C Chaussain
Overview
Explore the profile of C Chaussain including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
354
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0
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Recent Articles
1.
Chatzopoulou E, Bousaidi N, Guilbert T, Rucher G, Rose J, Germain S, et al.
J Dent Res
. 2024 Sep;
103(13):1392-1402.
PMID: 39290146
Regeneration of orofacial tissues is hampered by the lack of adequate vascular supply. Implantation of in vitro engineered, prevascularized constructs has emerged as a strategy to allow the rapid vascularization...
2.
Pragnere S, Auregan J, Bosser C, Linglart A, Bensidhoum M, Hoc T, et al.
Acta Biomater
. 2020 Oct;
119:259-267.
PMID: 33122145
Osteogenesis imperfecta (OI), also known as "brittle bone disease", is a rare genetic disorder of the skeleton, whose most benign form I corresponds to autosomal dominant mutations in the genes...
3.
Ghighi M, Llorens A, Baroukh B, Chaussain C, Bouchard P, Gosset M
J Periodontal Res
. 2017 Sep;
53(1):29-39.
PMID: 28898426
Background And Objective: The aim of this study was to analyze the differences in inflammatory and catabolic mediators expressed in peri-implantitis compared to periodontitis lesions after non-surgical therapy. Peri-implantitis is...
4.
Coyac B, Hoac B, Chafey P, Falgayrac G, Slimani L, Rowe P, et al.
J Dent Res
. 2017 Sep;
97(2):184-191.
PMID: 28880715
X-linked hypophosphatemia (XLH) is a skeletal disease caused by inactivating mutations in the PHEX gene. Mutated or absent PHEX protein/enzyme leads to a decreased serum phosphate level, which cause mineralization...
5.
Mangione F, EzEldeen M, Bardet C, Lesieur J, Bonneau M, Decup F, et al.
J Dent Res
. 2017 Aug;
96(12):1406-1413.
PMID: 28796952
Cell-based partial pulp regeneration is one of the promising approaches to obtain newly formed functional dentin-pulp complex. It relies on the preservation of the healthy tissue while regenerating the damaged...
6.
Linglart A, Chaussain C
Ann Endocrinol (Paris)
. 2017 Jun;
77 Suppl 1:S36-S42.
PMID: 28645356
Phosphate is absorbed through the gut, stored in the bone and reabsorbed through the proximal renal tubule. More importantly, PTH and FGF23 have been identified as the main phosphaturic factors...
7.
Collignon A, Amri N, Lesieur J, Sadoine J, Ribes S, Menashi S, et al.
J Dent Res
. 2017 Jun;
96(7):815-821.
PMID: 28571484
In humans, the SOST gene encodes sclerostin, an inhibitor of bone growth and remodeling, which also negatively regulates the bone repair process. Sclerostin has also been implicated in tooth formation,...
8.
Biosse Duplan M, Coyac B, Bardet C, Zadikian C, Rothenbuhler A, Kamenicky P, et al.
J Dent Res
. 2016 Nov;
96(4):388-395.
PMID: 27821544
X-linked hypophosphatemia (XLH) is a rare genetic skeletal disease where increased phosphate wasting in the kidney leads to hypophosphatemia and prevents normal mineralization of bone and dentin. Here, we examined...
9.
Opsahl-Vital S, Gaucher C, Bardet C, Courson F, Linglart A, Chaussain C
Arch Pediatr
. 2015 Jun;
22(5 Suppl 1):151-2.
PMID: 26112566
No abstract available.
10.
Acuna-Mendoza S, Martin S, Ribes S, Keller L, Chaussain C, Lebrin L, et al.
Bull Group Int Rech Sci Stomatol Odontol
. 2014 Dec;
52(1):e7-16.
PMID: 25461448
Recent progresses in stem cell biology and tissue engineering allow considering the possible development of new therapies for compensating the dental tissue losses associated with traumas, pathologies or ageing. The...