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Integrative genome-wide analysis reveals a robust genomic glioblastoma signature associated with copy number driving changes in gene expression

Genes chromosomes & cancer, 2009-01, Vol.48 (1), p.55-68

2009

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Redox active plasma iron in C282Y/C282Y hemochromatosis

Blood, 2005-06, Vol.105 (11), p.4527-4531

2005

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Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations

Molecular human reproduction, 2000-12, Vol.6 (12), p.1063-1067

2000

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Five distinct biological processes and 14 differentially expressed genes characterize TEL/AML1-positive leukemia

BMC genomics, 2007-10, Vol.8 (1), p.385-385, Article 385

2007

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Iron-related transcriptomic variations in CaCo-2 cells, an in vitro model of intestinal absorptive cells

Physiological genomics, 2006-06, Vol.26 (1), p.55-67

2006

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Analytical performance of the serum free light chain assay

Clinical chemistry and laboratory medicine, 2010-01, Vol.48 (1), p.73-79

2010

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Serum Ceruloplasmin and Ferroxidase Activity Are Not Decreased in Hepatic Failure Related to Alcoholic Cirrhosis: Clinical and Pathophysiological Implications

Alcoholism, clinical and experimental research, 2004-05, Vol.28 (5), p.775-779

2004

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Altered Hepcidin Regulation in Hereditary Hemochromatosis and Dysmetabolic Hyperferritinemia

Blood, 2005-11, Vol.106 (11), p.3590-3590

2005

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Serum ceruloplasmin and ferroxidase activity are decreased in HFE C282Y homozygote male iron-overloaded patients

Journal of hepatology, 2002, Vol.36 (1), p.60-65

2002

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Promoter analysis of the human translation termination factor 1 gene

Gene, 2003-10, Vol.316, p.91-101

2003

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Don’t forget to test for D-lactic acid in short bowel syndrome

The American journal of gastroenterology, 2000, Vol.95 (12), p.3675-3677

2000

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Don't forget to test for D-lactic acid in short bowel syndrome

The American journal of gastroenterology, 2000-12, Vol.95 (12), p.3675-3677

2000

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Evaluation of ETF1/eRF1, mapping to 5q31, as a candidate myeloid tumor suppressor gene

Cancer genetics and cytogenetics, 2002-04, Vol.134 (1), p.33-37

2002

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Human release factor eRF1: structural organisation of the unique functional gene on chromosome 5 and of the three processed pseudogenes

FEBS letters, 1999-07, Vol.454 (1), p.131-136

1999

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Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE)

American journal of human genetics, 1994-02, Vol.54 (2), p.252-263

1994

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Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region : implications for mapping the hemochromatosis gene (HFE)

Human genetics, 1996, Vol.97 (1), p.103-113

1996

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Le dosage de l'enzyme de conversion de l'angiotensine i par methode spectrophotometrique

Clinica chimica acta, 1979-10, Vol.98 (1-2), p.1-4

1979

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In patients with cirrhosis, serum albumin determination should be carried out by immunonephelometry rather than by protein electrophoresis

European journal of gastroenterology & hepatology, 1999-12, Vol.11 (12), p.1405-1412

1999

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Structural analysis of CFTR gene in congenital bilateral absence of vas deferens

Clinical chemistry (Baltimore, Md.), 1995-06, Vol.41 (6 Pt 1), p.833-835

1995

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Identification of a novel mutation (A268G) in exon 8 of the HTRβ gene in a large family with thyroid hormone resistance

Human mutation, 1996, Vol.8 (4), p.396-396

1996

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Anonymous markers located on chromosome 6 in the HLA-A class I region : allelic distribution in genetic haemochromatosis

Human genetics, 1992-04, Vol.89 (1), p.33-36

1992

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1051 Labile plasma iron in C282Y/C282Y hemochromatosis: a reality of potential pathophysiological and clinical importance

Hepatology (Baltimore, Md.), 2003, Vol.38, p.661-661

2003

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Biochemical aspects of α‐L‐fucosidase in hepatocellular carcinoma

Hepatology (Baltimore, Md.), 1989-02, Vol.9 (2), p.249-252

1989

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Complex structure of human bronchial mucus glycoprotein

European journal of biochemistry, 1984-07, Vol.142 (2), p.209-218

1984

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Partial purification and characterization of a serine endopeptidase from rat liver plasma membranes

Biochimica et biophysica acta, 1986-04, Vol.881 (2), p.258-267

1986

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Integrative genome-wide analysis reveals a robust genomic glioblastoma signature associated with copy number driving changes in gene expression

Redox active plasma iron in C282Y/C282Y hemochromatosis

Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations

Five distinct biological processes and 14 differentially expressed genes characterize TEL/AML1-positive leukemia

Iron-related transcriptomic variations in CaCo-2 cells, an in vitro model of intestinal absorptive cells

Analytical performance of the serum free light chain assay

Serum Ceruloplasmin and Ferroxidase Activity Are Not Decreased in Hepatic Failure Related to Alcoholic Cirrhosis: Clinical and Pathophysiological Implications

Altered Hepcidin Regulation in Hereditary Hemochromatosis and Dysmetabolic Hyperferritinemia

Serum ceruloplasmin and ferroxidase activity are decreased in HFE C282Y homozygote male iron-overloaded patients

Promoter analysis of the human translation termination factor 1 gene

Don’t forget to test for D-lactic acid in short bowel syndrome

Don't forget to test for D-lactic acid in short bowel syndrome

Evaluation of ETF1/eRF1, mapping to 5q31, as a candidate myeloid tumor suppressor gene

Human release factor eRF1: structural organisation of the unique functional gene on chromosome 5 and of the three processed pseudogenes

Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE)

Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region : implications for mapping the hemochromatosis gene (HFE)

Le dosage de l'enzyme de conversion de l'angiotensine i par methode spectrophotometrique

In patients with cirrhosis, serum albumin determination should be carried out by immunonephelometry rather than by protein electrophoresis

Structural analysis of CFTR gene in congenital bilateral absence of vas deferens

Identification of a novel mutation (A268G) in exon 8 of the HTRβ gene in a large family with thyroid hormone resistance

Anonymous markers located on chromosome 6 in the HLA-A class I region : allelic distribution in genetic haemochromatosis

1051 Labile plasma iron in C282Y/C282Y hemochromatosis: a reality of potential pathophysiological and clinical importance

Biochemical aspects of α‐L‐fucosidase in hepatocellular carcinoma

Complex structure of human bronchial mucus glycoprotein

Partial purification and characterization of a serine endopeptidase from rat liver plasma membranes

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