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EMBO Reports
|
February 22, 2017
Activity-DEPendent Transposition
Andrew 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 neocortex
Mateusz 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 Development
Sami Zaqout, Paraskevi Bessa, Nadine Krämer, et al.
Frontiers in Neuroanatomy
|
February 1, 2024
Molecular mechanisms of corpus callosum development: a four-step journey
Maria 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 Neurod2/6
Kuo 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 Signaling
Srinivas 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 expression
A Ioana Weber, Srinivas Parthasarathy, Ekaterina Borisova, et al.
Nature Communications
|
August 16, 2024
Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiring
Paraskevi 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-140
Mateusz 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 disorders
Ethiraj Ravindran, Ramona Jühlen, Carlos H Vieira-Vieira, et al.
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Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
EMBO Reports
|
February 22, 2017
Activity-DEPendent Transposition
Andrew 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 neocortex
Mateusz 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 Development
Sami Zaqout, Paraskevi Bessa, Nadine Krämer, et al.
Frontiers in Neuroanatomy
|
February 1, 2024
Molecular mechanisms of corpus callosum development: a four-step journey
Maria 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 Neurod2/6
Kuo 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 Signaling
Srinivas 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 expression
A Ioana Weber, Srinivas Parthasarathy, Ekaterina Borisova, et al.
Nature Communications
|
August 16, 2024
Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiring
Paraskevi 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-140
Mateusz 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 disorders
Ethiraj Ravindran, Ramona Jühlen, Carlos H Vieira-Vieira, et al.
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