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A Renieri

Showing results (91-100 of 106) with videos related to

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Heliyon|November 25, 2024
A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profilingC Quadalti, M Sannia, N E Humphreys, et al.
Neuroscience|March 23, 2016
Visual impairment in FOXG1-mutated individuals and miceE M Boggio, L Pancrazi, M Gennaro, et al.
Environmental Research|June 30, 2018
Effects of carbon and silicon nanotubes and carbon nanofibers on marine microalgae Heterosigma akashiwoK S Pikula, A M Zakharenko, V V Chaika, et al.
Clinical Genetics|November 19, 2016
Alport syndrome: impact of digenic inheritance in patients managementC Fallerini, M Baldassarri, E Trevisson, et al.
Human Mutation|February 6, 1998
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndromeT M Neri, P Zanelli, G De Palma, et al.
Brain & Development|April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteriaR Artuso, M A Mencarelli, R Polli, et al.
American Journal of Medical Genetics|November 20, 1995
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndromeA Renieri, L Galli, A Grillo, et al.
American Journal of Human Genetics|June 1, 1996
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 geneA Renieri, M Bruttini, L Galli, et al.
Journal of Medical Genetics|July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndromeM A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 28, 2001
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome femalesM Vacca, F Filippini, A Budillon, et al.
Pageof 11

Showing results (91-100 of 106) with videos related to

Sort By:
Pageof 11
Heliyon|November 25, 2024
A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profilingC Quadalti, M Sannia, N E Humphreys, et al.
Neuroscience|March 23, 2016
Visual impairment in FOXG1-mutated individuals and miceE M Boggio, L Pancrazi, M Gennaro, et al.
Environmental Research|June 30, 2018
Effects of carbon and silicon nanotubes and carbon nanofibers on marine microalgae Heterosigma akashiwoK S Pikula, A M Zakharenko, V V Chaika, et al.
Clinical Genetics|November 19, 2016
Alport syndrome: impact of digenic inheritance in patients managementC Fallerini, M Baldassarri, E Trevisson, et al.
Human Mutation|February 6, 1998
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndromeT M Neri, P Zanelli, G De Palma, et al.
Brain & Development|April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteriaR Artuso, M A Mencarelli, R Polli, et al.
American Journal of Medical Genetics|November 20, 1995
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndromeA Renieri, L Galli, A Grillo, et al.
American Journal of Human Genetics|June 1, 1996
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 geneA Renieri, M Bruttini, L Galli, et al.
Journal of Medical Genetics|July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndromeM A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 28, 2001
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome femalesM Vacca, F Filippini, A Budillon, et al.
Pageof 11