Eric Clauser
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Explore the profile of Eric Clauser including associated specialties, affiliations and a list of published articles.
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49
Citations
1660
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Recent Articles
1.
Tetti M, Burrello J, Hureaux M, Billon C, Clauser E, Veglio F, et al.
Hypertension
. 2024 Sep;
81(11):2275-2285.
PMID: 39229746
Background: Hyperkalemia is a frequent electrolyte alteration whose prevalence varies widely, depending on the adopted cutoff, the setting (inpatients versus outpatients), and the characteristics of the study population. Familial hyperkalemic...
2.
Kouranti I, Abdel Khalek W, Mazurkiewicz S, Loisel-Ferreira I, Gautreau A, Pintard L, et al.
Int J Mol Sci
. 2022 May;
23(9).
PMID: 35563538
Cullin 3 (CUL3) is the scaffold of Cullin3 Ring E3-ligases (CRL3s), which use various BTB-adaptor proteins to ubiquitinate numerous substrates targeting their proteasomal degradation. mutations, responsible for a severe form...
3.
Vandestienne M, Zhang Y, Santos-Zas I, Al-Rifai R, Joffre J, Giraud A, et al.
J Clin Invest
. 2020 Dec;
131(2).
PMID: 33258804
The triggering receptor expressed on myeloid cells 1 (TREM-1) drives inflammatory responses in several cardiovascular diseases but its role in abdominal aortic aneurysm (AAA) remains unknown. Our objective was to...
4.
Louis-Dit-Picard H, Kouranti I, Rafael C, Loisel-Ferreira I, Chavez-Canales M, Abdel-Khalek W, et al.
J Clin Invest
. 2020 Aug;
130(12):6379-6394.
PMID: 32790646
Gain-of-function mutations in with no lysine (K) 1 (WNK1) and WNK4 genes are responsible for familial hyperkalemic hypertension (FHHt), a rare, inherited disorder characterized by arterial hypertension and hyperkalemia with...
5.
Hamzaoui N, Alarcon F, Leulliot N, Guimbaud R, Buecher B, Colas C, et al.
Genet Med
. 2020 May;
22(9):1533-1541.
PMID: 32424176
Purpose: Polymerase proofreading-associated polyposis is a dominantly inherited colorectal cancer syndrome caused by exonuclease domain missense variants in the DNA polymerases POLE and POLD1. Manifestations may also include malignancies at...
6.
Cavalcante I, Vaczlavik A, Drougat L, Lotfi C, Perlemoine K, Ribes C, et al.
Endocr Relat Cancer
. 2020 Feb;
27(4):221-230.
PMID: 32023208
ARMC5 (Armadillo repeat containing 5 gene) was identified as a new tumor suppressor gene responsible for hereditary adrenocortical tumors and meningiomas. ARMC5 is ubiquitously expressed and encodes a protein which...
7.
Abdel Khalek W, Rafael C, Loisel-Ferreira I, Kouranti I, Clauser E, Hadchouel J, et al.
J Am Soc Nephrol
. 2019 Apr;
30(5):811-823.
PMID: 30967423
Background: Mutations in four genes, WNK lysine deficient protein kinase 1 and 4 ( and ), kelch like family member 3 (), or Cullin 3 (), can result in familial...
8.
Lamour V, Bessereau J, Thalabard J, Gressens P, Bessis A, Barbour B, et al.
Med Sci (Paris)
. 2018 Jun;
34(5):462-463.
PMID: 29900851
No abstract available.
9.
Lecoq A, Stratakis C, Viengchareun S, Chaligne R, Tosca L, Demeocq V, et al.
JCI Insight
. 2017 Sep;
2(18).
PMID: 28931750
GIP-dependent Cushing's syndrome is caused by ectopic expression of glucose-dependent insulinotropic polypeptide receptor (GIPR) in cortisol-producing adrenal adenomas or in bilateral macronodular adrenal hyperplasias. Molecular mechanisms leading to ectopic GIPR...
10.
Jouinot A, Assie G, Libe R, Fassnacht M, Papathomas T, Barreau O, et al.
J Clin Endocrinol Metab
. 2016 Dec;
102(3):923-932.
PMID: 27967600
Context: Adrenocortical cancer (ACC) is an aggressive tumor with a heterogeneous outcome. Prognostic stratification is difficult even based on tumor stage and Ki67. Recently integrated genomics studies have demonstrated that...