Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment. - Wikidata - wikimedia - TriplyDB

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

http://www.wikidata.org/entity/Q34028117

about

Oxidative Stress Implications in the Affective Disorders: Main Biomarkers, Animal Models Relevance, Genetic Perspectives, and Antioxidant Approaches Mottled Mice and Non-Mammalian Models of Menkes Disease Treatment of nongout joint deposition diseases: an update Metals, oxidative stress and neurodegeneration: a focus on iron, manganese and mercury Molecular basis of neurodegeneration and neurodevelopmental defects in Menkes disease Elemental and chemically specific X-ray fluorescence imaging of biological systems Hypocupremia: a possible association with late cortical cerebellar atrophy.The T1048I mutation in ATP7A gene causes an unusual Menkes disease presentation.The Features of Copper Metabolism in the Rat Liver during Development Celiac disease markers in patients with liver diseases: a single center large scale screening study.Diagnostic copper imaging of Menkes disease by synchrotron radiation-generated X-ray fluorescence analysis Effects of ATP7A overexpression in mice on copper transport and metabolism in lactation and gestation Inborn errors of metabolism causing epilepsy.Pathological mitochondrial copper overload in livers of Wilson's disease patients and related animal models.What has fluorescent sensing told us about copper and brain malfunction?Possible role of trace elements in epilepsy and febrile seizures: a meta-analysis.Psychiatric comorbidity in Wilson's disease.Drosophila melanogaster Models of Metal-Related Human Diseases and Metal Toxicity.Reduced glutathione biosynthesis in Drosophila melanogaster causes neuronal defects linked to copper deficiency.Wilson's disease in association with anetoderma.Characterization of ATP7A missense mutants suggests a correlation between intracellular trafficking and severity of Menkes disease Copper deficiency, a new triad: anemia, leucopenia, and myeloneuropathy.The Extracellular Domain of Human High Affinity Copper Transporter (hNdCTR1), Synthesized by E. coli Cells, Chelates Silver and Copper Ions In Vivo.Novel mutations and clinical outcomes of copper-histidine therapy in Menkes disease patients.Spontaneous retroperitoneal hemorrhage in Menkes disease: A rare case report.Toxic effects of copper sulfate on the brains of term Hubbard broiler chicks: a stereological and biochemical study.Menkes disease: importance of diagnosis with molecular analysis in the neonatal period

P2860

Q26738789-0CC27341-FA08-424E-A766-B0558BAFD7AD Q26770905-D7A596A5-855A-48BE-8ACD-927C1504B4F3 Q26852957-3924C289-19B5-46C3-B729-D4BA445AF449 Q26863224-EC771E7C-0357-4451-8FD6-9BA942AE8DC5 Q28088624-42CB17CA-CE63-4309-9DA9-F99B9D48C02F Q28655858-B20FC80A-FB61-4BD9-B0D5-6748F6BCE058 Q34200579-5E4C0EEE-FC82-4004-976B-DBB57B9A3737 Q34418390-7A273ABA-9D28-40D0-87D1-5C68859FF175 Q36170780-670AB68D-1427-4053-854D-6D90F5091C8F Q36410388-9981EE08-2FDF-446B-B7F7-95A779CB6522 Q37257560-840104DE-A869-4C4D-9CE2-C2DFF884D32D Q37668439-6B2255C7-CAF1-4232-9C70-5366B6CF1C3C Q38045430-921DBAC4-9D22-4AE7-AC96-9FD5D0B96269 Q38187164-BC930B99-C840-4317-8BC4-170388ADC777 Q38271378-0EE093C4-A319-499B-90B5-325E2689073C Q38598305-93B63330-3C56-474D-976B-48B6CC3BDE41 Q39417676-FE62BB83-9B00-4C5B-A23A-580C55B21C24 Q39419474-A2D1E4C4-12C2-4DCF-B78B-669BE64395F3 Q40018327-3A94925B-C36C-4FA7-9A64-1D90480FA9BF Q42174218-350F7177-D7D7-4492-AC84-36D518C79C36 Q42189067-CE55F2FD-724A-40FF-8775-C755B467AE54 Q42375475-AE9D8C3A-EC26-40EB-89A7-7B74728F0F82 Q47111192-DAC8EF97-2DED-4CCD-9DCA-F169AC9820C4 Q48720813-04DB3197-F9DB-4F08-8682-5D52535E44DC Q50117791-4F939526-9D07-4E02-8C7E-CDDC0A1C6F79 Q50734326-CC77FCC3-2699-4924-AACB-A51C7272AE7A Q57234886-4674FC1D-273F-4941-ADFB-626AFEF0C6AF

P2860

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

http://www.wikidata.org/entity/Q34028117

description

2012 nî lūn-bûn

@nan

2012 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի մարտին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@ast

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@en

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@nl

type

label

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@ast

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@en

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@nl

prefLabel

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@ast

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@en

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@nl

P1433

Q34028117-22B0C90E-10A8-4A89-96C7-38B05A52DFDE

P1476

Q34028117-E5527BED-93F4-451D-A540-BBF14439E2F9

P2093

Q34028117-3BCA725C-D3F6-487E-A062-D9E2EB59DF54

Q34028117-9970EA8D-FB85-4EE1-9004-7F58B02899F2

Q34028117-AE52F40F-D2FF-4A43-BD59-96994CACC49C

P275

Q34028117-0DF322BF-F9CF-4B32-B33B-B480203120D2

P2860

Q34028117-00CE6C28-366B-463F-8076-FF07C09532FA

Q34028117-03917034-41C4-4496-ADAB-90B18EE38F3C

Q34028117-07FF2D80-6C1C-469D-B72E-D918414B1667

Q34028117-0B56CDA0-AC12-4DEF-BE23-E22C87EDBC75

Q34028117-0D99B6F8-A0DF-46D1-A220-D0BD2B313230

Q34028117-0DA1C1E3-9480-4848-990B-350531685E42

Q34028117-15E29BF8-9996-4014-8956-5B7485B5B489

Q34028117-15FF7E40-8D88-4C9C-B5B8-6784C33AF902

Q34028117-16D9F112-9667-47B7-9868-BD10D58499CC

Q34028117-1EA27228-F3A4-49C5-A2FC-ACEE98A4C433

P304

Q34028117-C86E075B-C479-43E0-87F0-CA36F10B1338

P31

Q34028117-5215B1C3-7597-40C2-A156-43ED05C5222D

Q34028117-E7DE6122-0F2B-4B66-B60F-B20D97FB4D77

P356

Q34028117-F82CB2EF-93BF-4F61-B9AC-C6639DB9059F

P407

Q34028117-B4308963-91ED-4921-A4EC-D12A39996811

P433

Q34028117-389C9AC7-7EC5-453D-8C53-770F36136FD1

P478

Q34028117-A392AFAA-D502-43BA-9924-B1376EEF65FA

P5008

Q34028117-F8C50918-E84B-469B-BFBD-DFF16BAA0B80

P577

Q34028117-51159850-1A1D-416F-BCFD-5C7727921406

P5875

Q34028117-25D0D8CA-5A5A-4BA7-9F4F-0C741BE6E291

P698

Q34028117-C373E2C7-410F-4967-A660-A92FFA13A111

P921

Q34028117-0A2C79C8-BA15-451E-845D-DC3427BE7CDD

Q34028117-23CAC94B-D0C7-4101-B4B7-BD65EB50BAF5

Q34028117-A9252165-072A-46CC-B7D4-925E35860B30

Q34028117-DD147799-F2D5-4F44-9AD8-7CEDE346BBFA

Q34028117-F805A0F6-6932-4B63-917B-0584DC6D3E1A

P932

Q34028117-1B1D739B-F5CD-4027-B2A3-4AADC2891F5D

P356

138920012799320455

P1433

Current Drug Metabolism

P1476

Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

@en

P2093

Chie Fujisawa

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

Hiroko Kodama

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

Wattanaporn Bhadhprasit

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

P275

Creative Commons Attribution 2.5 Unported

P2860

Angiogenins: a new class of microbicidal proteins involved in innate immunity

Characterization and copper binding properties of human COMMD1 (MURR1)

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Neonatal diagnosis and treatment of Menkes disease

Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy

Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?

Molecular genetics and pathophysiology of Menkes disease

The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein

Identification of a new copper metabolism gene by positional cloning in a purebred dog population

Treatment of Wilson's disease with tetrathiomolybdate: V. Control of free copper by tetrathiomolybdate and a comparison with trientine

P304

237-250

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

P31

scholarly article

P356

10.2174/138920012799320455

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

P407

P433

3

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

P478

13

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

P5008

P577

2012-03-01T00:00:00Z

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

P5875

51568626

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

P698

21838703

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

P921

Ehlers-Danlos syndrome

inorganic compound

P932

3290776

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