leukemia patients with poor prognostic features.

Vrbacky F, Smolej L, Vroblova V, Pekova S, Hrudkova M, Cervinka M, Pecka M, Krejsek J, Maly J.

Hematology. 2010 Aug;15(4):210-4. doi: 10.1179/102453309X12583347113898.

PMID:
20670479
23.

Expression of the hippocampal NMDA receptor GluN1 subunit and its splicing isoforms in schizophrenia: postmortem study.

Vrajová M, Stastný F, Horácek J, Lochman J, Serý O, Peková S, Klaschka J, Höschl C.

Neurochem Res. 2010 Jul;35(7):994-1002. doi: 10.1007/s11064-010-0145-z. Epub 2010 Mar 5.

PMID:
20204507
24.

Molecular variability of FLT3/ITD mutants and their impact on the differentiation program of 32D cells: implications for the biological properties of AML blasts.

Pekova S, Ivanek R, Dvorak M, Rueggeberg S, Leicht S, Li X, Franz T, Kozak T, Vrba J, Koza V, Karas M, Schwarz J, Cetkovsky P, Prucha M.

Leuk Res. 2009 Oct;33(10):1409-16. doi: 10.1016/j.leukres.2009.01.004. Epub 2009 Jan 31.

PMID:
19181379
25.

Genomic polymorphism and sepsis--is there a reason for optimism?

Průcha M, Zazula R, Peková S.

Prague Med Rep. 2008;109(2-3):113-26. Review.

PMID:
19548592
26.

Quantitation of minimal residual disease in patients with chronic lymphocytic leukemia using locked nucleic acid-modified, fluorescently labeled hybridization probes and real-time PCR technology.

Peková S, Bezdícková L, Smolej L, Kozák T, Hochová I, Zák P, Tomsíková L, Průcha M.

Mol Diagn Ther. 2007;11(5):325-35.

PMID:
17963420
27.

Identification of somatic hypermutations in the TP53 gene in B-cell chronic lymphocytic leukemia.

Malcikova J, Smardova J, Pekova S, Cejkova S, Kotaskova J, Tichy B, Francova H, Doubek M, Brychtova Y, Janek D, Pospisilova S, Mayer J, Dvorakova D, Trbusek M.

Mol Immunol. 2008 Mar;45(5):1525-9. Epub 2007 Oct 24.

PMID:
17920683
28.

Most pediatric patients with essential thrombocythemia show hypersensitivity to erythropoietin in vitro, with rare JAK2 V617F-positive erythroid colonies.

Veselovska J, Pospisilova D, Pekova S, Horvathova M, Solna R, Cmejlova J, Cmejla R, Belickova M, Mihal V, Stary J, Divoky V.

Leuk Res. 2008 Mar;32(3):369-77. Epub 2007 Aug 23.

PMID:
17719087
29.

Identification of a novel, transactivation-defective splicing variant of p53 gene in patients with chronic lymphocytic leukemia.

Pekova S, Cmejla R, Smolej L, Kozak T, Spacek M, Prucha M.

Leuk Res. 2008 Mar;32(3):395-400. Epub 2007 Aug 3.

PMID:
17688945
31.
32.

[Isolated lymphadenopathy as the first presentation of systemic mastocytosis--description of two cases].

Kinkor Z, Síma R, Skálová A, Boudová L, Peková S, Dvoráková D, Dĕdic K, Kracík M, Janousek M, Michal M.

Cesk Patol. 2006 Jan;42(1):34-8. Czech.

PMID:
16506600
34.

Incidence of chromosomal anomalies detected with FISH and their clinical correlations in B-chronic lymphocytic leukemia.

Sindelárová L, Michalová K, Zemanová Z, Ransdorfová S, Brezinová J, Peková S, Schwarz J, Karban J, Cmunt E.

Cancer Genet Cytogenet. 2005 Jul 1;160(1):27-34.

PMID:
15949567
35.

A single administration of gemtuzumab ozogamicin for molecular relapse of acute promyelocytic leukemia.

Schwarz J, Marková J, Peková S, Trnková Z, Sponerová D, Cetkovský P.

Hematol J. 2004;5(3):279-80. No abstract available.

PMID:
15167917
36.

Type J CBFbeta/MYH11 transcript in the M4Eo subtype of acute myeloid leukemia.

Trnková Z, Peková S, Bedrlíková R, Záková D, Zemanová Z, Polák J, Michalová K, Cermák J, Schwarz J.

Hematology. 2003 Apr;8(2):115-7.

PMID:
12745661
37.

[Expression of cyclin-dependent kinase inhibitors in leukemia].

Polák J, Peková S, Schwarz J, Kozák T, Haskovec C.

Cas Lek Cesk. 2003 Jan 20;142(1):25-8. Czech.

PMID:
12693294

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