Query author contributions in Reactome

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Details on Person Jassal, B, 2013-05-21

Class:Id	InstanceEdit:3560797
_displayName	Jassal, B, 2013-05-21
_timestamp	2013-05-21 12:48:00
author	[Person:73447] Jassal, Bijay
dateTime	2013-05-21 16:47:35
(authored)	[Pathway:3560782] Diseases associated with glycosaminoglycan metabolism [Homo sapiens] [Pathway:3560783] Defective B4GALT7 causes EDS, progeroid type [Homo sapiens] [FailedReaction:3560785] Defective PAPSS2 does not transfer PO4(2-) group from ATP to APS to form PAPS [Homo sapiens] [FailedReaction:3560789] Defective SLC26A2 does not cotransport extracellular SO4(2-), H+ to cytosol [Homo sapiens] [Pathway:3560792] Defective SLC26A2 causes chondrodysplasias [Homo sapiens] [FailedReaction:3560794] Defective PAPSS2 does not transfer SO4(2-) group to ATP to form APS [Homo sapiens] [Pathway:3560796] Defective PAPSS2 causes SEMD-PA [Homo sapiens] [Pathway:3560801] Defective B3GAT3 causes JDSSDHD [Homo sapiens] [FailedReaction:3560802] Defective B3GAT3 does not transfer GlcA to tetrasaccharide linker [Homo sapiens] [FailedReaction:3560804] Defective B4GALT7 does not transfer Gal to xylosyl-unit of the tetrasaccharide linker [Homo sapiens] List all 16 refering instances
(created)	[Pathway:3560782] Diseases associated with glycosaminoglycan metabolism [Homo sapiens] [Pathway:3560783] Defective B4GALT7 causes EDS, progeroid type [Homo sapiens] [Summation:3560784] The SLC26A1 and 2 genes encode proteins that facilitate sulf... [FailedReaction:3560785] Defective PAPSS2 does not transfer PO4(2-) group from ATP to APS to form PAPS [Homo sapiens] [EntityWithAccessionedSequence:3560786] SLC26A2 V340del [plasma membrane] [Homo sapiens] [ReplacedResidue:3560787] L-arginine 279 replaced with L-tryptophan [ReplacedResidue:3560788] L-leucine 587 replaced with L-serine [FailedReaction:3560789] Defective SLC26A2 does not cotransport extracellular SO4(2-), H+ to cytosol [Homo sapiens] [EntityWithAccessionedSequence:3560790] SLC26A2 R279W [plasma membrane] [Homo sapiens] [ReplacedResidue:3560791] L-valine 340 replaced with unknown List all 23 refering instances
(edited)	[Pathway:3560782] Diseases associated with glycosaminoglycan metabolism [Homo sapiens] [Pathway:3560783] Defective B4GALT7 causes EDS, progeroid type [Homo sapiens] [FailedReaction:3560785] Defective PAPSS2 does not transfer PO4(2-) group from ATP to APS to form PAPS [Homo sapiens] [FailedReaction:3560789] Defective SLC26A2 does not cotransport extracellular SO4(2-), H+ to cytosol [Homo sapiens] [Pathway:3560792] Defective SLC26A2 causes chondrodysplasias [Homo sapiens] [FailedReaction:3560794] Defective PAPSS2 does not transfer SO4(2-) group to ATP to form APS [Homo sapiens] [Pathway:3560796] Defective PAPSS2 causes SEMD-PA [Homo sapiens] [Pathway:3560801] Defective B3GAT3 causes JDSSDHD [Homo sapiens] [FailedReaction:3560802] Defective B3GAT3 does not transfer GlcA to tetrasaccharide linker [Homo sapiens] [FailedReaction:3560804] Defective B4GALT7 does not transfer Gal to xylosyl-unit of the tetrasaccharide linker [Homo sapiens] List all 16 refering instances
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No pathways have been reviewed or authored by Jassal, B, 2013-05-21 (3560797)