Viterbo et al., 2008 - Google Patents
Mutational characterization of pancreatitis-associated protein 2 domains involved in mediating cytokine secretion in macrophages and the NF-κB pathwayViterbo et al., 2008
View PDF- Document ID
- 15036275904069293781
- Author
- Viterbo D
- Bluth M
- Mueller C
- Zenilman M
- Publication year
- Publication venue
- The Journal of Immunology
External Links
- 101700006219 REG3A 0 title abstract description 229
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Schlingmann et al. | Defects in KCNJ16 cause a novel tubulopathy with hypokalemia, salt wasting, disturbed acid-base homeostasis, and sensorineural deafness | |
| Gollwitzer et al. | A Rag GTPase dimer code defines the regulation of mTORC1 by amino acids | |
| Di Donato et al. | Mutations in CRADD result in reduced caspase-2-mediated neuronal apoptosis and cause megalencephaly with a rare lissencephaly variant | |
| Blackburn et al. | Bi-allelic alterations in AEBP1 lead to defective collagen assembly and connective tissue structure resulting in a variant of Ehlers-Danlos syndrome | |
| Ojala et al. | Crystal structure of the cysteine-rich domain of scavenger receptor MARCO reveals the presence of a basic and an acidic cluster that both contribute to ligand recognition | |
| Xue et al. | Regulator-dependent mechanisms of C3b processing by factor I allow differentiation of immune responses | |
| Ferreira et al. | Factor H–mediated cell surface protection from complement is critical for the survival of PNH erythrocytes | |
| Aspberg | The different roles of aggrecan interaction domains | |
| Williams et al. | Targeted β-adrenergic receptor kinase (βARK1) inhibition by gene transfer in failing human hearts | |
| Shi et al. | The MIG-2/integrin interaction strengthens cell-matrix adhesion and modulates cell motility | |
| Pasutto et al. | Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation | |
| Angel et al. | Structural insight into the bacterial mucinase StcE essential to adhesion and immune evasion during enterohemorrhagic E. coli infection | |
| Ormsby et al. | Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degeneration | |
| Elphick et al. | Recombinant human activated protein C inhibits integrin-mediated neutrophil migration | |
| Chaudary | Triplet CFTR modulators: future prospects for treatment of cystic fibrosis | |
| Gaida et al. | Evidence of the TNF-α system in the human Achilles tendon: expression of TNF-α and TNF receptor at both protein and mRNA levels in the tenocytes | |
| Dremina et al. | Heat-shock proteins attenuate SERCA inactivation by the anti-apoptotic protein Bcl-2: possible implications for the ER Ca2+-mediated apoptosis | |
| Shao et al. | Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia | |
| Zhang et al. | Sensing ceramides by CYSLTR2 and P2RY6 to aggravate atherosclerosis | |
| Gesteira et al. | Lumican peptides: rational design targeting ALK5/TGFBRI | |
| Wichmann et al. | Dimer-tetramer transition controls RUNX1/ETO leukemogenic activity | |
| Mandt et al. | SLC41A1 Mg2+ transport is regulated via Mg2+-dependent endosomal recycling through its N-terminal cytoplasmic domain | |
| Dreßen et al. | A novel de novo TBX 5 mutation in a patient with Holt–Oram syndrome leading to a dramatically reduced biological function | |
| Yang et al. | Structure of GPR101–Gs enables identification of ligands with rejuvenating potential | |
| Dharmat et al. | IFT81 as a candidate gene for nonsyndromic retinal degeneration |