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

D Seripa

Showing results (11-20 of 32) with videos related to

Pageof 4
Sort By:
Journal of the National Cancer Institute|July 17, 1998
Identification of a possible somatic BRCA1 mutation affecting translation efficiency in an early-onset sporadic breast cancer patientS Papa, D Seripa, G Merla, et al.
Biochemical and Biophysical Research Communications|April 15, 1994
Accumulation of human apolipoprotein-E in rat plasma after in vivo intramuscular injection of naked DNAV M Fazio, S Fazio, M Rinaldi, et al.
Cancer Research|August 15, 1994
PML/RAR alpha+ U937 mutant and NB4 cell lines: retinoic acid restores the monocytic differentiation response to vitamin D3U Testa, F Grignani, T Barberi, et al.
Current Alzheimer Research|May 25, 2011
Mediterranean diet in predementia and dementia syndromesV Solfrizzi, V Frisardi, D Seripa, et al.
Neuroscience Letters|April 20, 2001
The Apolipoprotein E genotype in patients affected by syndromes with focal cortical atrophyC Masullo, A Daniele, V M Fazio, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from southern ItalyD Seripa, C Gravina, R Volpe, et al.
Current Alzheimer Research|November 27, 2009
Towards disease-modifying treatment of Alzheimer's disease: drugs targeting beta-amyloidV Frisardi, V Solfrizzi, P B Imbimbo, et al.
Stroke|February 24, 1998
Prevalence of apolipoprotein E alleles in healthy subjects and survivors of ischemic stroke: an Italian Case-Control StudyM Margaglione, D Seripa, C Gravina, et al.
Journal of Medical Genetics|September 10, 2003
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromesA Sarkozy, E Conti, D Seripa, et al.
Blood|September 26, 2000
A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicingM Margaglione, R Santacroce, D Colaizzo, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Journal of the National Cancer Institute|July 17, 1998
Identification of a possible somatic BRCA1 mutation affecting translation efficiency in an early-onset sporadic breast cancer patientS Papa, D Seripa, G Merla, et al.
Biochemical and Biophysical Research Communications|April 15, 1994
Accumulation of human apolipoprotein-E in rat plasma after in vivo intramuscular injection of naked DNAV M Fazio, S Fazio, M Rinaldi, et al.
Cancer Research|August 15, 1994
PML/RAR alpha+ U937 mutant and NB4 cell lines: retinoic acid restores the monocytic differentiation response to vitamin D3U Testa, F Grignani, T Barberi, et al.
Current Alzheimer Research|May 25, 2011
Mediterranean diet in predementia and dementia syndromesV Solfrizzi, V Frisardi, D Seripa, et al.
Neuroscience Letters|April 20, 2001
The Apolipoprotein E genotype in patients affected by syndromes with focal cortical atrophyC Masullo, A Daniele, V M Fazio, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from southern ItalyD Seripa, C Gravina, R Volpe, et al.
Current Alzheimer Research|November 27, 2009
Towards disease-modifying treatment of Alzheimer's disease: drugs targeting beta-amyloidV Frisardi, V Solfrizzi, P B Imbimbo, et al.
Stroke|February 24, 1998
Prevalence of apolipoprotein E alleles in healthy subjects and survivors of ischemic stroke: an Italian Case-Control StudyM Margaglione, D Seripa, C Gravina, et al.
Journal of Medical Genetics|September 10, 2003
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromesA Sarkozy, E Conti, D Seripa, et al.
Blood|September 26, 2000
A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicingM Margaglione, R Santacroce, D Colaizzo, et al.
Pageof 4