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Bijay Jassal

 ORCID
https://orcid.org/0000-0002-5039-5405
Project
Reactome
Affiliation
Ontario Institute for Cancer Research
Authored Pathways (512)
Date Identifier Pathway Reference
2021-09-30 R-HSA-9754706 Atorvastatin ADME BibTex
2021-09-06 R-HSA-9753281 Paracetamol ADME BibTex
2021-07-27 R-HSA-9748787 Azathioprine ADME BibTex
2021-07-27 R-HSA-9748784 Drug ADME BibTex
2020-07-13 R-HSA-9694516 SARS-CoV-2 Infection BibTex
2020-03-23 R-HSA-9679191 Potential therapeutics for SARS BibTex
2020-02-05 R-HSA-9658195 Leishmania infection BibTex
2020-01-09 R-HSA-9673324 WNT5:FZD7-mediated leishmania damping BibTex
2020-01-07 R-HSA-9664424 Cell recruitment (pro-inflammatory response) BibTex
2020-01-07 R-HSA-9660826 Purinergic signaling in leishmaniasis infection BibTex
2020-01-07 R-HSA-9664420 Killing mechanisms BibTex
2020-01-07 R-HSA-9664407 Parasite infection BibTex
2020-01-07 R-HSA-9664417 Leishmania phagocytosis BibTex
2020-01-07 R-HSA-9664422 FCGR3A-mediated phagocytosis BibTex
2020-01-07 R-HSA-9664433 Leishmania parasite growth and survival BibTex
2020-01-07 R-HSA-9662851 Anti-inflammatory response favouring Leishmania parasite infection BibTex
2020-01-07 R-HSA-9660821 ADORA2B mediated anti-inflammatory cytokines production BibTex
2020-01-07 R-HSA-9664323 FCGR3A-mediated IL10 synthesis BibTex
2020-01-07 R-HSA-9662834 CD163 mediating an anti-inflammatory response BibTex
2020-01-07 R-HSA-9664535 LTC4-CYSLTR mediated IL4 production BibTex
2018-02-20 R-HSA-9037628 Rhesus blood group biosynthesis BibTex
2018-02-20 R-HSA-9037629 Lewis blood group biosynthesis BibTex
2017-12-28 R-HSA-9033807 ABO blood group biosynthesis BibTex
2017-12-27 R-HSA-9033658 Blood group systems biosynthesis BibTex
2017-11-03 R-HSA-9027604 Biosynthesis of electrophilic ?-3 PUFA oxo-derivatives BibTex
2017-10-30 R-HSA-9027307 Biosynthesis of maresin-like SPMs BibTex
2017-10-23 R-HSA-9026766 Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) BibTex
2017-10-23 R-HSA-9026762 Biosynthesis of maresin conjugates in tissue regeneration (MCTR) BibTex
2017-10-19 R-HSA-9026395 Biosynthesis of DHA-derived sulfido conjugates BibTex
2017-10-19 R-HSA-9026403 Biosynthesis of DPAn-3-derived 13-series resolvins BibTex
2017-10-19 R-HSA-9026290 Biosynthesis of DPAn-3-derived maresins BibTex
2017-10-19 R-HSA-9026286 Biosynthesis of DPAn-3-derived protectins and resolvins BibTex
2017-10-12 R-HSA-9025094 Biosynthesis of DPAn-3 SPMs BibTex
2017-10-12 R-HSA-9025106 Biosynthesis of DPAn-6 SPMs BibTex
2017-09-28 R-HSA-9023661 Biosynthesis of E-series 18(R)-resolvins BibTex
2017-09-05 R-HSA-9020265 Biosynthesis of aspirin-triggered D-series resolvins BibTex
2017-09-05 R-HSA-9018896 Biosynthesis of E-series 18(S)-resolvins BibTex
2017-09-04 R-HSA-9018678 Biosynthesis of specialized proresolving mediators (SPMs) BibTex
2017-09-04 R-HSA-9018679 Biosynthesis of EPA-derived SPMs BibTex
2017-09-04 R-HSA-9018677 Biosynthesis of DHA-derived SPMs BibTex
2017-09-04 R-HSA-9018676 Biosynthesis of D-series resolvins BibTex
2017-09-04 R-HSA-9018682 Biosynthesis of maresins BibTex
2017-09-04 R-HSA-9018681 Biosynthesis of protectins BibTex
2017-09-04 R-HSA-9018683 Biosynthesis of DPA-derived SPMs BibTex
2017-02-10 R-HSA-8964540 Alanine metabolism BibTex
2017-02-10 R-HSA-8964539 Glutamate and glutamine metabolism BibTex
2017-02-10 R-HSA-8963693 Aspartate and asparagine metabolism BibTex
2017-02-10 R-HSA-8963691 Phenylalanine and tyrosine metabolism BibTex
2017-02-10 R-HSA-8963684 Tyrosine catabolism BibTex
2016-10-11 R-HSA-8942233 Intestinal infectious diseases BibTex
2016-08-30 R-HSA-8937144 Aryl hydrocarbon receptor signalling BibTex
2016-08-15 R-HSA-8963743 Digestion and absorption BibTex
2016-08-15 R-HSA-8935690 Digestion BibTex
2016-06-27 R-HSA-8877627 Vitamin E BibTex
2016-04-01 R-HSA-8866427 VLDLR internalisation and degradation BibTex
2016-04-01 R-HSA-8866423 VLDL assembly BibTex
2016-03-31 R-HSA-8866376 Reelin signalling pathway BibTex
2016-02-11 R-HSA-8964572 Lipid particle organization BibTex
2016-02-10 R-HSA-8964038 LDL clearance BibTex
2016-02-10 R-HSA-8963889 Assembly of active LPL and LIPC lipase complexes BibTex
2016-01-27 R-HSA-8964046 VLDL clearance BibTex
2016-01-27 R-HSA-8964043 Plasma lipoprotein clearance BibTex
2016-01-22 R-HSA-8853383 Lysosomal oligosaccharide catabolism BibTex
2016-01-18 R-HSA-8852405 Signaling by MST1 BibTex
2015-12-14 R-HSA-8849175 Threonine catabolism BibTex
2015-09-22 R-HSA-6799198 Complex I biogenesis BibTex
2015-09-17 R-HSA-6798163 Choline catabolism BibTex
2015-07-15 R-HSA-6787639 GDP-fucose biosynthesis BibTex
2015-06-18 R-HSA-6783984 Glycine degradation BibTex
2015-04-28 R-HSA-5690338 Defective ABCC6 causes PXE BibTex
2015-04-20 R-HSA-5688890 Defective CSF2RA causes SMDP4 BibTex
2015-04-20 R-HSA-5688849 Defective CSF2RB causes SMDP5 BibTex
2015-04-16 R-HSA-5688399 Defective ABCA3 causes SMDP3 BibTex
2015-04-16 R-HSA-5688354 Defective pro-SFTPC causes SMDP2 and RDS BibTex
2015-04-13 R-HSA-5688031 Defective pro-SFTPB causes SMDP1 and RDS BibTex
2015-04-10 R-HSA-5687868 Defective SFTPA2 causes IPF BibTex
2015-04-08 R-HSA-5687613 Diseases associated with surfactant metabolism BibTex
2015-04-08 R-HSA-5687583 Defective SLC34A2 causes PALM BibTex
2015-03-18 R-HSA-5684045 Defective ABCD1 causes ALD BibTex
2015-03-17 R-HSA-5683826 Surfactant metabolism BibTex
2015-03-16 R-HSA-5683678 Defective ABCA3 causes SMDP3 BibTex
2015-03-13 R-HSA-5683371 Defective ABCB6 causes MCOPCB7 BibTex
2015-03-13 R-HSA-5683329 Defective ABCD4 causes MAHCJ BibTex
2015-03-12 R-HSA-5683177 Defective ABCC8 can cause hypo- and hyper-glycemias BibTex
2015-03-06 R-HSA-5682294 Defective ABCA12 causes ARCI4B BibTex
2015-03-05 R-HSA-5682113 Defective ABCA1 causes TGD BibTex
2015-03-02 R-HSA-5679096 Defective ABCG5 causes sitosterolemia BibTex
2015-03-02 R-HSA-5679090 Defective ABCG8 causes GBD4 and sitosterolemia BibTex
2015-02-27 R-HSA-5679001 Defective ABCC2 causes DJS BibTex
2015-02-26 R-HSA-5678895 Defective CFTR causes cystic fibrosis BibTex
2015-02-26 R-HSA-5678771 Defective ABCB4 causes PFIC3, ICP3 and GBD1 BibTex
2015-02-24 R-HSA-5678520 Defective ABCB11 causes PFIC2 and BRIC2 BibTex
2015-02-24 R-HSA-5678420 Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome BibTex
2015-01-30 R-HSA-5669034 TNFs bind their physiological receptors BibTex
2014-10-31 R-HSA-5633231 Defective ALG14 causes ALG14-CMS BibTex
2014-08-22 R-HSA-5619115 Disorders of transmembrane transporters BibTex
2014-08-22 R-HSA-5619102 SLC transporter disorders BibTex
2014-08-22 R-HSA-5619114 Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A) BibTex
2014-08-22 R-HSA-5619113 Defective SLC3A1 causes cystinuria (CSNU) BibTex
2014-08-22 R-HSA-5656364 Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM) BibTex
2014-08-22 R-HSA-5663020 Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) BibTex
2014-08-22 R-HSA-5619107 Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) BibTex
2014-08-22 R-HSA-5619104 Defective SLC12A1 causes Bartter syndrome 1 (BS1) BibTex
2014-08-22 R-HSA-5619110 Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) BibTex
2014-08-22 R-HSA-5619111 Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) BibTex
2014-08-22 R-HSA-5619108 Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS) BibTex
2014-08-22 R-HSA-5619109 Defective SLC6A2 causes orthostatic intolerance (OI) BibTex
2014-08-22 R-HSA-5660862 Defective SLC7A7 causes lysinuric protein intolerance (LPI) BibTex
2014-08-22 R-HSA-5660724 Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) BibTex
2014-08-22 R-HSA-5619083 Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) BibTex
2014-08-22 R-HSA-5619081 Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) BibTex
2014-08-22 R-HSA-5619087 Defective SLC12A3 causes Gitelman syndrome (GS) BibTex
2014-08-22 R-HSA-5660686 Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) BibTex
2014-08-22 R-HSA-5619085 Defective SLC26A3 causes congenital secretory chloride diarrhea 1 (DIAR1) BibTex
2014-08-22 R-HSA-5619072 Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M) BibTex
2014-08-22 R-HSA-5619073 Defective GCK causes maturity-onset diabetes of the young 2 (MODY2) BibTex
2014-08-22 R-HSA-5619078 Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C) BibTex
2014-08-22 R-HSA-5619079 Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria BibTex
2014-08-22 R-HSA-5619076 Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25) BibTex
2014-08-22 R-HSA-5619077 Defective SLC24A1 causes congenital stationary night blindness 1D (CSNB1D) BibTex
2014-08-22 R-HSA-5619098 Defective SLC2A2 causes Fanconi-Bickel syndrome (FBS) BibTex
2014-08-22 R-HSA-5619099 Defective AVP does not bind AVPR1A,B and causes neurohypophyseal diabetes insipidus (NDI) BibTex
2014-08-22 R-HSA-5619096 Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1) BibTex
2014-08-22 R-HSA-5619097 Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) BibTex
2014-08-22 R-HSA-5619101 Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) BibTex
2014-08-22 R-HSA-5619088 Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ) BibTex
2014-08-22 R-HSA-5619089 Defective SLC6A5 causes hyperekplexia 3 (HKPX3) BibTex
2014-08-22 R-HSA-5619094 Variant SLC6A14 may confer susceptibility towards obesity BibTex
2014-08-22 R-HSA-5619095 Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2) BibTex
2014-08-22 R-HSA-5619092 Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH) BibTex
2014-08-22 R-HSA-5619050 Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) BibTex
2014-08-22 R-HSA-5619048 Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1) BibTex
2014-08-22 R-HSA-5619049 Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages) BibTex
2014-08-22 R-HSA-5619054 Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) BibTex
2014-08-22 R-HSA-5619055 Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI) BibTex
2014-08-22 R-HSA-5619052 Defective SLC9A9 causes autism 16 (AUTS16) BibTex
2014-08-22 R-HSA-5619053 Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP) BibTex
2014-08-22 R-HSA-5619042 Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN) BibTex
2014-08-22 R-HSA-5658208 Defective SLC5A2 causes renal glucosuria (GLYS1) BibTex
2014-08-22 R-HSA-5619043 Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1) BibTex
2014-08-22 R-HSA-5619040 Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1) BibTex
2014-08-22 R-HSA-9036092 Defective AVP does not bind AVPR2 and causes neurohypophyseal diabetes insipidus (NDI) BibTex
2014-08-22 R-HSA-5619041 Defective SLC36A2 causes iminoglycinuria (IG) and hyperglycinuria (HG) BibTex
2014-08-22 R-HSA-5619046 Defective SLC26A4 causes Pendred syndrome (PDS) BibTex
2014-08-22 R-HSA-5619047 Defective SLC2A9 causes hypouricemia renal 2 (RHUC2) BibTex
2014-08-22 R-HSA-5619044 Defective SLC6A19 causes Hartnup disorder (HND) BibTex
2014-08-22 R-HSA-5658471 Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A) BibTex
2014-08-22 R-HSA-5619045 Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM) BibTex
2014-08-22 R-HSA-5619066 Defective SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1) BibTex
2014-08-22 R-HSA-5619067 Defective SLC1A1 is implicated in schizophrenia 18 (SCZD18) and dicarboxylic aminoaciduria (DCBXA) BibTex
2014-08-22 R-HSA-5619084 ABC transporter disorders BibTex
2014-08-22 R-HSA-5659735 Defective SLC6A19 causes Hartnup disorder (HND) BibTex
2014-08-22 R-HSA-5660883 Defective SLC7A9 causes cystinuria (CSNU) BibTex
2014-08-22 R-HSA-5659729 Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria BibTex
2014-08-22 R-HSA-5619037 Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) BibTex
2014-08-22 R-HSA-5619036 Defective SLC24A5 causes oculocutaneous albinism 6 (OCA6) BibTex
2014-08-22 R-HSA-5619039 Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) BibTex
2014-08-22 R-HSA-5619035 Defective SLC17A5 causes Salla disease (SD) and ISSD BibTex
2014-08-22 R-HSA-5619061 Defective SLC33A1 causes spastic paraplegia 42 (SPG42) BibTex
2014-08-22 R-HSA-5619060 Defective CP causes aceruloplasminemia (ACERULOP) BibTex
2014-08-22 R-HSA-5655799 Defective SLC40A1 causes hemochromatosis 4 (HFE4) (duodenum) BibTex
2014-08-22 R-HSA-5619063 Defective SLC29A3 causes histiocytosis-lymphadenopathy plus syndrome (HLAS) BibTex
2014-08-22 R-HSA-5619062 Defective SLC1A3 causes episodic ataxia 6 (EA6) BibTex
2014-08-22 R-HSA-5619056 Defective HK1 causes hexokinase deficiency (HK deficiency) BibTex
2014-08-22 R-HSA-5619058 Defective SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR) BibTex
2014-08-22 R-HSA-5619068 Defective SLC2A10 causes arterial tortuosity syndrome (ATS) BibTex
2014-08-22 R-HSA-5619071 Defective SLC22A12 causes renal hypouricemia 1 (RHUC1) BibTex
2014-08-22 R-HSA-5619070 Defective SLC16A1 causes symptomatic deficiency in lactate transport (SDLT) BibTex
2014-07-18 R-HSA-5609975 Diseases associated with glycosylation precursor biosynthesis BibTex
2014-07-18 R-HSA-5609978 Defective GALT can cause GALCT BibTex
2014-07-18 R-HSA-5609976 Defective GALK1 causes GALCT2 BibTex
2014-07-18 R-HSA-5609977 Defective GALE causes EDG BibTex
2014-07-18 R-HSA-5609974 Defective PGM1 causes PGM1-CDG BibTex
2014-06-06 R-HSA-5579031 Defective ACTH causes obesity and POMCD BibTex
2014-06-06 R-HSA-5579029 Metabolic disorders of biological oxidation enzymes BibTex
2014-06-06 R-HSA-5579002 Defective UGT1A1 causes hyperbilirubinemia BibTex
2014-06-06 R-HSA-5579000 Defective CYP1B1 causes Glaucoma BibTex
2014-06-06 R-HSA-5579006 Defective GSS causes GSS deficiency BibTex
2014-06-06 R-HSA-5579007 Defective ACY1 causes encephalopathy BibTex
2014-06-06 R-HSA-5579004 Defective CYP26C1 causes FFDD4 BibTex
2014-06-06 R-HSA-5579005 Defective CYP4F22 causes ARCI5 BibTex
2014-06-06 R-HSA-5578995 Defective TPMT causes TPMT deficiency BibTex
2014-06-06 R-HSA-5578998 Defective OPLAH causes OPLAHD BibTex
2014-06-06 R-HSA-5578999 Defective GCLC causes HAGGSD BibTex
2014-06-06 R-HSA-5578996 Defective CYP27A1 causes CTX BibTex
2014-06-06 R-HSA-5578997 Defective AHCY causes HMAHCHD BibTex
2014-06-06 R-HSA-5579019 Defective FMO3 causes TMAU BibTex
2014-06-06 R-HSA-5579016 Defective UGT1A4 causes hyperbilirubinemia BibTex
2014-06-06 R-HSA-5579017 Defective CYP11B1 causes AH4 BibTex
2014-06-06 R-HSA-5579022 Defective GGT1 causes GLUTH BibTex
2014-06-06 R-HSA-5579020 Defective SLC35D1 causes SCHBCKD BibTex
2014-06-06 R-HSA-5579028 Defective CYP17A1 causes AH5 BibTex
2014-06-06 R-HSA-5579030 Defective CYP19A1 causes AEXS BibTex
2014-06-06 R-HSA-5579024 Defective MAT1A causes MATD BibTex
2014-06-06 R-HSA-5579027 Defective CYP27B1 causes VDDR1B BibTex
2014-06-06 R-HSA-5579026 Defective CYP11A1 causes AICSR BibTex
2014-06-06 R-HSA-9035968 Defective GGT1 in aflatoxin detoxification causes GLUTH BibTex
2014-06-06 R-HSA-5579032 Defective TBXAS1 causes GHDD BibTex
2014-06-06 R-HSA-5579013 Defective CYP7B1 causes SPG5A and CBAS3 BibTex
2014-06-06 R-HSA-5579012 Defective MAOA causes BRUNS BibTex
2014-06-06 R-HSA-5579015 Defective CYP26B1 causes RHFCA BibTex
2014-06-06 R-HSA-5579014 Defective CYP27B1 causes VDDR1A BibTex
2014-06-06 R-HSA-5579009 Defective CYP11B2 causes CMO-1 deficiency BibTex
2014-06-06 R-HSA-5579011 Defective CYP2U1 causes SPG56 BibTex
2014-06-06 R-HSA-5579010 Defective CYP24A1 causes HCAI BibTex
2014-06-06 R-HSA-5579021 Defective CYP21A2 causes AH3 BibTex
2014-06-02 R-HSA-5578768 Physiological factors BibTex
2014-06-02 R-HSA-5578775 Ion homeostasis BibTex
2014-05-27 R-HSA-5576891 Cardiac conduction BibTex
2014-05-27 R-HSA-5576892 Phase 0 - rapid depolarisation BibTex
2014-05-27 R-HSA-5576894 Phase 1 - inactivation of fast Na+ channels BibTex
2014-05-27 R-HSA-5576893 Phase 2 - plateau phase BibTex
2014-05-27 R-HSA-5576890 Phase 3 - rapid repolarisation BibTex
2014-05-27 R-HSA-5576886 Phase 4 - resting membrane potential BibTex
2014-05-09 R-HSA-5423646 Aflatoxin activation and detoxification BibTex
2014-04-16 R-HSA-5362517 Signaling by Retinoic Acid BibTex
2014-04-16 R-HSA-5365859 RA biosynthesis pathway BibTex
2014-01-06 R-HSA-5223345 Miscellaneous transport and binding events BibTex
2013-11-25 R-HSA-5173105 O-linked glycosylation BibTex
2013-11-25 R-HSA-5173214 O-glycosylation of TSR domain-containing proteins BibTex
2013-11-07 R-HSA-5083635 Defective B3GALTL causes PpS BibTex
2013-11-07 R-HSA-5083632 Defective C1GALT1C1 causes TNPS BibTex
2013-11-07 R-HSA-5083633 Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1 BibTex
2013-11-07 R-HSA-5083636 Defective GALNT12 causes CRCS1 BibTex
2013-11-07 R-HSA-5083627 Defective LARGE causes MDDGA6 and MDDGB6 BibTex
2013-11-07 R-HSA-5083625 Defective GALNT3 causes HFTC BibTex
2013-11-07 R-HSA-5083630 Defective LFNG causes SCDO3 BibTex
2013-11-07 R-HSA-5083628 Defective POMGNT1 causes MDDGA3, MDDGB3 and MDDGC3 BibTex
2013-11-07 R-HSA-5083629 Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2 BibTex
2013-10-29 R-HSA-4793952 Defective MGAT2 causes CDG-2a BibTex
2013-10-25 R-HSA-4755583 Defective DOLK causes DOLK-CDG BibTex
2013-10-25 R-HSA-4755579 Defective SRD5A3 causes SRD5A3-CDG, KHRZ BibTex
2013-10-25 R-HSA-4755609 Defective DHDDS causes RP59 BibTex
2013-10-23 R-HSA-4724325 Defective ALG8 causes CDG-1h BibTex
2013-10-23 R-HSA-4724289 Defective ALG6 causes CDG-1c BibTex
2013-10-21 R-HSA-4720475 Defective ALG3 causes CDG-1d BibTex
2013-10-21 R-HSA-4720489 Defective ALG12 causes CDG-1g BibTex
2013-10-21 R-HSA-4720454 Defective ALG9 causes CDG-1l BibTex
2013-10-18 R-HSA-4719377 Defective DPM2 causes DPM2-CDG BibTex
2013-10-18 R-HSA-4719360 Defective DPM3 causes DPM3-CDG BibTex
2013-10-17 R-HSA-4717374 Defective DPM1 causes DPM1-CDG BibTex
2013-10-15 R-HSA-4687000 Defective MPDU1 causes CDG-1f BibTex
2013-09-23 R-HSA-4570571 Defective RFT1 causes CDG-1n BibTex
2013-09-13 R-HSA-4551295 Defective ALG11 causes CDG-1p BibTex
2013-09-12 R-HSA-4549356 Defective DPAGT1 causes CDG-1j, CMSTA2 BibTex
2013-09-12 R-HSA-4549380 Defective ALG1 causes CDG-1k BibTex
2013-09-12 R-HSA-4549349 Defective ALG2 causes CDG-1i BibTex
2013-09-03 R-HSA-4420332 Defective B3GALT6 causes EDSP2 and SEMDJL1 BibTex
2013-08-21 R-HSA-4341670 Defective NEU1 causes sialidosis BibTex
2013-08-01 R-HSA-4085011 Defective GNE causes sialuria, NK and IBM2 BibTex
2013-08-01 R-HSA-4085023 Defective GFPT1 causes CMSTA1 BibTex
2013-08-01 R-HSA-4085001 Sialic acid metabolism BibTex
2013-07-29 R-HSA-4793950 Defective MAN1B1 causes MRT15 BibTex
2013-07-29 R-HSA-4793954 Defective MOGS causes CDG-2b BibTex
2013-07-29 R-HSA-4793953 Defective B4GALT1 causes CDG-2d BibTex
2013-07-29 R-HSA-4043911 Defective PMM2 causes PMM2-CDG BibTex
2013-07-29 R-HSA-4043916 Defective MPI causes MPI-CDG BibTex
2013-07-17 R-HSA-3906995 Diseases associated with O-glycosylation of proteins BibTex
2013-06-28 R-HSA-3781865 Diseases of glycosylation BibTex
2013-06-28 R-HSA-3781860 Diseases associated with N-glycosylation of proteins BibTex
2013-05-31 R-HSA-3656234 Defective HEXA causes GM2G1 BibTex
2013-05-31 R-HSA-3656237 Defective EXT2 causes exostoses 2 BibTex
2013-05-31 R-HSA-3656225 Defective CHST6 causes MCDC1 BibTex
2013-05-31 R-HSA-3656248 Defective HEXB causes GM2G2 BibTex
2013-05-31 R-HSA-3656253 Defective EXT1 causes exostoses 1, TRPS2 and CHDS BibTex
2013-05-31 R-HSA-3656243 Defective ST3GAL3 causes MCT12 and EIEE15 BibTex
2013-05-31 R-HSA-3656244 Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) BibTex
2013-05-21 R-HSA-3560782 Diseases associated with glycosaminoglycan metabolism BibTex
2013-05-21 R-HSA-3595177 Defective CHSY1 causes TPBS BibTex
2013-05-21 R-HSA-3560783 Defective B4GALT7 causes EDS, progeroid type BibTex
2013-05-21 R-HSA-3560801 Defective B3GAT3 causes JDSSDHD BibTex
2013-05-21 R-HSA-3595172 Defective CHST3 causes SEDCJD BibTex
2013-05-21 R-HSA-3595174 Defective CHST14 causes EDS, musculocontractural type BibTex
2013-05-21 R-HSA-3560792 Defective SLC26A2 causes chondrodysplasias BibTex
2013-05-21 R-HSA-3560796 Defective PAPSS2 causes SEMD-PA BibTex
2013-05-13 R-HSA-9759785 Diseases of propionyl-CoA catabolism BibTex
2013-05-13 R-HSA-3359478 Defective MUT causes MMAM BibTex
2013-05-13 R-HSA-3359485 Defective CD320 causes MMATC BibTex
2013-05-13 R-HSA-3359469 Defective MTR causes HMAG BibTex
2013-05-13 R-HSA-3359454 Defective TCN2 causes TCN2 deficiency BibTex
2013-05-13 R-HSA-3359471 Defective MMAB causes MMA, cblB type BibTex
2013-05-13 R-HSA-3359467 Defective MTRR causes HMAE BibTex
2013-05-13 R-HSA-3359462 Defective AMN causes MGA1 BibTex
2013-05-13 R-HSA-3359463 Defective CUBN causes MGA1 BibTex
2013-05-13 R-HSA-3359473 Defective MMADHC causes MMAHCD BibTex
2013-05-13 R-HSA-3359457 Defective CBLIF causes IFD BibTex
2013-05-13 R-HSA-3359474 Defective MMACHC causes MAHCC BibTex
2013-05-13 R-HSA-3359475 Defective MMAA causes MMA, cblA type BibTex
2013-05-13 R-HSA-3371598 Defective BTD causes biotidinase deficiency BibTex
2013-05-13 R-HSA-3371599 Defective HLCS causes multiple carboxylase deficiency BibTex
2013-05-09 R-HSA-3323169 Defects in biotin (Btn) metabolism BibTex
2013-04-18 R-HSA-3296482 Defects in vitamin and cofactor metabolism BibTex
2013-04-18 R-HSA-3296469 Defects in cobalamin (B12) metabolism BibTex
2013-04-17 R-HSA-3295583 TRP channels BibTex
2012-11-27 R-HSA-2672351 Stimuli-sensing channels BibTex
2012-10-11 R-HSA-2514859 Inactivation, recovery and regulation of the phototransduction cascade BibTex
2012-10-11 R-HSA-2514856 The phototransduction cascade BibTex
2012-10-01 R-HSA-2485179 Activation of the phototransduction cascade BibTex
2012-09-25 R-HSA-2474795 Diseases associated with visual transduction BibTex
2012-09-12 R-HSA-2466712 Biosynthesis of A2E, implicated in retinal degradation BibTex
2012-08-17 R-HSA-2453864 Retinoid cycle disease events BibTex
2012-08-17 R-HSA-6809583 Retinoid metabolism disease events BibTex
2012-08-17 R-HSA-2453902 The canonical retinoid cycle in rods (twilight vision) BibTex
2012-04-26 R-HSA-2206281 Mucopolysaccharidoses BibTex
2012-04-26 R-HSA-2206302 MPS I - Hurler syndrome BibTex
2012-04-26 R-HSA-2206305 MPS IIID - Sanfilippo syndrome D BibTex
2012-04-26 R-HSA-2206307 MPS IIIA - Sanfilippo syndrome A BibTex
2012-04-26 R-HSA-2206291 MPS IIIC - Sanfilippo syndrome C BibTex
2012-04-26 R-HSA-2206290 MPS IV - Morquio syndrome A BibTex
2012-04-26 R-HSA-2206308 MPS IV - Morquio syndrome B BibTex
2012-04-26 R-HSA-2206292 MPS VII - Sly syndrome BibTex
2012-04-26 R-HSA-2206296 MPS II - Hunter syndrome BibTex
2012-04-26 R-HSA-2206280 MPS IX - Natowicz syndrome BibTex
2012-04-26 R-HSA-2206282 MPS IIIB - Sanfilippo syndrome B BibTex
2012-04-26 R-HSA-2206285 MPS VI - Maroteaux-Lamy syndrome BibTex
2012-04-09 R-HSA-2187338 Visual phototransduction BibTex
2012-04-09 R-HSA-2187335 The retinoid cycle in cones (daylight vision) BibTex
2012-04-04 R-HSA-881907 Gastrin-CREB signalling pathway via PKC and MAPK BibTex
2012-04-04 R-HSA-2179392 EGFR Transactivation by Gastrin BibTex
2012-03-05 R-HSA-2160916 Hyaluronan uptake and degradation BibTex
2012-02-24 R-HSA-2142845 Hyaluronan metabolism BibTex
2012-02-24 R-HSA-2142850 Hyaluronan biosynthesis and export BibTex
2011-12-14 R-HSA-2024101 CS/DS degradation BibTex
2011-12-14 R-HSA-2024096 HS-GAG degradation BibTex
2011-12-01 R-HSA-2022870 Chondroitin sulfate biosynthesis BibTex
2011-12-01 R-HSA-2022923 Dermatan sulfate biosynthesis BibTex
2011-12-01 R-HSA-2022928 HS-GAG biosynthesis BibTex
2011-12-01 R-HSA-2022857 Keratan sulfate degradation BibTex
2011-12-01 R-HSA-2022854 Keratan sulfate biosynthesis BibTex
2011-11-04 R-HSA-1971475 A tetrasaccharide linker sequence is required for GAG synthesis BibTex
2011-10-21 R-HSA-1793185 Chondroitin sulfate/dermatan sulfate metabolism BibTex
2011-10-14 R-HSA-1663150 The activation of arylsulfatases BibTex
2011-10-14 R-HSA-1660662 Glycosphingolipid metabolism BibTex
2011-10-07 R-HSA-1638091 Heparan sulfate/heparin (HS-GAG) metabolism BibTex
2011-10-05 R-HSA-1630316 Glycosaminoglycan metabolism BibTex
2011-10-05 R-HSA-1638074 Keratan sulfate/keratin metabolism BibTex
2011-08-17 R-HSA-1474151 Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation BibTex
2011-07-04 R-HSA-1369007 Mitochondrial ABC transporters BibTex
2011-07-04 R-HSA-1369062 ABC transporters in lipid homeostasis BibTex
2010-11-02 R-HSA-983712 Ion channel transport BibTex
2010-10-15 R-HSA-977068 Termination of O-glycan biosynthesis BibTex
2010-10-01 R-HSA-975634 Retinoid metabolism and transport BibTex
2010-08-24 R-HSA-936837 Ion transport by P-type ATPases BibTex
2010-07-19 R-HSA-913709 O-linked glycosylation of mucins BibTex
2010-06-18 R-HSA-879518 Transport of organic anions BibTex
2010-05-26 R-HSA-804914 Transport of fatty acids BibTex
2010-05-12 R-HSA-727802 Transport of nucleotide sugars BibTex
2010-03-25 R-HSA-561048 Organic anion transport BibTex
2010-03-17 R-HSA-549132 Organic cation/anion/zwitterion transport BibTex
2010-03-17 R-HSA-549127 Organic cation transport BibTex
2010-02-05 R-HSA-500792 GPCR ligand binding BibTex
2009-10-23 R-HSA-444411 Rhesus glycoproteins mediate ammonium transport. BibTex
2009-09-29 R-HSA-442660 Na+/Cl- dependent neurotransmitter transporters BibTex
2009-09-25 R-HSA-442380 Zinc influx into cells by the SLC39 gene family BibTex
2009-09-09 R-HSA-435354 Zinc transporters BibTex
2009-09-09 R-HSA-435368 Zinc efflux and compartmentalization by the SLC30 family BibTex
2009-08-25 R-HSA-433692 Proton-coupled monocarboxylate transport BibTex
2009-08-21 R-HSA-433137 Sodium-coupled sulphate, di- and tri-carboxylate transporters BibTex
2009-07-17 R-HSA-429593 Inositol transporters BibTex
2009-07-06 R-HSA-428559 Proton-coupled neutral amino acid transporters BibTex
2009-07-06 R-HSA-428643 Organic anion transporters BibTex
2009-06-30 R-HSA-427975 Proton/oligopeptide cotransporters BibTex
2009-06-23 R-HSA-427601 Multifunctional anion exchangers BibTex
2009-06-23 R-HSA-427652 Sodium-coupled phosphate cotransporters BibTex
2009-06-23 R-HSA-427589 Type II Na+/Pi cotransporters BibTex
2009-06-12 R-HSA-426117 Cation-coupled Chloride cotransporters BibTex
2009-06-11 R-HSA-425986 Sodium/Proton exchangers BibTex
2009-06-05 R-HSA-425561 Sodium/Calcium exchangers BibTex
2009-06-04 R-HSA-425407 SLC-mediated transmembrane transport BibTex
2009-06-04 R-HSA-425397 Transport of vitamins, nucleosides, and related molecules BibTex
2009-06-04 R-HSA-425366 Transport of bile salts and organic acids, metal ions and amine compounds BibTex
2009-06-04 R-HSA-425410 Metal ion SLC transporters BibTex
2009-06-04 R-HSA-425393 Transport of inorganic cations/anions and amino acids/oligopeptides BibTex
2009-06-04 R-HSA-425381 Bicarbonate transporters BibTex
2009-05-12 R-HSA-420499 Class C/3 (Metabotropic glutamate/pheromone receptors) BibTex
2009-05-11 R-HSA-420092 Glucagon-type ligand receptors BibTex
2009-05-07 R-HSA-419812 Calcitonin-like ligand receptors BibTex
2009-05-07 R-HSA-419771 Opsins BibTex
2009-04-30 R-HSA-419408 Lysosphingolipid and LPA receptors BibTex
2009-04-14 R-HSA-418038 Nucleotide-like (purinergic) receptors BibTex
2009-04-14 R-HSA-417957 P2Y receptors BibTex
2009-04-14 R-HSA-417973 Adenosine P1 receptors BibTex
2009-04-02 R-HSA-391908 Prostanoid ligand receptors BibTex
2009-03-26 R-HSA-391906 Leukotriene receptors BibTex
2009-02-27 R-HSA-392170 ADP signalling through P2Y purinoceptor 12 BibTex
2009-02-25 R-HSA-391903 Eicosanoid ligand-binding receptors BibTex
2009-02-23 R-HSA-375281 Hormone ligand-binding receptors BibTex
2009-02-12 R-HSA-390666 Serotonin receptors BibTex
2009-02-11 R-HSA-390650 Histamine receptors BibTex
2009-02-10 R-HSA-390651 Dopamine receptors BibTex
2009-02-10 R-HSA-390696 Adrenoceptors BibTex
2009-02-10 R-HSA-390648 Muscarinic acetylcholine receptors BibTex
2009-01-07 R-HSA-389397 Orexin and neuropeptides FF and QRFP bind to their respective receptors BibTex
2008-12-12 R-HSA-388479 Vasopressin-like receptors BibTex
2008-11-24 R-HSA-380095 Tachykinin receptors bind tachykinins BibTex
2008-11-24 R-HSA-186797 Signaling by PDGF BibTex
2008-11-24 R-HSA-186763 Downstream signal transduction BibTex
2008-11-07 R-HSA-380108 Chemokine receptors bind chemokines BibTex
2008-10-01 R-HSA-209952 Peptide hormone biosynthesis BibTex
2008-10-01 R-HSA-209822 Glycoprotein hormones BibTex
2008-10-01 R-HSA-196108 Pregnenolone biosynthesis BibTex
2008-10-01 R-HSA-193993 Mineralocorticoid biosynthesis BibTex
2008-10-01 R-HSA-193144 Estrogen biosynthesis BibTex
2008-10-01 R-HSA-193048 Androgen biosynthesis BibTex
2008-10-01 R-HSA-194002 Glucocorticoid biosynthesis BibTex
2008-10-01 R-HSA-209776 Metabolism of amine-derived hormones BibTex
2008-10-01 R-HSA-209931 Serotonin and melatonin biosynthesis BibTex
2008-10-01 R-HSA-209968 Thyroxine biosynthesis BibTex
2008-10-01 R-HSA-196791 Vitamin D (calciferol) metabolism BibTex
2008-10-01 R-HSA-209905 Catecholamine biosynthesis BibTex
2008-10-01 R-HSA-350864 Regulation of thyroid hormone activity BibTex
2008-08-21 R-HSA-375280 Amine ligand-binding receptors BibTex
2008-08-21 R-HSA-375276 Peptide ligand-binding receptors BibTex
2008-07-14 R-HSA-373080 Class B/2 (Secretin family receptors) BibTex
2008-07-03 R-HSA-373076 Class A/1 (Rhodopsin-like receptors) BibTex
2008-07-02 R-HSA-372790 Signaling by GPCR BibTex
2008-05-19 R-HSA-211859 Biological oxidations BibTex
2008-05-19 R-HSA-211945 Phase I - Functionalization of compounds BibTex
2008-05-19 R-HSA-211897 Cytochrome P450 - arranged by substrate type BibTex
2008-05-19 R-HSA-211916 Vitamins BibTex
2008-05-19 R-HSA-211981 Xenobiotics BibTex
2008-05-19 R-HSA-211999 CYP2E1 reactions BibTex
2008-05-19 R-HSA-211957 Aromatic amines can be N-hydroxylated or N-dealkylated by CYP1A2 BibTex
2008-05-19 R-HSA-211935 Fatty acids BibTex
2008-05-19 R-HSA-211976 Endogenous sterols BibTex
2008-05-19 R-HSA-211994 Sterols are 12-hydroxylated by CYP8B1 BibTex
2008-05-19 R-HSA-211979 Eicosanoids BibTex
2008-05-19 R-HSA-211958 Miscellaneous substrates BibTex
2008-05-19 R-HSA-71384 Ethanol oxidation BibTex
2008-05-19 R-HSA-140180 COX reactions BibTex
2008-05-19 R-HSA-217271 FMO oxidises nucleophiles BibTex
2008-05-19 R-HSA-141334 PAOs oxidise polyamines to amines BibTex
2008-05-19 R-HSA-141333 Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB BibTex
2008-05-19 R-HSA-140179 Amine Oxidase reactions BibTex
2008-02-28 R-HSA-177929 Signaling by EGFR BibTex
2008-02-13 R-HSA-212718 EGFR interacts with phospholipase C-gamma BibTex
2007-08-21 R-HSA-201556 Signaling by ALK BibTex
2007-05-02 R-HSA-197264 Nicotinamide salvaging BibTex
2007-04-24 R-HSA-196854 Metabolism of vitamins and cofactors BibTex
2007-04-24 R-HSA-196849 Metabolism of water-soluble vitamins and cofactors BibTex
2007-04-24 R-HSA-196780 Biotin transport and metabolism BibTex
2007-04-24 R-HSA-196783 Coenzyme A biosynthesis BibTex
2007-04-24 R-HSA-196807 Nicotinate metabolism BibTex
2007-04-24 R-HSA-196819 Vitamin B1 (thiamin) metabolism BibTex
2007-04-24 R-HSA-9758881 Uptake of dietary cobalamins into enterocytes BibTex
2007-04-24 R-HSA-9759218 Cobalamin (Cbl) metabolism BibTex
2007-04-24 R-HSA-9758890 Transport of RCbl within the body BibTex
2007-04-24 R-HSA-196741 Cobalamin (Cbl, vitamin B12) transport and metabolism BibTex
2007-04-24 R-HSA-196836 Vitamin C (ascorbate) metabolism BibTex
2007-04-21 R-HSA-196071 Metabolism of steroid hormones BibTex
2007-02-03 R-HSA-556833 Metabolism of lipids BibTex
2007-02-03 R-HSA-8978868 Fatty acid metabolism BibTex
2007-02-03 R-HSA-8979227 Triglyceride metabolism BibTex
2007-01-24 R-HSA-8957322 Metabolism of steroids BibTex
2007-01-24 R-HSA-191273 Cholesterol biosynthesis BibTex
2007-01-24 R-HSA-189451 Heme biosynthesis BibTex
2007-01-19 R-HSA-194068 Bile acid and bile salt metabolism BibTex
2007-01-19 R-HSA-192105 Synthesis of bile acids and bile salts BibTex
2007-01-19 R-HSA-193368 Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol BibTex
2006-02-17 R-HSA-174362 Transport and synthesis of PAPS BibTex
2006-02-02 R-HSA-170834 Signaling by TGF-beta Receptor Complex BibTex
2005-11-09 R-HSA-166187 Mitochondrial Uncoupling BibTex
2005-06-29 R-HSA-163210 Formation of ATP by chemiosmotic coupling BibTex
2005-06-16 R-DME-110523 TOR signaling pathway BibTex
2005-06-14 R-DME-5252538 Drosophila signaling pathways BibTex
2005-06-14 R-DME-110526 Insulin receptor mediated signaling BibTex
2005-04-21 R-HSA-163200 Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. BibTex
2005-04-21 R-HSA-611105 Respiratory electron transport BibTex
2005-03-10 R-HSA-156587 Amino Acid conjugation BibTex
2005-03-10 R-HSA-159424 Conjugation of carboxylic acids BibTex
2005-03-09 R-HSA-159418 Recycling of bile acids and salts BibTex
2005-02-03 R-HSA-156581 Methylation BibTex
2004-12-15 R-HSA-157118 Signaling by NOTCH BibTex
2004-12-15 R-HSA-1980145 Signaling by NOTCH2 BibTex
2004-12-15 R-HSA-9012852 Signaling by NOTCH3 BibTex
2004-12-15 R-HSA-9013694 Signaling by NOTCH4 BibTex
2004-12-15 R-HSA-1912420 Pre-NOTCH Processing in Golgi BibTex
2004-11-30 R-HSA-173599 Formation of the active cofactor, UDP-glucuronate BibTex
2004-11-30 R-HSA-174403 Glutathione synthesis and recycling BibTex
2004-11-30 R-HSA-177135 Conjugation of benzoate with glycine BibTex
2004-11-30 R-HSA-177128 Conjugation of salicylate with glycine BibTex
2004-11-30 R-HSA-177162 Conjugation of phenylacetate with glutamine BibTex
2004-11-30 R-HSA-156582 Acetylation BibTex
2004-11-30 R-HSA-156590 Glutathione conjugation BibTex
2004-11-29 R-HSA-156580 Phase II - Conjugation of compounds BibTex
2004-11-29 R-HSA-156588 Glucuronidation BibTex
2004-11-29 R-HSA-156584 Cytosolic sulfonation of small molecules BibTex
2004-03-31 R-HSA-111885 Opioid Signalling BibTex
2004-03-31 R-HSA-202040 G-protein activation BibTex
2004-03-31 R-HSA-180024 DARPP-32 events BibTex
2004-03-31 R-HSA-112040 G-protein mediated events BibTex
2004-03-31 R-HSA-112043 PLC beta mediated events BibTex
2004-03-31 R-HSA-111996 Ca-dependent events BibTex
2004-03-31 R-HSA-111995 phospho-PLA2 pathway BibTex
2004-03-31 R-HSA-170660 Adenylate cyclase activating pathway BibTex
2004-03-31 R-HSA-111957 Cam-PDE 1 activation BibTex
2004-03-31 R-HSA-163615 PKA activation BibTex
2004-03-31 R-HSA-111931 PKA-mediated phosphorylation of CREB BibTex
2004-03-31 R-HSA-111932 CaMK IV-mediated phosphorylation of CREB BibTex
2004-03-31 R-HSA-111933 Calmodulin induced events BibTex
2004-03-31 R-HSA-111997 CaM pathway BibTex
2004-03-31 R-HSA-170670 Adenylate cyclase inhibitory pathway BibTex
2004-02-11 R-DME-110478 Insulin signaling pathway BibTex
2003-07-17 R-HSA-74217 Purine salvage BibTex
2003-07-17 R-HSA-74259 Purine catabolism BibTex
2003-06-26 R-HSA-15869 Metabolism of nucleotides BibTex
2003-06-26 R-HSA-8956321 Nucleotide salvage BibTex
2003-06-26 R-HSA-8956320 Nucleotide biosynthesis BibTex
2003-06-26 R-HSA-73817 Purine ribonucleoside monophosphate biosynthesis BibTex
2003-06-26 R-HSA-8956319 Nucleotide catabolism BibTex
2003-06-17 R-HSA-73621 Pyrimidine catabolism BibTex
2003-06-17 R-HSA-73614 Pyrimidine salvage BibTex
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