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Author/Creator Houdusse, Anne

1. 2nd PSL Chemical Biology Symposium (2019): At the Crossroads of Chemistry and Biology. (25th February 2019)

Authors:
Lucchino, Marco; Billet, Anne; Versini, Antoine; Bavireddi, Harikrishna; Dasari, Bhanu‐Das; Debieu, Sylvain; Colombeau, Ludovic; Cañeque, Tatiana; Wagner, Alain; Masson, Géraldine; Taran, Frédéric; Karoyan, Philippe; Delepierre, Muriel; Gaillet, Christine; Houdusse, Anne; Britton, Sébastien; Schm...
Journal:
Chembiochem
Issue:
Volume 20:Number 7(2019)
Page Start:
968
Record Type:
Journal Article
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2. An Overview and Online Registry of Microvillus Inclusion Disease Patients and their MYO5B Mutations. Issue 12 (16th October 2013)

Authors:
van der, K. Joeri; Dhekne, Herschel S.; Swertz, Morris A.; Sirigu, Serena; Ropars, Virginie; Vinke, Petra C.; Rengaw, Trebor; van den, Peter C.; Rings, Edmond H. H. M.; Houdusse, Anne; van, Sven C. D.
Journal:
Human mutation
Issue:
Volume 34:Issue 12(2013:Dec.)
Page Start:
1597
Record Type:
Journal Article
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3. Coupling fission and exit of RAB6 vesicles at Golgi hotspots through kinesin-myosin interactions. Issue 1 (December 2017)

Authors:
Miserey-Lenkei, Stéphanie; Bousquet, Hugo; Pylypenko, Olena; Bardin, Sabine; Dimitrov, Ariane; Bressanelli, Gaëlle; Bonifay, Raja; Fraisier, Vincent; Guillou, Catherine; Bougeret, Cécile; Houdusse, Anne; Echard, Arnaud; Goud, Bruno
Journal:
Nature communications
Issue:
Volume 8:Issue 1(2017)
Page Start:
1
Record Type:
Journal Article
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6. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Issue 3 (17th January 2018)

Authors:
Dhekne, Herschel S.; Pylypenko, Olena; Overeem, Arend W.; Ferreira, Rosaria J.; van der Velde, K. Joeri; Rings, Edmond H.H.M.; Posovszky, Carsten; Swertz, Morris A.; Houdusse, Anne; van IJzendoorn, Sven C.D.
Journal:
Human mutation
Issue:
Volume 39:Issue 3(2018)
Page Start:
333
Record Type:
Journal Article
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