Detalhe da pesquisa
1.
UHMK1 is a novel splicing regulatory kinase.
J Biol Chem
; 299(4): 103041, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36803961
2.
DNA methylation epitypes highlight underlying developmental and disease pathways in acute myeloid leukemia.
Genome Res
; 31(5): 747-761, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33707228
3.
Genetics and beyond: Precision Medicine Real-World Data for Patients with Cervical, Vaginal or Vulvar Cancer in a Tertiary Cancer Center.
Int J Mol Sci
; 25(4)2024 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38397025
4.
Mutations in HID1 Cause Syndromic Infantile Encephalopathy and Hypopituitarism.
Ann Neurol
; 90(1): 143-158, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33999436
5.
Fusion gene detection by RNA-sequencing complements diagnostics of acute myeloid leukemia and identifies recurring NRIP1-MIR99AHG rearrangements.
Haematologica
; 107(1): 100-111, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34134471
6.
NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU.
Arch Gynecol Obstet
; 303(5): 1331-1345, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33277683
7.
GATA2 mutations in myeloid malignancies: Two zinc fingers in many pies.
IUBMB Life
; 72(1): 151-158, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31785092
8.
Loss of ISWI ATPase SMARCA5 (SNF2H) in Acute Myeloid Leukemia Cells Inhibits Proliferation and Chromatid Cohesion.
Int J Mol Sci
; 21(6)2020 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32197313
9.
Clonal evolution of acute myeloid leukemia from diagnosis to relapse.
Genes Chromosomes Cancer
; 58(12): 839-849, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31478278
10.
Controlled stem cell amplification by HOXB4 depends on its unique proline-rich region near the N terminus.
Blood
; 129(3): 319-323, 2017 01 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-27827825
11.
Spectrum and prognostic relevance of driver gene mutations in acute myeloid leukemia.
Blood
; 128(5): 686-98, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27288520
12.
A 29-gene and cytogenetic score for the prediction of resistance to induction treatment in acute myeloid leukemia.
Haematologica
; 103(3): 456-465, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29242298
13.
Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4.
Genes Chromosomes Cancer
; 56(1): 75-86, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27636548
14.
In-depth mutational analyses of colorectal neuroendocrine carcinomas with adenoma or adenocarcinoma components.
Mod Pathol
; 30(1): 95-103, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27586204
15.
Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosis.
Haematologica
; 102(1): 130-138, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27561722
16.
Close correlation of copy number aberrations detected by next-generation sequencing with results from routine cytogenetics in acute myeloid leukemia.
Genes Chromosomes Cancer
; 55(7): 553-67, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27015608
17.
Isolated trisomy 13 defines a homogeneous AML subgroup with high frequency of mutations in spliceosome genes and poor prognosis.
Blood
; 124(8): 1304-11, 2014 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-24923295
18.
Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations.
Blood
; 121(23): 4749-52, 2013 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23603912
19.
Exome sequencing identifies recurring FLT3 N676K mutations in core-binding factor leukemia.
Blood
; 122(10): 1761-9, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23878140
20.
The CATS (FAM64A) protein is a substrate of the Kinase Interacting Stathmin (KIS).
Biochim Biophys Acta
; 1833(5): 1269-79, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23419774