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Pierri

Showing results (111-120 of 929) with videos related to

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Human Genetics|May 4, 2010
Copy number variants at Williams-Beuren syndrome 7q11.23 regionGiuseppe Merla, Nicola Brunetti-Pierri, Lucia Micale, et al.
Journal of Inherited Metabolic Disease|January 21, 2015
Differential inhibition of PDKs by phenylbutyrate and enhancement of pyruvate dehydrogenase complex activity by combination with dichloroacetateRosa Ferriero, Clara Iannuzzi, Giuseppe Manco, et al.
American Journal of Medical Genetics. Part A|December 13, 2017
A child with Myhre syndrome presenting with corectopia and tetralogy of FallotMarianna Alagia, Gerarda Cappuccio, Michele Pinelli, et al.
Biochimica Et Biophysica Acta|February 14, 2016
The switching mechanism of the mitochondrial ADP/ATP carrier explored by free-energy landscapesAdriana Pietropaolo, Ciro Leonardo Pierri, Ferdinando Palmieri, et al.
Cardiologia (Rome, Italy)|December 1, 1993
[Unstable angina: the point of view of the surgeon]L Chiariello, A Penta de Peppo, M D Pierri
Journal of Inherited Metabolic Disease|September 22, 2006
Two familial cases of high blood galactose of unknown aetiologyNicola Brunetti-Pierri, Antone R Opekun, William J Craigen
Human Molecular Genetics|June 23, 2019
Progress and challenges in development of new therapies for urea cycle disordersLeandro R Soria, Nicholas Ah Mew, Nicola Brunetti-Pierri
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|April 15, 1986
Prevalence of hepatitis B virus infection in pregnant women in the Montreal areaG Delage, S Montplaisir, S Rémy-Prince, et al.
Gene Therapy|August 15, 2014
SR-A and SREC-I binding peptides increase HDAd-mediated liver transductionP Piccolo, P Annunziata, P Mithbaokar, et al.
Analytical Biochemistry|May 21, 2022
Multiclass determination of endocrine disruptors in urine by hollow fiber microporous membrane and liquid chromatographyMaria Eduarda Pierri, Lucas Morés, Gabrieli Bernardi, et al.
Pageof 93

Showing results (111-120 of 929) with videos related to

Sort By:
Pageof 93
Human Genetics|May 4, 2010
Copy number variants at Williams-Beuren syndrome 7q11.23 regionGiuseppe Merla, Nicola Brunetti-Pierri, Lucia Micale, et al.
Journal of Inherited Metabolic Disease|January 21, 2015
Differential inhibition of PDKs by phenylbutyrate and enhancement of pyruvate dehydrogenase complex activity by combination with dichloroacetateRosa Ferriero, Clara Iannuzzi, Giuseppe Manco, et al.
American Journal of Medical Genetics. Part A|December 13, 2017
A child with Myhre syndrome presenting with corectopia and tetralogy of FallotMarianna Alagia, Gerarda Cappuccio, Michele Pinelli, et al.
Biochimica Et Biophysica Acta|February 14, 2016
The switching mechanism of the mitochondrial ADP/ATP carrier explored by free-energy landscapesAdriana Pietropaolo, Ciro Leonardo Pierri, Ferdinando Palmieri, et al.
Cardiologia (Rome, Italy)|December 1, 1993
[Unstable angina: the point of view of the surgeon]L Chiariello, A Penta de Peppo, M D Pierri
Journal of Inherited Metabolic Disease|September 22, 2006
Two familial cases of high blood galactose of unknown aetiologyNicola Brunetti-Pierri, Antone R Opekun, William J Craigen
Human Molecular Genetics|June 23, 2019
Progress and challenges in development of new therapies for urea cycle disordersLeandro R Soria, Nicholas Ah Mew, Nicola Brunetti-Pierri
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|April 15, 1986
Prevalence of hepatitis B virus infection in pregnant women in the Montreal areaG Delage, S Montplaisir, S Rémy-Prince, et al.
Gene Therapy|August 15, 2014
SR-A and SREC-I binding peptides increase HDAd-mediated liver transductionP Piccolo, P Annunziata, P Mithbaokar, et al.
Analytical Biochemistry|May 21, 2022
Multiclass determination of endocrine disruptors in urine by hollow fiber microporous membrane and liquid chromatographyMaria Eduarda Pierri, Lucas Morés, Gabrieli Bernardi, et al.
Pageof 93