Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases. - Test2 - elhamkhani - TriplyDB

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

http://www.wikidata.org/entity/Q37623378

about

Targeting New Candidate Genes by Small Molecules Approaching Neurodegenerative Diseases Kynurenine 3-Monooxygenase: An Influential Mediator of Neuropathology Changing the face of kynurenines and neurotoxicity: therapeutic considerations Antioxidant Properties of Kynurenines: Density Functional Theory Calculations The kynurenine pathway is involved in bacterial meningitis.Tetrahydrobiopterin Biosynthesis as a Potential Target of the Kynurenine Pathway Metabolite Xanthurenic Acid Plasma Biomarkers of Inflammation, the Kynurenine Pathway, and Risks of All-Cause, Cancer, and Cardiovascular Disease Mortality: The Hordaland Health Study X-linked inhibitor of apoptosis protein mediates tumor cell resistance to antibody-dependent cellular cytotoxicity.Effects of Various Kynurenine Metabolites on Respiratory Parameters of Rat Brain, Liver and Heart Mitochondria.Tryptophan-kynurenine pathway is dysregulated in inflammation, and immune activation.Depressive symptoms as a side effect of Interferon-α therapy induced by induction of indoleamine 2,3-dioxygenase 1.The Kynurenine Pathway in the Acute and Chronic Phases of Cerebral Ischemia.3-Hydroxykynurenine and 3-Hydroxyanthranilic Acid Enhance the Toxicity Induced by Copper in Rat Astrocyte Culture.Redox Properties of Tryptophan Metabolism and the Concept of Tryptophan Use in Pregnancy.Kynurenine, a Tryptophan Metabolite That Accumulates With Age, Induces Bone Loss.Kynurenines and Glutamate: Multiple Links and Therapeutic Implications.Iron chelation and redox chemistry of anthranilic acid and 3-hydroxyanthranilic acid: A comparison of two structurally related kynurenine pathway metabolites to obtain improved insights into their potential role in neurological disease development.Oxidative Stress, Disrupted Energy Metabolism, and Altered Signaling Pathways in Glutaryl-CoA Dehydrogenase Knockout Mice: Potential Implications of Quinolinic Acid Toxicity in the Neuropathology of Glutaric Acidemia Type I.Structure of the PLP-Form of the Human Kynurenine Aminotransferase II in a Novel Spacegroup at 1.83 Å Resolution.Induction of Neuroinflammatory Response and Histopathological Alterations Caused by Quinolinic Acid Administration in the Striatum of Glutaryl-CoA Dehydrogenase Deficient Mice.Vitamin B6 Reduces Neurochemical and Long-Term Cognitive Alterations After Polymicrobial Sepsis: Involvement of the Kynurenine Pathway Modulation.An Expanded Neuroimmunomodulation Axis: sCD83-Indoleamine 2,3-Dioxygenase—Kynurenine Pathway and Updates of Kynurenine Pathway in Neurologic Diseases.Preparation and Characterization of Kynurenic Acid Occluded in Sol-Gel Silica and SBA-15 Silica as Release Reservoirs

P2860

Q26771812-98399AB5-71D7-481D-84EE-83798F8829AD Q26782867-85A5CEDD-EEAC-49AF-91D3-BC455498BBD7 Q28085041-D6C1983D-C528-4891-B281-D6FFBBD3EC15 Q28553594-BAA13815-83A8-4CA3-BFAB-9B34D856AC13 Q34306405-AC04E563-AB53-4139-922C-4C74B5613043 Q36442352-25CDBEB6-5E8C-4D48-B64C-A9A50566A383 Q36579036-03057409-977E-470A-8F03-58C6523124EB Q36751784-319D4CDA-6CD3-40FD-ABE6-A9DC9CEA305B Q36915988-EBC1A6C9-005A-4035-8A40-4BC62C3E5E08 Q37013795-064B9D97-AE0E-4B8E-9859-2C911ADD590E Q37111098-C3DA2413-E9D2-47E3-B4C1-81C418423002 Q38253558-80D442A8-498C-4609-A6D3-C2EE77BFF266 Q38613212-84B7C249-30D8-4495-AA1A-D40AAC8DE60E Q38652774-82DE316A-9776-4202-B30D-ADFEE9334483 Q38670358-D4C9A371-3F91-40D3-AE1B-F40B8205BB1D Q38861843-ED1D77A0-107A-4F9D-B0B1-7BB83C7886AE Q39630770-44044FDE-FE14-4BC0-B8B6-AB449A40C2BB Q40274773-40CB814F-5857-49CD-9CC1-3ADD05C96B9A Q40749076-60067DD3-EE0B-49A8-A231-EB1E413544C1 Q47299503-5224E22C-F160-4872-BE3A-4E89BE40B2A0 Q48114977-DD83AADD-9B26-43D4-9487-2724DBC95E5A Q55381445-05F91444-7F42-4F8C-93A7-D6D021666C72 Q59060399-3B8BACE4-EF6B-4F95-B37D-16AE25AD6DCF

P2860

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

http://www.wikidata.org/entity/Q37623378

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 17 February 2014

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

@en

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

@nl

type

label

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

@en

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

@nl

prefLabel

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

@en

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases.

@nl

P1433

Q37623378-C50887EC-4F66-43B8-AEBE-09E2DBE45E41

P1476

Q37623378-202BD721-8A91-4D1D-9B7D-12CCB7A553B1

P2093

Q37623378-1233F497-321F-43B8-BCEC-755E472798C2

Q37623378-15935504-2C15-4554-9C1B-7814648DB403

Q37623378-1880DD41-5D6F-41BD-A0B3-8A5146D3F89C

Q37623378-490F7946-AFA8-4A00-91D5-5E7419C77C4D

Q37623378-54870BA3-7AC5-4C5C-9C00-FC30C2FE27CC

Q37623378-D413AF10-D4CD-4EB0-ADD0-F28715A91329

Q37623378-F2C34EC5-9C0A-4FBC-A073-7B4528AC0380

Q37623378-F50C5FCD-5992-4433-8D08-A7E08C96C0CE

P275

Q37623378-0470C507-CC0E-41A3-90E1-A5EDBC236A8D

P2860

Q37623378-00F90D27-6480-4B6C-94B0-B23F6F25B17F

Q37623378-0389AC01-B1A5-46DC-9B3A-AAC66F8F4740

Q37623378-05C38E8F-FC3E-4970-9499-BB6280C5D1D4

Q37623378-05D0269A-4E18-4651-B15C-4BD17C44A224

Q37623378-08E7DD80-D76F-4C26-8390-0ACC094CEA0A

Q37623378-0B36F83F-F8C7-44FA-8EDA-736E33D999AC

Q37623378-0B764711-6603-428B-BA25-B4DB1AEDF844

Q37623378-0DA8272C-1A3E-4EF3-9249-D3111F06CB7D

Q37623378-0DBAE459-828C-4C81-BB55-B92970DCFAD4

Q37623378-0EF587A2-F1CC-4D4F-BC4A-AD6EF16127C2

P304

Q37623378-A0EECF22-C5FF-470D-A982-1211B24F1F75

P31

Q37623378-5649FB9A-CFC5-4FE5-97B5-3BFCEF9F7BD1

P356

Q37623378-699FF887-97E4-4C4B-AB09-BD2824243332

P478

Q37623378-02D6E473-25F2-4DCE-AEDD-785890053DBB

P50

Q37623378-162E4DCF-8D8A-45D6-8398-BBB51AB1A36C

P5008

Q37623378-BF71ADCB-9A77-4E10-A241-738D4953716E

P577

Q37623378-954235EB-F671-4C7F-AD8B-5A2AF2E2BF92

P5875

Q37623378-150B4582-B72A-43FF-BE6E-912972DE4C61

P698

Q37623378-2885DDC4-2AF8-48C1-A86E-5A610C6FCD8A

P921

Q37623378-46F1C4E1-BA10-4180-B720-E7FCB5460E05

Q37623378-4D5AE30F-7B40-4EED-8F60-B4A13A12BBC1

P932

Q37623378-0AE87204-23A3-472F-928F-06AA3B647DB8

P356

P1433

Oxidative medicine and cellular longevity

P1476

Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases

@en

P2093

Anabel Jiménez-Anguiano

http://www.w3.org/2001/XMLSchema#string

Benjamín Pineda

http://www.w3.org/2001/XMLSchema#string

Camilo Ríos

http://www.w3.org/2001/XMLSchema#string

Dinora González-Esquivel

http://www.w3.org/2001/XMLSchema#string

José Pedraza-Chaverri

http://www.w3.org/2001/XMLSchema#string

Perla Ugalde-Muñiz

http://www.w3.org/2001/XMLSchema#string

Rafael Lugo Huitrón

http://www.w3.org/2001/XMLSchema#string

Verónica Pérez de la Cruz

http://www.w3.org/2001/XMLSchema#string

P275

Creative Commons Attribution 3.0 Unported

P2860

Functional characterization and mechanism of action of recombinant human kynurenine 3-hydroxylase

Structural and kinetic characterization of quinolinate phosphoribosyltransferase (hQPRTase) from homo sapiens

Purification and biochemical characterization of some of the properties of recombinant human kynureninase

Cloning of human 3-hydroxyanthranilic acid dioxygenase in Escherichia coli: characterisation of the purified enzyme and its in vitro inhibition by Zn2+

Characterization of an indoleamine 2,3-dioxygenase-like protein found in humans and mice

Substrate specificity and structure of human aminoadipate aminotransferase/kynurenine aminotransferase II

Novel tryptophan catabolic enzyme IDO2 is the preferred biochemical target of the antitumor indoleamine 2,3-dioxygenase inhibitory compound D-1-methyl-tryptophan

Kynurenic acid as a ligand for orphan G protein-coupled receptor GPR35

Primary structure of human indoleamine 2,3-dioxygenase deduced from the nucleotide sequence of its cDNA

The physiological action of picolinic Acid in the human brain

P304

646909

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1155/2014/646909

http://www.w3.org/2001/XMLSchema#string

P478

2014

http://www.w3.org/2001/XMLSchema#string

P50

Jazmin Reyes Ocampo

P5008

P577

2014-02-17T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

261295396

http://www.w3.org/2001/XMLSchema#string

P698

24693337

http://www.w3.org/2001/XMLSchema#string

P921

P932

3945746

http://www.w3.org/2001/XMLSchema#string