CYTOCHALASIN B

CYTOCHALASIN B is a lipid of Polyketides (PK) class. Cytochalasin b is associated with abnormalities such as Renal tubular disorder and Chagas Disease. The involved functions are known as Membrane Protein Traffic, inhibitors, Metabolic Inhibition, Biochemical Pathway and Increased Sensitivy. Cytochalasin b often locates in Cytoplasmic matrix, Plasma membrane, Microtubules, Extracellular and Protoplasm. The associated genes with CYTOCHALASIN B are SLC2A2 gene, PFDN5 gene, SLC2A1 gene, OMG gene and SPEN gene. The related lipids are Steroids, Lipopolysaccharides and Liposomes. The related experimental models are Xenograft Model.

Cross Reference

Introduction

To understand associated biological information of CYTOCHALASIN B, 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 CYTOCHALASIN B?

CYTOCHALASIN B is suspected in Renal tubular disorder, Chagas Disease 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
Loading... please refresh the page if content is not showing up.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with CYTOCHALASIN B

MeSH term MeSH ID Detail
Congenital Abnormalities D000013 11 associated lipids
Adenocarcinoma D000230 166 associated lipids
Alzheimer Disease D000544 76 associated lipids
Anemia D000740 21 associated lipids
Arteriosclerosis D001161 86 associated lipids
Asthma D001249 52 associated lipids
Ataxia Telangiectasia D001260 6 associated lipids
Birth Weight D001724 23 associated lipids
Body Weight D001835 333 associated lipids
Burkitt Lymphoma D002051 15 associated lipids
Carbon Monoxide Poisoning D002249 9 associated lipids
Carcinoma 256, Walker D002279 22 associated lipids
Cell Transformation, Neoplastic D002471 126 associated lipids
Cell Transformation, Viral D002472 26 associated lipids
Chancroid D002602 4 associated lipids
Chondrosarcoma D002813 9 associated lipids
Colonic Neoplasms D003110 161 associated lipids
Dermatitis, Contact D003877 59 associated lipids
Diabetes Mellitus D003920 90 associated lipids
Diabetes Mellitus, Experimental D003921 85 associated lipids
Per page 10 20 50 100 | Total 79

PubChem Associated disorders and diseases

What pathways are associated with CYTOCHALASIN B

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with CYTOCHALASIN B?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
Loading... please refresh the page if content is not showing up.

What functions are associated with CYTOCHALASIN B?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with CYTOCHALASIN B?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
Loading... please refresh the page if content is not showing up.

What genes are associated with CYTOCHALASIN B?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with CYTOCHALASIN B?

Xenograft Model

Xenograft Model are used in the study 'Endofacial competitive inhibition of the glucose transporter 1 activity by gossypol.' (Pérez A et al., 2009).

Related references are published most in these journals:

Model Cross reference Weighted score Related literatures
Loading... please refresh the page if content is not showing up.

NCBI Entrez Crosslinks

All references with CYTOCHALASIN B

Download all related citations
Per page 10 20 50 100 | Total 4982
Authors Title Published Journal PubMed Link
Ciaraldi TP et al. Insulin-stimulated glucose transport in human adipocytes. 1979 Am. J. Physiol. pmid:443417
King PA et al. Glucose transport in skeletal muscle membrane vesicles from control and exercised rats. 1989 Am. J. Physiol. pmid:2610251
Singhal PC et al. Effects of vasoactive agents on uptake of immunoglobulin G complexes by mesangial cells. 1990 Am. J. Physiol. pmid:2156448
Renfro JL Calcium transport across peritubular surface of the marine teleost renal tubule. 1978 Am. J. Physiol. pmid:665777
Garland A et al. Activated eosinophils elicit substance P release from cultured dorsal root ganglion neurons. 1997 Am. J. Physiol. pmid:9374740
She ZW et al. Tumor necrosis factor primes neutrophils for hypochlorous acid production. 1989 Am. J. Physiol. pmid:2558582
Singhal PC et al. Endocytosis by cultured mesangial cells and associated changes in prostaglandin E2 synthesis. 1987 Am. J. Physiol. pmid:3105331
Mullin JM et al. Isolation of mutant renal (LLC-PK1) epithelia defective in basolateral, Na(+)-independent glucose transport. 1989 Am. J. Physiol. pmid:2603953
Mills JW and Lubin M Effect of adenosine 3',5'-cyclic monophosphate on volume and cytoskeleton of MDCK cells. 1986 Am. J. Physiol. pmid:3006500
Feuilloley M et al. Effects of selective disruption of cytoskeletal elements on steroid secretion by human adrenocortical slices. 1994 Am. J. Physiol. pmid:8141278
Renfro JL and Shustock E Peritubular uptake and brush border transport of 28Mg by flounder renal tubules. 1985 Am. J. Physiol. pmid:2413774
Hardy MA and DiBona DR Microfilaments and the hydrosmotic action of vasopressin in toad urinary bladder. 1982 Am. J. Physiol. pmid:6810708
Rosholt MN et al. High-fat diet reduces glucose transporter responses to both insulin and exercise. 1994 Am. J. Physiol. pmid:8304561
Johnson LW and Smith CH Monosaccharide transport across microvillous membrane of human placenta. 1980 Am. J. Physiol. pmid:6990781
Muller J and Kachadorian WA Aggregate-carrying membranes during ADH stimulation and washout in toad bladder. 1984 Am. J. Physiol. pmid:6430101
Mattana J and Singhal PC Macrophage Fc receptor activity modulates mesangial cell proliferation and matrix synthesis. 1994 Am. J. Physiol. pmid:8184889
Grisham MB et al. Endotoxemia and neutrophil activation in vivo. 1988 Am. J. Physiol. pmid:2834968
Goodyear LJ et al. Glucose transporter number, activity, and isoform content in plasma membranes of red and white skeletal muscle. 1991 Am. J. Physiol. pmid:1951679
Carter-Su C and Okamoto K Effect of insulin and glucocorticoids on glucose transporters in rat adipocytes. 1987 Am. J. Physiol. pmid:3551626
Reshkin SJ and Ahearn GA Basolateral glucose transport by intestine of teleost, Oreochromis mossambicus. 1987 Am. J. Physiol. pmid:3030144
Craik JD et al. GLUT-1 mediation of rapid glucose transport in dolphin (Tursiops truncatus) red blood cells. 1998 Am. J. Physiol. pmid:9458906
Mullin JM et al. Basolateral 3-O-methylglucose transport by cultured kidney (LLC-PK1) epithelial cells. 1992 Am. J. Physiol. pmid:1558165
Barnard RJ et al. Effects of maturation and aging on the skeletal muscle glucose transport system. 1992 Am. J. Physiol. pmid:1590372
Mercado CL et al. Enhanced glucose transport in response to inhibition of respiration in Clone 9 cells. 1989 Am. J. Physiol. pmid:2750888
Schneyer LH Differential effects of cytochalasin B on Na and K transport in a perfused salivary duct. 1974 Am. J. Physiol. pmid:4412815
Valant P and Erlij D K+-stimulated sugar uptake in skeletal muscle: role of cytoplasmic Ca2+. 1983 Am. J. Physiol. pmid:6346894
Malaisse WJ et al. Insulinotropic action of alpha-D-glucose pentaacetate: functional aspects. 1997 Am. J. Physiol. pmid:9435523
Lipowsky HH et al. Leukocyte rolling velocity and its relation to leukocyte-endothelium adhesion and cell deformability. 1996 Am. J. Physiol. pmid:8967378
Peralta Soler A et al. Tissue remodeling during tumor necrosis factor-induced apoptosis in LLC-PK1 renal epithelial cells. 1996 Am. J. Physiol. pmid:8928850
Sakaida I et al. Phospholipid metabolism and intracellular Ca2+ homeostasis in cultured rat hepatocytes intoxicated with cyanide. 1992 Am. J. Physiol. pmid:1415517
Grinstein S et al. Phorbol ester-induced changes of cytoplasmic pH in neutrophils: role of exocytosis in Na+-H+ exchange. 1985 Am. J. Physiol. pmid:2579574
Wright G and Hurn E Cytochalasin inhibition of slow tension increase in rat aortic rings. 1994 Am. J. Physiol. pmid:7943389
Sumpio BE and Maack T Kinetics, competition, and selectivity of tubular absorption of proteins. 1982 Am. J. Physiol. pmid:7124951
Henquin JC and Lambert AE Bicarbonate modulation of glucose-9nduced biphasic insulin release by rat islets. 1976 Am. J. Physiol. pmid:788525
Youn JH et al. Calcium stimulates glucose transport in skeletal muscle by a pathway independent of contraction. 1991 Am. J. Physiol. pmid:2003578
Stetson DL and Steinmetz PR Role of membrane fusion in CO2 stimulation of proton secretion by turtle bladder. 1983 Am. J. Physiol. pmid:6408926
Bentzel CJ et al. Cytoplasmic regulation of tight-junction permeability: effect of plant cytokinins. 1980 Am. J. Physiol. pmid:7435552
Ismail-Beigi F et al. Stimulation of glucose transport in Clone 9 cells by exposure to alkaline pH. 1990 Am. J. Physiol. pmid:2305872
Kimmich GA et al. Energetics of Na+-dependent sugar transport by isolated intestinal cells: evidence for a major role for membrane potentials. 1977 Am. J. Physiol. pmid:562624
Wang WH et al. Involvement of actin cytoskeleton in modulation of apical K channel activity in rat collecting duct. 1994 Am. J. Physiol. pmid:7943357
Tseng S et al. F-actin disruption attenuates agonist-induced [Ca2+], myosin phosphorylation, and force in smooth muscle. 1997 Am. J. Physiol. pmid:9227425
Salans LB et al. Effects of dietary composition on glucose metabolism in rat adipose cells. 1981 Am. J. Physiol. pmid:7008628
Strek ME et al. Effect of mode of activation of human eosinophils on tracheal smooth muscle contraction in guinea pigs. 1993 Am. J. Physiol. pmid:8498524
Ajubi NE et al. Signal transduction pathways involved in fluid flow-induced PGE2 production by cultured osteocytes. 1999 Am. J. Physiol. pmid:9886964
Goldblum SE et al. TNF-alpha induces endothelial cell F-actin depolymerization, new actin synthesis, and barrier dysfunction. 1993 Am. J. Physiol. pmid:8476021
Franceschi RT et al. Requirement for Na(+)-dependent ascorbic acid transport in osteoblast function. 1995 Am. J. Physiol. pmid:7611363
Longo N et al. Influx and efflux of 3-O-methyl-D-glucose by cultured human fibroblasts. 1988 Am. J. Physiol. pmid:3364550
Cheung PT and Hammerman MR Na+-independent D-glucose transport in rabbit renal basolateral membranes. 1988 Am. J. Physiol. pmid:3364579
Guerin MA and Loizzi RF Inhibition of mammary gland lactose secretion by colchicine and vincristine. 1978 Am. J. Physiol. pmid:645891
Kachadorian WA et al. Possible roles for microtubules and microfilaments in ADH action on toad urinary bladder. 1979 Am. J. Physiol. pmid:107810