De nouveaux gènes suppresseurs de tumeurs intervenant dans la régulation de cycle cellulaire = New suppressor genes witch regulate the cell cycleGRANDCHAMP, B.Annales de génétique (Paris). 1994, Vol 37, Num 3, pp 117-120, issn 0003-3995Article

DECREASED LYMPHOCYTE COPROPORPHYRINOGEN III OXIDASE ACTIVITY IN HEREDITARY COPROPORPHYRIA.GRANDCHAMP B; NORDMANN Y.1977; BIOCHEM. BIOPHYS. RES. COMMUNIC.; U.S.A.; DA. 1977; VOL. 74; NO 3; PP. 1089-1095; BIBL. 18 REF.Article

DOSAGE DE L'ACTIVITE DE L'UROPORPHYRINOGENE SYNTHETASE (UROSYNTHETASE) DANS LES GLOBULES ROUGES. (DIAGNOSTIC DE LA PORPHYRIE AIGUE INTERMITTENTE)GRANDCHAMP B; NORDMANN Y.sdIN: JOURN. BIOL. CLIN. NECKER-INST. PASTEUR. PROGRAMME SEANCES TRAV. PRAT.; PARIS; 1976; S.L.; DA. S.D.; PP. 31-33Conference Paper

Marqueurs moléculaires de clonalité = Molecular markers of clonalityGRANDCHAMP, B.Thérapie (Paris). 2001, Vol 56, Num 4, pp 387-388, issn 0040-5957Conference Paper

Hémophilie et myopathie de Duchenne de Boulogne : génétique = Haemophilia and Duchenne muscular dystrophy: geneticsGRANDCHAMP, B.La Revue du praticien (Paris). 1991, Vol 41, Num 23, pp 2367-2370, issn 0035-2640Article

BIOSYNTHESE DE L'HEME: REGULATION; PORPHYRIES HEREDITAIRES ET EXPERIMENTALESGRANDCHAMP B; NORDMANN Y.1980; EXPOSES ANNU. BIOCHIM. MED.; FRA; DA. 1980; VOL. 34; PP. 45-80; BIBL. 3 P.Article

CONJUGATED EFFECT OF LIGHT AND UROPORPHYRIN ON PORPHOBILINOGEN.NORDMANN Y; GRANDCHAMP B.1976; BIOCHEM. MED.; U.S.A.; DA. 1976; VOL. 15; NO 2; PP. 119-125; BIBL. 12 REF.Article

THE MITOCHONDRIAL LOCALIZATION OF COPROPORPHYRINOGEN III OXIDASEGRANDCHAMP B; NHU PHUNG; NORDMANN Y et al.1978; BIOCHEM. J.; GBR; DA. 1978; VOL. 176; NO 1; PP. 97-102; BIBL. 16 REF.Article

PORPHYRIE AIGUE INTERMITTENTE. DETECTION DES PORTEURS ASYMPTOMATIQUES DE LA TARE.GRANDCHAMP B; GRELIER M; NORDMANN Y et al.1975; NOUV. PRESSE MED.; FR.; DA. 1975; VOL. 4; NO 24; PP. 1801-1802; ABS. ANGL.; BIBL. 2 REF.Article

SOME KINETIC PROPERTIES OF HUMAN RED CELL UROPORPHYRINOGEN DECARBOXYLASEDE VERNEUIL H; GRANDCHAMP B; NORDMANN Y et al.1980; BIOCHIM. BIOPHYS. ACTA; NLD; DA. 1980; VOL. 611; NO 1; PP. 174-186; BIBL. 25 REF.Article

Structure of the mouse H2A.X gene and physical linkage to the UPS locus on chromosome 9 : assignment of the human H2A.X gene to 11q23 by sequence analysisPORCHER, C; GRANDCHAMP, B.Genomics (San Diego, Calif.). 1995, Vol 25, Num 1, pp 312-313, issn 0888-7543Article

FORMATION AND DISPOSITION OF NEWLY SYNTHESIZED HEME IN ADULT RAT HEPATOCYTES IN PRIMARY CULTUREGRANDCHAMP B; BISSELL DM; LICKO V et al.1981; J. BIOL. CHEM.; ISSN 0021-9258; USA; DA. 1981; VOL. 256; NO 22; PP. 11677-11683; BIBL. 35 REF.Article

ASPECTS BIOCHIMIQUES ACTUELS ET PHYSIOPATHOLOGIE DES PORPHYRIESNORDMANN Y; DEYBACH JC; GRANDCHAMP B et al.1983; REVUE DE MEDECINE (PARIS); ISSN 0035-1512; FRA; DA. 1983; VOL. 24; NO 17; PP. 763-770; ABS. ENG; BIBL. 18 REF.Article

THE SPECTROPHOTOMETRIC DETERMINATION OF UROPORPHYRINOGEN I SYNTHETASE ACTIVITY.GRANDCHAMP B; N'GUYEN PHLING; GRELIER M et al.1976; CLIN. CHIM. ACTA; PAYS BAS; DA. 1976; VOL. 70; NO 1; PP. 113-118; BIBL. 12 REF.Article

DETECTION DE LA PORPHYRIE AIGUE INTERMITTENTE PAR LE DOSAGE DE L'UROSYNTHETASE. BILAN DE 2 ANNEES.GRELIER M; GRANDCHAMP B; PHUNG N et al.1977; NOUV. PRESSE MED.; FR.; DA. 1977; VOL. 6; NO 12; PP. 1045-1047; ABS. ANGL.; BIBL. 6 REF.Article

PRENATAL EXCLUSION OF CONGENITAL ERYTHROPOIETIC PORPHYRIA (GUENTHER'S DISEASE) IN A FETUS AT RISKDEYBACH JC; GRANDCHAMP B; GRELIER M et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 217-221; BIBL. 18 REF.Article

FAMILIAL AND SPORADIC PORPHYSIA CUTANEA: TWO DIFFERENT DISEASESDE VERNEUIL H; NORDMANN Y; PHUNG N et al.1978; INTERNATION. J. BIOCHEM.; GBR; DA. 1978; VOL. 9; NO 12; PP. 927-931; BIBL. 14 REF.Article

Clonage, caractérisation et expression du gène de la sous-unité L ferritine de souris = Cloning, characterization and expression of the mouse ferritin L subunit geneRENAUDIE, F; BOULANGER, L; GRANDCHAMP, B et al.Comptes rendus de l'Académie des sciences. Série 3, Sciences de la vie. 1995, Vol 318, Num 4, pp 431-437, issn 0764-4469Article

Coproporphyrinogene oxidase: gene organization and description of a mutation leading to exon 6 skippingDELFAY-LARUE, M.-H; MARTASEK, P; GRANDCHAMP, B et al.Human molecular genetics (Print). 1994, Vol 3, Num 8, pp 1325-1330, issn 0964-6906Article

Pathologie moléculaire de la biosynthèse de l'hème = Molecular pathology of heme biosynthsisGRANDCHAMP, B.Nouvelle revue française d'hématologie. 1993, Vol 35, Num 3, pp 313-315, issn 0029-4810Conference Paper

PCR detection of a C/T polymorphism in exon 1 of the prophobilinogen deaminase gene (PBGD)PICAT, C; BOURGEOIS, F; GRANDCHAMP, B et al.Nucleic acids research. 1991, Vol 19, Num 18, issn 0305-1048, 5099Article

Etude de la famille multigénique codant pour les sous-unités de type L ferritine de souris = Study of the multigenic family encoding the mouse L ferritin subunitsRenaudie, Françoise; Grandchamp, B.1994, 101 p.Thesis

Contribution à l'étude moléculaire des porphyries hépatiques graves = Contribution to molecular studies of acute hepatic porphyriasDelfau-Larue, Marie-Hélène; Grandchamp, B.1995, 124 p.Thesis

Accumulation of porphobilinogen deaminase, uroporphyrinogen decarboxylase, and α- and β-globin mRNAs during differentiation of mouse erythroleukemic cells: effects of succinylacetoneGRANDCHAMP, B; BEAUMONT, C; DE VERNEUIL, H et al.The Journal of biological chemistry (Print). 1985, Vol 260, Num 17, pp 9630-9635, issn 0021-9258Article

Two-dimensional DC simulation methodology for InP/GaAs_0.51Sb_0.49/InP heterojunction bipolar transistorMANEUX, C; BELHAI, M; GRANDCHAMP, B et al.Solid-state electronics. 2005, Vol 49, Num 6, pp 956-964, issn 0038-1101, 9 p.Article