|
🐜
|
Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome
22 auth.
Nikki M. Plaster,
R. Tawil,
M. Tristani-Firouzi,
S. Canún,
S. Bendahhou,
Akiko Tsunoda,
Matthew R. Donaldson,
S. Iannaccone,
E. Brunt,
R. Barohn,
...
John Clark,
F. Deymeer,
A. George,
F. Fish,
A. Hahn,
Alexandru Nitu,
C. Õzdemir,
P. Serdarog̃lu,
S. Subramony,
G. Wolfe,
Ying-Hui Fu,
L. Ptáček
|
9 |
2001 |
9
🐜
|
|
🐜
|
KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation
20 auth.
Yi-Han Chen,
Shi-jie Xu,
S. Bendahhou,
Xiao-liang Wang,
Ying Wang,
Wenyuan Xu,
Hong-wei Jin,
Hao Sun,
Xiaoyan Su,
Q. Zhuang,
...
Yiqing Yang,
Yue-bin Li,
Yi Liu,
Hong-Ju Xu,
Xiao-Fei Li,
Ning Ma,
Chun-Ping Mou,
Zhu Chen,
J. Barhanin,
Wei Huang
|
9 |
2003 |
9
🐜
|
|
🐜
|
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).
13 auth.
M. Tristani-Firouzi,
J. L. Jensen,
Matthew R. Donaldson,
V. Sansone,
G. Meola,
A. Hahn,
S. Bendahhou,
H. Kwiecinski,
A. Fidziańska,
Nikki M. Plaster,
...
Ying-Hui Fu,
L. Ptáček,
R. Tawil
|
9 |
2002 |
9
🐜
|
|
🐜
|
KCNQ1 gain-of-function mutation in familial atrial fibrillation.
20 auth.
Yi-Han Chen,
Shi-jie Xu,
S. Bendahhou,
Xiao-liang Wang,
Ying Wang,
Wenyuan Xu,
Hong-wei Jin,
Hao Sun,
Xiaoyan Su,
Q. Zhuang,
...
Yiqing Yang,
Yue-bin Li,
Yi Liu,
Hong-Ju Xu,
Xiao-Fei Li,
Ning Ma,
Chun-Ping Mou,
Zhu Chen,
J. Barhanin,
Wei Huang
|
8 |
2003 |
8
🐜
|
|
🐜
|
Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.
23 auth.
Yiqing Yang,
Min Xia,
Qingfeng Jin,
S. Bendahhou,
Jingyi Shi,
Yiping Chen,
Bo Liang,
Jie Lin,
Yi Liu,
Ban Liu,
...
Qinshu Zhou,
Dongwei Zhang,
Rong Wang,
Ning Ma,
Xiaoyan Su,
Kaiya Niu,
Yan-Zhi Pei,
Wenyuan Xu,
Zhao-hong Chen,
Haiying Wan,
J. Cui,
J. Barhanin,
Yi-han Chen
|
8 |
2004 |
8
🐜
|
|
🐜
|
A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
24 auth.
Min Xia,
Qingfeng Jin,
S. Bendahhou,
Yusong He,
Marie-Madeleine Larroque,
Yiping Chen,
Qinshu Zhou,
Yiqing Yang,
Yi Liu,
Ban Liu,
...
Qian Zhu,
Yan Zhou,
Jie Lin,
Bo Liang,
Li Li,
Xiongjian Dong,
Zhiwen Pan,
Rongrong Wang,
Haiying Wan,
Weiqin Qiu,
Wenyuan Xu,
Petra M. H. Eurlings,
J. Barhanin,
Yihan Chen
|
8 |
2005 |
8
🐜
|
|
🐬
|
MiRP2 Forms Potassium Channels in Skeletal Muscle with Kv3.4 and Is Associated with Periodic Paralysis
G. Abbott,
M. Butler,
S. Bendahhou,
M. Dalakas,
L. Ptáček,
S. Goldstein
|
8 |
2001 |
8
🐬
|
|
🐜
|
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome
17 auth.
Matthew R. Donaldson,
J. L. Jensen,
M. Tristani-Firouzi,
R. Tawil,
S. Bendahhou,
W. Suarez,
A. Cobo,
J. Poza,
E. Behr,
John F. Wagstaff,
...
P. Szepetowski,
S. Pereira,
T. Mozaffar,
D. Escolar,
Ying-Hui Fu,
L. Ptáček,
L. Ptáček
|
7 |
2003 |
7
🐜
|
|
🐜
|
Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis
20 auth.
D. Heitzmann,
R. Dérand,
S. Jungbauer,
S. Bandulik,
C. Sterner,
F. Schweda,
A. E. Wakil,
E. Lalli,
N. Guy,
R. Mengual,
...
M. Reichold,
I. Tegtmeier,
S. Bendahhou,
C. Gomez-Sanchez,
M. Isabel Aller,
W. Wisden,
A. Weber,
F. Lesage,
R. Warth,
J. Barhanin
|
7 |
2008 |
7
🐜
|
|
🦁
|
Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome*
S. Bendahhou,
Matthew R. Donaldson,
Nikki M. Plaster,
M. Tristani-Firouzi,
Ying-Hui Fu,
L. Ptáček
|
7 |
2003 |
7
🦁
|
|
🦁
|
In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart.
9 auth.
S. Bendahhou,
Céline Marionneau,
Karinne Haurogne,
Marie-Madeleine Larroque,
R. Dérand,
V. Szűts,
...
D. Escande,
S. Demolombe,
J. Barhanin
|
7 |
2005 |
7
🦁
|
|
🐜
|
Proximal renal tubular acidosis in TASK2 K+ channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport.
15 auth.
R. Warth,
H. Barriere,
P. Meneton,
M. Bloch,
Jörg Thomas,
M. Tauc,
D. Heitzmann,
E. Romeo,
F. Verrey,
R. Mengual,
...
N. Guy,
S. Bendahhou,
F. Lesage,
P. Poujeol,
J. Barhanin
|
7 |
2004 |
7
🐜
|
