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Sandrine Wallerich

Showing results (1-10 of 6) with videos related to

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Cell Reports|September 27, 2018
Stochastic Gene Choice during Cellular DifferentiationTakeo Wada, Sandrine Wallerich, Attila Becskei
ACS Synthetic Biology|January 10, 2019
Synthetic Transcription Factors Switch from Local to Long-Range Control during Cell DifferentiationTakeo Wada, Sandrine Wallerich, Attila Becskei
Cell Reports|March 28, 2019
Contribution of RNA Degradation to Intrinsic and Extrinsic Noise in Gene ExpressionAntoine Baudrimont, Vincent Jaquet, Sandrine Wallerich, et al.
Nucleic Acids Research|January 12, 2022
Determinants of the temperature adaptation of mRNA degradationVincent Jaquet, Sandrine Wallerich, Sylvia Voegeli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 29, 2024
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degenerationJi Hoon Han, Kim Rodenburg, Tamar Hayman, et al.
American Journal of Human Genetics|February 20, 2026
Bi-allelic variants in FSD1L cause retinitis pigmentosa with or without neurological involvementSiying Lin, Francesca Cancellieri, Yexuan Cao, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Cell Reports|September 27, 2018
Stochastic Gene Choice during Cellular DifferentiationTakeo Wada, Sandrine Wallerich, Attila Becskei
ACS Synthetic Biology|January 10, 2019
Synthetic Transcription Factors Switch from Local to Long-Range Control during Cell DifferentiationTakeo Wada, Sandrine Wallerich, Attila Becskei
Cell Reports|March 28, 2019
Contribution of RNA Degradation to Intrinsic and Extrinsic Noise in Gene ExpressionAntoine Baudrimont, Vincent Jaquet, Sandrine Wallerich, et al.
Nucleic Acids Research|January 12, 2022
Determinants of the temperature adaptation of mRNA degradationVincent Jaquet, Sandrine Wallerich, Sylvia Voegeli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 29, 2024
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degenerationJi Hoon Han, Kim Rodenburg, Tamar Hayman, et al.
American Journal of Human Genetics|February 20, 2026
Bi-allelic variants in FSD1L cause retinitis pigmentosa with or without neurological involvementSiying Lin, Francesca Cancellieri, Yexuan Cao, et al.
Pageof 1