HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

ribosomal protein S19

Higher level expression is seen in the colon carcinoma tissue than normal colon tissue in human; defects in RPS19 are a cause of DIAMOND-BLACKFAN ANEMIA (DBA) in human; RefSeq NM_001022 (human); XM_218456 (rat)
Also Known As:
30S ribosomal subunit protein S19, E coli; DBA protein, human; RPS19 protein, human; RPS19A protein, S cerevisiae; Ribosomal protein S19, Drosophila; RpS19a protein, Drosophila; Rps19 protein, Drosophila; Rps19 protein, Xenopus; Rps19 protein, rat; RpsS protein, E coli; S19 ribosomal protein; S19 ribosomal protein, Xenopus; YOL121C protein, S cerevisiae; ribosomal protein S19 protein, human; ribosomal protein S19, rat; ribosomal protein S19A , S cerevisiae
Networked: 43 relevant articles (1 outcomes, 1 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Dahl, Niklas: 8 articles (01/2011 - 05/2003)
2. Flygare, Johan: 6 articles (12/2014 - 05/2003)
3. Karlsson, Stefan: 6 articles (12/2014 - 05/2003)
4. Badhai, Jitendra: 6 articles (01/2011 - 01/2009)
5. Schuster, Jens: 6 articles (01/2011 - 01/2009)
6. Richter, Johan: 5 articles (12/2011 - 05/2003)
7. Fröjmark, Anne-Sophie: 5 articles (06/2010 - 01/2009)
8. Tchernia, Gil: 5 articles (11/2008 - 01/2003)
9. Da Costa, Lydie: 5 articles (11/2008 - 01/2003)
10. Dianzani, Irma: 4 articles (10/2014 - 12/2004)

Related Diseases

1. Kidney Diseases (Kidney Disease)
2. Diamond-Blackfan Anemia (Anemia, Diamond Blackfan)
3. Neoplasms (Cancer)
4. Inflammation
5. Carcinoma (Carcinomatosis)
02/15/1992 - "Differential expression of S19 ribosomal protein, laminin-binding protein, and human lymphocyte antigen class I messenger RNAs associated with colon carcinoma progression and differentiation."
06/01/2005 - "The 20 genes with at least a 3-fold change, annotated with known phenotypic associations in the current gene databank (phenotype association, fold change) were aspartoacylase (Canavan disease, 9.96), growth hormone receptor (Laron dwarfism, idiopathic short stature, 8.25), lipoprotein lipase (familial chylomicronemia syndrome, lipoprotein lipase deficiency, 8.00), vitamin D (1,25- dihydroxyvitamin D3) receptor (involutional osteoporosis, vitamin D resistant rickets, 7.94), intercellular adhesion molecule 1 human rhinovirus receptor (cerebral malaria susceptibility, 7.16), peroxisomal membrane protein 3 35-kDa (Refsum disease, infantile form, Zellweger syndrome-3, 6.00), Bardet-Biedl syndrome 2 (Bardet-Biedl syndrome, 5.87), ribosomal protein S19 (Diamond Blackfan anemia, 5.85), apolipoprotein C-III (hypertriglyceridemia, 5.44), argininosuccinate lyase (argininosuccinicaciduria, 5.22), myosin VA (Griscelli syndrome-type pigmentary dilution with mental retardation, 4.92), lysozyme (renal amyloidosis, 4.17), SAM domain, SH3 domain and nuclear localisation signals 1 (Cherubism, 4.12 ), von Hippel-Lindau syndrome (hemangioblastoma, cerebellar, somatic, von Hippel-Lindau syndrome, 3.94), early-onset breast cancer 1 (BRCA1, papillary serous carcinoma of the peritoneum, 3.73), UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (inclusion body myopathy, autosomal recessive, sialuria, 3.53), apolipoprotein A-I (amyloidosis, 3 or more types, hypoalphalipoproteinemia, 3.29), midline 1 Opitz/BBB syndrome (Opitz G syndrome, type I, 3.28), ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide (familial hemiplegic migraine, 3.05). "

Related Drugs and Biologics

1. Proteasome Endopeptidase Complex (Proteasome)
2. Small Interfering RNA (siRNA)
3. Messenger RNA (mRNA)
4. Peroxiredoxins
5. Janus Kinase 2
6. Apolipoprotein C-III
7. TNF-Related Apoptosis-Inducing Ligand Receptors
8. 5' Untranslated Regions (5' UTR)
9. Thapsigargin
10. Intercellular Adhesion Molecule-1 (Intercellular Adhesion Molecule 1)

Related Therapies and Procedures

1. Transplantation (Transplant Recipients)