Benjamin Delprat
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Explore the profile of Benjamin Delprat including associated specialties, affiliations and a list of published articles.
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34
Citations
808
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Recent Articles
11.
Crouzier L, Richard E, Sourbron J, Lagae L, Maurice T, Delprat B
Int J Mol Sci
. 2021 Dec;
22(24).
PMID: 34948153
Rare genetic diseases are a group of pathologies with often unmet clinical needs. Even if rare by a single genetic disease (from 1/2000 to 1/more than 1,000,000), the total number...
12.
Abatematteo F, Mosier P, Niso M, Brunetti L, Berardi F, Loiodice F, et al.
Eur J Med Chem
. 2021 Dec;
228:114038.
PMID: 34902734
The sigma-1 (σ) receptor plays a significant role in many normal physiological functions and pathological disease states, and as such represents an attractive therapeutic target for both agonists and antagonists....
13.
Crouzier L, Denus M, Richard E, Tavernier A, Diez C, Cubedo N, et al.
Int J Mol Sci
. 2021 Oct;
22(20).
PMID: 34681705
The sigma-1 receptor (S1R) is a highly conserved transmembrane protein highly enriched in mitochondria-associated endoplasmic reticulum (ER) membranes, where it interacts with several partners involved in ER-mitochondria Ca transfer, activation...
14.
Crouzier L, Diez C, Richard E, Cubedo N, Barbereau C, Rossel M, et al.
Front Cell Dev Biol
. 2021 Jun;
9:675517.
PMID: 34095146
Retinitis pigmentosa (RP) is one of the most common forms of inherited retinal degeneration with 1/4,000 people being affected. The vision alteration primarily begins with rod photoreceptor degeneration, then the...
15.
Bassani S, van Beelen E, Rossel M, Voisin N, Morgan A, Arribat Y, et al.
Hum Mol Genet
. 2021 Jun;
30(19):1785-1796.
PMID: 34059922
Non-Syndromic Hereditary Hearing Loss (NSHHL) is a genetically heterogeneous sensory disorder with about 120 genes already associated. Through exome sequencing (ES) and data aggregation, we identified a family with six...
16.
Patergnani S, Marchi S, Delprat B, Wieckowski M
Front Cell Dev Biol
. 2021 Apr;
9:678307.
PMID: 33898471
No abstract available.
17.
Crouzier L, Couly S, Roques C, Peter C, Belkhiter R, Arguel Jacquemin M, et al.
Eur Neuropsychopharmacol
. 2020 Sep;
39:29-45.
PMID: 32893057
The sigma-1 receptor (S1R) is a membrane-associated protein expressed in neurons and glia at mitochondria-associated endoplasmic reticulum (ER) membranes (MAMs). S1R interacts with different partners to regulate cellular responses, including...
18.
Delprat B, Crouzier L, Su T, Maurice T
Adv Exp Med Biol
. 2019 Oct;
1131:699-718.
PMID: 31646531
Calcium exchanges and homeostasis are finely regulated between cellular organelles and in response to physiological signals. Besides ionophores, including voltage-gated Ca channels, ionotropic neurotransmitter receptors, or Store-operated Ca entry, activity...
19.
Angebault C, Fauconnier J, Patergnani S, Rieusset J, Danese A, Affortit C, et al.
Sci Signal
. 2018 Oct;
11(553).
PMID: 30352948
Communication between the endoplasmic reticulum (ER) and mitochondria plays a pivotal role in Ca signaling, energy metabolism, and cell survival. Dysfunction in this cross-talk leads to metabolic and neurodegenerative diseases....
20.
Delprat B, Maurice T, Delettre C
Cell Death Dis
. 2018 Mar;
9(3):364.
PMID: 29511163
Wolfram syndrome (WS) is a rare neurodegenerative disease, the main pathological hallmarks of which associate with diabetes, optic atrophy, and deafness. Other symptoms may be identified in some but not...