Sebastien Bender
Overview
Explore the profile of Sebastien Bender including associated specialties, affiliations and a list of published articles.
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Articles
25
Citations
373
Followers
0
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Recent Articles
1.
Thomas M, Bruzeau C, Martin O, Pollet J, Bender S, Carrion C, et al.
Cell Mol Immunol
. 2023 Aug;
20(10):1114-1126.
PMID: 37544964
SATB1 (Special A-T rich Binding protein 1) is a cell type-specific factor that regulates the genetic network in developing T cells and neurons. In T cells, SATB1 is required for...
2.
Martin O, Thomas M, Marquet M, Bruzeau C, Garot A, Brousse M, et al.
Front Immunol
. 2023 Mar;
14:1030813.
PMID: 36865553
Intoduction: Two scaffold/matrix attachment regions (5'- and 3'- ) flank the intronic core enhancer (c) within the immunoglobulin heavy chain locus (). Besides their conservation in mice and humans, the...
3.
Martinez-Rivas G, Bender S, Sirac C
Front Immunol
. 2022 Dec;
13:1008449.
PMID: 36458006
Monoclonal immunoglobulin (Ig) light chain amyloidosis (AL) is a rare but severe disease that may occur when a B or plasma cell clone secretes an excess of free Ig light...
4.
Javaugue V, Pascal V, Bender S, Nasraddine S, Dargelos M, Alizadeh M, et al.
Kidney Int
. 2021 Nov;
101(2):331-337.
PMID: 34767830
The diagnostic approach of monoclonal gammopathy of renal significance is based on the detection of a monoclonal immunoglobulin in the blood and urine, and the identification of the underlying clone...
5.
Steinberg A, Fox L, Bender S, Batrouney A, Juneja S, Sirac C, et al.
Am J Kidney Dis
. 2021 Mar;
78(3):459-463.
PMID: 33774080
There is increasing recognition of monoclonal gammopathy as a cause of proliferative glomerulonephritis (GN), including cases in which glomerular deposition of monoclonal immunoglobulin is demonstrated. Recently, proliferative GN with monoclonal...
6.
Ayala M, Bender S, Anegon I, Menoret S, Bridoux F, Jaccard A, et al.
Amyloid
. 2021 Jan;
28(3):209-210.
PMID: 33480298
No abstract available.
7.
Bender S, Ayala M, Bonaud A, Javaugue V, Carrion C, Oblet C, et al.
Blood
. 2020 Jun;
136(14):1645-1656.
PMID: 32559766
Light chain (LC) deposition disease (LCDD) is a rare disorder characterized by glomerular and peritubular amorphous deposits of a monoclonal immunoglobulin LC, leading to nodular glomerulosclerosis and nephrotic syndrome. We...
8.
Bender S, Javaugue V, Saintamand A, Ayala M, Alizadeh M, Filloux M, et al.
Blood
. 2020 Apr;
135(20):1750-1758.
PMID: 32243509
Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome is a rare multisystem disease resulting from an underlying plasma cell (PC) dyscrasia. The pathophysiology of the disease remains unclear,...
9.
Nasr S, Sirac C, Bridoux F, Javaugue V, Bender S, Rinsant A, et al.
Am J Kidney Dis
. 2019 Apr;
74(2):276-280.
PMID: 30955945
Heavy chain amyloidosis and heavy chain deposition disease are the only known kidney diseases caused by the deposition of truncated immunoglobulin heavy chains. Fibrillary glomerulonephritis typically results from deposition of...
10.
Joly F, Cohen C, Javaugue V, Bender S, Belmouaz M, Arnulf B, et al.
Blood
. 2018 Dec;
133(6):576-587.
PMID: 30578255
Monoclonal immunoglobulin deposition disease (MIDD) is a rare complication of B-cell clonal disorders, defined by Congo red negative-deposits of monoclonal light chain (LCDD), heavy chain (HCDD), or both (LHCDD). MIDD...