About: Torsten Haferlach

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Torsten Haferlach Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky)
rdfs:label	Torsten Haferlach (en) Torsten Haferlach (nl) Torsten Haferlach (ast)
skos:prefLabel	Torsten Haferlach (en) Torsten Haferlach (nl) Torsten Haferlach (ast)
name	Torsten Haferlach (en) Torsten Haferlach (nl) Torsten Haferlach (ast)
given name	wds:Q66370751-06E16FEF-8BE7-4969-BA14-409DB288ED22
given name	Torsten
instance of	wds:Q66370751-CC5F2D0A-C551-4226-8588-215E2D79CC42
instance of	Homo sapiens
ResearchGate profile ID	wds:Q66370751-20df6e11-422d-d224-73c1-3079ad68281c
ResearchGate profile ID	Torsten_Haferlach
skos:altLabel	Haferlach (en) Haferlach T (en) Haferlach T. (en) T Haferlach (en) T. Haferlach (en)
Nationale Thesaurus voor Auteursnamen ID	wds:Q66370751-62e05203-8035-4b3a-9aa2-e39b253327c8
occupation	wds:Q66370751-A5E215C6-93D3-4739-A79D-EEA81A2B2FF4
NUKAT ID	wds:Q66370751-22BC8A2C-03E8-4282-BEFD-6FB5C169507D
sex or gender	wds:Q66370751-3f855f18-490e-302c-dd6d-7d942bf55d20
ISNI	wds:Q66370751-C74B5CB9-5CD6-43BE-BEE7-7F7B7C8A0907
VIAF ID	wds:Q66370751-E541A61D-2018-4D89-AF2E-0AB328DC1C58
Library of Congress authority ID	wds:Q66370751-B8B3B843-D490-4DB4-89F6-18E102BD5EDC
Bibliothèque nationale de France ID	wds:Q66370751-E219B42A-A370-4002-8195-0D54FF387CDA
IdRef ID	wds:Q66370751-BAA97FD7-6058-48C0-B054-A59746E4B74B
National Library of Korea ID	wds:Q66370751-FEF891EC-AA95-4AC0-AD4E-2141C3BB0BC8
date of birth	wds:Q66370751-BBAFFD7D-ACA3-4B8B-9E3A-1B95BBD9F235
WorldCat Identities ID (superseded)	wds:Q66370751-755A1360-E4C2-4100-81DD-D9E38088DB29
National Library of Israel J9U ID	wds:Q66370751-19CF59D5-7AD5-4ACC-83CA-3D7967D4302D
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p329034367
VIAF ID	http://viaf.org/viaf/41958595
Library of Congress authority ID	http://id.loc.gov/authorities/names/nr92042635
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb12570562p#about
IdRef ID	http://www.idref.fr/035017341/id
National Library of Korea ID	http://lod.nl.go.kr/resource/KAC200711667
Nationale Thesaurus voor Auteursnamen ID	329034367
occupation	researcher
NUKAT ID	n2006148741
sex or gender	male
ISNI	0000000116284878
VIAF ID	41958595
Library of Congress authority ID	nr92042635
Bibliothèque nationale de France ID	12570562p
IdRef ID	035017341
National Library of Korea ID	KAC200711667
date of birth	1900-01-01 00:00:00Z (xsd:dateTime)
WorldCat Identities ID (superseded)	lccn-nr92042635
National Library of Israel J9U ID	987007376773305171
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q66370751
is author of	Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms Early blast clearance by remission induction therapy is a major independent prognostic factor for both achievement of complete remission and long-term outcome in acute myeloid leukemia: data from the German AML Cooperative Group (AMLCG) 1992 Trial Response to azacitidine is independent of p53 expression in higher-risk myelodysplastic syndromes and secondary acute myeloid leukemia Implications of NRAS mutations in AML: a study of 2502 patients Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML. Prognostic impact of FLT3-ITD load in NPM1 mutated acute myeloid leukemia ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype Diversity of the juxtamembrane and TKD1 mutations (exons 13-15) in the FLT3 gene with regards to mutant load, sequence, length, localization, and correlation with biological data Identification of a novel type of ITD mutations located in nonjuxtamembrane domains of the FLT3 tyrosine kinase receptor SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations A novel hierarchical prognostic model of AML solely based on molecular mutations AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic features. WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups. AML with translocation t(8;16)(p11;p13) demonstrates unique cytomorphological, cytogenetic, molecular and prognostic features. Acute myeloid leukemia with a complex aberrant karyotype is a distinct biological entity characterized by genomic imbalances and a specific gene expression profile The detection of TP53 mutations in chronic lymphocytic leukemia independently predicts rapid disease progression and is highly correlated with a complex aberrant karyotype Frequency and prognostic impact of CEBPA proximal, distal and core promoter methylation in normal karyotype AML: a study on 623 cases Expression of IGFBP7 in acute leukemia is regulated by DNA methylation. Definitions and standards in the diagnosis and treatment of the myelodysplastic syndromes: Consensus statements and report from a working conference Distinctive microRNA signature of acute myeloid leukemia bearing cytoplasmic mutated nucleophosmin KIT-D816 mutations in AML1-ETO-positive AML are associated with impaired event-free and overall survival Correlation of protein expression and gene expression in acute leukemia Clinical utility of microarray-based gene expression profiling in the diagnosis and subclassification of leukemia: report from the International Microarray Innovations in Leukemia Study Group Conventional cytogenetics of myeloproliferative diseases other than CML contribute valid information. Age-related risk profile and chemotherapy dose response in acute myeloid leukemia: a study by the German Acute Myeloid Leukemia Cooperative Group BRAF mutations in hairy-cell leukemia Insight into the molecular pathogenesis of myeloid malignancies Molecular genetics in acute myeloid leukemia Molecular genetics of adult acute myeloid leukemia: prognostic and therapeutic implications Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype Recurrent SETBP1 mutations in atypical chronic myeloid leukemia SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML) Age, JAK2(V617F) and SF3B1 mutations are the main predicting factors for survival in refractory anaemia with ring sideroblasts and marked thrombocytosis Both carboxy-terminus NES motif and mutated tryptophan(s) are crucial for aberrant nuclear export of nucleophosmin leukemic mutants in NPMc+ AML. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes High dose ara-C in the treatment of newly diagnosed acute promyelocytic leukemia: long-term results of the German AMLCG.

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software