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RNA Biology
|
April 10, 2025
Alternative splicing of the Snap23 microexon is regulated by MBNL, QKI, and RBFOX2 in a tissue-specific manner and is altered in striated muscle diseases
Gabrielle M Gentile, R Eric Blue, Grant A Goda, et al.
Human Genetics
|
August 14, 1998
The familial adenomatous polyposis region exhibits many different haplotypes
A Stella, N Resta, A Polizzi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
January 21, 2012
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011
A Novelli, F R Grati, L Ballarati, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin
|
February 27, 2010
A case of dengue type 3 virus infection imported from Africa to Italy, October 2009
C Nisii, F Carletti, C Castilletti, et al.
Blood Cancer Journal
|
September 10, 2016
lncRNA profiling in early-stage chronic lymphocytic leukemia identifies transcriptional fingerprints with relevance in clinical outcome
D Ronchetti, M Manzoni, L Agnelli, et al.
Leukemia
|
February 5, 2015
Diagnostic and prognostic role of PET/CT in patients with chronic lymphocytic leukemia and progressive disease
F R Mauro, S Chauvie, F Paoloni, et al.
Archives of Toxicology
|
June 14, 2025
Buccal micronucleus cytome assay to evaluate cyto-genotoxic effects of occupational exposure to antineoplastic drugs: application on a large sample size of workers furnished by an Italian network of oncological hospitals
C L Ursini, E Omodeo-Salè, G Di Gennaro, et al.
Clinical and Experimental Medicine
|
November 25, 2025
A multicenter observational retrospective study of second-line treatment with daratumumab-bortezomib-dexamethasone (DaraVd) in multiple myeloma patients refractory to lenalidomide
I Rizzello, I Sacchetti, S Barbato, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
January 25, 2018
Genetic landscape of ultra-stable chronic lymphocytic leukemia patients
S Raponi, I Del Giudice, M Marinelli, et al.
Journal of Medical Genetics
|
July 4, 2009
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)
D Doherty, M A Parisi, L S Finn, et al.
Page
of 32
Search research articles
Search
Showing results (301-310 of 317) with videos related to
Sort By:
Page
of 32
RNA Biology
|
April 10, 2025
Alternative splicing of the Snap23 microexon is regulated by MBNL, QKI, and RBFOX2 in a tissue-specific manner and is altered in striated muscle diseases
Gabrielle M Gentile, R Eric Blue, Grant A Goda, et al.
Human Genetics
|
August 14, 1998
The familial adenomatous polyposis region exhibits many different haplotypes
A Stella, N Resta, A Polizzi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
January 21, 2012
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011
A Novelli, F R Grati, L Ballarati, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin
|
February 27, 2010
A case of dengue type 3 virus infection imported from Africa to Italy, October 2009
C Nisii, F Carletti, C Castilletti, et al.
Blood Cancer Journal
|
September 10, 2016
lncRNA profiling in early-stage chronic lymphocytic leukemia identifies transcriptional fingerprints with relevance in clinical outcome
D Ronchetti, M Manzoni, L Agnelli, et al.
Leukemia
|
February 5, 2015
Diagnostic and prognostic role of PET/CT in patients with chronic lymphocytic leukemia and progressive disease
F R Mauro, S Chauvie, F Paoloni, et al.
Archives of Toxicology
|
June 14, 2025
Buccal micronucleus cytome assay to evaluate cyto-genotoxic effects of occupational exposure to antineoplastic drugs: application on a large sample size of workers furnished by an Italian network of oncological hospitals
C L Ursini, E Omodeo-Salè, G Di Gennaro, et al.
Clinical and Experimental Medicine
|
November 25, 2025
A multicenter observational retrospective study of second-line treatment with daratumumab-bortezomib-dexamethasone (DaraVd) in multiple myeloma patients refractory to lenalidomide
I Rizzello, I Sacchetti, S Barbato, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
January 25, 2018
Genetic landscape of ultra-stable chronic lymphocytic leukemia patients
S Raponi, I Del Giudice, M Marinelli, et al.
Journal of Medical Genetics
|
July 4, 2009
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)
D Doherty, M A Parisi, L S Finn, et al.
Page
of 32