Search Results - "Lalouette, Alexis"

Mef2 interacts with the Notch pathway during adult muscle development in Drosophila melanogaster by Caine, Charlotte, Kasherov, Petar, Silber, Joël, Lalouette, Alexis

“…Myogenesis of indirect flight muscles (IFMs) in Drosophila melanogaster follows a well-defined cellular developmental scheme. During embryogenesis, a set of…”
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Hotfoot Mouse Mutations Affect the δ2 Glutamate Receptor Gene and Are Allelic to Lurcher by Lalouette, Alexis, Guénet, Jean-Louis, Vriz, Sophie

“…Hotfoot (ho) is a recessive mouse mutation characterized by cerebellar ataxia associated with relatively mild abnormalities of the cerebellum. It has been…”
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Male Sterility Caused by Sperm Cell-Specific Structural Abnormalities in Ebouriffé, a New Mutation of the House Mouse1 by Lalouette, Alexis, Lablack, Abdesselam, Guenet, Jean-Louis, Montagutelli, Xavier, Segretain, Dominique

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Mef2 Interacts with the Notch Pathway during Adult Muscle Development in Drosophila melanogaster: e108149 by Caine, Charlotte, Kasherov, Petar, Silber, Joeel, Lalouette, Alexis

“…Myogenesis of indirect flight muscles (IFMs) in Drosophila melanogaster follows a well-defined cellular developmental scheme. During embryogenesis, a set of…”
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Integration of differentiation signals during indirect flight muscle formation by a novel enhancer of Drosophila vestigial gene by Bernard, Frédéric, Kasherov, Petar, Grenetier, Sabrina, Dutriaux, Annie, Zider, Alain, Silber, Joël, Lalouette, Alexis

“…The gene vestigial ( vg) plays a key role in indirect flight muscle (IFM) development. We show here that vg is controlled by the Notch anti-myogenic signaling…”
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Lurcher GRID2-Induced Death and Depolarization Can Be Dissociated in Cerebellar Purkinje Cells by Selimi, Fekrije, Lohof, Ann M., Heitz, Stéphane, Lalouette, Alexis, Jarvis, Christopher I., Bailly, Yannick, Mariani, Jean

“…The Lurcher mutation transforms the GRID2 receptor into a constitutively opened channel. In Lurcher heterozygous mice, cerebellar Purkinje cells are…”
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Lurcher GRID2 induced death and depolarization can be dissociate in cerebellar Purkinje cells by Selimi, Fekrije, Lohof, Ann, Heitz, Stéphane, Lalouette, Alexis, I. Jarvis, Christopher, Bailly, Yannick, Mariani, Jean

“…The Lurcher mutation transforms the GRID2 receptor into a constitutively opened channel. In Lurcher heterozygous mice, cerebellar Purkinje cells are…”
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Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus by Montagutelli, Xavier, Lalouette, Alexis, Boulouis, Henri-Jean, Guénet, Jean-Louis, Sundberg, John P.

“…The balding (bal) mutation of the mouse is an auto-somal recessive mutation that causes alopecia and immunologic anomalies. A new allele was identified by…”
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Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair by Montagutelli, Xavier, Hogan, Margaret E., Aubin, Geneviève, Lalouette, Alexis, Guénet, Jean-Louis, King, Lloyd E., Sundberg, John P.

“…A new autosomal recessive mutation of the house mouse developed generalized alopecia associated with breakage of abnormal hair shafts. This mutation, named…”
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aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16 by Montagutelli, X, Lalouette, A, Coudé, M, Kamoun, P, Forest, M, Guénet, J L

“…Alkaptonuria is a human hereditary metabolic disease characterized by a very high urinary excretion of homogentisic acid, an intermediary product in the…”
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Male sterility caused by sperm cell-specific structural abnormalities in ébouriffé, a new mutation of the house mouse by LALOUETTE, A, LABLACK, A, GUENET, J.-L, MONTAGUTELLI, X, SEGRETAIN, D

“…We have investigated the male sterility associated with a new recessive mutation of the house mouse: ébouriffé (ebo). All spermatozoa present in the epididymis…”
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Construction of a high-resolution genetic map encompassing the hotfoot locus by Lalouette, A, Christians, E, Guénet, J L, Vriz, S

“…Hotfoot (ho) is a mutation affecting posture and movement. We report a new allele associated with the insertion of a transgene and its high-resolution mapping…”
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