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Items: 1 to 50 of 65

1.

Letter by Peran et al Regarding Article, "Public Perceptions on Why Women Receive Less Bystander Cardiopulmonary Resuscitation Than Men in Out-of-Hospital Cardiac Arrest".

Peran D, Vesela K, Franek O.

Circulation. 2019 Aug 27;140(9):e510. doi: 10.1161/CIRCULATIONAHA.119.040792. Epub 2019 Aug 26. No abstract available.

PMID:
31449455
2.

Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic.

Soukupová J, Lhotová K, Zemánková P, Vočka M, Janatová M, Stolařová L, Borecká M, Kleiblová P, Macháčková E, Foretová L, Koudová M, Lhota F, Tavandzis S, Zikán M, Stránecký V, Veselá K, Panczak A, Kotlas J, Kleibl Z.

Klin Onkol. 2019 Summer;32(Supplementum2):72-78. doi: 10.14735/amko2019S72.

PMID:
31409082
3.

Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance.

Kleiblová P, Stolařová L, Křížová K, Lhota F, Hojný J, Zemánková P, Havránek O, Vočka M, Černá M, Lhotová K, Borecká M, Janatová M, Soukupová J, Ševčík J, Zimovjanová M, Kotlas J, Panczak A, Veselá K, Červenková J, Schneiderová M, Burócziová M, Burdová K, Stránecký V, Foretová L, Macháčková E, Tavandzis S, Kmoch S, Macůrek L, Kleibl Z.

Klin Onkol. 2019 Summer;32(Supplementum2):36-50. doi: 10.14735/amko2019S36.

PMID:
31409080
4.

Endometrial Receptivity Analysis - a tool to increase an implantation rate in assisted reproduction.

Hromadová L, Tokareva I, Veselá K, Trávník P, Veselý J.

Ceska Gynekol. 2019 Spring;84(3):177-183.

PMID:
31324106
5.

Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer.

Kleiblova P, Stolarova L, Krizova K, Lhota F, Hojny J, Zemankova P, Havranek O, Vocka M, Cerna M, Lhotova K, Borecka M, Janatova M, Soukupova J, Sevcik J, Zimovjanova M, Kotlas J, Panczak A, Vesela K, Cervenkova J, Schneiderova M, Burocziova M, Burdova K, Stranecky V, Foretova L, Machackova E, Tavandzis S, Kmoch S, Macurek L, Kleibl Z.

Int J Cancer. 2019 Oct 1;145(7):1782-1797. doi: 10.1002/ijc.32385. Epub 2019 May 20.

PMID:
31050813
6.

Incidence and origin of meiotic whole and segmental chromosomal aneuploidies detected by karyomapping.

Kubicek D, Hornak M, Horak J, Navratil R, Tauwinklova G, Rubes J, Vesela K.

Reprod Biomed Online. 2019 Mar;38(3):330-339. doi: 10.1016/j.rbmo.2018.11.023. Epub 2018 Dec 23.

7.

Peripheral Inflammation Enhances Microglia Response and Nigral Dopaminergic Cell Death in an in vivo MPTP Model of Parkinson's Disease.

García-Domínguez I, Veselá K, García-Revilla J, Carrillo-Jiménez A, Roca-Ceballos MA, Santiago M, de Pablos RM, Venero JL.

Front Cell Neurosci. 2018 Nov 6;12:398. doi: 10.3389/fncel.2018.00398. eCollection 2018.

8.

Multiple haploids, triploids, and tetraploids found in modern-day "living fossil" Ginkgo biloba.

Šmarda P, Horová L, Knápek O, Dieck H, Dieck M, Ražná K, Hrubík P, Orlóci L, Papp L, Veselá K, Veselý P, Bureš P.

Hortic Res. 2018 Oct 1;5:55. doi: 10.1038/s41438-018-0055-9. eCollection 2018.

9.

[Mutations in genes affecting fertility of men - current routine laboratory genetic diagnostics and searching for more DNA segments and genes influencing spermatogenesis].

Hrdlička I, Chylíková B, Veselá K, Danková M, Janků M, Řežábek K, Mihalová R, Liška F.

Ceska Gynekol. Winter 2016;81(6):437-443. Czech.

PMID:
27918162
10.

[Current issues of reproductive medicine in the Czech Republic].

Ventruba P, Žáková J, Ješeta M, Rumpík D, Brandejská M, Crha I, Hlinka D, Jelínková L, Oráčová E, Pavelková J, Řežábek K, Veselá K.

Ceska Gynekol. Summer 2016;81(3):234-240. Czech.

PMID:
27882769
11.

Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population.

Chylíková B, Hrdlička I, Veselá K, Řežábek K, Liška F.

PLoS One. 2016 Jun 3;11(6):e0156102. doi: 10.1371/journal.pone.0156102. eCollection 2016.

12.

[Assisted Reproduction and Preimplantation Genetic Diagnosis in Patients Susceptible to Breast Cancer].

Veselá K, Kocur T, Horák J, Horňák M, Oráčová E, Hromadová L, Veselý J, Trávník P.

Klin Onkol. 2016;29 Suppl 1:S93-9. Review. Czech.

PMID:
26691949
13.

[PALB2 as Another Candidate Gene for Genetic Testing in Patients with Hereditary Breast Cancer in Czech Republic].

Janatová M, Borecká M, Soukupová J, Kleiblová P, Stříbrná J, Vočka M, Zemánková P, Panczak A, Veselá K, Souček P, Foretová L, Kleibl Z.

Klin Onkol. 2016;29 Suppl 1:S31-4. Czech.

PMID:
26691940
14.

Frameshift mutations in the insulin gene leading to prolonged molecule of insulin in two families with Maturity-Onset Diabetes of the Young.

Dusatkova L, Dusatkova P, Vosahlo J, Vesela K, Cinek O, Lebl J, Pruhova S.

Eur J Med Genet. 2015 Apr;58(4):230-4. doi: 10.1016/j.ejmg.2015.02.004. Epub 2015 Feb 23.

PMID:
25721872
15.

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
16.

Comprehensive meiotic segregation analysis of a 4-breakpoint t(1;3;6) complex chromosome rearrangement using single sperm array comparative genomic hybridization and FISH.

Hornak M, Vozdova M, Musilova P, Prinosilova P, Oracova E, Linkova V, Vesela K, Rubes J.

Reprod Biomed Online. 2014 Oct;29(4):499-508. doi: 10.1016/j.rbmo.2014.06.014. Epub 2014 Jul 10.

PMID:
25154015
17.

ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010.

Moutou C, Goossens V, Coonen E, De Rycke M, Kokkali G, Renwick P, SenGupta SB, Vesela K, Traeger-Synodinos J.

Hum Reprod. 2014 May;29(5):880-903. doi: 10.1093/humrep/deu012. Epub 2014 Mar 11.

PMID:
24619432
18.

Progress of sperm IZUMO1 relocation during spontaneous acrosome reaction.

Sebkova N, Ded L, Vesela K, Dvorakova-Hortova K.

Reproduction. 2013 Dec 28;147(2):231-40. doi: 10.1530/REP-13-0193. Print 2014 Feb.

PMID:
24277869
19.

The PALB2 gene is a strong candidate for clinical testing in BRCA1- and BRCA2-negative hereditary breast cancer.

Janatova M, Kleibl Z, Stribrna J, Panczak A, Vesela K, Zimovjanova M, Kleiblova P, Dundr P, Soukupova J, Pohlreich P.

Cancer Epidemiol Biomarkers Prev. 2013 Dec;22(12):2323-32. doi: 10.1158/1055-9965.EPI-13-0745-T. Epub 2013 Oct 17.

20.

[Current issues of assisted reproduction in the Czech Republic].

Ventruba P, Žáková J, Trávník P, Crha I, Mrázek M, Rumpík D, Štěpán J, Režábek K, Mardešić T, Malenovská A, Veselá K, Brandejská M.

Ceska Gynekol. 2013 Aug;78(4):392-8. Review. Czech.

PMID:
24040990
21.

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.

22.

RFT1-CDG in adult siblings with novel mutations.

Ondruskova N, Vesela K, Hansikova H, Magner M, Zeman J, Honzik T.

Mol Genet Metab. 2012 Dec;107(4):760-2. doi: 10.1016/j.ymgme.2012.10.002. Epub 2012 Oct 13.

PMID:
23111317
23.

Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families.

Schwarzová L, Štekrová J, Florianová M, Novotný A, Schneiderová M, Lněnička P, Kebrdlová V, Kotlas J, Veselá K, Kohoutová M.

Fam Cancer. 2013 Mar;12(1):35-42. doi: 10.1007/s10689-012-9569-8.

PMID:
22987206
24.

Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency.

Honzík T, Magner M, Krijt J, Sokolová J, Vugrek O, Belužić R, Barić I, Hansíkova H, Elleder M, Veselá K, Bauerová L, Ondrušková N, Ješina P, Zeman J, Kožich V.

Mol Genet Metab. 2012 Nov;107(3):611-3. doi: 10.1016/j.ymgme.2012.08.014. Epub 2012 Aug 23.

PMID:
22959829
25.

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
26.

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
27.

Ancestral mutations may cause a significant proportion of GCK-MODY.

Dusatkova P, Pruhova S, Borowiec M, Vesela K, Antosik K, Lebl J, Mlynarski W, Cinek O.

Pediatr Diabetes. 2012 Sep;13(6):489-98. doi: 10.1111/j.1399-5448.2011.00845.x. Epub 2012 Feb 15.

PMID:
22332836
28.

Multiple meiotic errors caused by predivision of chromatids in women of advanced maternal age undergoing in vitro fertilisation.

Handyside AH, Montag M, Magli MC, Repping S, Harper J, Schmutzler A, Vesela K, Gianaroli L, Geraedts J.

Eur J Hum Genet. 2012 Jul;20(7):742-7. doi: 10.1038/ejhg.2011.272. Epub 2012 Feb 8.

29.

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
30.

Polar body array CGH for prediction of the status of the corresponding oocyte. Part II: technical aspects.

Magli MC, Montag M, Köster M, Muzi L, Geraedts J, Collins J, Goossens V, Handyside AH, Harper J, Repping S, Schmutzler A, Vesela K, Gianaroli L.

Hum Reprod. 2011 Nov;26(11):3181-5. doi: 10.1093/humrep/der295. Epub 2011 Sep 9.

31.

Polar body array CGH for prediction of the status of the corresponding oocyte. Part I: clinical results.

Geraedts J, Montag M, Magli MC, Repping S, Handyside A, Staessen C, Harper J, Schmutzler A, Collins J, Goossens V, van der Ven H, Vesela K, Gianaroli L.

Hum Reprod. 2011 Nov;26(11):3173-80. doi: 10.1093/humrep/der294. Epub 2011 Sep 9.

32.

Cryptic chromosomal rearrangements in children with idiopathic mental retardation in the Czech population.

Hirschfeldova K, Baxova A, Kebrdlova V, Solc R, Mihalova R, Lnenicka P, Vesela K, Stekrova J.

Genet Test Mol Biomarkers. 2011 Sep;15(9):607-11. doi: 10.1089/gtmb.2010.0218. Epub 2011 Apr 7.

PMID:
21473681
33.

Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I.

Guillard M, Wada Y, Hansikova H, Yuasa I, Vesela K, Ondruskova N, Kadoya M, Janssen A, Van den Heuvel LP, Morava E, Zeman J, Wevers RA, Lefeber DJ.

J Inherit Metab Dis. 2011 Aug;34(4):901-6. doi: 10.1007/s10545-011-9311-y. Epub 2011 Mar 23.

34.

Lack of PAX4 mutations in 53 Czech MODYX families.

Dusatkova P, Vesela K, Pruhova S, Lebl J, Cinek O.

Diabet Med. 2010 Dec;27(12):1459-60. doi: 10.1111/j.1464-5491.2010.03126.x. No abstract available.

PMID:
21059099
35.

ESHRE PGD consortium best practice guidelines for fluorescence in situ hybridization-based PGD.

Harton GL, Harper JC, Coonen E, Pehlivan T, Vesela K, Wilton L; European Society for Human Reproduction and Embryology (ESHRE) PGD Consortium.

Hum Reprod. 2011 Jan;26(1):25-32. doi: 10.1093/humrep/deq230. Epub 2010 Oct 21.

PMID:
20966461
36.

Monozygotic twins with discordant karyotypes following preimplantation genetic screening and single embryo transfer: case report.

Tauwinklova G, Gaillyova R, Travnik P, Oracova E, Vesela K, Hromadova L, Vesely J, Musilova P, Rubes J, Kadlecova J, Slamova I, Makaturova E, Vranova V.

J Assist Reprod Genet. 2010 Nov;27(11):649-55. doi: 10.1007/s10815-010-9462-z. Epub 2010 Aug 11.

37.

What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium Steering Committee.

Harper J, Coonen E, De Rycke M, Fiorentino F, Geraedts J, Goossens V, Harton G, Moutou C, Pehlivan Budak T, Renwick P, Sengupta S, Traeger-Synodinos J, Vesela K.

Hum Reprod. 2010 Apr;25(4):821-3. doi: 10.1093/humrep/dep476. Epub 2010 Feb 2.

PMID:
20124394
38.

Accreditation of the PGD laboratory.

Harper JC, Sengupta S, Vesela K, Thornhill A, Dequeker E, Coonen E, Morris MA.

Hum Reprod. 2010 Apr;25(4):1051-65. doi: 10.1093/humrep/dep450. Epub 2010 Jan 23.

PMID:
20097923
39.

Cytosine-Adenosine (CA)n repeats polymorphism in IGF-I gene and early growth in infants born appropriate and small for gestational age.

Kytnarova J, Vesela K, Zlatohlavkova B, Dohnalova A, Fedorova M, Krsek M, Zeman J.

Neuro Endocrinol Lett. 2009;30(4):501-5.

PMID:
20010501
40.

SURF1 missense mutations promote a mild Leigh phenotype.

Piekutowska-Abramczuk D, Magner M, Popowska E, Pronicki M, Karczmarewicz E, Sykut-Cegielska J, Kmiec T, Jurkiewicz E, Szymanska-Debinska T, Bielecka L, Krajewska-Walasek M, Vesela K, Zeman J, Pronicka E.

Clin Genet. 2009 Aug;76(2):195-204. doi: 10.1111/j.1399-0004.2009.01195.x.

PMID:
19780766
41.

A new case of ALG8 deficiency (CDG Ih).

Vesela K, Honzik T, Hansikova H, Haeuptle MA, Semberova J, Stranak Z, Hennet T, Zeman J.

J Inherit Metab Dis. 2009 Dec;32 Suppl 1. doi: 10.1007/s10545-009-1203-z. Epub 2009 Aug 18. Review.

42.

Loss of function of Sco1 and its interaction with cytochrome c oxidase.

Stiburek L, Vesela K, Hansikova H, Hulkova H, Zeman J.

Am J Physiol Cell Physiol. 2009 May;296(5):C1218-26. doi: 10.1152/ajpcell.00564.2008. Epub 2009 Mar 18.

43.

Sperm and embryo analysis in a carrier of supernumerary inv dup(15) marker chromosome.

Oracova E, Musilova P, Kopecna O, Rybar R, Vozdova M, Vesela K, Rubes J.

J Androl. 2009 May-Jun;30(3):233-9. doi: 10.2164/jandrol.108.006783. Epub 2008 Dec 4.

44.

Hybridization of the 18 alpha-satellite probe to chromosome 1 revealed in PGD.

Musilova P, Rybar R, Oracova E, Veselá K, Rubes J.

Reprod Biomed Online. 2008 Nov;17(5):695-8.

PMID:
18983755
45.

Structural analysis of tissues affected by cytochrome C oxidase deficiency due to mutations in the SCO2 gene.

Vesela K, Hulkova H, Hansikova H, Zeman J, Elleder M.

APMIS. 2008 Jan;116(1):41-9. doi: 10.1111/j.1600-0463.2008.00772.x.

PMID:
18254779
46.

What next for preimplantation genetic screening?

Harper J, Sermon K, Geraedts J, Vesela K, Harton G, Thornhill A, Pehlivan T, Fiorentino F, SenGupta S, de Die-Smulders C, Magli C, Moutou C, Wilton L.

Hum Reprod. 2008 Mar;23(3):478-80. doi: 10.1093/humrep/dem424. Epub 2008 Jan 17.

PMID:
18203706
47.

Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.

Stekrova J, Sulova M, Kebrdlova V, Zidkova K, Kotlas J, Ilencikova D, Vesela K, Kohoutova M.

BMC Med Genet. 2007 Apr 5;8:16.

48.

Plasma cysteine concentrations in uncomplicated pregnancies.

Viskova H, Vesela K, Janosikova B, Krijt J, Visek JA, Calda P.

Fetal Diagn Ther. 2007;22(4):254-8. Epub 2007 Mar 16.

PMID:
17369690
49.

ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004.

Sermon KD, Michiels A, Harton G, Moutou C, Repping S, Scriven PN, SenGupta S, Traeger-Synodinos J, Vesela K, Viville S, Wilton L, Harper JC.

Hum Reprod. 2007 Feb;22(2):323-36. Epub 2006 Nov 28.

PMID:
17132677
50.

Central data collection on PGD and screening.

Repping S, Geraedts J, Scriven P, Harton G, Veselá K, Kearns W, Viville S, Sermon K.

Reprod Biomed Online. 2006 Mar;12(3):389; author reply 390. No abstract available.

PMID:
16569335

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