Wissenschaftliche Publikationen

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

Extracellular matrix in heart failure: role of ADAMTS5 in proteoglycan remodeling

J. Barallobre-Barreiro
T. Radovits
M. Fava
U. Mayr
W.Y. Lin
E. Ermolaeva
D. Martínez-López
E.L. Lindberg
E. Duregotti
L. Daróczi
M. Hasman
L.E. Schmidt
B. Singh
R. Lu
F. Baig
A.M. Siedlar
F. Cuello
N. Catibog
K. Theofilatos
A.M. Shah
M.G. Crespo-Leiro
N. Doménech
N. Hübner
B. Merkely
M. Mayr

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

Endophilin A2 deficiency protects rodents from autoimmune arthritis by modulating T cell activation

U. Norin
C. Rintisch
L. Meng
F. Forster
D. Ekman
J. Tuncel
K. Klocke
J. Bäcklund
M. Yang
M.Y Bonner
G.F. Lahore
J. James
K. Shchetynsky
M. Bergquist
I. Gjertsson
N. Hubner
L. Bäckdahl
R. Holmdahl

Activation of tripartite motif containing 63 expression by transcription factor EB and transcription factor binding to immunoglobulin heavy chain enhancer 3 is regulated by protein kinase D and class IIa histone deacetylases

C. Pablo Tortola
B. Fielitz
Y. Li
J. Rüdebusch
F.C. Luft
J. Fielitz

Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure

J. Kovarik
N. Morisawa
J. Wild
A. Marton
K. Takase-Minegishi
S. Minegishi
S. Daub
J.M. Sands
J.D. Klein
J.L. Bailey
J.P. Kovalik
M. Rauh
S. Karbach
K.F. Hilgers
F. Luft
A. Nishiyama
D. Nakano
K. Kitada
J. Titze

Aestivation motifs explain hypertension and muscle mass loss in mice with psoriatic skin barrier defect

J. Wild
R. Jung
T. Knopp
P. Efentakis
D. Benaki
A. Grill
J. Wegner
M. Molitor
V. Garlapati
N. Rakova
L. Markó
A. Marton
E. Mikros
T. Muenzel
S. Kossmann
M. Rauh
D. Nakano
K. Kitada
F. Luft
A. Waisman
P. Wenzel
J. Titze
S. Karbach

Molekulargenetik der humanen Hypertonie [Molecular genetics of human hypertension]

F.C. Luft

Apple peel and flesh contain pro-neurogenic compounds

M. Ichwan
T.L. Walker
Z. Nicola
J. Ludwig-Müller
C. Böttcher
R.W. Overall
V.S. Adusumilli
M. Bulut
A.M. Sykes
N. Hübner
G. Ramirez-Rodriguez
L. Ortiz-López
E.A. Lugo-Hernández
G. Kempermann

14. Juli 2020 / Circulation

Phosphodiesterase 3A and arterial hypertension

M. Ercu
L. Markó
C. Schächterle
D. Tsvetkov
Y. Cui
S. Maghsodi
T.U.P. Bartolomaeus
P.G. Maass
K. Zühlke
N. Gregersen
N. Hübner
R. Hodge
A. Mühl
B. Pohl
R. Molé-Illas
A. Geelhaar
S. Walter
H. Napieczynska
S. Schelenz
M. Taube
A. Heuser
Y.M. Anistan
F. Qadri
M. Todiras
R. Plehm
E. Popova
R. Langanki
J. Eichhorst
M. Lehmann
B. Wiesner
M. Russwurm
S.K. Forslund
I. Kamer
D.N. Müller
M. Gollasch
A. Aydin
S. Bähring
M. Bader
F.C. Luft
E. Klussmann