HEMATOXYLIN
HEMATOXYLIN is a lipid of Polyketides (PK) class. Hematoxylin is associated with abnormalities such as Eosinophilia, Duodenal Adenoma, Senile Plaques, Morphologically altered structure and Cervical abscess. The involved functions are known as Uptake, Apoptosis, Amplification, Necrosis and Karyopyknosis. Hematoxylin often locates in Body tissue, Extracellular, Compact bone, Skin and Basement membrane. The associated genes with HEMATOXYLIN are GAPDH gene, Genome, Elastin, MERTK wt Allele and P4HTM gene.
Cross Reference
Introduction
To understand associated biological information of HEMATOXYLIN, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.
What diseases are associated with HEMATOXYLIN?
HEMATOXYLIN is suspected in Senile Plaques, Eosinophilia, Duodenal Adenoma, Morphologically altered structure, Cervical abscess and other diseases in descending order of the highest number of associated sentences.
Related references are mostly published in these journals:
| Disease | Cross reference | Weighted score | Related literature |
|---|
Possible diseases from mapped MeSH terms on references
We collected disease MeSH terms mapped to the references associated with HEMATOXYLIN
PubChem Associated disorders and diseases
What pathways are associated with HEMATOXYLIN
There are no associated biomedical information in the current reference collection.
PubChem Biomolecular Interactions and Pathways
Link to PubChem Biomolecular Interactions and PathwaysWhat cellular locations are associated with HEMATOXYLIN?
Visualization in cellular structure
Associated locations are in red color. Not associated locations are in black.
Related references are published most in these journals:
- Am. J. Physiol. Heart Circ. Physiol. (3)
- Proc. Natl. Acad. Sci. U.S.A. (1)
- Stem Cells Transl Med (1)
- Others (13)
| Location | Cross reference | Weighted score | Related literatures |
|---|
What functions are associated with HEMATOXYLIN?
Related references are published most in these journals:
| Function | Cross reference | Weighted score | Related literatures |
|---|
What lipids are associated with HEMATOXYLIN?
There are no associated biomedical information in the current reference collection.
What genes are associated with HEMATOXYLIN?
Related references are published most in these journals:
| Gene | Cross reference | Weighted score | Related literatures |
|---|
What common seen animal models are associated with HEMATOXYLIN?
There are no associated biomedical information in the current reference collection.
NCBI Entrez Crosslinks
All references with HEMATOXYLIN
Download all related citations| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Rothkamm K et al. | In situ biological dose mapping estimates the radiation burden delivered to 'spared' tissue between synchrotron X-ray microbeam radiotherapy tracks. | 2012 | PLoS ONE | pmid:22238667 |
| Giaretti W et al. | Genomic aberrations in normal appearing mucosa fields distal from oral potentially malignant lesions. | 2012 | Cell Oncol (Dordr) | pmid:22144094 |
| Zhang Z et al. | Diagnostic significance of immunocytochemistry on fine needle aspiration biopsies processed by thin-layer cytology. | 2012 | Diagn. Cytopathol. | pmid:21563326 |
| Hůlková H and Elleder M | Distinctive histopathological features that support a diagnosis of cholesterol ester storage disease in liver biopsy specimens. | 2012 | Histopathology | pmid:22621222 |
| Tian L et al. | AAV2-mediated combined subretinal delivery of IFN-α and IL-4 reduces the severity of experimental autoimmune uveoretinitis. | 2012 | PLoS ONE | pmid:22685550 |
| Klinge U and Klosterhalfen B | Modified classification of surgical meshes for hernia repair based on the analyses of 1,000 explanted meshes. | 2012 | Hernia | pmid:22562353 |
| Kerecuk L et al. | Expression of Fraser syndrome genes in normal and polycystic murine kidneys. | 2012 | Pediatr. Nephrol. | pmid:21993971 |
| Binello E et al. | Stemness of the CT-2A Immunocompetent Mouse Brain Tumor Model: Characterization In Vitro. | 2012 | J Cancer | pmid:22514559 |
| Ten Berge B et al. | Evidence for local dendritic cell activation in pulmonary sarcoidosis. | 2012 | Respir. Res. | pmid:22513006 |
| Di Bari MA et al. | The mouse model for scrapie: inoculation, clinical scoring, and histopathological techniques. | 2012 | Methods Mol. Biol. | pmid:22528109 |
| Hua Y et al. | IGF-1 deficiency resists cardiac hypertrophy and myocardial contractile dysfunction: role of microRNA-1 and microRNA-133a. | 2012 | J. Cell. Mol. Med. | pmid:21418519 |
| Jacob F et al. | Loss of secreted frizzled-related protein 4 correlates with an aggressive phenotype and predicts poor outcome in ovarian cancer patients. | 2012 | PLoS ONE | pmid:22363760 |
| Manning L et al. | A histopathologic study of fatal paediatric cerebral malaria caused by mixed Plasmodium falciparum/Plasmodium vivax infections. | 2012 | Malar. J. | pmid:22472013 |
| Onul A et al. | Application of immunohistochemical staining to detect antigen destruction as a measure of tissue damage. | 2012 | J. Histochem. Cytochem. | pmid:22723525 |
| Galve J et al. | A 32-year-old man with grouped papules and vesicles. | 2012 | Arch Dermatol | pmid:22801624 |
| Akhmetshina A et al. | Activation of canonical Wnt signalling is required for TGF-β-mediated fibrosis. | 2012 | Nat Commun | pmid:22415826 |
| Nowaczyk P et al. | Analysis of sentinel lymph node biopsy results in colon cancer in regard of the anthropometric features of the population and body composition assessment formulas. | 2012 | Langenbecks Arch Surg | pmid:22415154 |
| Cornish GH et al. | Tissue specific deletion of inhibitor of kappa B kinase 2 with OX40-Cre reveals the unanticipated expression from the OX40 locus in skin epidermis. | 2012 | PLoS ONE | pmid:22363815 |
| Faga A et al. | Effects of thermal water on skin regeneration. | 2012 | Int. J. Mol. Med. | pmid:22344563 |
| Kawai C et al. | A novel mutation of human liver alanine:glyoxylate aminotransferase causes primary hyperoxaluria type 1: immunohistochemical quantification and subcellular distribution. | 2012 | Acta Histochem Cytochem | pmid:22685354 |