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Showing results (31-40 of 46) with videos related to

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Clinical Genetics|September 12, 2013
Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex IS Assereto, A Robbiano, M Di Rocco, et al.
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists|October 20, 2022
Implementation of a pharmacological prophylaxis bundle to prevent obstetric-associated venous thromboembolismRonald E Iverson, Min Zhang, Emily M Jansen, et al.
Neurology|September 27, 2013
Copy number variants are frequent in genetic generalized epilepsy with intellectual disabilitySaul A Mullen, Gemma L Carvill, Susannah Bellows, et al.
Journal of Neurology|April 9, 2013
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvementRoberta Biancheri, Denise Cassandrini, Francesca Pinto, et al.
Epilepsia|January 15, 2014
A common SCN1A splice-site polymorphism modifies the effect of carbamazepine on cortical excitability--a pharmacogenetic transcranial magnetic stimulation studyKatja Menzler, Anke Hermsen, Katharina Balkenhol, et al.
Human Molecular Genetics|July 14, 2009
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritanceLeanne M Dibbens, Saul Mullen, Ingo Helbig, et al.
Neurobiology of Disease|February 25, 2014
Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsyBorislav Dejanovic, Dennis Lal, Claudia B Catarino, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
Epilepsia|January 9, 2013
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsyRikke S Møller, Yvonne G Weber, Laura L Klitten, et al.
Biomolecular NMR Assignments|November 7, 2020
<sup>1</sup>H, <sup>13</sup>C, and <sup>15</sup>N backbone chemical shift assignments of coronavirus-2 non-structural protein Nsp10N Kubatova, N S Qureshi, N Altincekic, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Clinical Genetics|September 12, 2013
Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex IS Assereto, A Robbiano, M Di Rocco, et al.
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists|October 20, 2022
Implementation of a pharmacological prophylaxis bundle to prevent obstetric-associated venous thromboembolismRonald E Iverson, Min Zhang, Emily M Jansen, et al.
Neurology|September 27, 2013
Copy number variants are frequent in genetic generalized epilepsy with intellectual disabilitySaul A Mullen, Gemma L Carvill, Susannah Bellows, et al.
Journal of Neurology|April 9, 2013
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvementRoberta Biancheri, Denise Cassandrini, Francesca Pinto, et al.
Epilepsia|January 15, 2014
A common SCN1A splice-site polymorphism modifies the effect of carbamazepine on cortical excitability--a pharmacogenetic transcranial magnetic stimulation studyKatja Menzler, Anke Hermsen, Katharina Balkenhol, et al.
Human Molecular Genetics|July 14, 2009
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritanceLeanne M Dibbens, Saul Mullen, Ingo Helbig, et al.
Neurobiology of Disease|February 25, 2014
Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsyBorislav Dejanovic, Dennis Lal, Claudia B Catarino, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
Epilepsia|January 9, 2013
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsyRikke S Møller, Yvonne G Weber, Laura L Klitten, et al.
Biomolecular NMR Assignments|November 7, 2020
<sup>1</sup>H, <sup>13</sup>C, and <sup>15</sup>N backbone chemical shift assignments of coronavirus-2 non-structural protein Nsp10N Kubatova, N S Qureshi, N Altincekic, et al.
Pageof 5