Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA. - Wikidata - wikimedia - TriplyDB

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.

http://www.wikidata.org/entity/Q36979961

about

Revisiting Crohn's disease as a primary immunodeficiency of macrophages Genetic interstitial lung disease Interstitial Lung Disease in Childhood: Clinical and Genetic Aspects An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy Respiratory epithelial cells orchestrate pulmonary innate immunity.Genetic disorders of surfactant dysfunction Alveolar surfactant homeostasis and the pathogenesis of pulmonary disease Orphan G protein-coupled receptor GPR116 regulates pulmonary surfactant pool size Alveolar macrophages are essential for protection from respiratory failure and associated morbidity following influenza virus infection.Novel primary immunodeficiencies relevant to internal medicine: novel phenotypes.Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I Autoimmune pulmonary proteinosis in a Chilean teenager, a rare aetiology of interstitial lung disease.Autoimmunity as a predisposition for infectious diseases The molecular basis of pulmonary alveolar proteinosis The molecular era of surfactant biology.Inhaled granulocyte/macrophage-colony stimulating factor as therapy for pulmonary alveolar proteinosis.Patient-derived granulocyte/macrophage colony-stimulating factor autoantibodies reproduce pulmonary alveolar proteinosis in nonhuman primates.Long-term follow-up and treatment of congenital alveolar proteinosis.The GM-CSF/IL-3/IL-5 cytokine receptor family: from ligand recognition to initiation of signaling.Efficacy and safety of mavrilimumab in subjects with rheumatoid arthritis Diffuse lung disease in infancy and childhood: expanding the chILD classification.Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapy.Diseases of pulmonary surfactant homeostasis.Pulmonary macrophage transplantation therapy Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis.A standardized blood test for the routine clinical diagnosis of impaired GM-CSF signaling using flow cytometry.Genetic Basis of Children's Interstitial Lung Disease.Outcome of corticosteroid administration in autoimmune pulmonary alveolar proteinosis: a retrospective cohort study Pulmonary alveolar proteinosis in a cat.The GM-CSF receptor utilizes β-catenin and Tcf4 to specify macrophage lineage differentiation Elderly-onset hereditary pulmonary alveolar proteinosis and its cytokine profile.Out of breath: GM-CSFRalpha mutations disrupt surfactant homeostasis.Autoantibody-Mediated Pulmonary Alveolar Proteinosis in Rasgrp1-Deficient Mice.Alveolar macrophages develop from fetal monocytes that differentiate into long-lived cells in the first week of life via GM-CSF.The granulocyte-macrophage colony-stimulating factor receptor: linking its structure to cell signaling and its role in disease.Acute Respiratory Distress Syndrome Neutrophils Have a Distinct Phenotype and Are Resistant to Phosphoinositide 3-Kinase Inhibition.Pulmonary alveolar proteinosis, a primary immunodeficiency of impaired GM-CSF stimulation of macrophages.Use of induced pluripotent stem cells to recapitulate pulmonary alveolar proteinosis pathogenesis.Update in pediatric lung disease 2009.Review: The intersection of surfactant homeostasis and innate host defense of the lung: lessons from newborn infants.

P2860

be7248706156cb6fdd1efa3a1f35deabb5d032b0

P248

Q22242983-C880D413-B0E0-49F5-B9BC-14EAE1A8418C Q24626239-CACE47D4-49FE-410E-9FFD-414366D3CED5 Q26778109-FDFE388F-435F-46CF-AC16-25B682D97C31 Q26824718-9977186F-296C-4E9D-AFC6-95C0BDD33258 Q27687743-DC6C9A0C-7A3D-4BF9-82F2-05B694A8C157 Q28235256-907BDD6E-5295-49CB-AD53-8DDD430A9CC3 Q28261260-D2B3BAC5-3A01-4937-808E-95F984FE464F Q28508878-063230EE-9CE1-4001-929C-DDC698B9A88D Q31157006-7FBA8C49-C46B-4671-9BF4-21CBEB4A215E Q33387136-1EE2F876-A702-4F36-BC87-654133FF07FC Q33656182-ED5C1F1B-8106-4220-8F78-5C145820F181 Q33691075-FAFB1628-E43E-4774-A901-FF7B81FDC7DF Q33747588-E9AF33F0-E67B-49E9-8FD5-F7667E0FCCBE Q33835843-4335BB18-5DD8-40F2-A207-E422317BFBA3 Q33942221-EB4CF440-AA56-4C46-8A6F-0B1C04552022 Q33950106-EF2C99F7-952A-4F07-9256-944BDCD5726D Q33988125-45B5BAEB-AAF5-4E33-B422-8980453E1B64 Q33995121-ADDF28EF-E1A2-40BE-B806-E3E69523FF84 Q34304678-E77251A2-85F4-4EB4-AA19-ADEFAB8DA9B4 Q34317197-516CCA12-043D-4842-A9C5-4B9C83BE77F5 Q34377177-F3A1C100-27BF-4FD2-8B2E-AC3207CF4119 Q34402453-EDC827B6-5F58-482D-83D0-EF04121D2B7C Q34459713-BD35AAF6-CFFB-478B-BC0D-F8DA1D38C19A Q34539736-0921F16A-DE95-48D4-B46E-CBC832A7E914 Q34623826-DDA3F71A-B101-40ED-BA48-2FE95EC515B3 Q35078403-9B42221A-3F85-4F48-8FC7-698AAB094FB5 Q35513452-10A57273-23B2-4471-BE18-E46C741C2AAE Q35743143-4ABF1DDA-0A04-46EA-9ED9-953188D06425 Q35863387-77316A99-E262-4247-90D6-9895B1CEA133 Q36089825-EDE9F336-58A0-4A89-821D-AFBC3085B3D4 Q36284490-C373FC12-C957-488A-96A7-BDDF1A4CBA45 Q36979933-52C6E8DE-0DF4-46AA-BE80-9685A5E5C773 Q37072048-11CEE436-1159-4014-A305-0725329150F8 Q37194936-B5CA8E52-C7B1-422A-BA9D-580292CE78D3 Q37306641-8B5DBDA2-0EB6-4E5E-A802-A2DBBAF24BE0 Q37345975-C27A309F-BAFB-4A7D-A437-06BFDECE2C40 Q37427088-19A0299A-79A5-41B9-9B20-996883A0C71E Q37698322-3A34DD03-2D8E-4B7F-B9F4-9959A78646F3 Q37718407-A989EBBB-14E6-4AA6-A7C2-6B3CA4B883E2 Q37721029-98894441-65AC-4105-94B7-1DD7F1FCD0F2

P2860

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.

http://www.wikidata.org/entity/Q36979961

description

2008 nî lūn-bûn

@nan

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

2008年论文

@zh

2008年论文

@zh-cn

name

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.

@en

type

label

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.

@en

prefLabel

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.

@en

P1433

Q36979961-DCF6FC53-ECC9-4D5A-A75E-B55B71ABD39C

P1476

Q36979961-D796D950-BC19-4F7A-A0C3-11D7608C75EC

P2093

Q36979961-05D32975-1A89-4D90-A4EA-483292B517EF

Q36979961-15DA8A3E-3ED4-4B62-A5F3-90CD112C9C5F

Q36979961-18EE6512-9FF3-4FA4-8DB5-5A821CDD62E2

Q36979961-1C1106EB-E062-408C-A027-57F107FC21E6

Q36979961-2D31C311-6EEE-462C-BF9B-25DCCB912DA8

Q36979961-4F18E8BE-0486-49DC-8B81-426BCEB644FA

Q36979961-7222C86D-0365-4CF6-BD1A-41907469B3CF

Q36979961-89D517B4-1F0E-4568-9506-FAF804D244F5

Q36979961-9863D24F-E85C-42F0-9D8D-B73C14E0793D

Q36979961-A7FCF76A-A037-4244-B221-4134A5AC7D13

P2860

Q36979961-041B84D6-ADEC-43E0-B68D-EE8A159CA3E9

Q36979961-11B17D5B-1522-49DB-A074-FC41FA795F05

Q36979961-2F44CCD4-E3DA-4BE8-8F3E-CFD44A2A2F55

Q36979961-3A0F77E2-219E-4C99-B513-A41D19F7F743

Q36979961-3F375CB0-ED28-450F-B372-8AF5EE478A2D

Q36979961-3FDFBE90-B717-4046-B591-FD563DC3C694

Q36979961-407C29AF-A628-4461-991F-457424C20FE8

Q36979961-4BD29E52-314E-4BB9-9A18-2C28833B191E

Q36979961-5BCA60CC-5160-4414-95D6-0435EDD19D22

Q36979961-65554D25-B315-433F-AFC5-8120B87AF8CE

P304

Q36979961-769B5B21-B07E-4D5B-BDBD-60A953E80B21

P31

Q36979961-0E20C8F9-5C7C-4D65-A026-F312F8E7086C

P356

Q36979961-63B8FCDB-CF89-4007-B10B-DD2D8DF16BA4

P407

Q36979961-9F1876F7-DD04-473D-A0A2-DE31520B5A78

P433

Q36979961-7B6E3BF6-E77D-41B3-8D40-E6AE5D3E937E

P478

Q36979961-1B948D2C-BDB6-4988-995D-0D7FEF35971C

P577

Q36979961-77056B0B-0E8D-489A-8577-6DB6196CA3E6

P5875

Q36979961-9EED0D0D-A40C-4894-BC08-0A92D663484B

P698

Q36979961-4F466ECD-CD05-4ECA-B3FA-F73A02AF6C44

P932

Q36979961-540AB00B-1F07-45D2-BACE-F2BDBB7FCF80

P356

P1433

Journal of Experimental Medicine

P1476

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA.

@en

P2093

Brenna C Carey

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

Bruce C Trapnell

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

Bruce K Rubin

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

Carrie Stevens

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

Gregory Grabowski

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

Jeffrey A Whitsett

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

Johannes C M van der Loo

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

Lawrence M Nogee

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

Megan K Dishop

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

Robert E Wood

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

P2860

Growth factor pleiotropy is controlled by a receptor Tyr/Ser motif that acts as a binary switch

Human pulmonary alveolar proteinosis associated with a defect in GM-CSF/IL-3/IL-5 receptor common beta chain expression

Granulocyte/macrophage colony-stimulating factor-deficient mice show no major perturbation of hematopoiesis but develop a characteristic pulmonary pathology

Characteristics of a large cohort of patients with autoimmune pulmonary alveolar proteinosis in Japan.

Global variation in copy number in the human genome

A mutation in the surfactant protein C gene associated with familial interstitial lung disease

Alterations in SP-B and SP-C expression in neonatal lung disease

Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

Hematopoietic and lung abnormalities in mice with a null mutation of the common beta subunit of the receptors for granulocyte-macrophage colony-stimulating factor and interleukins 3 and 5.

P304

2703-2710

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

P31

scholarly article

P356

10.1084/JEM.20080990

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

P407

P433

12

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

P478

205

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

P577

2008-10-27T00:00:00Z

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

P5875

23423350

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

P698

18955570

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

P932

2585845

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