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Items: 1 to 20 of 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

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