C. Laclef

发表

Altered myogenesis in Six1-deficient mice

G. Hamard, C. Laclef, J. Demignon, 2003, Development.

Conserved rules in embryonic development of cortical interneurons.

C. Métin, C. Laclef, 2017, Seminars in cell & developmental biology.

Six1 is required for the early organogenesis of mammalian kidney

C. Laclef, P. Maire, P. Xu, 2003, Development.

A transient role of primary cilia in controlling direct versus indirect neurogenesis in the developing cerebral cortex

S. Schneider-Maunoury, J. Reiter, C. Laclef, 2020, bioRxiv.

A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development

S. Schneider-Maunoury, J. Reiter, C. Laclef, 2020, eLife.

Eya1 and Eya2 proteins are required for hypaxial somitic myogenesis in the mouse embryo.

C. Laclef, J. Demignon, E. Souil, 2007, Developmental biology.

Six1 is not involved in limb tendon development, but is expressed in limb connective tissue under Shh regulation

M. Bonnin, C. Laclef, P. Maire, 2005, Mechanisms of Development.

[The transcriptional activator Eya is a tyrosine phosphatase].

C. Laclef, 2004, Medecine sciences : M/S.

The Ciliopathy Gene Ftm/Rpgrip1l Controls Mouse Forebrain Patterning via Region-Specific Modulation of Hedgehog/Gli Signaling

S. Schneider-Maunoury, C. Laclef, M. Catala, 2018, The Journal of Neuroscience.

Six Homeoproteins Directly Activate Myod Expression in the Gene Regulatory Networks That Control Early Myogenesis

M. Buckingham, M. Lagha, Marc Santolini, 2013, PLoS genetics.

Phenotype into the Fast-Twitch Phenotype Adult Muscle from the Slow-Twitch Six 1 and Eya 1 Expression Can Reprogram

J. Concordet, F. Spitz, K. Kawakami, 2004 .

The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathies

R. Roepman, M. Ueffing, B. Durand, 2015, Cilia.

The ciliopathy gene Rpgrip1l is essential for hair follicle development

S. Schneider-Maunoury, R. Paus, K. Takemaru, 2014, The Journal of investigative dermatology.

Thymus, kidney and craniofacial abnormalities in Six1 deficient mice

C. Laclef, J. Demignon, E. Souil, 2003, Mechanisms of Development.

Six1 and Eya1 Expression Can Reprogram Adult Muscle from the Slow-Twitch Phenotype into the Fast-Twitch Phenotype

Kiyoshi Kawakami, Jean-Paul Concordet, Pascal Maire, 2004, Molecular and Cellular Biology.

Modifying transcript lengths of cycling mouse segmentation genes

D. Ish-Horowicz, C. Laclef, M. Stauber, 2012, Mechanisms of Development.

Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid.

R. Maas, H. Peters, C. Laclef, 2002, Development.

Defects in brain patterning and head morphogenesis in the mouse mutant Fused toes.

S. Schneider-Maunoury, U. Rüther, C. Laclef, 2007, Developmental biology.

Primary cilia are required for cerebellar development and Shh-dependent expansion of progenitor pool.

J. García-Verdugo, A. Álvarez-Buylla, N. Spassky, 2008, Developmental biology.

Altered myogenesis in Six 1-deficient mice

G. Hamard, C. Laclef, J. Demignon, 2003 .

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

Colin A. Johnson, Nathalie Boddaert, Sophie Saunier, 2007, Nature Genetics.

Primary cilia control telencephalic patterning and morphogenesis via Gli3 proteolytic processing

Sylvie Schneider-Maunoury, S. Schneider-Maunoury, U. Rüther, 2011, Development.

The role of primary cilia in corpus callosum formation is mediated by production of the Gli3 repressor.

Martin Catala, Sylvie Schneider-Maunoury, C. Métin, 2015, Human molecular genetics.

[Primary cilia control different steps of brain development].

C. Laclef, 2014, Medecine sciences : M/S.

RPGRIP1L is required for stabilizing epidermal keratinocyte adhesion through regulating desmoglein endocytosis

Y. Hannun, K. Shroyer, S. Schneider-Maunoury, 2019, PLoS genetics.