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Diana Baralle

Showing results (1-10 of 129) with videos related to

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The FEBS Journal|January 20, 2010
Novel aspects of alternative splicingDiana Baralle
Archives of Disease in Childhood|January 10, 2024
Epidemiology of Robin sequence: geographical variation in the UK/IrelandGiles Atton, Diana Baralle
RNA Biology|June 5, 2010
Novel roles of U1 snRNP in alternative splicing regulationEmanuele Buratti, Diana Baralle
Biochemical Society Transactions|May 17, 2008
Can donor splice site recognition occur without the involvement of U1 snRNP?Michela Raponi, Diana Baralle
Clinical Science (London, England : 1979)|February 17, 2017
RNA splicing in human disease and in the clinicDiana Baralle, Emanuele Buratti
Clinical Dysmorphology|February 15, 2011
Anophthalmia in fronto-facial-nasal dysplasiaMoira Blyth, Diana Baralle
Methods in Molecular Biology (Clifton, N.J.)|March 29, 2012
Exon skipping mutations in neurofibromatosisEmanuele Buratti, Diana Baralle
Frontiers in Genetics|July 19, 2021
Splicing in the Diagnosis of Rare Disease: Advances and ChallengesJenny Lord, Diana Baralle
Archives of Disease in Childhood|October 30, 2020
'Next Generation Sequencing' as a diagnostic tool in paediatricsDiana Baralle, Vardha Ismail
EMBO Reports|August 4, 2009
Missed threads. The impact of pre-mRNA splicing defects on clinical practiceDiana Baralle, Anneke Lucassen, Emanuele Buratti
Pageof 13

Showing results (1-10 of 129) with videos related to

Sort By:
Pageof 13
The FEBS Journal|January 20, 2010
Novel aspects of alternative splicingDiana Baralle
Archives of Disease in Childhood|January 10, 2024
Epidemiology of Robin sequence: geographical variation in the UK/IrelandGiles Atton, Diana Baralle
RNA Biology|June 5, 2010
Novel roles of U1 snRNP in alternative splicing regulationEmanuele Buratti, Diana Baralle
Biochemical Society Transactions|May 17, 2008
Can donor splice site recognition occur without the involvement of U1 snRNP?Michela Raponi, Diana Baralle
Clinical Science (London, England : 1979)|February 17, 2017
RNA splicing in human disease and in the clinicDiana Baralle, Emanuele Buratti
Clinical Dysmorphology|February 15, 2011
Anophthalmia in fronto-facial-nasal dysplasiaMoira Blyth, Diana Baralle
Methods in Molecular Biology (Clifton, N.J.)|March 29, 2012
Exon skipping mutations in neurofibromatosisEmanuele Buratti, Diana Baralle
Frontiers in Genetics|July 19, 2021
Splicing in the Diagnosis of Rare Disease: Advances and ChallengesJenny Lord, Diana Baralle
Archives of Disease in Childhood|October 30, 2020
'Next Generation Sequencing' as a diagnostic tool in paediatricsDiana Baralle, Vardha Ismail
EMBO Reports|August 4, 2009
Missed threads. The impact of pre-mRNA splicing defects on clinical practiceDiana Baralle, Anneke Lucassen, Emanuele Buratti
Pageof 13