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C Julien

Showing results (141-150 of 150) with videos related to

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The Journal of Physiology|June 3, 2010
Does obesity reduce load-induced muscle hypertrophy?Madhusudhan R Papasani, Kara Thornton, Zhan Yinggian, et al.
American Journal of Hypertension|July 1, 1988
Patients with congenital dopamine beta-hydroxylase deficiency. A lesson in catecholamine physiologyA Man in 't Veld, F Boomsma, J Lenders, et al.
Journal of Medicinal Chemistry|June 29, 2001
Utilization of an intramolecular hydrogen bond to increase the CNS penetration of an NK(1) receptor antagonistV A Ashwood, M J Field, D C Horwell, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 3, 2000
In vivo 129Xe NMR in rat brain during intra-arterial injection of hyperpolarized 129Xe dissolved in a lipid emulsionG Duhamel, P Choquet, J L Leviel, et al.
Neurology|March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patientsG Stevanin, A Camuzat, S E Holmes, et al.
American Journal of Medical Genetics|August 9, 1996
Trinucleotide repeat expansion in the FRAXE locus is not common among institutionalized individuals with non-specific developmental disabilitiesJ J Holden, C Julien-Inalsingh, M Chalifoux, et al.
Journal of Medical Genetics|July 10, 2007
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal gangliaY Saillour, G Zanni, V Des Portes, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|April 22, 2017
Atrial fibrillation is associated with hypermethylation in human left atrium, and treatment with decitabine reduces atrial tachyarrhythmias in spontaneously hypertensive ratsR Doñate Puertas, E Meugnier, C Romestaing, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
The apolipoprotein E epsilon4 allele selectively increases the risk of frontotemporal lobar degeneration in malesR Srinivasan, Y Davidson, L Gibbons, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Genetic associations between cathepsin D exon 2 C-->T polymorphism and Alzheimer's disease, and pathological correlations with genotypeY Davidson, L Gibbons, A Pritchard, et al.
Pageof 15

Showing results (141-150 of 150) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 150 results.
The Journal of Physiology|June 3, 2010
Does obesity reduce load-induced muscle hypertrophy?Madhusudhan R Papasani, Kara Thornton, Zhan Yinggian, et al.
American Journal of Hypertension|July 1, 1988
Patients with congenital dopamine beta-hydroxylase deficiency. A lesson in catecholamine physiologyA Man in 't Veld, F Boomsma, J Lenders, et al.
Journal of Medicinal Chemistry|June 29, 2001
Utilization of an intramolecular hydrogen bond to increase the CNS penetration of an NK(1) receptor antagonistV A Ashwood, M J Field, D C Horwell, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 3, 2000
In vivo 129Xe NMR in rat brain during intra-arterial injection of hyperpolarized 129Xe dissolved in a lipid emulsionG Duhamel, P Choquet, J L Leviel, et al.
Neurology|March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patientsG Stevanin, A Camuzat, S E Holmes, et al.
American Journal of Medical Genetics|August 9, 1996
Trinucleotide repeat expansion in the FRAXE locus is not common among institutionalized individuals with non-specific developmental disabilitiesJ J Holden, C Julien-Inalsingh, M Chalifoux, et al.
Journal of Medical Genetics|July 10, 2007
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal gangliaY Saillour, G Zanni, V Des Portes, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|April 22, 2017
Atrial fibrillation is associated with hypermethylation in human left atrium, and treatment with decitabine reduces atrial tachyarrhythmias in spontaneously hypertensive ratsR Doñate Puertas, E Meugnier, C Romestaing, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
The apolipoprotein E epsilon4 allele selectively increases the risk of frontotemporal lobar degeneration in malesR Srinivasan, Y Davidson, L Gibbons, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Genetic associations between cathepsin D exon 2 C-->T polymorphism and Alzheimer's disease, and pathological correlations with genotypeY Davidson, L Gibbons, A Pritchard, et al.
Pageof 15