Maria Eugenia Chollet
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Explore the profile of Maria Eugenia Chollet including associated specialties, affiliations and a list of published articles.
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12
Citations
87
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Recent Articles
1.
Westerberg N, Atneosen-Asegg M, Melheim M, Chollet M, Harrison S, Siller R, et al.
Pediatr Res
. 2024 Jul;
97(1):195-201.
PMID: 38951656
Objectives: Hepatic ischemia and hypoxia are accompanied by reduced bile flow, biliary sludge and cholestasis. Hepatobiliary transport systems, nuclear receptors and aquaporins were studied after hypoxia and reoxygenation in human...
2.
Harrison S, Siller R, Tanaka Y, Chollet M, de la Morena-Barrio M, Xiang Y, et al.
Exp Mol Med
. 2023 Aug;
55(9):2005-2024.
PMID: 37653039
The lack of physiological parity between 2D cell culture and in vivo culture has led to the development of more organotypic models, such as organoids. Organoid models have been developed...
3.
Roman G, Stavik B, Lauritzen K, Sandset P, Harrison S, Sullivan G, et al.
Front Physiol
. 2023 Jan;
14:1094249.
PMID: 36711019
The bleeding phenotype of hereditary coagulation disorders is caused by the low or undetectable activity of the proteins involved in hemostasis, due to a broad spectrum of genetic alterations. Most...
4.
Andersen E, Chollet M, Sletten M, Stavik B, Skarpen E, Backe P, et al.
Thromb Haemost
. 2021 Mar;
121(12):1588-1598.
PMID: 33742435
Clinical parameters have been extensively studied in factor (F) VII deficiency, but the knowledge of molecular mechanisms of this disease is scarce. We report on three probands with intracranial bleeds...
5.
Andersen E, Chollet M, Baroni M, Pinotti M, Bernardi F, Skarpen E, et al.
Cell Biosci
. 2019 Aug;
9:69.
PMID: 31467667
Background: Congenital coagulation factor (F) VII deficiency is a rare bleeding disorder caused by mutations in the gene. The missense factor FVII variant p.Q160R is the disease-causing mutation in all...
6.
Andersen E, Chollet M, Myklebust C, Pinotti M, Bernardi F, Chuansumrit A, et al.
Thromb Haemost
. 2018 Apr;
118(4):664-675.
PMID: 29618153
Congenital factor (F) VII deficiency is a bleeding disorder caused by a heterogeneous pattern of mutations in the gene. Protein misfolding due to mutations is a strong candidate mechanism to...
7.
Chollet M, Andersen E, Skarpen E, Myklebust C, Koehler C, Morth J, et al.
Biochim Biophys Acta Mol Basis Dis
. 2017 Dec;
1864(3):660-667.
PMID: 29246447
Activated factor (F) VII is a vitamin K-dependent glycoprotein that initiates blood coagulation upon interaction with tissue factor. FVII deficiency is the most common of the rare congenital bleeding disorders....
8.
Chollet M, Skarpen E, Iversen N, Sandset P, Skretting G
Cell Biosci
. 2015 Oct;
5:57.
PMID: 26457178
Some inherited coagulation factor deficiencies are caused by intracellular retention or degradation of misfolded proteins, and chemical chaperones have been shown to reverse protein misfolding. The purpose of the present...
9.
Woldt E, Terrand J, Mlih M, Matz R, Bruban V, Coudane F, et al.
Nat Commun
. 2012 Sep;
3:1077.
PMID: 23011131
Vascular calcification is a hallmark of advanced atherosclerosis. Here we show that deletion of the nuclear receptor PPARγ in vascular smooth muscle cells of low density lipoprotein receptor (LDLr)-deficient mice...
10.
Tristano A, Chollet M, Willson M, Perez J, Troccoli M
Invest Clin
. 2004 Oct;
45(3):277-88.
PMID: 15469072
Paracoccidioidomycosis is a systemic infection caused by a dimorphic fungus (Paracoccidioides brasiliensis). The most common lesions frequently occur in the bucopharinx mucosa. Other lesions occur in the adrenal glands, liver,...