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1.
A mutation of the human EPHB2 gene leads to a major platelet functional defect.
Blood
; 132(19): 2067-2077, 2018 11 08.
Article
in English
| MEDLINE | ID: mdl-30213874
2.
Relevance of platelet desialylation and thrombocytopenia in type 2B von Willebrand disease: preclinical and clinical evidence.
Haematologica
; 104(12): 2493-2500, 2019 12.
Article
in English
| MEDLINE | ID: mdl-30819911
3.
A mouse model of pseudohypoaldosteronism type II reveals a novel mechanism of renal tubular acidosis.
Kidney Int
; 94(3): 514-523, 2018 09.
Article
in English
| MEDLINE | ID: mdl-30146013
4.
Acute genetic ablation of pendrin lowers blood pressure in mice.
Nephrol Dial Transplant
; 32(7): 1137-1145, 2017 Jul 01.
Article
in English
| MEDLINE | ID: mdl-28064162
5.
A fate-mapping approach reveals the composite origin of the connecting tubule and alerts on "single-cell"-specific KO model of the distal nephron.
Am J Physiol Renal Physiol
; 311(5): F901-F906, 2016 11 01.
Article
in English
| MEDLINE | ID: mdl-27582101
6.
WNK1-related Familial Hyperkalemic Hypertension results from an increased expression of L-WNK1 specifically in the distal nephron.
Proc Natl Acad Sci U S A
; 110(35): 14366-71, 2013 Aug 27.
Article
in English
| MEDLINE | ID: mdl-23940364
7.
Decreased ENaC expression compensates the increased NCC activity following inactivation of the kidney-specific isoform of WNK1 and prevents hypertension.
Proc Natl Acad Sci U S A
; 107(42): 18109-14, 2010 Oct 19.
Article
in English
| MEDLINE | ID: mdl-20921400
8.
New insights into regulation of αIIbß3 integrin signaling by filamin A.
Res Pract Thromb Haemost
; 6(2): e12672, 2022 Feb.
Article
in English
| MEDLINE | ID: mdl-35316942
9.
A gain-of-function filamin A mutation in mouse platelets induces thrombus instability.
J Thromb Haemost
; 20(11): 2666-2678, 2022 11.
Article
in English
| MEDLINE | ID: mdl-36006037
10.
Conditional glucocorticoid receptor expression in the heart induces atrio-ventricular block.
FASEB J
; 21(12): 3133-41, 2007 Oct.
Article
in English
| MEDLINE | ID: mdl-17517920
11.
Consequences of SPAK inactivation on Hyperkalemic Hypertension caused by WNK1 mutations: evidence for differential roles of WNK1 and WNK4.
Sci Rep
; 8(1): 3249, 2018 02 19.
Article
in English
| MEDLINE | ID: mdl-29459793
12.
Conditional mineralocorticoid receptor expression in the heart leads to life-threatening arrhythmias.
Circulation
; 111(23): 3025-33, 2005 Jun 14.
Article
in English
| MEDLINE | ID: mdl-15939817
13.
LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B.
JCI Insight
; 1(16): e88643, 2016 Oct 06.
Article
in English
| MEDLINE | ID: mdl-27734030
14.
WNK-SPAK-NCC cascade revisited: WNK1 stimulates the activity of the Na-Cl cotransporter via SPAK, an effect antagonized by WNK4.
Hypertension
; 64(5): 1047-53, 2014 Nov.
Article
in English
| MEDLINE | ID: mdl-25113964
15.
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.
Nat Genet
; 44(4): 456-60, S1-3, 2012 Mar 11.
Article
in English
| MEDLINE | ID: mdl-22406640
16.
Cross-talk between mineralocorticoid and angiotensin II signaling for cardiac remodeling.
Hypertension
; 52(6): 1060-7, 2008 Dec.
Article
in English
| MEDLINE | ID: mdl-18981328
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