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Paraskevi Bessa

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

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EMBO Reports|February 22, 2017
Activity-DEPendent TranspositionAndrew G Newman, Paraskevi Bessa, Victor Tarabykin, et al.
Journal of Neuroscience Methods|August 8, 2017
Satb2<sup>Cre/+</sup> mouse as a tool to investigate cell fate determination in the developing neocortexMateusz Cyryl Ambrozkiewicz, Paraskevi Bessa, Andrea Salazar-Lázaro, et al.
Stem Cell Reports|February 7, 2017
CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic DevelopmentSami Zaqout, Paraskevi Bessa, Nadine Krämer, et al.
Frontiers in Neuroanatomy|February 1, 2024
Molecular mechanisms of corpus callosum development: a four-step journeyMaria Gavrish, Angelina Kustova, Juan C Celis Suescún, et al.
Cerebral Cortex (New York, N.Y. : 1991)|April 24, 2022
TrkB-dependent EphrinA reverse signaling regulates callosal axon fasciculate growth downstream of Neurod2/6Kuo Yan, Ingo Bormuth, Olga Bormuth, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 14, 2021
TrkC-T1, the Non-Catalytic Isoform of TrkC, Governs Neocortical Progenitor Fate Specification by Inhibition of MAP Kinase SignalingSrinivas Parthasarathy, Swathi Srivatsa, A Ioana Weber, et al.
Nucleic Acids Research|September 12, 2023
Srsf1 and Elavl1 act antagonistically on neuronal fate choice in the developing neocortex by controlling TrkC receptor isoform expressionA Ioana Weber, Srinivas Parthasarathy, Ekaterina Borisova, et al.
Nature Communications|August 16, 2024
Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiringParaskevi Bessa, Andrew G Newman, Kuo Yan, et al.
Neuron|November 6, 2018
Polarity Acquisition in Cortical Neurons Is Driven by Synergistic Action of Sox9-Regulated Wwp1 and Wwp2 E3 Ubiquitin Ligases and Intronic miR-140Mateusz C Ambrozkiewicz, Manuela Schwark, Mika Kishimoto-Suga, et al.
Human Molecular Genetics|June 25, 2021
Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disordersEthiraj Ravindran, Ramona Jühlen, Carlos H Vieira-Vieira, et al.
Pageof 1

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

Sort By:
Pageof 1
EMBO Reports|February 22, 2017
Activity-DEPendent TranspositionAndrew G Newman, Paraskevi Bessa, Victor Tarabykin, et al.
Journal of Neuroscience Methods|August 8, 2017
Satb2<sup>Cre/+</sup> mouse as a tool to investigate cell fate determination in the developing neocortexMateusz Cyryl Ambrozkiewicz, Paraskevi Bessa, Andrea Salazar-Lázaro, et al.
Stem Cell Reports|February 7, 2017
CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic DevelopmentSami Zaqout, Paraskevi Bessa, Nadine Krämer, et al.
Frontiers in Neuroanatomy|February 1, 2024
Molecular mechanisms of corpus callosum development: a four-step journeyMaria Gavrish, Angelina Kustova, Juan C Celis Suescún, et al.
Cerebral Cortex (New York, N.Y. : 1991)|April 24, 2022
TrkB-dependent EphrinA reverse signaling regulates callosal axon fasciculate growth downstream of Neurod2/6Kuo Yan, Ingo Bormuth, Olga Bormuth, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 14, 2021
TrkC-T1, the Non-Catalytic Isoform of TrkC, Governs Neocortical Progenitor Fate Specification by Inhibition of MAP Kinase SignalingSrinivas Parthasarathy, Swathi Srivatsa, A Ioana Weber, et al.
Nucleic Acids Research|September 12, 2023
Srsf1 and Elavl1 act antagonistically on neuronal fate choice in the developing neocortex by controlling TrkC receptor isoform expressionA Ioana Weber, Srinivas Parthasarathy, Ekaterina Borisova, et al.
Nature Communications|August 16, 2024
Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiringParaskevi Bessa, Andrew G Newman, Kuo Yan, et al.
Neuron|November 6, 2018
Polarity Acquisition in Cortical Neurons Is Driven by Synergistic Action of Sox9-Regulated Wwp1 and Wwp2 E3 Ubiquitin Ligases and Intronic miR-140Mateusz C Ambrozkiewicz, Manuela Schwark, Mika Kishimoto-Suga, et al.
Human Molecular Genetics|June 25, 2021
Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disordersEthiraj Ravindran, Ramona Jühlen, Carlos H Vieira-Vieira, et al.
Pageof 1