Výsledky vyhledávání - "Mathilde Bonnet des Claustres"

Emerging drugs for the treatment of epidermolysis bullosa

Autor: Araksya Izmiryan, Alain Hovnanian, Matthias Titeux, Mathilde Bonnet des Claustres, Hélène Ragot

Publikováno v: Expert opinion on emerging drugs. 25(4)

Epidermolysis Bullosa (EB) form a heterogeneous group of rare, sometimes life-threatening inherited skin diseases characterized by skin and mucosal blistering after mild trauma from birth. They display a wide range of disease severity, with multiple

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1320b87886e2b8021e5e7e7aab66091f
https://pubmed.ncbi.nlm.nih.gov/33094671

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Secukinumab Therapy for Netherton Syndrome

Autor: Corinne Brunner, Barbara Meier-Schiesser, Nicole Knöpfel, Claire Barbieux, Mathilde Bonnet des Claustres, Alain Hovnanian, Davide Donghi, Agnes Schwieger-Briel, Lisa Weibel, Isabelle Luchsinger, Martin Theiler, Michael Buettcher

Publikováno v: JAMA Dermatology
JAMA Dermatology, American Medical Association, 2020, 156 (8), pp.907-911. ⟨10.1001/jamadermatol.2020.1019⟩

International audience; ImportanceNetherton syndrome (NS) is a rare, severe genetic disorder of cornification with high morbidity. Treatment for NS has been notoriously difficult. Recent studies showed an upregulated helper T cell (TH) 17/interleukin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21e29f3e79cda5984c5a1feb6ef77af5
https://www.zora.uzh.ch/id/eprint/199692/

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Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature

Autor: Mathilde Bonnet des Claustres, Alain Hovnanian, Florent Leturcq, Claire Barbieux, Olivier Gouin, Evgeniya Petrova

Publikováno v: Journal of Investigative Dermatology
Journal of Investigative Dermatology, Nature Publishing Group, 2020, 140, pp.1184-1194. ⟨10.1016/j.jid.2019.10.026⟩

Netherton syndrome is a rare autosomal recessive skin disease caused by loss-of-function mutations in SPINK5 encoding LEKTI protein that results in unopposed activity of epidermal kallikrein-related peptidases (KLKs), mainly KLK5, KLK7, and KLK14. Al

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da63b0550cd3895bde529ac36dbaf93c
https://hal.archives-ouvertes.fr/hal-03490223/document

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Transgenic kallikrein 14 mice display major hair defects associated with desmoglein 3 and 4 degradation and an inflammatory signature

Autor: Hovnanian Alain, Evgeniya Petrova, Mathilde Bonnet des Claustres, Florent Leturcq, Claire Barbieux, Olivier Gouin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8cf673f2a15ac380a8283a55d88fd3e9
https://doi.org/10.26226/morressier.5d4980cc8fb7e44098e72d3f

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Akademický článek

Citrullinated Histone H3, a Marker for Neutrophil Extracellular Traps, Is Associated with Poor Prognosis in Cutaneous Squamous Cell Carcinoma Developing in Patients with Recessive Dystrophic Epidermolysis Bullosa.

Autor: Ragot, Hélène¹ (AUTHOR) helene.ragot@inserm.fr, Gaucher, Sonia¹ (AUTHOR) sonia.gaucher@aphp.fr, Bonnet des Claustres, Mathilde¹ (AUTHOR) mathilde.bonnet-des-claustres@inserm.fr, Basset, Justine¹ (AUTHOR) justine.basset@inserm.fr, Boudan, Rose² (AUTHOR) emmanuelle.bourrat@aphp.fr, Battistella, Maxime³ (AUTHOR) maxime.battistella@aphp.fr, Bourrat, Emmanuelle² (AUTHOR), Hovnanian, Alain^1,4 (AUTHOR) alain.hovnanian@inserm.fr, Titeux, Matthias¹ (AUTHOR) alain.hovnanian@inserm.fr

Publikováno v: Cancers. Jul2024, Vol. 16 Issue 13, p2476. 17p.

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