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The response of sea turtles to vocalizations opens new perspectives to reduce their bycatch

Scientific reports, 2024-07, Vol.14 (1), p.16519-7, Article 16519

2024

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Gender‐specific phenotypic expression and screening strategies in C282Y‐linked haemochromatosis: a study of 9396 French people

British journal of haematology, 2002-09, Vol.118 (4), p.1170-1178

2002

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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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Insulin resistance–associated hepatic iron overload

Gastroenterology (New York, N.Y. 1943), 1999-11, Vol.117 (5), p.1155-1163

1999

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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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Identification of an endogenous RNA transcribed from the antisense strand of the HFE gene

Human molecular genetics, 2001-08, Vol.10 (17), p.1859-1866

2001

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Polymorphisms in the HFE Gene

Human heredity, 1999-01, Vol.49 (1), p.21-26

1999

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Haemochromatosis and HLA-H

Nature genetics, 1996-11, Vol.14 (3), p.251-252

1996

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Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload

Journal of hepatology, 2003-08, Vol.39 (2), p.286-289

2003

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Over-expression of wild-type and mutant HFE in a human melanocytic cell line reveals an intracellular bridge between MHC class I pathway and transferrin iron uptake

Biology of the cell, 2003-07, Vol.95 (5), p.243-255

2003

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A genotypic study of 217 unrelated probands diagnosed as “genetic hemochromatosis” on “classical” phenotypic criteria

Journal of hepatology, 1999-04, Vol.30 (4), p.588-593

1999

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A candidate gene for hemochromatosis : frequency of the C282Y and H63D mutations

Human genetics, 1997-10, Vol.100 (5-6), p.544-547

1997

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Transcriptome variations in human CaCo-2 cells: a model for enterocyte differentiation and its link to iron absorption

Genomics (San Diego, Calif.), 2004-05, Vol.83 (5), p.772-789

2004

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A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes

Immunogenetics (New York), 1992-02, Vol.35 (3), p.183-189

1992

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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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Should one screen systematically for genetic haemochromatosis?

La Presse médicale (1983), 2003-10, Vol.32 (34), p.1588-1590

Le Gall, Jean-Yves

2003

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Genome sequencing and personalized medicine: perspectives and limitations

Bulletin de l'Académie nationale de médecine, 2014-01, Vol.198 (1), p.101-117

2014

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Low Penetrant Hemochromatosis Phenotype in Eight Families: No Evidence of Modifiers in the MHC Region

Blood cells, molecules, & diseases, 2001-03, Vol.27 (2), p.518-529

2001

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Intestinal microbiota

Bulletin de l'Académie nationale de médecine, 2014-12, Vol.198 (9), p.1667-1684

2014

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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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Iron Overload in Mice Expressing HFE Exclusively in the Intestinal Villi Provides Evidence That HFE Regulates a Functional Cross-Talk between Crypt and Villi Enterocytes

Blood cells, molecules, & diseases, 2002-05, Vol.28 (3), p.348-360

2002

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The biology of aging

Bulletin de l'Académie nationale de médecine, 2009-02, Vol.193 (2), p.365

2009

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Genetics of Hemochromatosis: HLA Association and Mode of Inheritance

Annals of the New York Academy of Sciences, 1988, Vol.526 (1), p.11-22

1988

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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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Phenotypic expression of HFE mutations: A French study of 1110 unrelated iron-overloaded patients and relatives

Gastroenterology (New York, N.Y. 1943), 1999-02, Vol.116 (2), p.372-377

1999

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The response of sea turtles to vocalizations opens new perspectives to reduce their bycatch

Gender‐specific phenotypic expression and screening strategies in C282Y‐linked haemochromatosis: a study of 9396 French people

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

Insulin resistance–associated hepatic iron overload

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

Identification of an endogenous RNA transcribed from the antisense strand of the HFE gene

Polymorphisms in the HFE Gene

Haemochromatosis and HLA-H

Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload

Over-expression of wild-type and mutant HFE in a human melanocytic cell line reveals an intracellular bridge between MHC class I pathway and transferrin iron uptake

A genotypic study of 217 unrelated probands diagnosed as “genetic hemochromatosis” on “classical” phenotypic criteria

A candidate gene for hemochromatosis : frequency of the C282Y and H63D mutations

Transcriptome variations in human CaCo-2 cells: a model for enterocyte differentiation and its link to iron absorption

A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes

Promoter analysis of the human translation termination factor 1 gene

Should one screen systematically for genetic haemochromatosis?

Genome sequencing and personalized medicine: perspectives and limitations

Low Penetrant Hemochromatosis Phenotype in Eight Families: No Evidence of Modifiers in the MHC Region

Intestinal microbiota

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

Iron Overload in Mice Expressing HFE Exclusively in the Intestinal Villi Provides Evidence That HFE Regulates a Functional Cross-Talk between Crypt and Villi Enterocytes

The biology of aging

Genetics of Hemochromatosis: HLA Association and Mode of Inheritance

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

Phenotypic expression of HFE mutations: A French study of 1110 unrelated iron-overloaded patients and relatives

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