C. Beaumont

发表

Serum ferritin as a possible marker of the hemochromatosis allele.

R. Fauchet, C. Beaumont, M. Simon, 1979, The New England journal of medicine.

Two novel mutations in the L ferritin coding sequence associated with benign hyperferritinaemia unmasked by glycosylated ferritin assay

C. Beaumont, B. Grandchamp, V. Thurlow, 2012, Annals of clinical biochemistry.

Bilateral cataract and high serum ferritin: a new dominant genetic disorder?

C. Beaumont, D. Bonneau, D. Oriot, 1995 .

Bilateral cataract and high serum ferritin: a new dominant genetic disorder?

C. Beaumont, D. Bonneau, D. Oriot, 1995, Journal of medical genetics.

Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract

C. Beaumont, J. Scoazec, D. Bonneau, 1995, Nature Genetics.

Analysis of Ferritins in Lymphoblastoid Cell Lines and in the Lens of Subjects With Hereditary Hyperferritinemia-Cataract Syndrome

D. Girelli, C. Beaumont, F. Perrone, 1998 .

Hemolytic anemia repressed hepcidin level without hepatocyte iron overload: lesson from Günther disease model

C. Beaumont, C. Ged, T. Lefèbvre, 2017, Haematologica.

Maintenance and reversibility of active albumin secretion by adult rat hepatocytes co-cultured with another liver epithelial cell type.

A. Guillouzo, C. Beaumont, C. Guguen-Guillouzo, 1983, Experimental cell research.

Hepcidin and anemia of the critically ill patient: bench to bedside.

C. Beaumont, S. Lasocki, D. Longrois, 2011, Anesthesiology.

Erythropoietin stimulates spleen BMP4-dependent stress erythropoiesis and partially corrects anemia in a mouse model of generalized inflammation.

C. Beaumont, S. Lasocki, Z. Karim, 2010, Blood.

Inactive matriptase‐2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activity

C. Beaumont, C. Oudin, B. Grandchamp, 2012, Human mutation.

Intestinal DMT1 cotransporter is down-regulated by hepcidin via proteasome internalization and degradation.

C. Beaumont, A. Bado, Z. Karim, 2011, Gastroenterology.

Late introduction of sirolimus induces anemia in renal transplant recipients.

C. Beaumont, E. Morelon, O. Thaunat, 2007, Transplantation.

Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyria.

C. Beaumont, P. Romeo, B. Grandchamp, 1986, The Journal of clinical investigation.

Hepcidin and Anemia of the Critically Ill Patient: Bench to Bedside

C. Beaumont, S. Lasocki, D. Longrois, 2011 .

The mouse porphobilinogen deaminase gene. Structural organization, sequence, and transcriptional analysis.

C. Beaumont, B. Grandchamp, Y. Nordmann, 1989, The Journal of biological chemistry.

Epistasis in iron metabolism: complex interactions between Cp, Mon1a, and Slc40a1 loci and tissue iron in mice

C. Beaumont, J. Deybach, L. Gouya, 2013, Mammalian Genome.

Genetic study of variation in normal mouse iron homeostasis reveals ceruloplasmin as an HFE-hemochromatosis modifier gene.

C. Beaumont, J. Deybach, L. Gouya, 2007, Gastroenterology.

Impaired retinal iron homeostasis associated with defective phagocytosis in Royal College of Surgeons rats.

C. Sergeant, X. Guillonneau, Y. Courtois, 2002, Investigative ophthalmology & visual science.

Inactivation of Iron Responsive Element–binding Capacity and Aconitase Function of Iron Regulatory Protein-1 of Skin Cells by Ultraviolet A

C. Beaumont, P. Morlière, R. Santus, 2000, Photochemistry and photobiology.

Denaturing gradient gel electrophoresis screening for mutations in the hereditary hyperferritinaemia cataract syndrome

C. Beaumont, G. Hetet, J. Schved, 2001, British journal of haematology.

Overexpression of the ferritin H subunit in cultured erythroid cells changes the intracellular iron distribution.

M. Hentze, C. Beaumont, B. Grandchamp, 1996, Blood.

A hemin-inducible enhancer lies 4.5 Kb upstream of the mouse ferritin H subunit gene.

C. Beaumont, A. Seyhan, B. Grandchamp, 1994, Advances in experimental medicine and biology.

Light-induced retinal degeneration correlates with changes in iron metabolism gene expression, ferritin level, and aging.

Y. Courtois, F. Behar-Cohen, C. Beaumont, 2011, Investigative ophthalmology & visual science.

LC-MS/MS method for hepcidin-25 measurement in human and mouse serum: clinical and research implications in iron disorders

C. Beaumont, T. Lefèbvre, L. Gouya, 2015, Clinical chemistry and laboratory medicine.

Monoclonal immunoglobulin with antitransferrin activity: A rare cause of hypersideremia with increased transferrin saturation.

C. Beaumont, M. Alyanakian, J. Delanghe, 2007, Blood.

Function and regulation of transferrin and ferritin.

C. Beaumont, D. Richardson, P. Ponka, 1998, Seminars in hematology.

[Iron therapy: Indications, limitations and modality].

J. Pouchot, C. Beaumont, S. Lasocki, 2013, La Revue de medecine interne.

Transcriptional regulation of ferritin H and L subunits in adult erythroid and liver cells from the mouse. Unambiguous identification of mouse ferritin subunits and in vitro formation of the ferritin shells.

C. Beaumont, B. Grandchamp, F. Renaudie, 1989, The Journal of biological chemistry.

Iron Insufficiency Compromises Motor Neurons and Their Mitochondrial Function in Irp2-Null Mice

James B. Mitchell, R. Sougrat, C. Beaumont, 2011, PloS one.

Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single gene.

C. Beaumont, B. Grandchamp, O. Walter, 1987, European journal of biochemistry.

Molecular mechanisms of the defective hepcidin inhibition in TMPRSS6 mutations associated with iron-refractory iron deficiency anemia.

C. Beaumont, C. Oudin, B. Grandchamp, 2009, Blood.

Two nonsense mutations in the TMPRSS6 gene in a patient with microcytic anemia and iron deficiency.

C. Beaumont, B. Grandchamp, M. Westerman, 2008, Blood.

Immunoassay for human serum hemojuvelin

C. Beaumont, A. Lavoinne, B. Grandchamp, 2010, Haematologica.

Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis.

C. Beaumont, B. Grandchamp, J. Wagner, 2006, Clinical and laboratory haematology.

Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans.

C. Beaumont, P. Brissot, D. Valla, 2016, Gastroenterology.

Heterozygous Mutations in BMP 6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans Running title : BMP 6 , gene for moderate hemochromatosis

C. Beaumont, P. Brissot, D. Valla, 2016 .

Severe iron deficiency anemia in transgenic mice expressing liver hepcidin

C. Beaumont, B. Grandchamp, S. Vaulont, 2002, Proceedings of the National Academy of Sciences of the United States of America.

A physiological model to study iron recycling in macrophages.

C. Beaumont, B. Grandchamp, G. Hetet, 2005, Experimental cell research.

Assessment of liver iron content in 271 patients: A reevaluation of direct and indirect methods

Michel Bourel, C. Beaumont, M. Simon, 1981 .

Assessment of liver iron content in 271 patients: a reevaluation of direct and indirect methods.

C. Beaumont, M. Simon, P. Brissot, 1981, Gastroenterology.

Efficacy and toxicity of intravenous iron in a mouse model of critical care anemia*

E. Denamur, C. Beaumont, S. Lasocki, 2012, Critical care medicine.

Wild-type and mutant ferroportins do not form oligomers in transfected cells.

C. Beaumont, G. Hetet, C. Delaby, 2006, The Biochemical journal.

microcytic anemia and iron deficiency Two nonsense mutations in the TMPRSS6 gene in a patient with

C. Beaumont, B. Grandchamp, M. Westerman, 2013 .

Hepcidin levels in hereditary hyperferritinemia: Insights into the iron-sensing mechanism in hepatocytes.

C. Beaumont, M. Thursz, M. Busbridge, 2010, World journal of gastroenterology.

Not all DMT1 mutations lead to iron overload.

C. Beaumont, B. Grandchamp, C. Kannengiesser, 2009, Blood cells, molecules & diseases.

Natural history of recessive inheritance of DMT1 mutations.

C. Beaumont, A. Iolascon, D. Pospíšilová, 2008, The Journal of pediatrics.

Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload.

C. Beaumont, B. Grandchamp, G. Hetet, 2006, Blood.

Is the HLA‐linked haemochromatosis allele implicated in idiopathic refractory sideroblastic anaemia?

M. Krempf, R. Fauchet, B. Grosbois, 1985, British journal of haematology.

Idiopathic hemochromatosis: a study of biochemical expression in 247 heterozygous members of 63 families: evidence for a single major HLA-linked gene.

R. Fauchet, C. Beaumont, M. Simon, 1980, Gastroenterology.

HLA-linked hemochromatosis and sporadic porphyria cutanea tarda.

R. Fauchet, C. Beaumont, Y. Nordmann, 1986, Gastroenterology.

New variant of unclassified congenital dyserythropoietic anaemia: the concept of the erythroid regulator?

C. Beaumont, M. Fontenay, P. Mayeux, 2012, British journal of haematology.

Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis

N. Andrews, C. Beaumont, S. Vaulont, 2003, Nature Genetics.

Influence of garlic or its main active component diallyl disulfide on iron bioavailability and toxicity.

C. Beaumont, M. E. El May, M. Hamdaoui, 2010, Nutrition research.

Porphyria cutanea tarda and HLA-linked hemochromatosis. Evidence against a systematic association.

R. Fauchet, C. Beaumont, H. de Verneuil, 1987, Gastroenterology.

[Diagnosis of hypochromic microcytic anemia in children].

C. Beaumont, H. Puy, J. Bresson, 2012, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Can erythroblasts donate iron?

C. Beaumont, 2011, Blood.

Multiple regulatory mechanisms act in concert to control ferroportin expression and heme iron recycling by macrophages

C. Beaumont, 2010, Haematologica.

[How is iron prescribed in French ICUs: a practice survey].

C. Beaumont, S. Lasocki, P. Montravers, 2008, Annales francaises d'anesthesie et de reanimation.

Is EPO therapy able to correct iron deficiency anaemia caused by matriptase‐2 deficiency?

G. Velasco, C. Beaumont, B. Grandchamp, 2011, British journal of haematology.

Hepcidin, a key regulator of iron metabolism

C. Beaumont, S. Vaulont, G. Nicolas, 2003 .

Serum pantetheinase/vanin levels regulate erythrocyte homeostasis and severity of malaria.

C. Beaumont, A. Viallat, G. Chimini, 2015, The American journal of pathology.

Uroporphyrinogen decarboxylase structural mutant (Gly281----Glu) in a case of porphyria.

C. Beaumont, B. Grandchamp, H. de Verneuil, 1986, Science.

Transient overexpression of human H- and L-ferritin chains in COS cells.

C. Beaumont, F. Perrone, M. Bourgeois, 1998, The Biochemical journal.

A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria.

C. Beaumont, F. D. de Rooij, J. Deybach, 1989, Nucleic acids research.

Serum Iron Protects from Renal Postischemic Injury.

N. Câmara, C. Beaumont, E. Daugas, 2017, Journal of the American Society of Nephrology : JASN.

All normal rat hepatocytes produce albumin at a rate related to their degree of ploidy.

M. Rissel, A. Guillouzo, C. Beaumont, 1981, Biochemical and biophysical research communications.

Ferritin is increased in diethylnitrosamine-altered rat hepatocytes.

A. Guillouzo, C. Beaumont, M. Bourel, 1981, Biochemical and biophysical research communications.

Ultrastructural Localization of α-fetoprotein in isolated and cultured rat hepatocytes

M. Rissel, A. Guillouzo, C. Beaumont, 1981 .

Cellular and subcellular immunolocalization of alpha1-fetoprotein and albumin in rat liver. Reevaluation of various experimental conditions.

A. Guillouzo, C. Beaumont, J. Chiu, 1978, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Light and Electron Microscope Immunolocalization of Alpha‐fetoprotein in Rat Liver Cells in vivo and in vitro

A. Guillouzo, C. Beaumont, S. Fleischer, 1978 .

FETOPROTEIN AND ALBUMIN IN RAT LIVER. REEVALUATION OF VARIOUS EXPERIMENTAL CONDITIONS

A. Guillouzo, C. Beaumont, J. Chiu, 1978 .

A second ferritin L subunit is encoded by an intronless gene in the mouse

C. Beaumont, B. Grandchamp, F. Renaudie, 2004, Mammalian Genome.

Porphyria cutanea tarda and HLA-linked hemochromatosis

R. Fauchet, C. Beaumont, Y. Nordmann, 1987 .

Novel Properties of L-type Polypeptide Subunits in Mouse Ferritin Molecules (*)

C. Beaumont, F. Torti, S. Torti, 1996, The Journal of Biological Chemistry.

ALAS2 acts as a modiﬁer gene in patients with congenital erythropoietic porphyria

C. Beaumont, C. Ged, S. Ducamp, 2011 .

Porphobilinogen deaminase is unstable in the absence of its substrate.

C. Beaumont, B. Grandchamp, H. de Verneuil, 1986, Biochimica et biophysica acta.

Effects of succinylacetone on dimethylsulfoxide-mediated induction of heme pathway enzymes in mouse friend virus-transformed erythroleukemia cells.

C. Beaumont, J. Deybach, B. Grandchamp, 1984, Experimental cell research.

Antisense oligonucleotide-based therapy in human erythropoietic protoporphyria.

C. Beaumont, F. Moreau-Gaudry, J. Marie, 2014, American journal of human genetics.

Epistasis in iron metabolism: complex interactions between Cp, Mon1a, and Slc40a1 loci and tissue iron in mice

C. Beaumont, J. Deybach, L. Gouya, 2013, Mammalian Genome.

Mouse ferritin H multigene family is polymorphic and contains a single multiallelic functional gene located on chromosome 19.

J. Guénet, C. Beaumont, B. Grandchamp, 1991, Genomics.

Crystallization and preliminary X-ray diffraction data of mouse L-chain apoferritin crystals.

C. Beaumont, B. Gallois, A. Dautant, 2000, Acta crystallographica. Section D, Biological crystallography.

Iron metabolism, free radicals, and oxidative injury.

C. Beaumont, F. Trivin, J Emerit, 2001, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Ferritin heavy chain upregulation by NF-kappaB inhibits TNFalpha-induced apoptosis by suppressing reactive oxygen species.

Francesca Zazzeroni, Salvatore Papa, C. Beaumont, 2004, Cell.

Neuromelanin associated redox‐active iron is increased in the substantia nigra of patients with Parkinson's disease

E. Hirsch, Y. Agid, J. Hauw, 2003, Journal of neurochemistry.

Recycling iron in normal and pathological states.

C. Beaumont, C. Delaby, 2009, Seminars in hematology.

Targeting iron homeostasis induces cellular differentiation and synergizes with differentiating agents in acute myeloid leukemia

Philippe Dessen, Olivier Hermine, Nicolas Boissel, 2010, The Journal of experimental medicine.

A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload

C. Beaumont, P. Brissot, B. Grandchamp, 2009, Haematologica.

The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation.

Gaël Nicolas, Isabelle Devaux, C. Beaumont, 2002, The Journal of clinical investigation.

[Cloning, characterization and expression of mouse ferritin L subunit gene].

C. Beaumont, B. Grandchamp, L. Boulanger, 1995, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria.

C. Beaumont, J. Deybach, L. Gouya, 2006, American journal of human genetics.

Sideroblastic anemia: molecular analysis of the ALAS2 gene in a series of 29 probands and functional studies of 10 missense mutations

H. Heimpel, C. Beaumont, S. Ducamp, 2011, Human mutation.

overload H ferritin knockout mice: a model of hyperferritinemia in the absence of iron

C. Beaumont, G. Feldmann, M. Martín, 2013 .

H ferritin knockout mice: a model of hyperferritinemia in the absence of iron overload.

C. Beaumont, G. Feldmann, M. Martín, 2001, Blood.

Early Embryonic Lethality of H Ferritin Gene Deletion in Mice*

C. Beaumont, B. Grandchamp, P. Arosio, 2000, The Journal of Biological Chemistry.

H-ferritin subunit overexpression in erythroid cells reduces the oxidative stress response and induces multidrug resistance properties.

C. Beaumont, I. Slotki, W. Breuer, 1999, Blood.

Ferritin Heavy Chain Upregulation by NF-κB Inhibits TNFα-Induced Apoptosis by Suppressing Reactive Oxygen Species

Francesca Zazzeroni, Salvatore Papa, Suzy V. Torti, 2004, Cell.

Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice

C. Beaumont, B. Grandchamp, S. Vaulont, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Diagnostic accuracy of serum hepcidin for iron deficiency in critically ill patients with anemia

I. Boutron, G. Baron, C. Beaumont, 2010, Intensive Care Medicine.

Ferritin synthesis in differentiating Friend erythroleukemic cells.

S. Jain, C. Beaumont, Y. Nordmann, 1987, The Journal of biological chemistry.

Role of Ferritin in the Control of the Labile Iron Pool in Murine Erythroleukemia Cells*

C. Beaumont, Z. Cabantchik, V. Picard, 1998, The Journal of Biological Chemistry.

Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase allele.

C. Beaumont, J. Deybach, L. Gouya, 1996, American journal of human genetics.

Miscellaneous Iron-Related Disorders

C. Beaumont, 2012 .

Hepcidin, a new iron regulatory peptide.

C. Beaumont, S. Vaulont, A. Kahn, 2002, Blood cells, molecules & diseases.

Lack of up‐regulation of ferritin is associated with sustained iron regulatory protein‐1 binding activity in the substantia nigra of patients with Parkinson's disease

E. Hirsch, Y. Agid, J. Hauw, 2002, Journal of neurochemistry.

Iron metabolism in patients with anorexia nervosa: elevated serum hepcidin concentrations in the absence of inflammation.

C. Beaumont, H. Puy, B. Chevallier, 2012, The American journal of clinical nutrition.

Role for NF-κB in the Regulation of Ferritin H by Tumor Necrosis Factor-α (*)

C. Beaumont, D. Larochelle, F. Torti, 1995, The Journal of Biological Chemistry.

Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia

C. Beaumont, Érica Morán, B. Grandchamp, 2011, Haematologica.

C-terminal deletions in the ALAS2 gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or iron overload.

Joanne, J. Marsden, G. Mieli-Vergani, 2008, American journal of human genetics.

Hepcidin as a Major Component of Renal Antibacterial Defenses against Uropathogenic Escherichia coli.

E. Denamur, M. Sari, C. Beaumont, 2016, Journal of the American Society of Nephrology : JASN.

Iron refractory iron deficiency anemia

M. Muckenthaler, C. Beaumont, A. Iolascon, 2013, Haematologica.

Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis

C. Beaumont, A. Iolascon, L. De Falco, 2009, Haematologica.

Structure of mouse L-chain ferritin at 1.6 A resolution.

C. Beaumont, B. Gallois, A. Dautant, 2001, Acta crystallographica. Section D, Biological crystallography.

The haptoglobin 2-2 phenotype affects serum markers of iron status in healthy males.

H. Neels, M. D. De Buyzere, C. Beaumont, 2000, Clinical chemistry.

A point mutation in the bulge of the iron-responsive element of the L ferritin gene in two families with the hereditary hyperferritinemia-cataract syndrome.

C. Beaumont, P. Brissot, M. Martín, 1998, Blood.

Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyria.

C. Beaumont, H. de Verneuil, Y. Nordmann, 1984, American journal of human genetics.

nonsense mutation in the A novel type of congenital hypochromic anemia associated with a

H. Heimpel, C. Beaumont, C. Oudin, 2012 .

A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene.

H. Heimpel, C. Beaumont, C. Oudin, 2011, Blood.

Functional and Clinical Impact of Novel Tmprss6 Variants in Iron‐Refractory Iron‐Deficiency Anemia Patients and Genotype–Phenotype Studies

Mayka Sanchez, Achille Iolascon, Clara Camaschella, 2014, Human mutation.

Transferrin receptor 1 mRNA is downregulated in placenta of hepcidin transgenic embryos

C. Beaumont, B. Grandchamp, S. Vaulont, 2004, FEBS letters.

Mouse ferritin H sequences map to chromosomes 3, 6, and 19.

M. Mattei, C. Beaumont, B. Grandchamp, 1991, Genomics.

ALAS2 acts as a modifier gene in patients with congenital erythropoietic porphyria.

C. Beaumont, C. Ged, S. Ducamp, 2011, Blood.

Increased plasma transferrin, altered body iron distribution, and microcytic hypochromic anemia in ferrochelatase-deficient mice.

C. Beaumont, J. Deybach, L. Gouya, 2007, Blood.

Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large‐scale analysis of disorders of iron metabolism

M. Cazzola, C. Beaumont, M. Ferrari, 2006, Human mutation.

Functional Analysis of DNase-I Hypersensitive Sites at the Mouse Porphobilinogen Deaminase Gene Locus

C. Beaumont, B. Grandchamp, C. Porcher, 1995, The Journal of Biological Chemistry.

Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome.

D. Girelli, C. Beaumont, F. Perrone, 1998, Blood.

Excessive erythrocyte PPIX influences the hematologic status and iron metabolism in patients with dominant erythropoietic protoporphyria.

C. Beaumont, S. Ducamp, L. Gouya, 2009, Cellular and molecular biology.

Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria.

C. Beaumont, J. Deybach, L. Gouya, 2005, Human molecular genetics.

Expression of the two mRNA isoforms of the iron transporter Nramp2/DMTI in mice and function of the iron responsive element.

C. Beaumont, D. Tchernitchko, Marie‐Elise Martin, 2002, The Biochemical journal.

Accumulation of porphobilinogen deaminase, uroporphyrinogen decarboxylase, and alpha- and beta-globin mRNAs during differentiation of mouse erythroleukemic cells. Effects of succinylacetone.

C. Beaumont, B. Grandchamp, H. de Verneuil, 1985, The Journal of biological chemistry.

The identification of ferritin in the nucleus of K562 cells, and investigation of a possible role in the transcriptional regulation of adult beta-globin gene expression.

C. Beaumont, M. Bourgeois, G. Trugnan, 1999, Journal of cell science.

Phlebotomies or erythropoietin injections allow mobilization of iron stores in a mouse model mimicking intensive care anemia

C. Beaumont, S. Lasocki, P. Montravers, 2008, Critical care medicine.

Anemia after Late Introduction of Sirolimus May Correlate with Biochemical Evidence of a Chronic Inflammatory State

C. Beaumont, L. Chatenoud, M. Mamzer-Bruneel, 2005, Transplantation.

Protoporphyrin retention in hepatocytes and Kupffer cells prevents sclerosing cholangitis in erythropoietic protoporphyria mouse model.

C. Beaumont, G. Berdeaux, J. Deybach, 2011, Gastroenterology.

Presence of the iron exporter ferroportin at the plasma membrane of macrophages is enhanced by iron loading and down-regulated by hepcidin.

C. Beaumont, C. Delaby, Nathalie Pilard, 2005, Blood.

Hepatic and Serum Ferritin Concentrations in Patients with Idiopathic Hemochromatosis

M. Worwood, C. Beaumont, M. Simon, 1980 .

Differential subcellular localization of hZip1 in adherent and non‐adherent cells

C. Beaumont, D. Dhermy, D. Pountney, 2001, FEBS letters.

Preoperative iron deficiency increases transfusion requirements and fatigue in cardiac surgery patients: a prospective observational study

C. Beaumont, S. Lasocki, D. Longrois, 2011, European journal of anaesthesiology.

Hepatic and serum ferritin concentrations in patients with idiopathic hemochromatosis.

M. Worwood, C. Beaumont, M. Simon, 1980, Gastroenterology.

Hereditary hepatic porphyria with delta aminolevulinate dehydrase deficiency: Immunologic characterization of the non-catalytic enzyme

C. Beaumont, Y. Nordmann, H. Verneuil, 2004, Human Genetics.

Assignment of the human gene for δ aminolevulinate dehydrase to chromosome 9 by somatic cell hybridization and specific enzyme immunoassay

M. Gross, V. C. N'guyen, D. Weil, 1984, Annals of human genetics.

Idiopathic hemochromatosis: A study of biochemical expression in 247 heterozygous members of 63 families: Evidence for a single major HLA-linked gene

R. Fauchet, C. Beaumont, M. Simon, 1980 .

Inactivation of Iron Responsive Element–binding Capacity and Aconitase Function of Iron Regulatory Protein‐1 of Skin Cells by Ultraviolet A

C. Beaumont, P. Morlière, R. Santus, 2000 .

Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations.

C. Beaumont, B. Grandchamp, N. Soufir, 2003, Blood.

Stress Response and Induces Multidrug Resistance Properties H-Ferritin Subunit Overexpression in Erythroid Cells Reduces the Oxidative

C. Beaumont, I. Slotki, W. Breuer, 1999 .

Albumin secretion and protein synthesis by cultured diploid and tetraploid rat hepatocytes separated by elutriation.

A. Guillouzo, C. Beaumont, C. Guguen-Guillouzo, 1983, Experimental cell research.

[Erythrophagocytosis and recycling of heme iron in normal and pathological conditions; regulation by hepcidin].

C. Beaumont, F. Canonne-Hergaux, 2005, Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine.

Ultrastructural localization of alpha-fetoprotein in isolated and cultured rat hepatocytes.

M. Rissel, A. Guillouzo, C. Beaumont, 1981, Journal of ultrastructure research.

The hepatic biosynthesis of rat thyroxine binding globulin (TBG): demonstration, ontogenesis, and up-regulation in experimental hypothyroidism.

C. Beaumont, R. Vranckx, I. Flink, 1990, Biochemical and biophysical research communications.

[Serum hepcidin assay in 2011: where do we stand?].

C. Beaumont, C. Delaby, 2012, Annales de biologie clinique.

STAT5 proteins are involved in down-regulation of iron regulatory protein 1 gene expression by nitric oxide.

C. Beaumont, J. Drapier, F. Muzeau, 2006, The Biochemical journal.

A point mutation GA in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria

C. Beaumont, J. Deybach, P. Wilson, 2022 .

Duodenal expression of NF‐E2 in mouse models of altered iron metabolism

C. Beaumont, B. Gérard, B. Grandchamp, 1995, British journal of haematology.

Mouse ferritin H subunit gene. Functional analysis of the promoter and identification of an upstream regulatory element active in erythroid cells.

C. Beaumont, A. Seyhan, B. Grandchamp, 1994, The Journal of biological chemistry.

[Molecular genetics of hereditary cataract-hyperferritinemia syndrome].

C. Beaumont, B. Milon, 1998, Annales de biologie clinique.