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Author/Creator Keck, Mathilde

1. A new Kunitz‐type snake toxin family associated with an original mode of interaction with the vasopressin 2 receptor. (28th February 2022)

Authors:
Droctové, Laura; Ciolek, Justyna; Mendre, Christiane; Chorfa, Amélia; Huerta, Paola; Carvalho, Chrystelle; Gouin, Charlotte; Lancien, Manon; Stanajic‐Petrovic, Goran; Braco, Lorine; Blanchet, Guillaume; Upert, Gregory; De Pauw, Gregory; Barbe, Peggy; Keck, Mathilde; Mourier, Gilles; Mouillac, Ber...
Other Names:
Lother Achim guestEditor.; Wenzel Ulrich guestEditor.; Jaisser Frédéric guestEditor.
Journal:
British journal of pharmacology
Issue:
Volume 179:Number 13(2022)
Page Start:
3470
Record Type:
Journal Article
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2. Analysis of CLCNKB mutations at dimer‐interface, calcium‐binding site, and pore reveals a variety of functional alterations in ClC‐Kb channel leading to Bartter syndrome. Issue 4 (24th December 2019)

Authors:
Bignon, Yohan; Sakhi, Imene; Bitam, Sara; Bakouh, Naziha; Keck, Mathilde; Frachon, Nadia; Paulais, Marc; Planelles, Gabrielle; Teulon, Jacques; Andrini, Olga
Journal:
Human mutation
Issue:
Volume 41:Issue 4(2020)
Page Start:
774
Record Type:
Journal Article
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3. Brain renin-angiotensin system blockade with orally active aminopeptidase A inhibitor prevents cardiac dysfunction after myocardial infarction in mice. (February 2019)

Authors:
Boitard, Solène Emmanuelle; Marc, Yannick; Keck, Mathilde; Mougenot, Nathalie; Agbulut, Onnik; Balavoine, Fabrice; Llorens-Cortes, Catherine
Journal:
Journal of molecular and cellular cardiology
Issue:
Volume 127(2019)
Page Start:
215
Record Type:
Journal Article
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5. Emergence of Orai3 activity during cardiac hypertrophy. (11th September 2014)

Authors:
Saliba, Youakim; Keck, Mathilde; Marchand, Alexandre; Atassi, Fabrice; Ouillé, Aude; Cazorla, Olivier; Trebak, Mohamed; Pavoine, Catherine; Lacampagne, Alain; Hulot, Jean-Sébastien; Farès, Nassim; Fauconnier, Jérémy; Lompré, Anne-Marie
Journal:
Cardiovascular research
Issue:
Volume 105:Number 3(2015)
Page Start:
248
Record Type:
Journal Article
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7. Novel CLCNKB Mutations Causing Bartter Syndrome Affect Channel Surface Expression. Issue 9 (12th June 2013)

Authors:
Keck, Mathilde; Andrini, Olga; Lahuna, Olivier; Burgos, Johanna; Cid, L. Pablo; Sepúlveda, Francisco V.; L'Hoste, Sébastien; Blanchard, Anne; Vargas‐Poussou, Rosa; Lourdel, Stéphane; Teulon, Jacques
Journal:
Human mutation
Issue:
Volume 34:Issue 9(2013:Sep.)
Page Start:
1269
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗