Wissenschaftliche Publikationen | Max Delbrück Center

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28. Oktober 2020 / J Genet Genomics

Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation

X. Su
Y. Feng
S.A. Rahman
S. Wu
G. Li
F. Rüschendorf
L. Zhao
H. Cui
J. Liang
L. Fang
H. Hu
S. Froehler
Y. Yu
G. Patone
O. Hummel
Q. Chen
K. Raile
F.C. Luft
S. Bähring
K. Hussain
W. Chen
J. Zhang
M. Gong

20. Oktober 2020 / J Genet Genomics

Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation

X. Su
Y. Feng
S.A. Rahman
S. Wu
G. Li
F. Rüschendorf
L. Zhao
H. Cui
J. Liang
L. Fang
H. Hu
S. Froehler
Y. Yu
G. Patone
O. Hummel
Q. Chen
K. Raile
F.C. Luft
S. Bähring
K. Hussain
W. Chen
J. Zhang
M. Gong

01. Januar 2021 / Cancers

Gene expression signatures of a preclinical mouse model during colorectal cancer progression under low-dose metronomic chemotherapy

H. Ho-Xuan
G. Lehmann
P. Glazar
F. Gypas
N. Eichner
K. Heizler
H.J. Schlitt
M. Zavolan
N. Rajewsky
G. Meister
C. Hackl

01. März 2022 / Eur J Pharm Sci

Suicide nanoplasmids coding for ribosome-inactivating proteins

H. Mitdank
M. Tröger
A. Sonntag
N.A. Shirazi
E. Woith
H. Fuchs
D. Kobelt
W. Walther
A. Weng

04. Januar 2021 / microPubl Biol

Estimation of C. elegans cell- and tissue volumes

J.J. Froehlich
N. Rajewsky
C.Y. Ewald

15. März 2021 / EMBO J

Transcriptional repression of NFKBIA triggers constitutive IKK- and proteasome-independent p65/RelA activation in senescence

M. Kolesnichenko
N. Mikuda
U.E. Höpken
E. Kärgel
B. Uyar
A.B. Tufan
M. Milanovic
W. Sun
I. Krahn
K. Schleich
L. von Hoff
M. Hinz
M. Willenbrock
S. Jungmann
A. Akalin
S. Lee
R. Schmidt-Ullrich
C.A. Schmitt
C. Scheidereit

01. April 2021 / Cell Mol Life Sci

MACC1 regulates clathrin-mediated endocytosis and receptor recycling of transferrin receptor and EGFR in colorectal cancer

F. Imbastari
M. Dahlmann
A. Sporbert
C. Ciolli Mattioli
T. Mari
F. Scholz
L. Timm
S. Twamley
R. Migotti
W. Walther
G. Dittmar
A. Rehm
U. Stein

01. Juni 2021 / Hum Genet

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

B. Vona
N. Mazaheri
S.J. Lin
L.A. Dunbar
R. Maroofian
H. Azaiez
K.T. Booth
S. Vitry
A. Rad
F. Rüschendorf
P. Varshney
B. Fowler
C. Beetz
K.N. Alagramam
D. Murphy
G. Shariati
A. Sedaghat
H. Houlden
C. Petree
S. VijayKumar
R.J.H. Smith
T. Haaf
A. El-Amraoui
M.R. Bowl
G.K. Varshney
H. Galehdari

19. März 2021 / iScience

Transcriptomic profiling of SARS-CoV-2 infected human cell lines identifies HSP90 as target for COVID-19 therapy

E. Wyler
K. Mösbauer
V. Franke
A. Diag
L.T. Gottula
R. Arsiè
F. Klironomos
D. Koppstein
K. Hönzke
S. Ayoub
C. Buccitelli
K. Hoffmann
A. Richter
I. Legnini
A. Ivanov
T. Mari
S. Del Giudice
J. Papies
S. Praktiknjo
T.F. Meyer
M.A. Müller
D. Niemeyer
A. Hocke
M. Selbach
A. Akalin
N. Rajewsky
C. Drosten
M. Landthaler

30. Juni 2020 / PLoS Genet

Age-of-onset information helps identify 76 genetic variants associated with allergic disease