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Items: 13

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.

Parental origin of deletions and duplications - about the necessity to check for cryptic inversions.

Liehr T, Schreyer I, Kuechler A, Manolakos E, Singer S, Dufke A, Wilhelm K, Jančušková T, Čmejla R, Othman MAK, Al-Rikabi AH, Mrasek K, Ziegler M, Kankel S, Kreskowski K, Weise A.

Mol Cytogenet. 2018 Mar 9;11:20. doi: 10.1186/s13039-018-0369-1. eCollection 2018.

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.

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.

7.

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
8.

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.

9.

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
10.

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
11.

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
12.

Feasibility of fetal-derived hypermethylated RASSF1A sequence quantification in maternal plasma--next step toward reliable non-invasive prenatal diagnostics.

Zejskova L, Jancuskova T, Kotlabova K, Doucha J, Hromadnikova I.

Exp Mol Pathol. 2010 Dec;89(3):241-7. doi: 10.1016/j.yexmp.2010.09.002. Epub 2010 Sep 22.

PMID:
20868679
13.

Quantification of extracellular DNA using hypermethylated RASSF1A, SRY, and GLO sequences--evaluation of diagnostic possibilities for predicting placental insufficiency.

Hromadnikova I, Zejskova L, Kotlabova K, Jancuskova T, Doucha J, Dlouha K, Krofta L, Jirasek JE, Vlk R.

DNA Cell Biol. 2010 Jun;29(6):295-301. doi: 10.1089/dna.2009.0971.

PMID:
20235876

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