Suchergebnisse - "Opatz, Sabrina"

PubPharm (10)

1

Enhancing Transsectoral Interdisciplinary Patient-Centered Care for Patients With Rare Cancers : Protocol for a Mixed Methods Process Evaluation

enthalten in: JMIR research protocols | 2023

von Hinneburg, J. | Zacher, S. | Berger-Höger, B. | +31

2

The clinical mutatome of core binding factor leukemia

enthalten in: Leukemia | 2020

von Opatz, S. | Bamopoulos, S. | Metzeler, K. | +28

3

Akute myeloische Leukämie mit rekurrenten chromosomalen Translokationen, Analyse der Fusionsproteine und kooperierender molekularer Mutationen auf dem Weg zu einer zielgerichteten, personalisierten Therapie

Erschienen: Dissertation, München, Ludwig-Maximilians-Universität, 2018

von Opatz, S. | Bohlander, S.

4

Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4

enthalten in: Genes, chromosomes & cancer | 2017

von Herold, T. | Metzeler, K. | Vosberg, S. | +19

5

Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4

enthalten in: Genes, chromosomes & cancer | 2017

von Herold, T. | Metzeler, K. | Vosberg, S. | +19

6

Close correlation of copy number aberrations detected by next-generation sequencing with results from routine cytogenetics in acute myeloid leukemia

enthalten in: Genes, chromosomes & cancer | 2016

von Vosberg, S. | Herold, T. | Hartmann, L. | +13

7

ZBTB7A mutations in acute myeloid leukaemia with t(8;21) translocation

enthalten in: Nature communications | 2016

von Hartmann, L. | Dutta, S. | Opatz, S. | +31

8

Close correlation of copy number aberrations detected by next‐generation sequencing with results from routine cytogenetics in acute myeloid leukemia

enthalten in: Genes, chromosomes & cancer | 2016

von Vosberg, S. | Herold, T. | Hartmann, L. | +13

9

Exome sequencing identifies recurring FLT3 N676K mutations in core-binding factor leukemia

enthalten in: Blood | 2013

von Opatz, S. | Polzer, H. | Herold, T. | +20

10

Exome sequencing identifies recurring FLT3 N676K mutations in core-binding factor leukemia

enthalten in: Blood | 2013

von Opatz, S. | Polzer, H. | Herold, T. | +20

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