Query author contributions in Reactome

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Details on Person Hardelin, Jean-Pierre

Class:Id	Person:5653995
_displayName	Hardelin, Jean-Pierre
_timestamp	2014-12-03 16:20:27
created	[InstanceEdit:5653996] Rothfels, Karen, 2014-12-03
firstname	Jean-Pierre
initial	JP
surname	Hardelin
(author)	[LiteratureReference:5653990] Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner [LiteratureReference:5654002] Kallmann syndrome [LiteratureReference:5654100] Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome [LiteratureReference:9664035] Otoferlin acts as a Ca²⁺ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses [LiteratureReference:9664736] Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery [LiteratureReference:9664742] Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids [LiteratureReference:9671857] Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane
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No pathways have been reviewed or authored by Hardelin, Jean-Pierre (5653995)