Dirsė V - Search Results

1

Multiple Myeloma Immunophenotype Related to Chromosomal Abnormalities Used in Risk Assessment.

Radzevičius M, Dirsė V, Klimienė I, Matuzevičienė R, Kučinskienė ZA, Pečeliūnas V. Radzevičius M, et al. Among authors: dirse v. Diagnostics (Basel). 2022 Aug 24;12(9):2049. doi: 10.3390/diagnostics12092049. Diagnostics (Basel). 2022. PMID: 36140450 Free PMC article.

2

ETV6 and NOTCH1 germline variants in adult acute leukemia.

Dirse V, Norvilas R, Gineikiene E, Matuzevičienė R, Griskevicius L, Preiksaitiene E. Dirse V, et al. Leuk Lymphoma. 2018 Apr;59(4):1022-1024. doi: 10.1080/10428194.2017.1359742. Epub 2017 Aug 4. Leuk Lymphoma. 2018. PMID: 28776427 No abstract available.

3

Outcomes of relapsed or refractory acute myeloid leukemia patients failing venetoclax-based salvage therapies.

Zucenka A, Pileckyte R, Trociukas I, Peceliunas V, Vaitekenaite V, Maneikis K, Davainis L, Zvirblis T, Stoskus M, Gineikiene E, Norvilas R, Dirse V, Surauciute A, Zucenkiene E, Griskevicius L. Zucenka A, et al. Among authors: dirse v. Eur J Haematol. 2021 Jan;106(1):105-113. doi: 10.1111/ejh.13527. Epub 2020 Oct 27. Eur J Haematol. 2021. PMID: 32997830

4

Acute Pre-B Lymphoblastic Leukemia and Congenital Anomalies in a Child with a de Novo 22q11.1q11.22 Duplication.

Vaisvilas M, Dirse V, Aleksiuniene B, Tamuliene I, Cimbalistiene L, Utkus A, Rascon J. Vaisvilas M, et al. Among authors: dirse v. Balkan J Med Genet. 2018 Oct 29;21(1):87-91. doi: 10.2478/bjmg-2018-0002. eCollection 2018 Jun. Balkan J Med Genet. 2018. PMID: 30425917 Free PMC article.

5

Population-based targeted RNA sequencing reveals novel disease-related gene fusions in pediatric and adult T-ALL.

Norvilas R, Batiuskaite R, Dirse V, Semaskeviciene R, Gineikiene E, Stoskus M, Vaitkeviciene G, Rascon J, Griskevicius L. Norvilas R, et al. Among authors: dirse v. Leuk Res. 2022 May;116:106825. doi: 10.1016/j.leukres.2022.106825. Epub 2022 Mar 12. Leuk Res. 2022. PMID: 35339799

6

A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital Defects.

Kalinauskiene R, Brazdziunaite D, Burokiene N, Dirsė V, Morkuniene A, Utkus A, Preiksaitiene E. Kalinauskiene R, et al. Among authors: dirse v. Medicina (Kaunas). 2023 Jun 15;59(6):1156. doi: 10.3390/medicina59061156. Medicina (Kaunas). 2023. PMID: 37374360 Free PMC article.

7

A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients.

Dirse V, Bertasiute A, Gineikiene E, Zvirblis T, Dambrauskiene R, Gerbutavicius R, Juozaityte E, Malciute L, Paulsson K, Griskevicius L. Dirse V, et al. Genes Chromosomes Cancer. 2015 May;54(5):326-33. doi: 10.1002/gcc.22246. Epub 2015 Feb 23. Genes Chromosomes Cancer. 2015. PMID: 25706938

8

Case Report: Specific ABL-Inhibitor Imatinib Is an Effective Targeted Agent as the First Line Therapy to Treat B-Cell Acute Lymphoblastic Leukemia With a Cryptic NUP214::ABL1 Gene Fusion.

Stukaite-Ruibiene E, Norvilas R, Dirse V, Stankeviciene S, Vaitkeviciene GE. Stukaite-Ruibiene E, et al. Among authors: dirse v. Pathol Oncol Res. 2022 Sep 12;28:1610570. doi: 10.3389/pore.2022.1610570. eCollection 2022. Pathol Oncol Res. 2022. PMID: 36172171 Free PMC article.

9

A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features.

Preiksaitiene E, Männik K, Dirse V, Utkus A, Ciuladaite Z, Kasnauskiene J, Kurg A, Kučinskas V. Preiksaitiene E, et al. Among authors: dirse v. Eur J Med Genet. 2012 Nov;55(11):656-9. doi: 10.1016/j.ejmg.2012.07.008. Epub 2012 Jul 27. Eur J Med Genet. 2012. PMID: 22842074

10

A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardation.

Dirse V, Burnyte B, Gineikiene E, Griskevicius L, Utkus A. Dirse V, et al. J Genet. 2014 Aug;93(2):501-3. doi: 10.1007/s12041-014-0369-9. J Genet. 2014. PMID: 25189247 Free article. No abstract available.

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