Wissenschaftliche Publikationen

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

Transgenic rat with overproduction of ubiquitous angiotensin-(1-7) presents neuroprotection in a model of ischemia and reperfusion

L.M. Kangussu
A.F. Almeida-Santos
L.F. Fernandes
N. Alenina
M. Bader
R.A.S. Santos
A.R. Massensini
M.J. Campagnole-Santos

Systemic outcomes of (Pyr(1))-apelin-13 infusion at mid-late pregnancy in a rat model with preeclamptic features

L.M. Yamaleyeva
K.B. Brosnihan
E. Elsangeedy
C. McGee
S. Shi
D. Caudell
C. Miller
J. Varagic
M. Bader
R. Dechend
H.A. Shaltout

Interactions between carboxypeptidase M and kinin B1 receptor in endothelial cells

P.B. Guimarães
R.F. da Silva
C.C. Hoff
L. Fernandes
C.R. Nakaie
J.R. Chagas
A. Karaoglanovic Carmona
M. Bader
J.B. Pesquero

The role of receptor MAS in microglia-driven retinal vascular development

S. Foulquier
V. Caolo
G. Swennen
I. Milanova
S. Reinhold
C. Recarti
N. Alenina
M. Bader
U M. Steckelings
T. Vanmierlo
M.J. Post
E.A. Jones
R.J. van Oostenbrugge
T. Unger

Linkage evidence for a two-locus inheritance of LQT-associated seizures in a multigenerational LQT family with a novel KCNQ1 loss-of-function mutation

H. Prüss
G. Gessner
S.H. Heinemann
F. Rüschendorf
A.K. Ruppert
H. Schulz
T. Sander
W. Rimpau

Targeted manipulation of brain serotonin: RNAi-mediated knockdown of tryptophan hydroxylase 2 in rats

S. Matthes
V. Mosienko
E. Popova
M. Rivalan
M. Bader
N. Alenina

Endothelial B2-receptor overexpression as an alternative animal model for hereditary angioedema

C. Lopes Veronez
S. Maghsodi
M. Todiras
E. Popova
A.F. Rodrigues
F. Qadri
J.B. Pesquero
M. Bader

Serotonin synthesis protects the mouse colonic crypt from DNA damage and colorectal tumorigenesis

J.Y. Sakita
M. Bader
E.S. Santos
S.B. Garcia
S.B. Minto
N. Alenina
M.O. Brunaldi
M.C. Carvalho
T. Vidotto
B. Gasparotto
R.B. Martins
W.A. Silva
M.L. Brandão
C.A. Leite
F.Q. Cunha
G. Karsenty
J.A. Squire
S.A. Uyemura
V. Kannen

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