The effects of sodium butyrate on transcription are mediated through activation of a protein phosphatase.

PubWeight™: 0.93‹?›

🔗 View Article (PMID 9305863)

Published in J Biol Chem on September 26, 1997

Authors

L Cuisset1, L Tichonicky, P Jaffray, M Delpech

Author Affiliations

1: Laboratoire de Biologie Moléculaire des Cellules Eucaryotes, I.C.G. M-EA 1501, Université Paris V, René Descartes, Faculté de Médecine Cochin Port-Royal, 24 rue du Faubourg Saint-Jacques, 75014 Paris, France.

Articles by these authors

Association of TNF2, a TNF-alpha promoter polymorphism, with septic shock susceptibility and mortality: a multicenter study. JAMA (1999) 3.51

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group. Nat Genet (1999) 3.44

Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44. Am J Hum Genet (1999) 1.68

Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A gene. Ann Rheum Dis (2006) 1.67

Factor VIII gene inversions in severe hemophilia A: results of an international consortium study. Blood (1995) 1.59

Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). Hum Mol Genet (1998) 1.55

MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications. Am J Hum Genet (1999) 1.44

Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome. Eur J Hum Genet (2001) 1.34

Mutations in the autoinflammatory cryopyrin-associated periodic syndrome gene: epidemiological study and lessons from eight years of genetic analysis in France. Ann Rheum Dis (2010) 1.26

Clinical versus genetic diagnosis of familial Mediterranean fever. QJM (2000) 1.17

Molecular analysis of the mevalonate kinase gene in a cohort of patients with the hyper-igd and periodic fever syndrome: its application as a diagnostic tool. Ann Intern Med (2001) 1.11

Detoxification of reactive oxygen species by a nonpeptidyl mimic of superoxide dismutase cures acetaminophen-induced acute liver failure in the mouse. Hepatology (2001) 1.11

Structural features of the central cannabinoid CB1 receptor involved in the binding of the specific CB1 antagonist SR 141716A. J Biol Chem (1996) 1.09

Nucleotide sequence of the bla(RTG-2) (CARB-5) gene and phylogeny of a new group of carbenicillinases. Antimicrob Agents Chemother (2000) 1.08

The superoxide dismutase mimetic MnTBAP prevents Fas-induced acute liver failure in the mouse. Gastroenterology (2001) 1.07

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1. Am J Pathol (1999) 1.05

Characterization and nucleotide sequence of CARB-6, a new carbenicillin-hydrolyzing beta-lactamase from Vibrio cholerae. Antimicrob Agents Chemother (1999) 1.03

Diagnostic value of serum immunoglobulinaemia D level in patients with a clinical suspicion of hyper IgD syndrome. Rheumatology (Oxford) (2007) 1.01

Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid Communication. Kidney Int (2001) 0.98

Histologic phenotype-genotype correlation of corneal dystrophies associated with eight distinct mutations in the TGFBI gene. Ophthalmology (2001) 0.97

A new mutation (A546T) of the betaig-h3 gene responsible for a French lattice corneal dystrophy type IIIA. Am J Ophthalmol (2000) 0.97

Monoclonal antibodies to the human immunodeficiency virus p18 protein cross-react with normal human tissues. AIDS (1988) 0.96

Characterization, purification and cDNA cloning of a rat perchloric-acid-soluble 23-kDa protein present only in liver and kidney. Eur J Biochem (1993) 0.94

Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations. Eur J Hum Genet (2001) 0.94

Interleukin 1 gene cluster polymorphisms in multiplex families with spondylarthropathies. Cytokine (2001) 0.93

A novel variant of granular corneal dystrophy caused by association of 2 mutations in the TGFBI gene-R124L and DeltaT125-DeltaE126. Arch Ophthalmol (2000) 0.93

Fas/CD95 pathway induces mouse liver regeneration and allows for highly efficient retrovirus-mediated gene transfer. Hepatology (2001) 0.92

Dual intracellular signaling pathways mediated by the human cannabinoid CB1 receptor. Eur J Pharmacol (1999) 0.92

Clinical, histologic, and ultrastructural features of the corneal dystrophy caused by the R124L mutation of the BIGH3 gene. Ophthalmology (2000) 0.90

Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial Mediterranean fever. Am J Med Genet (2000) 0.90

A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family. Arthritis Rheum (2000) 0.89

Preliminary clinical studies of a biological skin equivalent in burned patients. Burns Incl Therm Inj (1988) 0.88

Hereditary fevers. Curr Opin Rheumatol (1999) 0.88

Renal amyloidosis with a frame shift mutation in fibrinogen aalpha-chain gene producing a novel amyloid protein. Blood (1997) 0.88

Presence of non-histone proteins in nucleosomes. Eur J Biochem (1978) 0.87

Expression of c-fos oncogene during hepatocarcinogenesis, liver regeneration and in synchronized HTC cells. Exp Cell Res (1985) 0.87

Selective inhibition by sodium butyrate of glucocorticoid-induced tyrosine aminotransferase synthesis in hepatoma tissue-cultured cells. Eur J Biochem (1981) 0.87

Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu). Neurology (2001) 0.87

[Molecular and cellular action of butyrate]. C R Seances Soc Biol Fil (1992) 0.86

Spontaneous transient outward currents and delayed rectifier K+ current: effects of hypoxia. Am J Physiol (1998) 0.84

PEG1 expression in maternal uniparental disomy 7. Ann Genet (1997) 0.84

Correlated increase of the expression of the c-ras genes in chemically induced hepatocarcinomas. Biochem Biophys Res Commun (1984) 0.84

Increased level of the mitochondrial ND5 transcript in chemically induced rat hepatomas. Exp Cell Res (1989) 0.84

Changes in some chromatin and cytoplasmic enzymes of perinatal rat hepatocytes during culture. In Vitro (1980) 0.83

Effects of dexamethasone on the growth of cultured rabbit articular chondrocytes:relation with the nuclear glucocorticoid-receptor complex. Ann Rheum Dis (1987) 0.83

Characteristics of homogeneously small keratinocytes from newborn rat skin: possible epidermal stem cells. Am J Physiol (1991) 0.83

Rat liver nuclear protein kinases NI and NII. Purification, subunit composition, substrate specificity, possible levels of regulation. Eur J Biochem (1986) 0.82

Nuclear accumulation of HMG1 protein is correlated to DNA synthesis. Biol Cell (1986) 0.82

Hypoxia enhances agonist-induced pulmonary arterial contraction by increasing calcium sequestration. Am J Physiol (1997) 0.81

Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndrome. J Med Genet (1999) 0.81

CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromes. Dermatology (2003) 0.80

Single-strandedness of the majority of DNA sequences complementary to mRNA-coding sites isolated from rat hepatoma tissue cultured cells. Exp Cell Res (1981) 0.80

Characterization of an arginine-specific protein kinase tightly bound to rat liver DNA. Eur J Biochem (1987) 0.80

A protein phosphatase is involved in the inhibition of histone deacetylation by sodium butyrate. Biochem Biophys Res Commun (1998) 0.80

Epidermal keratinocyte-derived basophil promoting activity. Role of interleukin 3 and soluble CD23. J Clin Invest (1992) 0.80

Expression of human F8B, a gene nested within the coagulation factor VIII gene, produces multiple eye defects and developmental alterations in chimeric and transgenic mice. Hum Mol Genet (1999) 0.80

Effects of donor's age on growth kinetics of rabbit articular chondrocytes in culture. Mech Ageing Dev (1983) 0.79

Complement component C4 deficiencies and gene alterations in patients with systemic lupus erythematosus. Eur J Immunogenet (1993) 0.79

Study of C4A mRNA in mononuclear blood cells from a patient with SLE and C4A homozygous deficiency without C4A gene deletion. Clin Exp Rheumatol (1995) 0.79

Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female. Blood (2000) 0.79

Localization of phosphoproteins and of protein kinases in chromatin from butyrate treated HTC cells. Biochem Biophys Res Commun (1980) 0.79

Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria. Hum Genet (1990) 0.79

Genotypic diagnosis of familial Mediterranean fever (FMF) using new microsatellite markers: example of two extensive non-Ashkenazi Jewish pedigrees. J Med Genet (1997) 0.79

Proliferation kinetics of rabbit articular chondrocytes in primary culture and at the first passage. Cell Tissue Kinet (1983) 0.79

Multiple forms of protein kinase in liver cell. II. Nuclear kinases and cytosol phosvitin kinase. Biochimie (1974) 0.79

Purification and comparison of liver microsomal flavin-containing monooxygenase from normal and streptozotocin-diabetic rats. Biochem Pharmacol (1988) 0.78

The small chromatin fragments released by micrococcal nuclease from hepatoma tissue cultured cell nuclei are strongly enriched in coding DNA sequences and are related to an actively transcribed single-stranded DNA fraction. Biochim Biophys Acta (1982) 0.78

Separation of nuclear cAMP independent protein kinases NI and NII from their chromosomal protein substrates and enzyme inhibitors by the use of a casein-phosvitin-Sepharose column. Anal Biochem (1986) 0.78

Analysis of the complete coding region of the CFTR gene in ten Algerian cystic fibrosis families. Hum Hered (1999) 0.78

DNA sequences homologous to mitochondrial genes in nuclei from normal rat tissues and from rat hepatoma cells. Biochem Biophys Res Commun (1989) 0.78

A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia A. Hum Mutat (1992) 0.78

[Tumor necrosis factor receptor superfamily 1A-associated periodic syndrome (TRAPS)]. Rev Med Interne (2003) 0.78

Effect of sodium butyrate on chromatin structure. Biochem Biophys Res Commun (1980) 0.78

Localization of phosphoproteins and of protein kinases in chromatin from hepatoma tissue-cultured cells. Eur J Biochem (1980) 0.77

Potential pitfall in Prader-Willi syndrome and Angelman syndrome molecular diagnosis. Am J Med Genet (1998) 0.77

Effect of sodium cis-beta-4-methoxybenzoyl-beta-bromacrylate (Cytembena) on HeLa cell kinetics. Cancer Res (1982) 0.77

Hepatocyte chromosomal non-histone proteins in developing rats. Eur J Biochem (1979) 0.77

Early reversible nuclear alterations induced by sodium butyrate in cultured hepatoma cells. Cell Biol Int Rep (1980) 0.77

[Proposed law on protection of personal rights concerning personal information. Position of the French National Civil Rights Commission (CCTIR)]. Rev Epidemiol Sante Publique (2003) 0.77

[Cancer genetics: estimation of the needs of the population in France for the next ten years]. Bull Cancer (2009) 0.77

Chromatin protein kinases and phosphoproteins during myoblast growth and differentiation. Biochem Biophys Res Commun (1978) 0.77

Isolation and characterization of complementary DNA clones for genes overexpressed in chemically induced rat hepatomas. Cancer Res (1986) 0.77

A transcriptional Map of the FMF region. Genomics (1998) 0.77

Upregulation of rat P23 (a member of the YjgF protein family) by fasting, glucose diet and fatty acid feeding. Cell Mol Life Sci (2004) 0.76

In vitro, non enzymatic labelling of histone H1 with [14C] acetyl CoA. Biochimie (1983) 0.76

Molecular studies of liver aldolase B in hereditary fructose intolerance using blotting and immunological techniques. Ann Hum Genet (1982) 0.76

Fibrinogen A alpha chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French family. Amyloid (1998) 0.75

A novel variant of transthyretin (Glu42Asp) associated with sporadic late-onset cardiac amyloidosis. Amyloid (1998) 0.75

Effects of D-penicillamine on growth and cell cycle kinetics of cultured rabbit articular chondrocytes. Ann Rheum Dis (1984) 0.75

RNAs containing mitochondrial ND6 and COI sequences present an abnormal structure in chemically induced rat hepatomas. Nucleic Acids Res (1989) 0.75

A new TaqI allele at DXS52 frequent in Algeria. Nucleic Acids Res (1989) 0.75

Interleukin-1 beta-mediated glucose uptake by chondrocytes. Inhibition by cortisol. Osteoarthritis Cartilage (1996) 0.75

Mechanism of action of specific soluble inhibitors of protein synthesis in differentiated cells. Biochimie (1972) 0.75

[Acidic protein extracted from liver cell cytoplasm which inhibits the cell-free synthesis of hemoglobin]. Biochim Biophys Acta (1970) 0.75

Isolation of a reticulocyte protein which specifically inhibits the cell free synthesis of liver proteins. Biochimie (1971) 0.75

[Glycated hemoglobin: assay methods and problems of standardization]. Ann Biol Clin (Paris) (1994) 0.75

[Comparison of the proteins of chromatin from the nucleus and cytoplasm, and of RNA from 3 types of differentiated cells]. Bull Soc Chim Biol (Paris) (1970) 0.75

[Histones, acid proteins of chromatin and biosynthesis of hemoglobin]. Bull Soc Chim Biol (Paris) (1970) 0.75