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Patrick Reed

Showing results (11-20 of 18) with videos related to

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Clinical Orthopaedics and Related Research|October 24, 2002
Costameres: repeating structures at the sarcolemma of skeletal muscleRobert J Bloch, Yassemi Capetanaki, Andrea O'Neill, et al.
Annals of Neurology|January 27, 2006
Sarcolemmal reorganization in facioscapulohumeral muscular dystrophyPatrick Reed, Neil C Porter, John Strong, et al.
Molecular Psychiatry|February 1, 2024
Human iN neuronal model of schizophrenia displays dysregulation of chromogranin B and related neuropeptide transmitter signaturesSonia Podvin, Jeffrey Jones, Austin Kang, et al.
Journal of Virology|September 29, 2004
Anti-Vpr activity of a yeast chaperone proteinZsigmond Benko, Dong Liang, Emmanuel Agbottah, et al.
Nature Genetics|June 2, 2022
Genetic correlates of phenotypic heterogeneity in autismVarun Warrier, Xinhe Zhang, Patrick Reed, et al.
Molecular Psychiatry|May 4, 2024
Monozygotic twins discordant for schizophrenia differ in maturation and synaptic transmissionShani Stern, Lei Zhang, Meiyan Wang, et al.
American Journal of Human Genetics|May 23, 2020
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and OsteochondromasDara Tolchin, Jessica P Yeager, Priya Prasad, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt SignalingLot Snijders Blok, Erik Madsen, Jane Juusola, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Clinical Orthopaedics and Related Research|October 24, 2002
Costameres: repeating structures at the sarcolemma of skeletal muscleRobert J Bloch, Yassemi Capetanaki, Andrea O'Neill, et al.
Annals of Neurology|January 27, 2006
Sarcolemmal reorganization in facioscapulohumeral muscular dystrophyPatrick Reed, Neil C Porter, John Strong, et al.
Molecular Psychiatry|February 1, 2024
Human iN neuronal model of schizophrenia displays dysregulation of chromogranin B and related neuropeptide transmitter signaturesSonia Podvin, Jeffrey Jones, Austin Kang, et al.
Journal of Virology|September 29, 2004
Anti-Vpr activity of a yeast chaperone proteinZsigmond Benko, Dong Liang, Emmanuel Agbottah, et al.
Nature Genetics|June 2, 2022
Genetic correlates of phenotypic heterogeneity in autismVarun Warrier, Xinhe Zhang, Patrick Reed, et al.
Molecular Psychiatry|May 4, 2024
Monozygotic twins discordant for schizophrenia differ in maturation and synaptic transmissionShani Stern, Lei Zhang, Meiyan Wang, et al.
American Journal of Human Genetics|May 23, 2020
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and OsteochondromasDara Tolchin, Jessica P Yeager, Priya Prasad, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt SignalingLot Snijders Blok, Erik Madsen, Jane Juusola, et al.
Pageof 2