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Showing results (71-80 of 93) with videos related to

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American Journal of Human Genetics|May 1, 1988
An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequenceM D'Urso, L Luzzatto, L Perroni, et al.
Differentiation; Research in Biological Diversity|March 29, 2001
Emerin expression at the early stages of myogenic differentiationG Lattanzi, A Ognibene, P Sabatelli, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Unusual expression of emerin in a patient with X-linked Emery-Dreifuss muscular dystrophyC Di Blasi, L Morandi, M Raffaele di Barletta, et al.
American Journal of Human Genetics|April 29, 1998
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityS Bione, C Sala, C Manzini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 21, 2005
Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathyS Benedetti, E Bertini, S Iannaccone, et al.
Human Reproduction (Oxford, England)|January 29, 2019
High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian functionI Bestetti, C Castronovo, A Sironi, et al.
Acta Neuropathologica|August 31, 2000
Emerin presence in plateletsS Squarzoni, P Sabatelli, C Capanni, et al.
La Radiologia Medica|September 6, 2011
Hypoxic liver perfusion with mitomycin-C for treating multifocal metastases and unresectable primary tumours: a single-centre series of 42 patientsA Bagliani, A Baggiani, A M Ierardi, et al.
Human Molecular Genetics|March 21, 1998
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophyL Cartegni, M R di Barletta, R Barresi, et al.
Annals of Neurology|August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleM Mora, L Cartegni, C Di Blasi, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|May 1, 1988
An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequenceM D'Urso, L Luzzatto, L Perroni, et al.
Differentiation; Research in Biological Diversity|March 29, 2001
Emerin expression at the early stages of myogenic differentiationG Lattanzi, A Ognibene, P Sabatelli, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Unusual expression of emerin in a patient with X-linked Emery-Dreifuss muscular dystrophyC Di Blasi, L Morandi, M Raffaele di Barletta, et al.
American Journal of Human Genetics|April 29, 1998
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityS Bione, C Sala, C Manzini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 21, 2005
Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathyS Benedetti, E Bertini, S Iannaccone, et al.
Human Reproduction (Oxford, England)|January 29, 2019
High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian functionI Bestetti, C Castronovo, A Sironi, et al.
Acta Neuropathologica|August 31, 2000
Emerin presence in plateletsS Squarzoni, P Sabatelli, C Capanni, et al.
La Radiologia Medica|September 6, 2011
Hypoxic liver perfusion with mitomycin-C for treating multifocal metastases and unresectable primary tumours: a single-centre series of 42 patientsA Bagliani, A Baggiani, A M Ierardi, et al.
Human Molecular Genetics|March 21, 1998
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophyL Cartegni, M R di Barletta, R Barresi, et al.
Annals of Neurology|August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleM Mora, L Cartegni, C Di Blasi, et al.
Pageof 10