Amrit Singh-Estivalet
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Explore the profile of Amrit Singh-Estivalet including associated specialties, affiliations and a list of published articles.
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8
Citations
132
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Recent Articles
1.
Gagliardini M, Mechaussier S, Campos Pina C, Morais M, Postal O, Jean P, et al.
Adv Sci (Weinh)
. 2025 Feb;
:e2410776.
PMID: 39965080
Auditory neuropathies affect the spiral ganglion neurons of the auditory nerve or their synapses with the sensory hair cells, distorting the sound information transmitted from the ear to the brain....
2.
Salame M, Bonnet C, Singh-Estivalet A, Brahim S, Roux S, Boussaty E, et al.
J Appl Genet
. 2024 Sep;
PMID: 39230647
PJVK gene was recently shown to create hypervulnerability to sound in humans and was the first human gene implicated in non-syndromic hearing impairment due to neural defect. Targeted next-generation sequencing...
3.
Jean P, Wong Jun Tai F, Singh-Estivalet A, Lelli A, Scandola C, Megharba S, et al.
Proc Natl Acad Sci U S A
. 2023 Jun;
120(26):e2221744120.
PMID: 37339214
Functional molecular characterization of the cochlea has mainly been driven by the deciphering of the genetic architecture of sensorineural deafness. As a result, the search for curative treatments, which are...
4.
Boucher S, Wong Jun Tai F, Delmaghani S, Lelli A, Singh-Estivalet A, Dupont T, et al.
Proc Natl Acad Sci U S A
. 2020 Nov;
117(49):31278-31289.
PMID: 33229591
Presbycusis, or age-related hearing loss (ARHL), is a major public health issue. About half the phenotypic variance has been attributed to genetic factors. Here, we assessed the contribution to presbycusis...
5.
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, et al.
Eur J Hum Genet
. 2016 Jul;
24(12):1730-1738.
PMID: 27460420
Usher syndrome (USH), the most prevalent cause of hereditary deafness-blindness, is an autosomal recessive and genetically heterogeneous disorder. Three clinical subtypes (USH1-3) are distinguishable based on the severity of the...
6.
Ebou M, Singh-Estivalet A, Launay J, Callebert J, Tronche F, Ferre P, et al.
PLoS One
. 2016 May;
11(5):e0155174.
PMID: 27144400
[This corrects the article DOI: 10.1371/journal.pone.0149343.].
7.
Ebou M, Singh-Estivalet A, Launay J, Callebert J, Tronche F, Ferre P, et al.
PLoS One
. 2016 Feb;
11(2):e0149343.
PMID: 26901633
Diabetes is a major complication of chronic Glucocorticoids (GCs) treatment. GCs induce insulin resistance and also inhibit insulin secretion from pancreatic beta cells. Yet, a full understanding of this negative...
8.
Valtat B, Riveline J, Zhang P, Singh-Estivalet A, Armanet M, Venteclef N, et al.
Diabetes
. 2013 Jan;
62(4):1206-16.
PMID: 23274887
Adult β-cell dysfunction, a hallmark of type 2 diabetes, can be programmed by adverse fetal environment. We have shown that fetal glucocorticoids (GCs) participate in this programming through inhibition of...
9.
Blondeau B, Sahly I, Massourides E, Singh-Estivalet A, Valtat B, Dorchene D, et al.
PLoS One
. 2012 Feb;
7(2):e30210.
PMID: 22363422
Conditional gene deletion in specific cell populations has helped the understanding of pancreas development. Using this approach, we have shown that deleting the glucocorticoid receptor (GR) gene in pancreatic precursor...