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Jean-Louis Guénet
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17
Montagutelli, Xavier
15
Poirier, Christophe
6
Szatanik, Marek
6
Simon-Chazottes, Dominique
6
Lalouette, A
5
Mashimo, Tomoji
4
Lucas, Marianne
4
Desprès, Philippe
4
Jaubert, Jérôme
3
Frenkiel, Marie-Pascale
3
Benavides, Fernando
3
Bagot, Sébastien
3
Cazenave, Pierre-André
3
Ceccaldi, Pierre-Emmanuel
3
Conti, Claudio
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All Publications
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2008: Szatanik Marek; Vibert Nicolas; Vassias Isabelle; Guénet Jean-Louis; Eugène Daniel; de Waele Catherine; Jaubert Jean
Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channels.
Neurogenetics 2008;9(4):237-48.
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2008: Vanlaere Ineke; Vanderrijst Ananza; Guénet Jean-Louis; De Filette Marina; Libert Claude
Mx1 causes resistance against influenza A viruses in the Mus spretus-derived inbred mouse strain SPRET/Ei.
Cytokine 2008;42(1):62-70.
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2008: Maltecca Francesca; Aghaie Asadollah; Schroeder David G; Cassina Laura; Taylor Benjamin A; Phillips Sandra J; Malaguti Mariachiara; Previtali Stefano; Guénet Jean-Louis; Quattrini Angelo; Cox Gregory A; Casari Giorgio
The mitochondrial protease AFG3L2 is essential for axonal development.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2008;28(11):2827-36.
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2007: Burgio Gaëtan; Szatanik Marek; Guénet Jean-Louis; Arnau Maria-Rosa; Panthier Jean-Jacques; Montagutelli Xavier
Interspecific recombinant congenic strains between C57BL/6 and mice of the Mus spretus species: a powerful tool to dissect genetic control of complex traits.
Genetics 2007;177(4):2321-33.
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2007: Schaefer Michael K E; Schmalbruch Henning; Buhler Emmanuelle; Lopez Catherine; Martin Natalia; Guénet Jean-Louis; Haase Georg
Progressive motor neuronopathy: a critical role of the tubulin chaperone TBCE in axonal tubulin routing from the Golgi apparatus.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2007;27(33):8779-89.
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2006: Mashimo Tomoji; Erven Alexandra E; Spiden Sarah L; Guénet Jean-Louis; Steel Karen P
Two quantitative trait loci affecting progressive hearing loss in 101/H mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(8):841-50.
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2006: Adam Sonia Girard; Caraux Anouk; Fodil-Cornu Nassima; Loredo-Osti J Concepcion; Lesjean-Pottier Sarah; Jaubert Jean; Bubic Ivan; Jonjic Stipan; Guénet Jean-Louis; Vidal Silvia M; Colucci Francesco
Cmv4, a new locus linked to the NK cell gene complex, controls innate resistance to cytomegalovirus in wild-derived mice.
Journal of immunology (Baltimore, Md. : 1950) 2006;176(9):5478-85.
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2006: Simon-Chazottes Dominique; Tutois Sylvie; Kuehn Michael; Evans Martin; Bourgade Franck; Cook Sue; Davisson Muriel T; Guénet Jean-Louis
Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse.
Genomics 2006;87(5):673-7.
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2006: Kajaste-Rudnitski Anna; Mashimo Tomoji; Frenkiel Marie-Pascale; Guénet Jean-Louis; Lucas Marianne; Desprès Philippe
The 2',5'-oligoadenylate synthetase 1b is a potent inhibitor of West Nile virus replication inside infected cells.
The Journal of biological chemistry 2006;281(8):4624-37.
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2006: Benavides Fernando; Perez Carlos; Blando Jorge; Guénet Jean-Louis; Conti Claudio J
The radiation-induced nackt (nkt) allele is a loss-of-function mutation of the mouse cathepsin L gene.
Journal of immunology (Baltimore, Md. : 1950) 2006;176(2):702-3.
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2006: Abitbol M; Puy H; Sabaté J-M; Guénet J-L; Deybach J-Ch; Montagutelli X
Ursodesoxycholic acid and heme-arginate are unable to improve hematopoiesis and liver injury in an erythropoietic protoporphyria mouse model.
Physiological research / Academia Scientiarum Bohemoslovaca 2006;55 Suppl 2():S93-101.
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2005: Guénet Jean Louis
The mouse genome.
Genome research 2005;15(12):1729-40.
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2005: Aubin Isabelle; Guénet Jean-Louis
[Sphingomyelinases and osteogenesis imperfecta]
Médecine sciences : M/S 2005;21(12):1034-5.
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2005: Guénet Jean-Louis
Assessing the genetic component of the susceptibility of mice to viral infections.
Briefings in functional genomics & proteomics 2005;4(3):225-40.
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2005: Aubin Isabelle; Adams Carolyn P; Opsahl Sibylle; Septier Dominique; Bishop Colin E; Auge Nathalie; Salvayre Robert; Negre-Salvayre Anne; Goldberg Michel; Guénet Jean-Louis; Poirier Christophe
A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.
Nature genetics 2005;37(8):803-5.
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2005: Abitbol Marie; Bernex Florence; Puy Hervé; Jouault Hélène; Deybach Jean-Charles; Guénet Jean-Louis; Montagutelli Xavier
A mouse model provides evidence that genetic background modulates anemia and liver injury in erythropoietic protoporphyria.
American journal of physiology. Gastrointestinal and liver physiology 2005;288(6):G1208-16.
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2005: Kuwamura Mitsuru; Muraguchi Takehiko; Matsui Tamiko; Ueno Mayumi; Takenaka Shigeo; Yamate Jyoji; Kotani Takao; Kuramoto Takashi; Guénet Jean-Louis; Kitada Kazuhiro; Serikawa Tadao
Mutation at the Lmx1a locus provokes aberrant brain development in the rat.
Brain research. Developmental brain research 2005;155(2):99-106.
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2004: Guénet Jean-Louis
Chemical mutagenesis of the mouse genome: an overview.
Genetica 2004;122(1):9-24.
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2004: Lucas Marianne; Frenkiel Marie-Pascale; Mashimo Tomoji; Guénet Jean-Louis; Deubel Vincent; Desprès Philippe; Ceccaldi Pierre-Emmanuel
The Israeli strain IS-98-ST1 of West Nile virus as viral model for West Nile encephalitis in the Old World.
Virology journal 2004;1():9.
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2003: Blanc Isabelle; Bach Antoine; Lallemand Yvan; Perrin-Schmitt Fabienne; Guénet Jean-Louis; Robert Benoît
A new mouse limb mutation identifies a Twist allele that requires interacting loci on chromosome 4 for its phenotypic expression.
Mammalian genome : official journal of the International Mammalian Genome Society 2003;14(12):797-804.
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2003: Mashimo Tomoji; Glaser Philippe; Lucas Marianne; Simon-Chazottes Dominique; Ceccaldi Pierre Emmanuel; Montagutelli Xavier; Desprès Philippe; Guénet Jean Louis
Structural and functional genomics and evolutionary relationships in the cluster of genes encoding murine 2',5'-oligoadenylate synthetases.
Genomics 2003;82(5):537-52.
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2003: Gonçalves-Mendes Nicolas; Simon-Chazottes Dominique; Creveaux Isabelle; Meiniel Annie; Guénet Jean-Louis; Meiniel Robert
Mouse SCO-spondin, a gene of the thrombospondin type 1 repeat (TSR) superfamily expressed in the brain.
Gene 2003;312():263-70.
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2003: Lucas Marianne; Mashimo Tomoji; Frenkiel Marie-Pascale; Simon-Chazottes Dominique; Montagutelli Xavier; Ceccaldi Pierre-Emmanuel; Guénet Jean-Louis; Desprès Philippe
Infection of mouse neurones by West Nile virus is modulated by the interferon-inducible 2'-5' oligoadenylate synthetase 1b protein.
Immunology and cell biology 2003;81(3):230-6.
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2003: Besse Sylvie; Allamand Valérie; Vilquin Jean-Thomas; Li Zhenlin; Poirier Christophe; Vignier Nicolas; Hori Hisae; Guénet Jean-Louis; Guicheney Pascale
Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain gene.
Neuromuscular disorders : NMD 2003;13(3):216-22.
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2003: Guénet Jean-Louis; Després Philippe
[OAS genes and susceptibility to West Nile virus]
Médecine sciences : M/S 2003;19(1):9-12.
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2003: Guénet Jean Louis; Bonhomme François
Wild mice: an ever-increasing contribution to a popular mammalian model.
Trends in genetics : TIG 2003;19(1):24-31.
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2002: Martin Natalia; Jaubert Jean; Gounon Pierre; Salido Eduardo; Haase Georg; Szatanik Marek; Guénet Jean-Louis
A missense mutation in Tbce causes progressive motor neuronopathy in mice.
Nature genetics 2002;32(3):443-7.
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2002: Poirier Christophe; Yoshiki Atsushi; Fujiwara Kyoko; Guénet Jean-Louis; Kusakabe Moriaki
Hague (Hag). A new mouse hair mutation with an unstable semidominant allele.
Genetics 2002;162(2):831-40.
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2002: Santos Javier; Montagutelli Xavier; Acevedo Abraham; López Pilar; Vaquero Concepción; Fernández Mónica; Arnau Maria-Rosa; Szatanik Marek; Salido Eduardo; Guénet Jean-Louis; Fernández-Piqueras José
A new locus for resistance to gamma-radiation-induced thymic lymphoma identified using inter-specific consomic and inter-specific recombinant congenic strains of mice.
Oncogene 2002;21(43):6680-3.
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2002: Benavides Fernando; Starost Matthew F; Flores Mónica; Gimenez-Conti Irma B; Guénet Jean-Louis; Conti Claudio J
Impaired hair follicle morphogenesis and cycling with abnormal epidermal differentiation in nackt mice, a cathepsin L-deficient mutation.
The American journal of pathology 2002;161(2):693-703.
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2002: Staelens Jan; Wielockx Ben; Puimège Leen; Van Roy Frans; Guénet Jean-Louis; Libert Claude
Hyporesponsiveness of SPRET/Ei mice to lethal shock induced by tumor necrosis factor and implications for a TNF-based antitumor therapy.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(14):9340-5.
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2002: Gorgette Olivier; Existe Alexandre; Boubou Mariama Idrissa; Bagot Sébastien; Guénet Jean-Louis; Mazier Dominique; Cazenave Pierre-André; Pied Sylviane
Deletion of T cells bearing the V beta8.1 T-cell receptor following mouse mammary tumor virus 7 integration confers resistance to murine cerebral malaria.
Infection and immunity 2002;70(7):3701-6.
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2002: Campino Susana; Behrschmidt Catja; Bagot Sébastien; Guénet Jean-Louis; Cazenave Pierre-André; Holmberg Dan; Penha-Gonçalves Carlos
Unique genetic variation revealed by a microsatellite polymorphism survey in ten wild-derived inbred strains.
Genomics 2002;79(5):618-20.
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2002: Bagot S; Idrissa Boubou M; Campino S; Behrschmidt C; Gorgette O; Guénet J-L; Penha-Gonçalves C; Mazier D; Pied S; Cazenave P-A
Susceptibility to experimental cerebral malaria induced by Plasmodium berghei ANKA in inbred mouse strains recently derived from wild stock.
Infection and immunity 2002;70(4):2049-56.
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2002: Kiernan Amy E; Erven Alexandra; Voegeling Stéphanie; Peters Jo; Nolan Pat; Hunter Jackie; Bacon Yvonne; Steel Karen P; Brown Steve D M; Guénet Jean-Louis
ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(3):142-8.
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2001: Martin N; Jaubert J; Glaser P; Szatanik M; Guénet J L
Genetic and physical delineation of the region overlapping the progressive motor neuropathy (pmn) locus on mouse chromosome 13.
Genomics 2001;75(1-3):9-16.
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2001: Benavides F; Venables A; Poetschke Klug H; Glasscock E; Rudensky A; Gómez M; Martin Palenzuela N; Guénet J L; Richie E R; Conti C J
The CD4 T cell-deficient mouse mutation nackt (nkt) involves a deletion in the cathepsin L (CtsI) gene.
Immunogenetics 2001;53(3):233-42.
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2001: Lalouette A; Lohof A; Sotelo C; Guénet J; Mariani J
Neurobiological effects of a null mutation depend on genetic context: comparison between two hotfoot alleles of the delta-2 ionotropic glutamate receptor.
Neuroscience 2001;105(2):443-55.
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2001: Benavides F; Guénet J L
[Murine models for human diseases]
Medicina 2001;61(2):215-31.
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2000: Sipilä L; Szatanik M; Vainionpää H; Ruotsalainen H; Myllylä R; Guénet J L
The genes encoding mouse lysyl hydroxylase isoforms map to chromosomes 4,5, and 9.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(12):1132-4.
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2000: Barton P J; Mullen A J; Cullen M E; Dhoot G K; Simon-Chazottes D; Guénet J L
Genes encoding troponin I and troponin T are organized as three paralogous pairs in the mouse genome.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(10):926-9.
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2000: Simon-Chazottes D; Paces-Fessy M; Lamour-Isnard C; Guénet J L; Blanchet-Tournier M F
Genomic organization, chromosomal assignment, and expression analysis of the mouse suppressor of fused gene (Sufu) coding a Gli protein partner.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(8):614-21.
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1999: Jaubert J; Jaubert F; Martin N; Washburn L L; Lee B K; Eicher E M; Guénet J L
Three new allelic mouse mutations that cause skeletal overgrowth involve the natriuretic peptide receptor C gene (Npr3).
Proceedings of the National Academy of Sciences of the United States of America 1999;96(18):10278-83.
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1999: Benavides F; Giordano M; Fiette L; Bueno Brunialti A L; Martin Palenzuela N; Vanzulli S; Baldi P; Schmidt R; Dosne Pasqualini C; Guénet J
Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency.
Immunogenetics 1999;49(5):413-9.
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1998: Guénet J L
Wild mice as a source of genetic polymorphism.
Pathologie-biologie 1998;46(9):685-8.
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1998: Lalouette A; Guénet J L; Vriz S
Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher.
Genomics 1998;50(1):9-13.
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1998: Poirier C; Blot S; Fernandes M; Carle G F; Stanescu V; Stanescu R; Guénet J L
A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(5):390-1.
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1998: Poirier C; Poussard S; Faust D M; Imaizumi-Scherrer T; Weiss M C; Ducastaing A; Montarras D; Pinset C; Guénet J L
Mapping, cloning, cDNA sequence, and expression of the gene encoding the mouse micromolar calpain large subunit.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(5):388-9.
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1998: Poirier C; Guénet J L
Encyclopedia of the mouse genome VII. Mouse chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;8 Spec No():S353-60.
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1997: Lalouette A; Christians E; Guénet J L; Vriz S
Construction of a high-resolution genetic map encompassing the hotfoot locus.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(12):903-6.
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1997: Montagutelli X; Lalouette A; Boulouis H J; Guénet J L; Sundberg J P
Vesicle formation and follicular root sheath separation in mice homozygous for deleterious alleles at the balding (bal) locus.
The Journal of investigative dermatology 1997;109(3):324-8.
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1997: Fernandes M; Poirier C; Lassam N J; Larsson C; Guénet J; Gaudray P; Carle G F
The mouse homologs of RELA and MLK3 are located within a 120-kb fragment on chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(7):513-5.
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1997: Poirier C; Lalouette A; Foletta V C; Cohen D R; Guénet J L
The gene encoding the Fos-related antigen 2 (Fosl2) maps to mouse chromosome 5.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(3):223.
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1997: Viollet L; Bertrandy S; Bueno Brunialti A L; Lefebvre S; Burlet P; Clermont O; Cruaud C; Guénet J L; Munnich A; Melki J
cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn).
Genomics 1997;40(1):185-8.
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1997: Montagutelli X; Guénet J L
[Animal models of hereditary diseases]
La Revue du praticien 1997;47(2):162-8.
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1997: Benavides F; Guénet J L
[Gene mapping in mice]
Medicina 1997;57(4):507-10.
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1997: Poirier C; Guénet J L
Mouse chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;7 Spec No():S305-12.
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1996: Brunialti A L; Harding C O; Wolff J A; Guénet J L
The mouse mutation sarcosinemia (sar) maps to chromosome 2 in a region homologous to human 9q33-q34.
Genomics 1996;36(1):182-4.
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1996: Montagutelli X; Hogan M E; Aubin G; Lalouette A; Guénet J L; King L E; Sundberg J P
Lanceolate hair (lah): a recessive mouse mutation with alopecia and abnormal hair.
The Journal of investigative dermatology 1996;107(1):20-5.
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1996: Poirier C; O'Brien E P; Bueno Brunialti A L; Chambard J; Swank R T; Guénet J
The gene encoding the thrombin receptor (Cf2r) maps to mouse chromosome 13.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(4):322.
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1995: Guénet J L; Simon-Chazottes D; de Robertis E; Blum M
The mouse goosecoïd gene (Gsc) maps to the telomeric part of mouse chromosome 12.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(11):816-7.
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1995: Brunialti A L; Poirier C; Schmalbruch H; Guénet J L
The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13.
Genomics 1995;29(1):131-5.
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1995: Guénet J L; Simon-Chazottes D; Ringwald M; Kemler R
The genes coding for alpha and beta catenin (Catna1 and Catnb) and plakoglobin (Jup) map to mouse chromosomes 18, 9, and 11, respectively.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(5):363-6.
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1994: Beckers M C; Bar I; Huynh-Thu T; Dernoncourt C; Brunialti A L; Montagutelli X; Guénet J L; Goffinet A M
A high-resolution genetic map of mouse chromosome 5 encompassing the reeler (rl) locus.
Genomics 1994;23(3):685-90.
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1994: Robert B; Montagutelli X; Houzelstein D; Ferland L; Cohen A; Buckingham M; Guénet J L
Msx1 is close but not allelic to either Hm or Hx on mouse chromosome 5.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(7):446-9.
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1994: O'Brien E P; Novak E K; Keller S A; Poirier C; Guénet J L; Swank R T
Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(6):356-60.
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1994: Montagutelli X; Lalouette A; Coudé M; Kamoun P; Forest M; Guénet J L
aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16.
Genomics 1994;19(1):9-11.
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1994: Poirier C; Guénet J L
Mouse chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5 Spec No():S266-75.
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1993: Alonso S; Montagutelli X; Simon-Chazottes D; Guénet J L; Buckingham M
Re-localization of Actsk-1 to mouse chromosome 8, a new region of homology with human chromosome 1.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(1):15-20.
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1993: Simon-Chazottes D; Cloez-Tayarani I; Fillion M P; Guénet J L; Fillion G
The serotonin 5-HT1B receptor subtype (Htr1b) gene maps to mouse chromosome 9.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(7):397-8.
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1993: Guénet J L; Poirier C
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4 Spec No():S261-8.
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1992: Baron B; Poirier C; Simon-Chazottes D; Barnier C; Guénet J L
A new strategy useful for rapid identification of microsatellites from DNA libraries with large size inserts.
Nucleic acids research 1992;20(14):3665-9.
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1992: Serikawa T; Montagutelli X; Simon-Chazottes D; Guénet J L
Polymorphisms revealed by PCR with single, short-sized, arbitrary primers are reliable markers for mouse and rat gene mapping.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(2):65-72.
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1992: Guénet J L; Watson M; Seldin M F
Mouse chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3 Spec No():S266-73.
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1992: Simon-Chazottes D; Matsubara S; Miyauchi T; Muramatsu T; Guénet J L
Chromosomal localization of two cell surface-associated molecules of potential importance in development: midkine (Mdk) and basigin (Bsg).
Mammalian genome : official journal of the International Mammalian Genome Society 1992;2(4):269-71.
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1992: Baldacci P A; Richoux V; Renard J P; Guénet J L; Babinet C
The locus Om, responsible for the DDK syndrome, maps close to Sigje on mouse chromosome 11.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;2(2):100-5.
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1991: Boyer S; Montagutelli X; Gomès D; Simon-Chazottes D; Guénet J L; Dupouey P
Recent evolutionary origin of the expression of the glial fibrillary acidic protein (GFAP) in lens epithelial cells. A molecular and genetic analysis of various mouse species.
Brain research. Molecular brain research 1991;10(2):159-66.
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1991: Guénet J L
Mouse chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1 Spec No():S306-17.
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1991: Tutois S; Salaun J; Mattei M G; Guénet J L
Tg (9 HSA-MYC), a homozygous lethal insertion in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(3):184-90.
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1991: Montagutelli X; Serikawa T; Guénet J L
PCR-analyzed microsatellites: data concerning laboratory and wild-derived mouse inbred strains.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(4):255-9.
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1991: Melanitou E; Simon-Chazottes D; Guénet J L; Rougeon F
The gene coding for the kidney androgen-regulated protein (Kap), maps between the Gapd and Kras-2 genes on mouse chromosome 6.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(3):191-2.
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1990: Guénet J L; Nagamine C; Simon-Chazottes D; Montagutelli X; Bonhomme F
Hst-3: an X-linked hybrid sterility gene.
Genetical research 1990;56(2-3):163-5.
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1990: Babinet C; Richoux V; Guénet J L; Renard J P
The DDK inbred strain as a model for the study of interactions between parental genomes and egg cytoplasm in mouse preimplantation development.
Development (Cambridge, England). Supplement 1990;():81-7.
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1988: Maunoury R; Robine S; Pringault E; Huet C; Guénet J L; Gaillard J A; Louvard D
Villin expression in the visceral endoderm and in the gut anlage during early mouse embryogenesis.
The EMBO journal 1988;7(11):3321-9.
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1988: Rousseau-Merck M F; Simon-Chazottes D; Arpin M; Pringault E; Louvard D; Guénet J L; Berger R
Localization of the villin gene on human chromosome 2q35-q36 and on mouse chromosome 1.
Human genetics 1988;78(2):130-3.
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1987: Nagamine C M; Michot J L; Roberts C; Guénet J L; Bishop C E
Linkage of the murine steroid sulfatase locus, Sts, to sex reversed, Sxr: a genetic and molecular analysis.
Nucleic acids research 1987;15(22):9227-38.
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1987: Bishop C E; Roberts C; Michot J L; Nagamine C; Winking H; Guénet J L; Weith A
The use of specific DNA probes to analyse the Sxr mutation in the mouse.
Development (Cambridge, England) 1987;101 Suppl():167-75.
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