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Items: 18

1.

GATA3 germline variant is associated with CRLF2 expression and predicts outcome in pediatric B-cell precursor acute lymphoblastic leukemia.

Madzio J, Pastorczak A, Sedek L, Braun M, Taha J, Wypyszczak K, Trelinska J, Lejman M, Muszynska-Roslan K, Tomasik B, Derwich K, Koltan A, Kazanowska B, Irga-Jaworska N, Badowska W, Matysiak M, Kowalczyk J, Styczynski J, Fendler W, Szczepanski T, Mlynarski W.

Genes Chromosomes Cancer. 2019 Mar 11. doi: 10.1002/gcc.22748. [Epub ahead of print]

PMID:
30859636
2.

Comprehensive Investigation of miRNome Identifies Novel Candidate miRNA-mRNA Interactions Implicated in T-Cell Acute Lymphoblastic Leukemia.

Dawidowska M, Jaksik R, Drobna M, Szarzyńska-Zawadzka B, Kosmalska M, Sędek Ł, Machowska L, Lalik A, Lejman M, Ussowicz M, Kałwak K, Kowalczyk JR, Szczepański T, Witt M.

Neoplasia. 2019 Mar;21(3):294-310. doi: 10.1016/j.neo.2019.01.004. Epub 2019 Feb 11.

3.

The distinguishable DNA whole genome methylation profile of 2 cases of pediatric precursor B acute lymphoblastic leukaemia (BCP ALL) with prodromal, preleukemic phase: A case report.

Chaber R, Gurgul A, Wróbel G, Tomoń A, Paszek S, Potocka N, Haus O, Lejman M, Łach K, Szmatoła T, Jasielczuk I, Rybka B, Ryczan-Krawczyk R, Stąpor S, Ciebiera K, Arthur CJ, Zawlik I.

Medicine (Baltimore). 2018 Oct;97(42):e12763. doi: 10.1097/MD.0000000000012763.

4.

Clinical characteristics and analysis of treatment result in children with Ph-positive acute lymphoblastic leukaemia in Poland between 2005 and 2017.

Zawitkowska J, Lejman M, Zaucha-Prażmo A, Drabko K, Płonowski M, Bulsa J, Romiszewski M, Mizia-Malarz A, Kołtan A, Derwich K, Karolczyk G, Ociepa T, Ćwiklińska M, Trelińska J, Owoc-Lempach J, Niedźwiecki M, Kiermasz A, Kowalczyk J.

Eur J Haematol. 2018 Oct;101(4):542-548. doi: 10.1111/ejh.13142. Epub 2018 Aug 31.

PMID:
30007093
5.

Surface expression of Cytokine Receptor-Like Factor 2 increases risk of relapse in pediatric acute lymphoblastic leukemia patients harboring IKZF1 deletions.

Pastorczak A, Sedek L, Braun M, Madzio J, Sonsala A, Twardoch M, Fendler W, Nebral K, Taha J, Bielska M, Gorniak P, Romiszewska M, Matysiak M, Derwich K, Lejman M, Kowalczyk J, Badowska W, Niedzwiecki M, Kazanowska B, Muszynska-Roslan K, Sobol-Milejska G, Karolczyk G, Koltan A, Ociepa T, Szczepanski T, Młynarski W.

Oncotarget. 2018 May 25;9(40):25971-25982. doi: 10.18632/oncotarget.25411. eCollection 2018 May 25.

6.

Heterozygous carriers of germline c.657_661del5 founder mutation in NBN gene are at risk of central nervous system relapse of B-cell precursor acute lymphoblastic leukemia.

Tomasik B, Pastorczak A, Fendler W, Bartłomiejczyk M, Braun M, Mycko M, Madzio J, Polakowska E, Ulińska E, Matysiak M, Derwich K, Lejman M, Kowalczyk J, Badowska W, Kazanowska B, Szczepański T, Styczyński J, Irga-Jaworska N, Młynarski W; Polish Pediatric Leukemia/Lymphoma Study Group (PPLLSG).

Haematologica. 2018 May;103(5):e200-e203. doi: 10.3324/haematol.2017.181198. Epub 2018 Feb 1. No abstract available.

7.

Usefulness of Post-Transplant Hematopoietic Chimera Monitoring by Use of the Quantitative Fluorescence Polymerase Chain Reaction Method.

Lejman M, Drabko K, Styka B, Winnicka D, Babicz M, Jaszczuk I, Kowalczyk JR.

Transplant Proc. 2017 Oct;49(8):1903-1910. doi: 10.1016/j.transproceed.2017.04.013.

PMID:
28923646
8.

Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease.

Jaszczuk I, Schlotawa L, Dierks T, Ohlenbusch A, Koppenhöfer D, Babicz M, Lejman M, Radhakrishnan K, Ługowska A.

Mol Genet Metab. 2017 Jul;121(3):252-258. doi: 10.1016/j.ymgme.2017.05.013. Epub 2017 May 22.

PMID:
28566233
9.

Biallelic loss of CDKN2A is associated with poor response to treatment in pediatric acute lymphoblastic leukemia.

Braun M, Pastorczak A, Fendler W, Madzio J, Tomasik B, Taha J, Bielska M, Sedek L, Szczepanski T, Matysiak M, Derwich K, Lejman M, Kowalczyk J, Kazanowska B, Badowska W, Styczynski J, Irga-Jaworska N, Trelinska J, Zalewska-Szewczyk B, Pierlejewski F, Wlodarska I, Młynarski W; Polish Pediatric Leukemia/Lymphoma Study Group.

Leuk Lymphoma. 2017 May;58(5):1162-1171. doi: 10.1080/10428194.2016.1228925. Epub 2016 Oct 18.

PMID:
27756164
10.

Ultrafast acousto-optic mode conversion in optically birefringent ferroelectrics.

Lejman M, Vaudel G, Infante IC, Chaban I, Pezeril T, Edely M, Nataf GF, Guennou M, Kreisel J, Gusev VE, Dkhil B, Ruello P.

Nat Commun. 2016 Aug 5;7:12345. doi: 10.1038/ncomms12345.

11.

Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL.

Dawidowska M, Kosmalska M, Sędek Ł, Szczepankiewicz A, Twardoch M, Sonsala A, Szarzyńska-Zawadzka B, Derwich K, Lejman M, Pawelec K, Obitko-Płudowska A, Pawińska-Wąsikowska K, Kwiecińska K, Kołtan A, Dyla A, Grzeszczak W, Kowalczyk JR, Szczepański T, Ziętkiewicz E, Witt M.

Sci Rep. 2016 Jul 18;6:29427. doi: 10.1038/srep29427.

12.

Giant ultrafast photo-induced shear strain in ferroelectric BiFeO3.

Lejman M, Vaudel G, Infante IC, Gemeiner P, Gusev VE, Dkhil B, Ruello P.

Nat Commun. 2014 Jul 1;5:4301. doi: 10.1038/ncomms5301.

PMID:
24980954
13.

Polymorphism in IKZF1 gene affects age at onset of childhood acute lymphoblastic leukemia.

Górniak P, Pastorczak A, Zalewska-Szewczyk B, Lejman M, Trelińska J, Chmielewska M, Sokół-Jeżewska A, Kowalczyk J, Szczepanski T, Matysiak M, Kazanowska B, Mlynarski W; Polish Pediatric Leukemia/Lymphoma Study Group.

Leuk Lymphoma. 2014 Sep;55(9):2174-8. doi: 10.3109/10428194.2013.866661. Epub 2014 Apr 2.

PMID:
24597983
14.

Asparagine synthetase (ASNS) gene polymorphism is associated with the outcome of childhood acute lymphoblastic leukemia by affecting early response to treatment.

Pastorczak A, Fendler W, Zalewska-Szewczyk B, Górniak P, Lejman M, Trelińska J, Walenciak J, Kowalczyk J, Szczepanski T, Mlynarski W; Polish Pediatric Leukemia/Lymphoma Study Group.

Leuk Res. 2014 Feb;38(2):180-3. doi: 10.1016/j.leukres.2013.10.027. Epub 2013 Nov 5.

PMID:
24268318
15.

Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population.

Pastorczak A, Górniak P, Sherborne A, Hosking F, Trelińska J, Lejman M, Szczepański T, Borowiec M, Fendler W, Kowalczyk J, Houlston RS, Młynarski W.

Leuk Res. 2011 Nov;35(11):1534-6. doi: 10.1016/j.leukres.2011.07.034. Epub 2011 Sep 1.

PMID:
21889209
16.

Structural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute lymphoblastic leukemia.

Kowalczyk JR, Babicz M, Gaworczyk A, Lejman M, Winnicka D, Styka B, Jaszczuk I.

Cancer Genet Cytogenet. 2010 Jul 15;200(2):161-6. doi: 10.1016/j.cancergencyto.2010.04.016.

PMID:
20620600
17.

The effectiveness of high-resolution-comparative genomic hybridization in detecting the most common chromosomal abnormalities in pediatric myelodysplastic syndromes.

Babicz M, Kowalczyk JR, Winnicka D, Gaworczyk A, Lejman M, Dmowski R, Kaczanowska K.

Cancer Genet Cytogenet. 2005 Apr 1;158(1):49-54.

PMID:
15771904
18.

Fluorescence in situ hybridization BCR/ABL fusion signal rate in interphase nuclei of healthy volunteer donors: a test study for establishing false positive rate.

Kowalczyk JR, Gaworczyk A, Winnicka D, Lejman M, Babicz M.

Cancer Genet Cytogenet. 2003 Apr 1;142(1):51-5.

PMID:
12660033

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