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Gilles Hetet

Research Profile

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Disorders

Chemicals & Drugs

Physiology

Genes & Molecular Sequences

Amino Acid Sequences

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France

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Publications

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Agnes Bourillon; Vincent Descamps; Nicolas Dumaz; Bernard Grandchamp; Gilles Hetet; Hui-Han Hu; Jean-Jacques Lacapere; Zighereda Ogbah; Susana Puig; philippe saiag; Jocelyne André; Martine Bagot; Nicole Basset-Seguin; Armand Bensussan; Nadem Soufir
Genetic variation at KIT locus may predispose to melanoma.
T Spica; P Wolkenstein; N Basset-Seguin; G Bertrand; F Cambien; V Descamps; N Dupin; Maria Concetta Fargnoli; Federica Formicone; B Grandchamp; Gilles Hetet; C Lebbe; Ketty Peris; P Saiag; Nadem Soufir
EDNRB gene variants and melanoma risk in two southern European populations.
Caroline Kannengiesser; Mayka Sanchez; Marion Sweeney; Gilles Hetet; Briedgeen Kerr; Erica Moran; Jose L Fuster Soler; Karim Maloum; Thomas Matthes; Caroline Oudot; Axelle Lascaux; Corinne Pondarré; Julian Sevilla Navarro; Sudharma Vidyatilake; Carole Beaumont; Bernard Grandchamp; Alison May
Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia.

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All Publications

2013: Agnes Bourillon; Vincent Descamps; Nicolas Dumaz; Bernard Grandchamp; Gilles Hetet; Hui-Han Hu; Jean-Jacques Lacapere; Zighereda Ogbah; Susana Puig; philippe saiag; Jocelyne André; Martine Bagot; Nicole Basset-Seguin; Armand Bensussan; Nadem Soufir
Genetic variation at KIT locus may predispose to melanoma.
Pigment cell & melanoma research 2013;26(1):88-96.
2011: T Spica; P Wolkenstein; N Basset-Seguin; G Bertrand; F Cambien; V Descamps; N Dupin; Maria Concetta Fargnoli; Federica Formicone; B Grandchamp; Gilles Hetet; C Lebbe; Ketty Peris; P Saiag; Nadem Soufir
EDNRB gene variants and melanoma risk in two southern European populations.
Clinical and experimental dermatology 2011;36(7):782-7.
2011: Caroline Kannengiesser; Mayka Sanchez; Marion Sweeney; Gilles Hetet; Briedgeen Kerr; Erica Moran; Jose L Fuster Soler; Karim Maloum; Thomas Matthes; Caroline Oudot; Axelle Lascaux; Corinne Pondarré; Julian Sevilla Navarro; Sudharma Vidyatilake; Carole Beaumont; Bernard Grandchamp; Alison May
Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia.
Haematologica 2011;96(6):808-13.
2009: Caroline Kannengiesser; Anne-Marie Jouanolle; Gilles Hetet; Annick Mosser; Françoise Muzeau; Dominique Henry; Edouard Bardou-Jacquet; Martine Mornet; Pierre Brissot; Yves Deugnier; Bernard Grandchamp; Carole Beaumont
A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload.
Haematologica 2009;94(3):335-9.
2006: Jean-Jacques Kiladjian; N Elkassar; Bruno Cassinat; Gilles Hetet; Stéphane Giraudier; Nicole Balitrand; C Conejero; Jean Briere; Pierre Fenaux; Christine Chomienne; Bernard Grandchamp
Essential thrombocythemias without V617F JAK2 mutation are clonal hematopoietic stem cell disorders.
Leukemia 2006;20(6):1181-3.
2006: Ana Sofia Gonçalves; Françoise Muzeau; Rand Blaybel; Gilles Hetet; Fathi Driss; Constance Delaby; François Canonne-Hergaux; Carole Beaumont
Wild-type and mutant ferroportins do not form oligomers in transfected cells.
The Biochemical journal 2006;396(2):265-75.
2006: Carole Beaumont; Jean Delaunay; Gilles Hetet; Bernard Grandchamp; Mariane de Montalembert; Gil Tchernia
Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload.
Blood 2006;107(10):4168-70.
2005: Constance Delaby; Nathalie Pilard; Gilles Hetet; Fathi Driss; Bernard Grandchamp; Carole Beaumont; François Canonne-Hergaux
A physiological model to study iron recycling in macrophages.
Experimental cell research 2005;310(1):43-53.
2004: Marie Elise Martin; Gaël Nicolas; Gilles Hetet; Sophie Vaulont; Bernard Grandchamp; Carole Beaumont
Transferrin receptor 1 mRNA is downregulated in placenta of hepcidin transgenic embryos.
FEBS letters 2004;574(1-3):187-91.
2003: Gilles Hetet; Isabelle Devaux; Nadem Soufir; Bernard Grandchamp; Carole Beaumont
Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations.
Blood 2003;102(5):1904-10.
2002: Claire Borie; Francesca Gasparini; Patrice Verpillat; Anne-Marie Bonnet; Yves Agid; Gilles Hetet; Alexis Brice; Alexandra Dürr; Bernard Grandchamp
Association study between iron-related genes polymorphisms and Parkinson's disease.
Journal of neurology 2002;249(7):801-4.
2002: Birgitte Wuyts; Gilles Hetet; Bernard Grandchamp; Joris R Delanghe
Novel haptoglobin insertion/deletion polymorphism is associated with the lipid profile and C-reactive protein (CRP) concentration.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2002;40(5):469-74.
2002: Valérie Bardet; Nathalie Couque; Laurence Cattolico; Gilles Hetet; Isabelle Devaux; Simone Duprat; Laetitia Gressin; Etienne Vilmer; Hélène Cavé; Bernard Grandchamp
Molecular analysis of nonrandom 8q12 deletions in acute lymphoblastic leukemia: identification of two candidate genes.
Genes, chromosomes & cancer 2002;33(2):178-87.
2001: Gilles Hetet; Bernard Grandchamp; Christiane Bouchier; Viviane Nicaud; L Tiret; Gérard Roizès; Michel Desnos; Ketty Schwartz; R Dorent; Michel Komajda
Idiopathic dilated cardiomyopathy: lack of association with haemochromatosis gene in the CARDIGENE study.
Heart (British Cardiac Society) 2001;86(6):702-3.
2001: Gilles Hetet; Alexis Elbaz; J Gariepy; Viviane Nicaud; Dominique Arveiler; Caroline Morrison; Frank Kee; Alun Evans; A Simon; Pierre Amarenco; François Cambien; Bernard Grandchamp
Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases.
European journal of clinical investigation 2001;31(5):382-8.
2000: Didier Dhermy; J Steen-Johnsen; Odile Bournier; Gilles Hetet; Thérèse Cynober; Gil Tchernia; Bernard Grandchamp
Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis family.
Clinical and laboratory haematology 2000;22(6):329-36.
2000: Sandrine Vuillaumier-Barrot; Gilles Hetet; Anne Barnier; Thierry Dupré; Maryvonne Cuer; Pascale de Lonlay; V Cormier-Daire; Geneviève Durand; Bernard Grandchamp; Nathalie Seta
Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients.
Journal of medical genetics 2000;37(8):579-80.
2000: Gilles Hetet; Hélène Dastot; M Baens; A Brizard; François Sigaux; Bernard Grandchamp; Marc-Henri Stern
Recurrent molecular deletion of the 12p13 region, centromeric to ETV6/TEL, in T-cell prolymphocytic leukemia.
The hematology journal : the official journal of the European Haematology Association / EHA 2000;1(1):42-7.
1998: N el-Kassar; Gilles Hetet; J Brière; Bernard Grandchamp
Clonality analysis of hematopoiesis and thrombopoietin levels in patients with essential thrombocythemia.
Leukemia & lymphoma 1998;30(1-2):181-8.
1998: N el-Kassar; Gilles Hetet; J Brière; Bernard Grandchamp
X-chromosome inactivation in healthy females: incidence of excessive lyonization with age and comparison of assays involving DNA methylation and transcript polymorphisms.
Clinical chemistry 1998;44(1):61-7.
1997: Jean-Jacques Kiladjian; N Elkassar; Gilles Hetet; Jean Briere; Bernard Grandchamp; Claude Gardin
Study of the thrombopoitin receptor in essential thrombocythemia.
Leukemia 1997;11(11):1821-6.
1997: N el-Kassar; Gilles Hetet; J Brière; Bernard Grandchamp
Clonality analysis of hematopoiesis in essential thrombocythemia: advantages of studying T lymphocytes and platelets.
Blood 1997;89(1):128-34.
1995: N el Kassar; Gilles Hetet; Y Li; J Brière; Bernard Grandchamp
Clonal analysis of haemopoietic cells in essential thrombocythaemia.
British journal of haematology 1995;90(1):131-7.