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

E Nicolis

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Human Mutation|January 1, 1993
Screening of 62 mutations in a cohort of cystic fibrosis patients from north eastern Italy: their incidence and clinical features of defined genotypesP Gasparini, C Marigo, G Bisceglia, et al.
Gene Therapy|April 16, 1998
ICAM-1 induction in respiratory cells exposed to a replication-deficient recombinant adenovirus in vitro and in vivoE Nicolis, A Tamanini, P Melotti, et al.
Human Genetics|April 1, 1995
Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from north-eastern Italy: identification of 90% of the mutationsA Bonizzato, L Bisceglia, C Marigo, et al.
Current Medicinal Chemistry|October 14, 2010
Targeting transcription factor activity as a strategy to inhibit pro-inflammatory genes involved in cystic fibrosis: decoy oligonucleotides and low-molecular weight compoundsG Cabrini, V Bezzerri, I Mancini, et al.
Human Gene Therapy|February 15, 2001
Radioisotopic imaging allows optimization of adenovirus lung deposition for cystic fibrosis gene therapyS Lerondel, A Le Pape, C Sené, et al.
The Annals of Pharmacotherapy|February 26, 1998
Doctorline: a private toll-free telephone medical information service. Five years of activity: old problems and new perspectivesA Nobili, F Gebru, A Rossetti, et al.
Leukemia|January 17, 2009
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndromeA Minelli, E Maserati, E Nicolis, et al.
Blood Cancer Journal|October 16, 2012
Mesenchymal stem cells from Shwachman-Diamond syndrome patients display normal functions and do not contribute to hematological defectsV André, D Longoni, S Bresolin, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Human Mutation|January 1, 1993
Screening of 62 mutations in a cohort of cystic fibrosis patients from north eastern Italy: their incidence and clinical features of defined genotypesP Gasparini, C Marigo, G Bisceglia, et al.
Gene Therapy|April 16, 1998
ICAM-1 induction in respiratory cells exposed to a replication-deficient recombinant adenovirus in vitro and in vivoE Nicolis, A Tamanini, P Melotti, et al.
Human Genetics|April 1, 1995
Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from north-eastern Italy: identification of 90% of the mutationsA Bonizzato, L Bisceglia, C Marigo, et al.
Current Medicinal Chemistry|October 14, 2010
Targeting transcription factor activity as a strategy to inhibit pro-inflammatory genes involved in cystic fibrosis: decoy oligonucleotides and low-molecular weight compoundsG Cabrini, V Bezzerri, I Mancini, et al.
Human Gene Therapy|February 15, 2001
Radioisotopic imaging allows optimization of adenovirus lung deposition for cystic fibrosis gene therapyS Lerondel, A Le Pape, C Sené, et al.
The Annals of Pharmacotherapy|February 26, 1998
Doctorline: a private toll-free telephone medical information service. Five years of activity: old problems and new perspectivesA Nobili, F Gebru, A Rossetti, et al.
Leukemia|January 17, 2009
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndromeA Minelli, E Maserati, E Nicolis, et al.
Blood Cancer Journal|October 16, 2012
Mesenchymal stem cells from Shwachman-Diamond syndrome patients display normal functions and do not contribute to hematological defectsV André, D Longoni, S Bresolin, et al.
Pageof 2