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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.

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Details on Person Jassal, Bijay, 2015-08-27

Class:IdInstanceEdit:6792750
_displayNameJassal, Bijay, 2015-08-27
_timestamp2015-08-27 08:27:17
author[Person:73447] Jassal, Bijay
dateTime2015-08-27 12:27:09
(modified)[PathwayDiagram:499927] Diagram of Transport of inorganic cations/anions and amino acids/oligopeptides
[PathwayDiagram:500171] Diagram of Transport of bile salts and organic acids, metal ions and amine compounds
[PathwayDiagram:532427] Diagram of Bile acid and bile salt metabolism, Defective ABCB11 causes PFIC2 and BRIC2, and Defective CYP27A1 causes CTX
[PathwayDiagram:541418] Diagram of Cellular hexose transport, Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1), Defective SLC2A9 causes hypouricemia renal 2 (RHUC2), Defective SLC2A10 causes arterial tortuosity syndrome (ATS), Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM), and Defective SLC5A2 causes renal glucosuria (GLYS1)
[PathwayDiagram:601857] Diagram of Transport of vitamins, nucleosides, and related molecules, Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS), Defective SLC29A3 causes histiocytosis-lymphadenopathy plus syndrome (HLAS), Defective SLC33A1 causes spastic paraplegia 42 (SPG42), Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M), Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS), Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C), and Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)
[PathwayDiagram:984845] Diagram of Ion channel transport
[Pathway:5619065] Defective SLC7A9 in vascular wall interactions causes cystinuria (CSNU) [Homo sapiens]
[Pathway:5619093] Defective SLC7A7 in vascular wall interactions causes lysinuric protein intolerance (LPI) [Homo sapiens]
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No pathways have been reviewed or authored by Jassal, Bijay, 2015-08-27 (6792750)
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