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Konstantina Fragaki

Showing results (1-10 of 37) with videos related to

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The Lancet. Infectious Diseases|February 1, 2005
Recombinant DNA-derived leishmania proteins: from the laboratory to the fieldJoanna Kubar, Konstantina Fragaki
Trends in Parasitology|February 1, 2006
Leishmania proteins derived from recombinant DNA: current status and next stepsJoanna Kubar, Konstantina Fragaki
BMC Microbiology|May 2, 2003
A novel Leishmania infantum nuclear phosphoprotein Lepp12 which stimulates IL1-beta synthesis in THP-1 transfectantsKonstantina Fragaki, Bernard Ferrua, Baharia Mograbi, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|February 21, 2006
Downregulation by a long-acting beta2-adrenergic receptor agonist and corticosteroid of Staphylococcus aureus-induced airway epithelial inflammatory mediator productionKonstantina Fragaki, Claire Kileztky, Chantal Trentesaux, et al.
Diabetes Care|October 14, 2011
A novel unstable mutation in mitochondrial DNA responsible for maternally inherited diabetes and deafnessSylvie Bannwarth, Meriame Abbassi, René Valéro, et al.
Molecular Genetics and Metabolism|May 23, 2017
Assembly defects of multiple respiratory chain complexes in a child with cardiac hypertrophy associated with a novel ACAD9 mutationKonstantina Fragaki, Annabelle Chaussenot, Audrey Boutron, et al.
Molecular Genetics and Metabolism Reports|December 3, 2019
A novel variant m.8561C>T in the overlapping region of <i>MT-ATP6</i> and <i>MT-ATP8</i> in a child with early-onset severe neurological signsKonstantina Fragaki, Annabelle Chaussenot, Valerie Serre, et al.
BMC Medical Genetics|April 8, 2018
Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseasesMorgane Plutino, Annabelle Chaussenot, Cécile Rouzier, et al.
Muscle & Nerve|July 21, 2016
Severe defect in mitochondrial complex I assembly with mitochondrial DNA deletions in ACAD9-deficient mild myopathyKonstantina Fragaki, Annabelle Chaussenot, Audrey Boutron, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|January 8, 2008
Presence of anti-Lepp12 antibody: a marker for diagnostic and prognostic evaluation of visceral leishmaniasisDhiraj Kumar, Gurumurthy Srividya, Sandeep Verma, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
The Lancet. Infectious Diseases|February 1, 2005
Recombinant DNA-derived leishmania proteins: from the laboratory to the fieldJoanna Kubar, Konstantina Fragaki
Trends in Parasitology|February 1, 2006
Leishmania proteins derived from recombinant DNA: current status and next stepsJoanna Kubar, Konstantina Fragaki
BMC Microbiology|May 2, 2003
A novel Leishmania infantum nuclear phosphoprotein Lepp12 which stimulates IL1-beta synthesis in THP-1 transfectantsKonstantina Fragaki, Bernard Ferrua, Baharia Mograbi, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|February 21, 2006
Downregulation by a long-acting beta2-adrenergic receptor agonist and corticosteroid of Staphylococcus aureus-induced airway epithelial inflammatory mediator productionKonstantina Fragaki, Claire Kileztky, Chantal Trentesaux, et al.
Diabetes Care|October 14, 2011
A novel unstable mutation in mitochondrial DNA responsible for maternally inherited diabetes and deafnessSylvie Bannwarth, Meriame Abbassi, René Valéro, et al.
Molecular Genetics and Metabolism|May 23, 2017
Assembly defects of multiple respiratory chain complexes in a child with cardiac hypertrophy associated with a novel ACAD9 mutationKonstantina Fragaki, Annabelle Chaussenot, Audrey Boutron, et al.
Molecular Genetics and Metabolism Reports|December 3, 2019
A novel variant m.8561C>T in the overlapping region of <i>MT-ATP6</i> and <i>MT-ATP8</i> in a child with early-onset severe neurological signsKonstantina Fragaki, Annabelle Chaussenot, Valerie Serre, et al.
BMC Medical Genetics|April 8, 2018
Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseasesMorgane Plutino, Annabelle Chaussenot, Cécile Rouzier, et al.
Muscle & Nerve|July 21, 2016
Severe defect in mitochondrial complex I assembly with mitochondrial DNA deletions in ACAD9-deficient mild myopathyKonstantina Fragaki, Annabelle Chaussenot, Audrey Boutron, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|January 8, 2008
Presence of anti-Lepp12 antibody: a marker for diagnostic and prognostic evaluation of visceral leishmaniasisDhiraj Kumar, Gurumurthy Srividya, Sandeep Verma, et al.
Pageof 4