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Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q

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Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q. / Panagiota, Victoria; Meggendorfer, Manja; Kubasch, Anne Sophie; Gabdoulline, Razif; Krönke, Jan; Mies, Anna; Shahswar, Rabia; Kandziora, Christian; Klement, Piroska; Schiller, Johannes; Göhring, Gudrun; Haferlach, Claudia; Ganster, Christina; Shirneshan, Katayoon; Gutermuth, Annika; Thiede, Christian; Germing, Ulrich; Schroeder, Thomas; Kobbe, Guido; Klesse, Sabrina; Koenecke, Christian; Schlegelberger, Brigitte; Kröger, Nicolaus; Haase, Detlef; Döhner, Konstanze; Sperr, Wolfgang R; Valent, Peter; Ganser, Arnold; Thol, Felicitas; Haferlach, Torsten; Platzbecker, Uwe; Heuser, Michael.

In: AM J HEMATOL, Vol. 96, No. 6, 01.06.2021, p. E207-E210.

Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

Harvard

Panagiota, V, Meggendorfer, M, Kubasch, AS, Gabdoulline, R, Krönke, J, Mies, A, Shahswar, R, Kandziora, C, Klement, P, Schiller, J, Göhring, G, Haferlach, C, Ganster, C, Shirneshan, K, Gutermuth, A, Thiede, C, Germing, U, Schroeder, T, Kobbe, G, Klesse, S, Koenecke, C, Schlegelberger, B, Kröger, N, Haase, D, Döhner, K, Sperr, WR, Valent, P, Ganser, A, Thol, F, Haferlach, T, Platzbecker, U & Heuser, M 2021, 'Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q', AM J HEMATOL, vol. 96, no. 6, pp. E207-E210. https://doi.org/10.1002/ajh.26162

APA

Panagiota, V., Meggendorfer, M., Kubasch, A. S., Gabdoulline, R., Krönke, J., Mies, A., Shahswar, R., Kandziora, C., Klement, P., Schiller, J., Göhring, G., Haferlach, C., Ganster, C., Shirneshan, K., Gutermuth, A., Thiede, C., Germing, U., Schroeder, T., Kobbe, G., ... Heuser, M. (2021). Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q. AM J HEMATOL, 96(6), E207-E210. https://doi.org/10.1002/ajh.26162

Vancouver

Panagiota V, Meggendorfer M, Kubasch AS, Gabdoulline R, Krönke J, Mies A et al. Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q. AM J HEMATOL. 2021 Jun 1;96(6):E207-E210. https://doi.org/10.1002/ajh.26162

Bibtex

@article{8dd7fe2387744414a180b01bd0cc3f0c,
title = "Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q",
keywords = "Abnormal Karyotype, Adult, Aged, Aged, 80 and over, Alleles, Anemia, Macrocytic/genetics, Chromosome Deletion, Chromosomes, Human, Pair 5/genetics, Clonal Evolution, Disease Progression, Drug Resistance, Neoplasm/genetics, Female, Genes, p53, Humans, Lenalidomide/pharmacology, Male, Middle Aged, Mutation, Myelodysplastic Syndromes/drug therapy, Protein Phosphatase 2C/genetics, Retrospective Studies",
author = "Victoria Panagiota and Manja Meggendorfer and Kubasch, {Anne Sophie} and Razif Gabdoulline and Jan Kr{\"o}nke and Anna Mies and Rabia Shahswar and Christian Kandziora and Piroska Klement and Johannes Schiller and Gudrun G{\"o}hring and Claudia Haferlach and Christina Ganster and Katayoon Shirneshan and Annika Gutermuth and Christian Thiede and Ulrich Germing and Thomas Schroeder and Guido Kobbe and Sabrina Klesse and Christian Koenecke and Brigitte Schlegelberger and Nicolaus Kr{\"o}ger and Detlef Haase and Konstanze D{\"o}hner and Sperr, {Wolfgang R} and Peter Valent and Arnold Ganser and Felicitas Thol and Torsten Haferlach and Uwe Platzbecker and Michael Heuser",
year = "2021",
month = jun,
day = "1",
doi = "10.1002/ajh.26162",
language = "English",
volume = "96",
pages = "E207--E210",
journal = "AM J HEMATOL",
issn = "0361-8609",
publisher = "Wiley-Liss Inc.",
number = "6",

}

RIS

TY - JOUR

T1 - Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q

AU - Panagiota, Victoria

AU - Meggendorfer, Manja

AU - Kubasch, Anne Sophie

AU - Gabdoulline, Razif

AU - Krönke, Jan

AU - Mies, Anna

AU - Shahswar, Rabia

AU - Kandziora, Christian

AU - Klement, Piroska

AU - Schiller, Johannes

AU - Göhring, Gudrun

AU - Haferlach, Claudia

AU - Ganster, Christina

AU - Shirneshan, Katayoon

AU - Gutermuth, Annika

AU - Thiede, Christian

AU - Germing, Ulrich

AU - Schroeder, Thomas

AU - Kobbe, Guido

AU - Klesse, Sabrina

AU - Koenecke, Christian

AU - Schlegelberger, Brigitte

AU - Kröger, Nicolaus

AU - Haase, Detlef

AU - Döhner, Konstanze

AU - Sperr, Wolfgang R

AU - Valent, Peter

AU - Ganser, Arnold

AU - Thol, Felicitas

AU - Haferlach, Torsten

AU - Platzbecker, Uwe

AU - Heuser, Michael

PY - 2021/6/1

Y1 - 2021/6/1

KW - Abnormal Karyotype

KW - Adult

KW - Aged

KW - Aged, 80 and over

KW - Alleles

KW - Anemia, Macrocytic/genetics

KW - Chromosome Deletion

KW - Chromosomes, Human, Pair 5/genetics

KW - Clonal Evolution

KW - Disease Progression

KW - Drug Resistance, Neoplasm/genetics

KW - Female

KW - Genes, p53

KW - Humans

KW - Lenalidomide/pharmacology

KW - Male

KW - Middle Aged

KW - Mutation

KW - Myelodysplastic Syndromes/drug therapy

KW - Protein Phosphatase 2C/genetics

KW - Retrospective Studies

U2 - 10.1002/ajh.26162

DO - 10.1002/ajh.26162

M3 - Other (editorial matter etc.)

C2 - 33725366

VL - 96

SP - E207-E210

JO - AM J HEMATOL

JF - AM J HEMATOL

SN - 0361-8609

IS - 6

ER -