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 Jassal, B, 2012-06-14
| Class:Id | InstanceEdit:2318591 |
| _displayName | Jassal, B, 2012-06-14 |
| _timestamp | 2012-06-14 11:34:12 |
| author | [Person:73447] Jassal, Bijay |
| dateTime | 2012-06-14 15:33:08 |
| (authored) | [FailedReaction:2318585] Defective HYAL1 does not hydrolyse Chondroitin chains [Homo sapiens] [FailedReaction:9036077] Defective HYAL1 does not hydrolyse (HA)50 [Homo sapiens] |
| (created) | [Person:2318583] Sims, K B [EntityWithAccessionedSequence:2318584] GUSB R216W [lysosomal lumen] [Homo sapiens] [FailedReaction:2318585] Defective HYAL1 does not hydrolyse Chondroitin chains [Homo sapiens] [Person:2318586] Triggs-Raine, B [Person:2318587] Dickersin, G R [Person:2318588] Short, M P [EntityWithAccessionedSequence:2318589] HYAL1 E268K [lysosomal lumen] [Homo sapiens] [EntityFunctionalStatus:2318590] loss_of_function of HYAL1 mutants [lysosomal lumen] [LiteratureReference:2318592] Clinical and biochemical manifestations of hyaluronidase deficiency [Person:2318593] Rosenberg, A E |
| (edited) | [FailedReaction:2318585] Defective HYAL1 does not hydrolyse Chondroitin chains [Homo sapiens] [FailedReaction:9036077] Defective HYAL1 does not hydrolyse (HA)50 [Homo sapiens] |
| (modified) | [Reaction:1793209] HYAL1-4 hydrolyze chondroitin chains [Homo sapiens] [Pathway:2206280] MPS IX - Natowicz syndrome (Hyaluronan metabolism) [Homo sapiens] [Pathway:2206281] Mucopolysaccharidoses [Homo sapiens] [Pathway:2206282] MPS IIIB - Sanfilippo syndrome B [Homo sapiens] [Pathway:2206285] MPS VI - Maroteaux-Lamy syndrome [Homo sapiens] [Summation:2206289] Mucopolysaccharidosis II (MPS II, Hunter syndrome, MIM:30990... [Pathway:2206290] MPS IV - Morquio syndrome A [Homo sapiens] [Pathway:2206291] MPS IIIC - Sanfilippo syndrome C [Homo sapiens] [Pathway:2206292] MPS VII - Sly syndrome (Hyaluronan metabolism) [Homo sapiens] [Summation:2206295] Absence of alpha-L-iduronidase (IDUA, MIM:252800), the enzym... |
|
[Change default viewing format]
|
No pathways have been reviewed or authored by Jassal, B, 2012-06-14 (2318591)