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Francis Jaubert

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Articles 81
Citations 1307
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Recent Articles
1.
Cheikhelard A, Thibaud E, Morel Y, Jaubert F, Lortat-Jacob S, Polak M, et al.
Expert Rev Endocrinol Metab . 2019 Feb; 4(6):565-573. PMID: 30780790
Complete androgen insensitivity syndrome (CAIS) is an X-linked genetic disorder affecting 46,XY individuals, characterized by the loss of function of the androgen receptor gene resulting in complete peripheral androgen resistance....
2.
Murakami I, Wada N, Nakashima J, Iguchi M, Toi M, Hashida Y, et al.
Cell Commun Signal . 2018 Aug; 16(1):49. PMID: 30134914
Background: The relationship between various external agents such as pollen, food, and infectious agents and human sensitivity exists and is variable depending upon individual's health conditions. For example, we believe...
3.
Lezmi G, Galmiche-Rolland L, Rioux S, Jaubert F, Tillie-Leblond I, Scheinmann P, et al.
Eur Respir J . 2016 Nov; 48(5):1320-1328. PMID: 27799385
The role of mast cells in the pathogenesis of childhood asthma is poorly understood. We aimed to estimate the implication of airway mucosal mast cells in severe asthma and their...
4.
Murakami I, Oh Y, Morimoto A, Sano H, Kanzaki S, Matsushita M, et al.
Clin Proteomics . 2015 Jun; 12(1):16. PMID: 26097443
Background: Langerhans cell histiocytosis (LCH) is a proliferative disorder in which abnormal Langerhans cell (LC)-like cells (LCH cells) intermingle with inflammatory cells. Whether LCH is reactive or neoplastic remains a...
5.
Murakami I, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Nagata K, et al.
Cell Commun Signal . 2015 Apr; 13:13. PMID: 25889448
We propose Langerhans cell histiocytosis (LCH) is an inflammatory process that is prolonged by mutations. We hypothesize that Merkel cell polyomavirus (MCPyV) infection triggers an interleukin-1 (IL-1) activation loop that...
6.
Gogusev J, Murakami I, Telvi L, Goguin A, Sarfati E, Jaubert F
Pathol Res Pract . 2015 Feb; 211(4):332-40. PMID: 25655355
Parathyroid carcinoma is a rare neoplasia associated with PTH-dependent hypercalcaemia. It is infrequent in primary hyperparathyroidism (HPT) and very rarely associated with uremic HPT. A continuous cell line named Pt.Kich-1...
7.
Murakami I, Gogusev J, Jaubert F, Matsushita M, Hayashi K, Miura I, et al.
Oncol Rep . 2014 Oct; 33(1):171-8. PMID: 25351656
A cell line named PRU-1, derived from a Langerhans cell (LC) histiocytosis (LCH) skull lesion of a 7-year-old boy, was established and characterized. PRU-1 is an adherent spindle-shaped cell line...
8.
Murakami I, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Horie Y, et al.
Infect Agent Cancer . 2014 May; 9:15. PMID: 24834110
Background: Langerhans cell (LC) sarcoma (LCS) is a high-grade neoplasm with overtly malignant cytologic features and an LC phenotype. We very recently suggested that LC behaves as a reservoir for...
9.
Murakami I, Matsushita M, Iwasaki T, Kuwamoto S, Kato M, Horie Y, et al.
Hum Pathol . 2013 Dec; 45(1):119-26. PMID: 24321520
Langerhans cell histiocytosis (LCH) is a group of granulomatous disorders in which abnormal Langerhans cells proliferate as either a localized lesion in a single bone or disseminated disease involving two...
10.
Murakami I, Morimoto A, Oka T, Kuwamoto S, Kato M, Horie Y, et al.
Virchows Arch . 2012 Dec; 462(2):219-28. PMID: 23269323
Langerhans cell histiocytosis (LCH) is a lymphoproliferative disorder consisting of abnormal Langerhans cell-like cells and other lymphoid cells. LCH presents as either a multisystem LCH (LCH-MS) or a single-system LCH...