Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alessandro De Luca

Showing results (111-120 of 192) with videos related to

Pageof 20
Sort By:
Digestive Diseases and Sciences|November 3, 2021
Coincidental or Causal? Concurrence of Colorectal Carcinoma with Primary Breast CancerDomenico Tripodi, Claudio Cannistra', Federica Gagliardi, et al.
Genes|August 6, 2021
Cardiac Defects and Genetic Syndromes: Old Uncertainties and New InsightsGiulio Calcagni, Flaminia Pugnaloni, Maria Cristina Digilio, et al.
Heart (British Cardiac Society)|November 26, 2009
Familial transposition of the great arteries caused by multiple mutations in laterality genesAlessandro De Luca, Anna Sarkozy, Federica Consoli, et al.
American Journal of Medical Genetics. Part A|August 5, 2011
Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1Maria Cristina Digilio, Laura Bernardini, Francesca Lepri, et al.
Gynecologic Oncology|June 13, 2008
Xenografts of primary human gynecological tumors grown under the renal capsule of NOD/SCID mice show genetic stability during serial transplantation and respond to cytotoxic chemotherapyJoshua Z Press, Jennifer A Kenyon, Hui Xue, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 15, 2020
Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle EastFerdinando Squitieri, Tommaso Mazza, Sabrina Maffi, et al.
European Journal of Medical Genetics|December 29, 2012
Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosisM Cristina Digilio, Laura Bernardini, Federica Consoli, et al.
Parkinsonism & Related Disorders|July 21, 2004
Mutational analysis of parkin gene by denaturing high-performance liquid chromatography (DHPLC) in essential tremorSimona Pigullo, Alessandro De Luca, Paolo Barone, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2002
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophreniaAlessandro De Luca, Emanuela Conti, Nicoletta Grifone, et al.
Stem Cell Research|June 17, 2022
Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 proteinAngela D'Anzi, Elisa Perciballi, Giorgia Ruotolo, et al.
Pageof 20

Showing results (111-120 of 192) with videos related to

Sort By:
Pageof 20
Digestive Diseases and Sciences|November 3, 2021
Coincidental or Causal? Concurrence of Colorectal Carcinoma with Primary Breast CancerDomenico Tripodi, Claudio Cannistra', Federica Gagliardi, et al.
Genes|August 6, 2021
Cardiac Defects and Genetic Syndromes: Old Uncertainties and New InsightsGiulio Calcagni, Flaminia Pugnaloni, Maria Cristina Digilio, et al.
Heart (British Cardiac Society)|November 26, 2009
Familial transposition of the great arteries caused by multiple mutations in laterality genesAlessandro De Luca, Anna Sarkozy, Federica Consoli, et al.
American Journal of Medical Genetics. Part A|August 5, 2011
Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1Maria Cristina Digilio, Laura Bernardini, Francesca Lepri, et al.
Gynecologic Oncology|June 13, 2008
Xenografts of primary human gynecological tumors grown under the renal capsule of NOD/SCID mice show genetic stability during serial transplantation and respond to cytotoxic chemotherapyJoshua Z Press, Jennifer A Kenyon, Hui Xue, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 15, 2020
Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle EastFerdinando Squitieri, Tommaso Mazza, Sabrina Maffi, et al.
European Journal of Medical Genetics|December 29, 2012
Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosisM Cristina Digilio, Laura Bernardini, Federica Consoli, et al.
Parkinsonism & Related Disorders|July 21, 2004
Mutational analysis of parkin gene by denaturing high-performance liquid chromatography (DHPLC) in essential tremorSimona Pigullo, Alessandro De Luca, Paolo Barone, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2002
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophreniaAlessandro De Luca, Emanuela Conti, Nicoletta Grifone, et al.
Stem Cell Research|June 17, 2022
Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 proteinAngela D'Anzi, Elisa Perciballi, Giorgia Ruotolo, et al.
Pageof 20