C Chevillard|N Duchene|J M Alexandre - JoVE Visualize

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Pathologie-Biologie|March 1, 1975

[Origin, nature, role and fate of prostaglandins liberated during the expansion of intravascular space in the anesthetized rat]N Papanicolaou, J M Alexandre, J Bariety, et al.

L'Encephale|October 16, 2012

[Similarities and differences between pathological gambling and substance dependance: A clarification]E Bosc, M Fatséas, J-M Alexandre, et al.

Genes and Immunity|November 17, 2006

Identification of a novel G245R polymorphism in the IL-2 receptor beta membrane proximal domain associated with human visceral leishmaniasisB Bucheton, L Argiro, C Chevillard, et al.

Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 1986

[Clinical pharmacology of enalapril in hypertension with chronic renal failure]M Chaignon, E Billaud-Mesguich, J M Alexandre, et al.

Molecular Cell|April 13, 1999

Evidence that a single replication fork proceeds from early to late replicating domains in the IgH locus in a non-B cell lineO V Ermakova, L H Nguyen, R D Little, et al.

Human Molecular Genetics|August 1, 1993

Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndromeC Chevillard, D Le Paslier, E Passage, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 22, 2001

Unequal VH gene rearrangement frequency within the large VH7183 gene family is not due to recombination signal sequence variation, and mapping of the genes shows a bias of rearrangement based on chromosomal locationG S Williams, A Martinez, A Montalbano, et al.

Journal of Chromatography|May 1, 1978

New electron-capture gas-liquid chromatographic method for the determination of mexiletine plasma levels in manA Frydman, J P Lafarge, F Vial, et al.

Journal of Cardiovascular Pharmacology|November 1, 1981

Dose dependency of captopril effects in severely hypertensive patientsJ C Aldigier, P F Plouin, J M Alexandre, et al.

Journal of Medical Genetics|July 4, 2001

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the diseaseL Villard, N Lévy, F Xiang, et al.

Pageof 12

Showing results (91-100 of 118) with videos related to

Sort By:

Pageof 12

Pathologie-Biologie|March 1, 1975

[Origin, nature, role and fate of prostaglandins liberated during the expansion of intravascular space in the anesthetized rat]N Papanicolaou, J M Alexandre, J Bariety, et al.

L'Encephale|October 16, 2012

[Similarities and differences between pathological gambling and substance dependance: A clarification]E Bosc, M Fatséas, J-M Alexandre, et al.

Genes and Immunity|November 17, 2006

Identification of a novel G245R polymorphism in the IL-2 receptor beta membrane proximal domain associated with human visceral leishmaniasisB Bucheton, L Argiro, C Chevillard, et al.

Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 1986

[Clinical pharmacology of enalapril in hypertension with chronic renal failure]M Chaignon, E Billaud-Mesguich, J M Alexandre, et al.

Molecular Cell|April 13, 1999

Evidence that a single replication fork proceeds from early to late replicating domains in the IgH locus in a non-B cell lineO V Ermakova, L H Nguyen, R D Little, et al.

Human Molecular Genetics|August 1, 1993

Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndromeC Chevillard, D Le Paslier, E Passage, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 22, 2001

Unequal VH gene rearrangement frequency within the large VH7183 gene family is not due to recombination signal sequence variation, and mapping of the genes shows a bias of rearrangement based on chromosomal locationG S Williams, A Martinez, A Montalbano, et al.

Journal of Chromatography|May 1, 1978

New electron-capture gas-liquid chromatographic method for the determination of mexiletine plasma levels in manA Frydman, J P Lafarge, F Vial, et al.

Journal of Cardiovascular Pharmacology|November 1, 1981

Dose dependency of captopril effects in severely hypertensive patientsJ C Aldigier, P F Plouin, J M Alexandre, et al.

Journal of Medical Genetics|July 4, 2001

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the diseaseL Villard, N Lévy, F Xiang, et al.

Pageof 12