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Y Sunada

Showing results (61-70 of 77) with videos related to

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Annals of Neurology|January 1, 1993
Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese familyY Sunada, T Shimizu, H Nakase, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
Congenital muscular dystrophy with merosin deficiencyF M Tomé, T Evangelista, A Leclerc, et al.
The Journal of Biological Chemistry|March 13, 1999
Characterization of the transmembrane molecular architecture of the dystroglycan complex in schwann cellsF Saito, T Masaki, K Kamakura, et al.
Annals of Neurology|December 1, 1996
Muscular dystrophy associated with beta-Dystroglycan deficiencyM A Salih, Y Sunada, M Al-Nasser, et al.
Human Molecular Genetics|August 1, 1995
Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophyD J Wells, K E Wells, E A Asante, et al.
Nature Genetics|November 1, 1995
Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12L E Lim, F Duclos, O Broux, et al.
Neurology|August 10, 2005
Reduced amplitude of the sural nerve sensory action potential in PARK2 patientsY Ohsawa, K Kurokawa, M Sonoo, et al.
Human Molecular Genetics|June 1, 1997
Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null miceR A Williamson, M D Henry, K J Daniels, et al.
The Review of Scientific Instruments|June 1, 2022
Discharge characteristics of steady-state high-density plasma source based on cascade arc discharge with hollow cathodeK Yamasaki, O Yanagi, Y Sunada, et al.
FEBS Letters|February 26, 1996
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
Annals of Neurology|January 1, 1993
Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese familyY Sunada, T Shimizu, H Nakase, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
Congenital muscular dystrophy with merosin deficiencyF M Tomé, T Evangelista, A Leclerc, et al.
The Journal of Biological Chemistry|March 13, 1999
Characterization of the transmembrane molecular architecture of the dystroglycan complex in schwann cellsF Saito, T Masaki, K Kamakura, et al.
Annals of Neurology|December 1, 1996
Muscular dystrophy associated with beta-Dystroglycan deficiencyM A Salih, Y Sunada, M Al-Nasser, et al.
Human Molecular Genetics|August 1, 1995
Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophyD J Wells, K E Wells, E A Asante, et al.
Nature Genetics|November 1, 1995
Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12L E Lim, F Duclos, O Broux, et al.
Neurology|August 10, 2005
Reduced amplitude of the sural nerve sensory action potential in PARK2 patientsY Ohsawa, K Kurokawa, M Sonoo, et al.
Human Molecular Genetics|June 1, 1997
Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null miceR A Williamson, M D Henry, K J Daniels, et al.
The Review of Scientific Instruments|June 1, 2022
Discharge characteristics of steady-state high-density plasma source based on cascade arc discharge with hollow cathodeK Yamasaki, O Yanagi, Y Sunada, et al.
FEBS Letters|February 26, 1996
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.
Pageof 8