K Peoc'h - JoVE Visualize

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Human Mutation|May 2, 2000

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotypeK Peoc'h, P Manivet, P Beaudry, et al.

The Journal of Pharmacology and Experimental Therapeutics|February 8, 2006

Evidence for a control of plasma serotonin levels by 5-hydroxytryptamine(2B) receptors in miceJ Callebert, J M Esteve, P Hervé, et al.

Annales De Biologie Clinique|November 27, 2009

["Standard" protocol for evaluating the impact of preanalytical variables on peptidic and proteic analytes and standard coding of preanalytical procedures]F Betsou, J-L Beaudeux, A Berthelaix, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2000

Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7J H d'Aignaux, J L Laplanche, N Delasnerie-Lauprêtre, et al.

FEBS Letters|February 15, 2003

Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob diseaseK Peoc'h, H Volland, A De Gassart, et al.

Brain : a Journal of Neurology|December 3, 1999

Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein geneJ L Laplanche, K H Hachimi, I Durieux, et al.

Medical Hypotheses|August 31, 2010

Could the inter-individual variability in cocaine-induced psychotic effects influence the development of cocaine addiction? Towards a new pharmacogenetic approach to addictionsG Brousse, F Vorspan, K Ksouda, et al.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 5, 2020

Maternal and neonatal outcomes and prognostic factors in acute fatty liver of pregnancyY Joueidi, K Peoc'h, M Le Lous, et al.

Nature Medicine|September 24, 2002

Function of the serotonin 5-hydroxytryptamine 2B receptor in pulmonary hypertensionJ-M Launay, P Hervé, K Peoc'h, et al.

Neurology|April 27, 2005

A novel mutation (G114V) in the prion protein gene in a family with inherited prion diseaseM-M Rodriguez, K Peoc'h, S Haïk, et al.

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Showing results (11-20 of 30) with videos related to

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Human Mutation|May 2, 2000

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotypeK Peoc'h, P Manivet, P Beaudry, et al.

The Journal of Pharmacology and Experimental Therapeutics|February 8, 2006

Evidence for a control of plasma serotonin levels by 5-hydroxytryptamine(2B) receptors in miceJ Callebert, J M Esteve, P Hervé, et al.

Annales De Biologie Clinique|November 27, 2009

["Standard" protocol for evaluating the impact of preanalytical variables on peptidic and proteic analytes and standard coding of preanalytical procedures]F Betsou, J-L Beaudeux, A Berthelaix, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2000

Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7J H d'Aignaux, J L Laplanche, N Delasnerie-Lauprêtre, et al.

FEBS Letters|February 15, 2003

Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob diseaseK Peoc'h, H Volland, A De Gassart, et al.

Brain : a Journal of Neurology|December 3, 1999

Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein geneJ L Laplanche, K H Hachimi, I Durieux, et al.

Medical Hypotheses|August 31, 2010

Could the inter-individual variability in cocaine-induced psychotic effects influence the development of cocaine addiction? Towards a new pharmacogenetic approach to addictionsG Brousse, F Vorspan, K Ksouda, et al.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 5, 2020

Maternal and neonatal outcomes and prognostic factors in acute fatty liver of pregnancyY Joueidi, K Peoc'h, M Le Lous, et al.

Nature Medicine|September 24, 2002

Function of the serotonin 5-hydroxytryptamine 2B receptor in pulmonary hypertensionJ-M Launay, P Hervé, K Peoc'h, et al.

Neurology|April 27, 2005

A novel mutation (G114V) in the prion protein gene in a family with inherited prion diseaseM-M Rodriguez, K Peoc'h, S Haïk, et al.

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