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Cell Reports
|
September 27, 2018
Stochastic Gene Choice during Cellular Differentiation
Takeo Wada, Sandrine Wallerich, Attila Becskei
ACS Synthetic Biology
|
January 10, 2019
Synthetic Transcription Factors Switch from Local to Long-Range Control during Cell Differentiation
Takeo Wada, Sandrine Wallerich, Attila Becskei
Cell Reports
|
March 28, 2019
Contribution of RNA Degradation to Intrinsic and Extrinsic Noise in Gene Expression
Antoine Baudrimont, Vincent Jaquet, Sandrine Wallerich, et al.
Nucleic Acids Research
|
January 12, 2022
Determinants of the temperature adaptation of mRNA degradation
Vincent 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 degeneration
Ji 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 involvement
Siying Lin, Francesca Cancellieri, Yexuan Cao, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Cell Reports
|
September 27, 2018
Stochastic Gene Choice during Cellular Differentiation
Takeo Wada, Sandrine Wallerich, Attila Becskei
ACS Synthetic Biology
|
January 10, 2019
Synthetic Transcription Factors Switch from Local to Long-Range Control during Cell Differentiation
Takeo Wada, Sandrine Wallerich, Attila Becskei
Cell Reports
|
March 28, 2019
Contribution of RNA Degradation to Intrinsic and Extrinsic Noise in Gene Expression
Antoine Baudrimont, Vincent Jaquet, Sandrine Wallerich, et al.
Nucleic Acids Research
|
January 12, 2022
Determinants of the temperature adaptation of mRNA degradation
Vincent 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 degeneration
Ji 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 involvement
Siying Lin, Francesca Cancellieri, Yexuan Cao, et al.
Page
of 1