Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1959 1
1965 1
1973 1
1975 1
1984 1
1988 1
1990 1
1992 1
1995 3
1997 1
1999 1
2001 2
2003 1
2004 3
2005 2
2006 1
2008 2
2009 2
2010 1
2011 1
2012 3
2013 1
2014 4
2015 3
2016 3
2017 11
2018 7
2019 11
2020 15
2021 7
2022 5
2023 3
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

94 results

Results by year

Filters applied: . Clear all
Page 1
Did you mean p grenier[Author] (954 results)?
Current mechanistic insights into the CCCP-induced cell survival response.
Kane MS, Paris A, Codron P, Cassereau J, Procaccio V, Lenaers G, Reynier P, Chevrollier A. Kane MS, et al. Among authors: reynier p. Biochem Pharmacol. 2018 Feb;148:100-110. doi: 10.1016/j.bcp.2017.12.018. Epub 2017 Dec 22. Biochem Pharmacol. 2018. PMID: 29277693 Free article. Review.
DRP1 haploinsufficiency attenuates cardiac ischemia/reperfusion injuries.
Bouche L, Kamel R, Tamareille S, Garcia G, Villedieu C, Pillot B, Gueguen N, Chehaitly A, Chao de la Barca JM, Beaumont J, Baetz D, Ovize M, Sesaki H, Henrion D, Reynier P, Lenaers G, Prunier F, Mirebeau-Prunier D. Bouche L, et al. Among authors: reynier p. PLoS One. 2021 Mar 25;16(3):e0248554. doi: 10.1371/journal.pone.0248554. eCollection 2021. PLoS One. 2021. PMID: 33765018 Free PMC article.
Following I/R, the infarct size was significantly smaller in Dnm1l+/- mice than in WT (34.63.1% vs. 44.53.3%, respectively; p<0.05) and the autophagic markers, LC3 II and P62 were significantly increased compared to baseline condition in Dnm1l+/- mice only. ...
Following I/R, the infarct size was significantly smaller in Dnm1l+/- mice than in WT (34.63.1% vs. 44.53.3%, respectively; p<0.05 …
Nicotinamide Deficiency in Primary Open-Angle Glaucoma.
Kouassi Nzoughet J, Chao de la Barca JM, Guehlouz K, Leruez S, Coulbault L, Allouche S, Bocca C, Muller J, Amati-Bonneau P, Gohier P, Bonneau D, Simard G, Milea D, Lenaers G, Procaccio V, Reynier P. Kouassi Nzoughet J, et al. Among authors: reynier p. Invest Ophthalmol Vis Sci. 2019 Jun 3;60(7):2509-2514. doi: 10.1167/iovs.19-27099. Invest Ophthalmol Vis Sci. 2019. PMID: 31185090
RESULTS: Using the semiquantitative method, the plasma nicotinamide concentration was significantly lower in the initial cohort of POAG individuals compared to controls and further confirmed in the same cohort, using the targeted quantitative method, with mean concentrations of 0 …
RESULTS: Using the semiquantitative method, the plasma nicotinamide concentration was significantly lower in the initial cohort of POAG indi …
Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria.
Chevrollier A, Bonnard AA, Ruaud L, Gueguen N, Perrin L, Desquiret-Dumas V, Guimiot F, Becker PH, Levy J, Reynier P, Gaignard P. Chevrollier A, et al. Among authors: reynier p. Brain. 2024 Jan 4;147(1):91-99. doi: 10.1093/brain/awad347. Brain. 2024. PMID: 37804319
Whole genome analysis revealed a homozygous deletion c.1717-274_1734 del (NM_014874.4) in the MFN2 gene, leading to exon 16 skipping and in-frame loss of 50 amino acids (p.Gln574_Val624del), removing the proline-rich domain and the transmembrane domain 1 (TM1). ...
Whole genome analysis revealed a homozygous deletion c.1717-274_1734 del (NM_014874.4) in the MFN2 gene, leading to exon 16 skipping and in- …
Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALS.
Blasco H, Veyrat-Durebex C, Bocca C, Patin F, Vourc'h P, Kouassi Nzoughet J, Lenaers G, Andres CR, Simard G, Corcia P, Reynier P. Blasco H, et al. Among authors: reynier p. Sci Rep. 2017 Dec 15;7(1):17652. doi: 10.1038/s41598-017-17389-9. Sci Rep. 2017. PMID: 29247199 Free PMC article.
We showed that ALS patients (n = 40) displayed a highly significant specific CSF lipidomic signature compared to controls (n = 45). Phosphatidylcholine PC(36:4), higher in ALS patients (p = 0.0003) was the most discriminant molecule, and ceramides and glucosylceramides wer …
We showed that ALS patients (n = 40) displayed a highly significant specific CSF lipidomic signature compared to controls (n = 45). Phosphat …
Primary antiphospholipid syndrome and antiphospholipid syndrome associated to systemic lupus: Are they different entities?
Belizna C, Stojanovich L, Cohen-Tervaert JW, Fassot C, Henrion D, Loufrani L, Nagy G, Muchardt C, Hasan M, Ungeheuer MN, Arnaud L, Alijotas-Reig J, Esteve-Valverde E, Nicoletti F, Saulnier P, Godon A, Reynier P, Chrétien JM, Damian L, Omarjee L, Mahé G, Pistorius MA, Meroni PL, Devreese K. Belizna C, et al. Among authors: reynier p. Autoimmun Rev. 2018 Aug;17(8):739-745. doi: 10.1016/j.autrev.2018.01.027. Epub 2018 Jun 6. Autoimmun Rev. 2018. PMID: 29885541 Free article. Review.
Maternal ageing impairs mitochondrial DNA kinetics during early embryogenesis in mice.
May-Panloup P, Brochard V, Hamel JF, Desquiret-Dumas V, Chupin S, Reynier P, Duranthon V. May-Panloup P, et al. Among authors: reynier p. Hum Reprod. 2019 Jul 8;34(7):1313-1324. doi: 10.1093/humrep/dez054. Hum Reprod. 2019. PMID: 31174209
We also noted a faster expression of CDX2 and NANOG in the aged mice than in the young mice during the second (P = 0.007 and P = 0.02, respectively) and the third phase (P = 0.01 and P = 0.008, respectively) of embryogenesis. ...PPARGC1A, NRF1, POLG, T …
We also noted a faster expression of CDX2 and NANOG in the aged mice than in the young mice during the second (P = 0.007 and P …
Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis.
Wiedemann A, Chery C, Coelho D, Flayac J, Gueguen N, Desquiret-Dumas V, Feillet F, Lavigne C, Neau JP, Fowler B, Baumgartner MR, Reynier P, Guéant JL, Oussalah A. Wiedemann A, et al. Among authors: reynier p. J Hum Genet. 2020 Jan;65(2):91-98. doi: 10.1038/s10038-019-0689-y. Epub 2019 Oct 23. J Hum Genet. 2020. PMID: 31645654 Review.
We found two pathogenic compound heterozygous variants in MTHFR, including a variant not referenced in international databases, c.197C>T (p.Pro66Leu) and a known variant, c.470G>A (p.Arg157Gln), and two heterozygous pathogenic variants in POLG, c.1760C>T ( …
We found two pathogenic compound heterozygous variants in MTHFR, including a variant not referenced in international databases, c.197C>T …
94 results