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Kaindl

Showing results (411-420 of 543) with videos related to

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Annals of Neurology|November 11, 2008
Sedative and anticonvulsant drugs suppress postnatal neurogenesisVanya G Stefovska, Ortrud Uckermann, Miroslaw Czuczwar, et al.
Neurobiology of Disease|May 19, 2019
Altered inhibition and excitation in neocortical circuits in congenital microcephalySami Zaqout, Kathrin Blaesius, Yuan-Ju Wu, et al.
Clinical Genetics|April 9, 2021
Zebrafish modeling mimics developmental phenotype of patients with RAPGEF1 mutationNa Li, Pei Zhou, Miaomiao Yang, et al.
Epilepsia Open|February 17, 2024
The importance of routine genetic testing in pediatric epilepsy surgeryLena-Luise Becker, Konstantin L Makridis, Angela T Abad-Perez, et al.
Oncogene|March 2, 2010
ETV6/RUNX1 abrogates mitotic checkpoint function and targets its key player MAD2L1G Krapf, U Kaindl, A Kilbey, et al.
European Journal of Neurology|March 4, 2008
Novel RYR1 missense mutation causes core rod myopathyM von der Hagen, W Kress, G Hahn, et al.
Science (New York, N.Y.)|February 9, 2018
Observation of chiral phononsHanyu Zhu, Jun Yi, Ming-Yang Li, et al.
Investigational New Drugs|February 15, 2023
Safety and anti-tumor activity of lisavanbulin administered as 48-hour infusion in patients with ovarian cancer or recurrent glioblastoma: a phase 2a studyMarkus Joerger, Thomas Hundsberger, Simon Haefliger, et al.
Neuropediatrics|October 19, 2019
Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular DisordersMaja von der Hagen, Lena-Luise Becker, Thomas F Wienker, et al.
Endocrinology|July 11, 2019
Estrogen Signaling Drives Ciliogenesis in Human Endometrial OrganoidsSandra Haider, Magdalena Gamperl, Thomas R Burkard, et al.
Pageof 55

Showing results (411-420 of 543) with videos related to

Sort By:
Pageof 55
Annals of Neurology|November 11, 2008
Sedative and anticonvulsant drugs suppress postnatal neurogenesisVanya G Stefovska, Ortrud Uckermann, Miroslaw Czuczwar, et al.
Neurobiology of Disease|May 19, 2019
Altered inhibition and excitation in neocortical circuits in congenital microcephalySami Zaqout, Kathrin Blaesius, Yuan-Ju Wu, et al.
Clinical Genetics|April 9, 2021
Zebrafish modeling mimics developmental phenotype of patients with RAPGEF1 mutationNa Li, Pei Zhou, Miaomiao Yang, et al.
Epilepsia Open|February 17, 2024
The importance of routine genetic testing in pediatric epilepsy surgeryLena-Luise Becker, Konstantin L Makridis, Angela T Abad-Perez, et al.
Oncogene|March 2, 2010
ETV6/RUNX1 abrogates mitotic checkpoint function and targets its key player MAD2L1G Krapf, U Kaindl, A Kilbey, et al.
European Journal of Neurology|March 4, 2008
Novel RYR1 missense mutation causes core rod myopathyM von der Hagen, W Kress, G Hahn, et al.
Science (New York, N.Y.)|February 9, 2018
Observation of chiral phononsHanyu Zhu, Jun Yi, Ming-Yang Li, et al.
Investigational New Drugs|February 15, 2023
Safety and anti-tumor activity of lisavanbulin administered as 48-hour infusion in patients with ovarian cancer or recurrent glioblastoma: a phase 2a studyMarkus Joerger, Thomas Hundsberger, Simon Haefliger, et al.
Neuropediatrics|October 19, 2019
Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular DisordersMaja von der Hagen, Lena-Luise Becker, Thomas F Wienker, et al.
Endocrinology|July 11, 2019
Estrogen Signaling Drives Ciliogenesis in Human Endometrial OrganoidsSandra Haider, Magdalena Gamperl, Thomas R Burkard, et al.
Pageof 55