CV Accueil - Archive ouverte HAL

	Disturbed expression of autophagy genes in blood of Parkinson’s disease patients Saïd El Haddad , Amandine Serrano , Fréderic Moal , Thierry Normand , Chloé Robin Gene, 2020, 738, pp.144454. ⟨10.1016/j.gene.2020.144454⟩ Article dans une revue hal-02501027v1
	LINGO family receptors are differentially expressed in the mouse brain and form native multimeric complexes Anthony Guillemain , Yousra Laouarem , Laetitia Cobret , Dora Štefok , Wanyin Chen FASEB Journal, 2020, pp.1-13. ⟨10.1096/fj.202000826R⟩ Article dans une revue hal-02943248v1
	Interaction of Alpha-synuclein with Cytogaligin, a protein encoded by the proapoptotic gene GALIG Saïd El Haddad , Amandine Serrano , Thierry Normand , Chloé Robin , Martine Dubois Biochemical and Biophysical Research Communications, 2018, 495 (1), pp.787-792. ⟨10.1016/j.bbrc.2017.11.078⟩ Article dans une revue hal-01966108v1
	Dysregulation of apoptosis and autophagy gene expression in peripheral blood mononuclear cells of efficiently treated HIV-infected patients Amandine Serrano , Saïd El Haddad , Fréderic Moal , Thierry Prazuck , Eric Legac AIDS. Official journal of the international AIDS Society, 2018, 32 (12), pp.1579 - 1587. ⟨10.1097/QAD.0000000000001851⟩ Article dans une revue hal-01936094v1
	Opposing Mcl-1, the GALIG proapoptotic gene is upregulated as neutrophils die and underexpressed in Acute Myeloid Leukemia cells. Lucile Mollet , Pauline Robinet , Martine Dubois , Axel Aurouet , Thierry Normand Molecular Immunology, 2013, 56 (1-2), pp.123-8. ⟨10.1016/j.molimm.2013.04.012⟩ Article dans une revue hal-00840170v1
	The mitogaligin protein is addressed to the nucleus via a non-classical localization signal Pauline Robinet , Lucile Mollet , Patrick Gonzalez , Thierry Normand , Stephane Charpentier Biochemical and Biophysical Research Communications, 2010, 392 (1), pp.53-57. ⟨10.1016/j.bbrc.2009.12.162⟩ Article dans une revue hal-00529397v1
	Apoptotic activity of a nuclear form of mitogaligin, a cell death protein Patrick Gonzalez , Pauline Robinet , Stéphane Charpentier , Lucile Mollet , Thierry Normand Biochemical and Biophysical Research Communications, 2009, 378 (4), pp.816-820. ⟨10.1016/j.bbrc.2008.11.133⟩ Article dans une revue hal-00522444v1
	Multiple reprobing of Western blots after inactivation of peroxidase activity by its substrate, hydrogen peroxide Alexis D. Sennepin , Stéphane Charpentier , Thierry Normand , Cedric Sarre , Alain Legrand Analytical Biochemistry, 2009, 393 (1), pp.129-131. ⟨10.1016/j.ab.2009.06.004⟩ Article dans une revue hal-00525339v1
	Destabilization of Membranes Containing Cardiolipin or Its Precursors by Peptides Derived from Mitogaligin, a Cell Death Protein Patrick Gonzalez , Mélanie Duneau , Stéphane Charpentier , Thierry Normand , Lucile Mollet Biochemistry, 2007, 46 (25), pp.7374-7382. ⟨10.1021/bi700213p⟩ Article dans une revue hal-00159568v1
	Galig, a novel cell death gene that encodes a mitochondrial protein promoting cytochrome c release M. Duneau , M. Boyer Guittaut , P. Gonzalez , S. Charpentier , T. Normand Experimental Cell Research, 2005, 302, pp.194-205 Article dans une revue hal-00088588v1
	Identification of an Internal Gene to the Human Galectin-3 Gene with Two Different Overlapping Reading Frames That Do Not Encode Galectin-3 Michaël Guittaut , Stéphane Charpentier , Thierry Normand , Martine Dubois , Jacques Raimond Journal of Biological Chemistry, 2001, 276 (4), pp.2652-2657. ⟨10.1074/jbc.m002523200⟩ Article dans une revue hal-02137994v1
	Genetic linkage mapping of the human steroid 5α-reductase type 2 gene (SRD5A2) close to D2S352 on chromosome region 2p23→p22 J. Morissette , F. Durocher , J. Leblanc , T. Normand , F. Labrie Cytogenetic and Genome Research, 1996, 73 (4), pp.304-307. ⟨10.1159/000134362⟩ Article dans une revue hal-02160041v1
	Molecular cloning of a novel widely expressed human 80 kDa 17 β -hydroxysteroid dehydrogenase IV J Adamski , Thierry Normand , F Leenders , D Monté , A. Bégué Biochemical Journal, 1995, 311 (2), pp.437-443. ⟨10.1042/bj3110437⟩ Article dans une revue hal-02160026v1
	Molecular characterization of mouse 17 beta-hydroxysteroid dehydrogenase IV. Thierry Normand , B. Husen , F Leenders , H Pelczar , J.L Baert Journal of Steroid Biochemistry and Molecular Biology, 1995, 55 (5-6), pp.541-8. ⟨10.1016/0960-0760(95)00204-9⟩ Article dans une revue hal-02160020v1
	Developmental and hormonal regulation of specific proteins in mouse seminal vesicles. Isolation and characterization of genomic and cDNA clones for androgen-regulated secretory protein A.M. Simon , C. Guilbault , Thierry Normand , Christiane Jean-Faucher , Georges Veyssière Experimental and Clinical Endocrinology, 1995, 14, pp.73-82 Article dans une revue hal-02167152v1
	Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12–21: exclusion of candidate genes EDH17B2 and RARA J Simard , Jean Feunteun , Gilbert Lenoir , T Tonin , Thierry Normand Human Molecular Genetics, 1993, 2 (8), pp.1193-1199. ⟨10.1093/hmg/2.8.1193⟩ Article dans une revue hal-02160208v1
	Detection of polymorphisms in the estradiol 17β-hydroxysteroid dehydrogenase II gene at the EDH17B2 locus on 17q11–q21 Thierry Normand , Steven Narod , Fernand Labrie , Jacques Simard Human Molecular Genetics, 1993, 2 (4), pp.479-483. ⟨10.1093/hmg/2.4.479⟩ Article dans une revue hal-02160210v1
	Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Québec. Thierry Normand , J. Bergeron , Teresa Fernandez-Margallo , Aoife Bharucha , R Ven Murthy Human Genetics, 1992, 89 (6), pp.671-5. ⟨10.1007/BF00221960⟩ Article dans une revue hal-02160222v1
	Adipose cell size and distribution in familial lipoprotein lipase deficiency. P Peeva , L Brun , M Ven Murthy , P Després , Thierry Normand International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity, 1992, 16 (10), pp.737-44 Article dans une revue hal-02160233v1
	Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of Québec. M. Bergeron , Thierry Normand , Aoife Bharucha , M Ven Murthy , P Julien Clinical Genetics, 1992, 41 (4), pp.206-10. ⟨10.1111/j.1399-0004.1992.tb03664.x⟩ Article dans une revue hal-02160230v1
	A Mutation in the Human Lipoprotein Lipase Gene as the Most Common Cause of Familial Chylomicronemia in French Canadians Y. Ma , Howard Henderson , V Murthy , Ghislaine Roederer , M. Monsalve New England Journal of Medicine, 1991, 324 (25), pp.1761-1766. ⟨10.1056/NEJM199106203242502⟩ Article dans une revue hal-02160241v1
	Neonatal exposure to oestrogens alters the protein profiles and gene expression in the genital tract of adult male mice Thierry Normand , Christiane Jean-Faucher , Claude Jean Journal of Steroid Biochemistry, 1990, 36 (5), pp.415-423. ⟨10.1016/0022-4731(90)90082-4⟩ Article dans une revue hal-02160254v1
	Developmental pattern of androgen-regulated proteins in seminal vesicles from the mouse. Thierry Normand , C. Jean-Faucher , C Jean International Journal of Andrology, 1989, 12 (3), pp.219-30 Article dans une revue hal-02160364v1

	Cytogaligin, an additional link between Parkinson’s disease and autophagy pathways? S. El Haddad , A. Serrano , Thierry Normand , Fabienne Brulé-Morabito , L. Mollet 7e Congrès du CFATG, Nov 2017, Paris, France Communication dans un congrès hal-02934905v1
	GALIG, gène inducteur de la mort cellulaire, s’exprime au cours de la différenciation myéloïde A Serrano , T Guery , S El Haddad , M Dubois , M Schoenwald 10es Journées du Cancéropole Grand Ouest, Jun 2016, Les Sables d'Olonne, France Communication dans un congrès hal-03661932v1
	Genes de l’autophagie : marqueurs sanguins potentiels de la maladie de Parkinson S El Haddad , A Serrano , C Ozsancak , P. Auzou , F Moal Journées de Neurologie de Langue Française, Apr 2016, Nantes, France Communication dans un congrès hal-03661930v1
	During efficient Anti-RetroViral (ARV) therapy, the expression of GALIG and its interacting partners involved in macroautophagy are deregulated A. Serrano , Thierry Normand , S. El Haddad , M. Dubois , Stéphane Charpentier 6es Journées Scientifiques du CFATG, Oct 2016, Bordeaux, France Communication dans un congrès hal-02934903v1

Thierry Normand

Publications

Disturbed expression of autophagy genes in blood of Parkinson’s disease patients

LINGO family receptors are differentially expressed in the mouse brain and form native multimeric complexes

Interaction of Alpha-synuclein with Cytogaligin, a protein encoded by the proapoptotic gene GALIG

Dysregulation of apoptosis and autophagy gene expression in peripheral blood mononuclear cells of efficiently treated HIV-infected patients

Opposing Mcl-1, the GALIG proapoptotic gene is upregulated as neutrophils die and underexpressed in Acute Myeloid Leukemia cells.

The mitogaligin protein is addressed to the nucleus via a non-classical localization signal

Apoptotic activity of a nuclear form of mitogaligin, a cell death protein

Multiple reprobing of Western blots after inactivation of peroxidase activity by its substrate, hydrogen peroxide

Destabilization of Membranes Containing Cardiolipin or Its Precursors by Peptides Derived from Mitogaligin, a Cell Death Protein

Galig, a novel cell death gene that encodes a mitochondrial protein promoting cytochrome c release

Identification of an Internal Gene to the Human Galectin-3 Gene with Two Different Overlapping Reading Frames That Do Not Encode Galectin-3

Genetic linkage mapping of the human steroid 5α-reductase type 2 gene (SRD5A2) close to D2S352 on chromosome region 2p23→p22

Molecular cloning of a novel widely expressed human 80 kDa 17 β -hydroxysteroid dehydrogenase IV

Molecular characterization of mouse 17 beta-hydroxysteroid dehydrogenase IV.

Developmental and hormonal regulation of specific proteins in mouse seminal vesicles. Isolation and characterization of genomic and cDNA clones for androgen-regulated secretory protein

Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12–21: exclusion of candidate genes EDH17B2 and RARA

Detection of polymorphisms in the estradiol 17β-hydroxysteroid dehydrogenase II gene at the EDH17B2 locus on 17q11–q21

Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Québec.

Adipose cell size and distribution in familial lipoprotein lipase deficiency.

Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of Québec.

A Mutation in the Human Lipoprotein Lipase Gene as the Most Common Cause of Familial Chylomicronemia in French Canadians

Neonatal exposure to oestrogens alters the protein profiles and gene expression in the genital tract of adult male mice

Developmental pattern of androgen-regulated proteins in seminal vesicles from the mouse.

Cytogaligin, an additional link between Parkinson’s disease and autophagy pathways?

GALIG, gène inducteur de la mort cellulaire, s’exprime au cours de la différenciation myéloïde

Genes de l’autophagie : marqueurs sanguins potentiels de la maladie de Parkinson

During efficient Anti-RetroViral (ARV) therapy, the expression of GALIG and its interacting partners involved in macroautophagy are deregulated