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Laurent Fasano

Showing results (21-30 of 32) with videos related to

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Development (Cambridge, England)|March 5, 2002
Grunge, related to human Atrophin-like proteins, has multiple functions in Drosophila developmentAlfrun Erkner, Agnès Roure, Bernard Charroux, et al.
Behavior Genetics|September 23, 2019
Construct Validity and Cross Validity of a Test Battery Modeling Autism Spectrum Disorder (ASD) in MicePierre L Roubertoux, Sylvie Tordjman, Xavier Caubit, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 12, 2009
Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstructionDagan Jenkins, Xavier Caubit, Aleksandar Dimovski, et al.
Diabetes|April 29, 2015
Tshz1 Regulates Pancreatic β-Cell MaturationJeffrey C Raum, Scott A Soleimanpour, David N Groff, et al.
Development (Cambridge, England)|September 9, 2008
Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4Xavier Caubit, Claire M Lye, Elise Martin, et al.
Translational Psychiatry|March 16, 2022
Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviorsXavier Caubit, Paolo Gubellini, Pierre L Roubertoux, et al.
Human Molecular Genetics|December 17, 2021
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defectsIrene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad, et al.
Biological Psychiatry|May 8, 2019
Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder-like BehaviorDorian Chabbert, Xavier Caubit, Pierre L Roubertoux, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Single-Nucleus Analysis of Human White Adipose Tissue Reveals Adipocyte Subsets with Distinct Metabolic ProfilesVissarion Efthymiou, Adhideb Ghosh, Sean D Kodani, et al.
European Journal of Human Genetics : EJHG|October 17, 2024
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tractEsra Kesdiren, Helge Martens, Frank Brand, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Development (Cambridge, England)|March 5, 2002
Grunge, related to human Atrophin-like proteins, has multiple functions in Drosophila developmentAlfrun Erkner, Agnès Roure, Bernard Charroux, et al.
Behavior Genetics|September 23, 2019
Construct Validity and Cross Validity of a Test Battery Modeling Autism Spectrum Disorder (ASD) in MicePierre L Roubertoux, Sylvie Tordjman, Xavier Caubit, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 12, 2009
Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstructionDagan Jenkins, Xavier Caubit, Aleksandar Dimovski, et al.
Diabetes|April 29, 2015
Tshz1 Regulates Pancreatic β-Cell MaturationJeffrey C Raum, Scott A Soleimanpour, David N Groff, et al.
Development (Cambridge, England)|September 9, 2008
Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4Xavier Caubit, Claire M Lye, Elise Martin, et al.
Translational Psychiatry|March 16, 2022
Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviorsXavier Caubit, Paolo Gubellini, Pierre L Roubertoux, et al.
Human Molecular Genetics|December 17, 2021
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defectsIrene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad, et al.
Biological Psychiatry|May 8, 2019
Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder-like BehaviorDorian Chabbert, Xavier Caubit, Pierre L Roubertoux, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Single-Nucleus Analysis of Human White Adipose Tissue Reveals Adipocyte Subsets with Distinct Metabolic ProfilesVissarion Efthymiou, Adhideb Ghosh, Sean D Kodani, et al.
European Journal of Human Genetics : EJHG|October 17, 2024
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tractEsra Kesdiren, Helge Martens, Frank Brand, et al.
Pageof 4