Marie-Christine de Vernejoul
Overview
Explore the profile of Marie-Christine de Vernejoul including associated specialties, affiliations and a list of published articles.
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56
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1261
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Recent Articles
1.
Coudert A, Redelsperger F, Chabbi-Achengli Y, Vernochet C, Marty C, Decrouy X, et al.
Bone Rep
. 2019 Jul;
11:100214.
PMID: 31360740
and are envelope genes of retroviral origin that have been captured in evolution for a role in placentation. They trigger cell-cell fusion and were shown to be essential for the...
2.
Howaldt A, Nampoothiri S, Quell L, Ozden A, Fischer-Zirnsak B, Collet C, et al.
Bone
. 2018 Dec;
120:495-503.
PMID: 30537558
The osteopetroses and related sclerosing bone dysplasias can have a broad range of manifestations. Especially in the milder forms, sandwich vertebrae are an easily recognizable and reliable radiological hallmark. We...
3.
Lhaneche L, Hald J, Domingues A, Hannouche D, Delepine M, Zelenika D, et al.
Bone
. 2016 Aug;
92:107-115.
PMID: 27519970
SOST encodes sclerostin, an inhibitor of bone formation that antagonizes canonical Wnt signaling. Variations of SOST expression have an impact on bone mineral density (BMD) and bone strength. We hypothesized...
4.
Chabbi-Achengli Y, Coman T, Collet C, Callebert J, Corcelli M, Lin H, et al.
Am J Pathol
. 2016 Mar;
186(4):927-37.
PMID: 26968113
Rheumatoid arthritis is a chronic disease that results in a disabling and painful condition as it progresses to destruction of the articular cartilage and ankylosis of the joints. Although the...
5.
Coudert A, de Vernejoul M, Muraca M, Del Fattore A
Int J Endocrinol
. 2015 Apr;
2015:372156.
PMID: 25873953
Osteopetrosis is a rare genetic disorder characterized by an increase of bone mass due to defective osteoclast function. Patients typically displayed spontaneous fractures, anemia, and in the most severe forms...
6.
London G, Marchais S, Guerin A, de Vernejoul M
J Am Soc Nephrol
. 2014 Sep;
26(2):476-83.
PMID: 25231881
An association between atherosclerosis and osteoporosis has been reported in several studies. This association could result from local intraosseous atherosclerosis and ischemia, which is shown by limb osteoporosis in patients...
7.
Coudert A, Del Fattore A, Baulard C, Olaso R, Schiltz C, Collet C, et al.
Lab Invest
. 2013 Dec;
94(3):275-85.
PMID: 24336069
Autosomal dominant osteopetrosis type II (ADO II) is a rare, heritable bone disorder characterized by a high bone mass and insufficient osteoclast activity. Mutations in the CLCN7 gene have been...
8.
de Vernejoul M, Collet C, Chabbi-Achengli Y
Bonekey Rep
. 2013 Aug;
1:120.
PMID: 23951501
Besides its action as a neurotransmitter, serotonin has multiple physiological functions in several peripheral organs. Recently, Yadav et al. suggested that peripheral serotonin produced in the gut was a major...
9.
Collet C, Laplanche J, de Vernejoul M
Am J Med Genet A
. 2013 Jul;
161A(8):2074-7.
PMID: 23824952
We report on a family affected by Camurati-Engelmann disease, characterized by radiological signs limited to the tibia, and associated with overweight or obesity, which is not a known feature of...
10.
Gualeni B, de Vernejoul M, Marty-Morieux C, De Leonardis F, Franchi M, Monti L, et al.
Bone
. 2013 Feb;
54(1):83-91.
PMID: 23369989
Diastrophic dysplasia (DTD) is a chondrodysplasia caused by mutations in the SLC26A2 gene, leading to reduced intracellular sulfate pool in chondrocytes, osteoblasts and fibroblasts. Hence, proteoglycans are undersulfated in the...