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Showing results (391-400 of 397) with videos related to

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Translational Psychiatry|May 18, 2016
Glucagon-like peptide 1 receptor activation regulates cocaine actions and dopamine homeostasis in the lateral septum by decreasing arachidonic acid levelsI A Reddy, J A Pino, P Weikop, et al.
Nature|May 1, 2024
Paternal microbiome perturbations impact offspring fitnessAyele Argaw-Denboba, Thomas S B Schmidt, Monica Di Giacomo, et al.
Molecular Psychiatry|December 21, 2011
Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disabilityL S Nguyen, L Jolly, C Shoubridge, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
G3 (Bethesda, Md.)|September 25, 2013
Construction of reference chromosome-scale pseudomolecules for potato: integrating the potato genome with genetic and physical mapsSanjeev Kumar Sharma, Daniel Bolser, Jan de Boer, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 40

Showing results (391-400 of 397) with videos related to

Sort By:
Pageof 40
You have reached the last page of results.This site can display upto 397 results.
Translational Psychiatry|May 18, 2016
Glucagon-like peptide 1 receptor activation regulates cocaine actions and dopamine homeostasis in the lateral septum by decreasing arachidonic acid levelsI A Reddy, J A Pino, P Weikop, et al.
Nature|May 1, 2024
Paternal microbiome perturbations impact offspring fitnessAyele Argaw-Denboba, Thomas S B Schmidt, Monica Di Giacomo, et al.
Molecular Psychiatry|December 21, 2011
Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disabilityL S Nguyen, L Jolly, C Shoubridge, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
G3 (Bethesda, Md.)|September 25, 2013
Construction of reference chromosome-scale pseudomolecules for potato: integrating the potato genome with genetic and physical mapsSanjeev Kumar Sharma, Daniel Bolser, Jan de Boer, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 40