Query author contributions in Reactome

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Details on Person Petit, Christine

Class:Id	Person:5653993
_displayName	Petit, Christine
_timestamp	2014-12-03 16:20:27
created	[InstanceEdit:5653996] Rothfels, Karen, 2014-12-03
firstname	Christine
initial	C
surname	Petit
(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:5654100] Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome [LiteratureReference:8931613] Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites [LiteratureReference:9663310] Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth [LiteratureReference:9664011] Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse [LiteratureReference:9664035] Otoferlin acts as a Ca²⁺ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses [LiteratureReference:9664114] Different Ca_V1.3 Channel Isoforms Control Distinct Components of the Synaptic Vesicle Cycle in Auditory Inner Hair Cells [LiteratureReference:9664150] Exocytotic machineries of vestibular type I and cochlear ribbon synapses display similar intrinsic otoferlin-dependent Ca2+ sensitivity but a different coupling to Ca2+ channels [LiteratureReference:9664158] Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane [LiteratureReference:9664694] Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle List all 17 refering instances
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No pathways have been reviewed or authored by Petit, Christine (5653993)