Query author contributions in Reactome
Reactome depends on collaboration between our curation team and outside experts to
assemble and peer-review its pathway modules. The integration of ORCID within Reactome
enables us to meet a key challenge with authoring, curating and reviewing biological
information by incentivizing and crediting the external experts that contribute their
expertise and time to the Reactome curation process. More information is available at
ORCID and Reactome.
If you have an ORCID ID that is not listed on this page, please
forward this information to us and we will update your Reactome pathway records.
Details on Person Bahloul, Amel
| Class:Id | Person:9664040 |
|---|
| _displayName | Bahloul, Amel |
|---|
| _timestamp | 2019-10-21 10:48:36 |
|---|
| created | [InstanceEdit:9664104] May, Bruce, 2019-10-21 |
|---|
| firstname | Amel |
|---|
| initial | A |
|---|
| surname | Bahloul |
|---|
| (author) | [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:9664694] Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle
[LiteratureReference:9664708] CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival
[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 |
|---|
|
[Change default viewing format]
|
No pathways have been reviewed or authored by Bahloul, Amel (9664040)
