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Auteur Saito F

Documents disponibles écrits par cet auteur (17)

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FASEB bioAdvances, 5, 11. Antioxidants restore store-operated Ca2+ entry in patient-iPSC-derived myotubes with tubular aggregate myopathy-associated Ile484ArgfsX21 STIM1 mutation via upregulation of binding immunoglobulin protein

Sakai-Takemura F ; Saito F ; Nogami K ; Maruyama Y ; Elhussieny A ; Matsumura K ; Takeda S ; Aoki Y ; Miyagoe-Suzuki Y | 26/10/2023

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Molecular therapy. Methods & clinical development, 18. Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach

Ikeda M ; Taniguchi-Ikeda M ; Kato T ; Shinkai Y ; Tanaka S ; Hagiwara H ; Sasaki N ; Masaki T ; Matsumura K ; Sonoo M ; Kurahashi H ; Saito F | 2020

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Proceedings of the national Academy of sciences of the United States of America, 113, 39. Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle

Rader EP, Auteur ; Turk R ; Willer T ; Beltran D ; Inamori K ; Peterson TA ; Engle J ; Prouty S ; Matsumura K ; Saito F ; Anderson ME ; Campbell KP | 2016

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Human molecular genetics, 23, 17. Overexpression of LARGE suppresses muscle regeneration via down-regulation of insulin-like growth factor 1 and aggravates muscular dystrophy in mice.

Saito F ; Kanagawa M ; Ikeda M ; Hagiwara H ; Masaki T ; Ohkuma H ; Katanosaka Y ; Shimizu T ; Sonoo M ; Toda T ; Matsumura K | 09/2014

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Neuromuscular disorders : NMD, 18, 9-10. Glycosylation of alpha-dystroglycan in cultured cells and its restoration by glycosyltransferase (Poster)

Collectif ; Saito F ; Arai Y ; Hagiwara H ; Shimizu T ; Matsumura K | 2008

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Journal of neurochemistry, 101, 6. Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice

Saito F ; Masaki T ; Saito Y ; Nakamura A ; Takeda S ; Shimizu T ; Toda T ; Matsumura K | 2007

Accès au résumé PubMed / to PubMed abstract 15/06/2007 - La fukutine joue un rôle crucial dans la myélinisation du nerf périphérique et la formation de la jonction neuromusculaire La dystrophie musculaire congénitale (DMC) de Fuku[...]

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FEBS Letters, 579, 11. Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy

Saito F ; Blank M ; Schroder J ; Manya H ; Shimizu T ; Campbell KP ; Endo T ; Mizutani M ; Kroger S ; Matsumura K | 2005

Accès au résumé PubMed / to PubMed abstract

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Cell, 117, 7. Molecular recognition by LARGE is essential for expression of functional dystroglycan

Kanagawa M ; Saito F ; Kunz S ; Yoshida-Moriguchi T ; Barresi R ; Kobayashi YM ; Muschler J ; Dumanski JP ; Michele DE ; Oldstone MBA ; Campbell KP | 25/06/2004

Accès au résumé PubMed / to PubMed abstract

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Neuromuscular disorders : NMD, 14, 2. A Japanese patient with distal myopathy with rimmed vacuoles : missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins

Saito F ; Tomimitsu H ; Araishi K ; Nakai S ; Kanda T ; Shimizu T ; Mizusawa H ; Matsumura K | 2004

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Nature, 418. Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

Michele DE ; Barresi R ; Kanagawa M ; Saito F ; Cohn RD ; Satz JS ; Dollar J ; Nishino I ; Kelley RI ; Somer H ; Straub V ; Mathews KD ; Moore SA ; Campbell KP | 25/07/2002

Accès au résumé PubMed / to PubMed abstract

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Cell, 110. Disruption of Dag1 in differentiated skeletal muscle reveals a role of dystroglycan in muscle regeneration

Cohn RD ; Henry MD ; Michele DE ; Barresi R ; Saito F ; Moore SA ; Flanagan JD ; Skwarchuk MW ; Robbins ME ; Mendell JR ; Williamson RA ; Campbell KP | 2002

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Journal of biological chemistry (The), 274, 12. Characterization of the transmembrane molecular architecture of the Dystroglycan complex in Schwann cells

Saito F ; Masaki T ; Kamakura K ; Anderson LVB ; Fujita S ; Fukuta-Ohi H ; Sunada Y ; Shimizu T ; Matsumura K | 19/03/1999

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Muscle & Nerve A 180-KDA protein is deficient in Fukuyama-type congenital muscular dystrophy skeletal muscle

IX International congress on neuromuscular diseases (30 Aout-4 Sept 1998; Adélaïde) ; Sunada Y ; Higuchi I ; Saito F ; Matsumura K ; Shimizu T | 1998

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Histology and histopathology, 12. The role of dystroglycan, a novel receptor of laminin and agrin, in cell differentiation

Matsumura K ; Yamada H ; Saito F ; Sunada Y ; Shimizu T | 1997

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Neuromuscular disorders : NMD, 7, 1. Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

Matsumura K ; Yamada H ; Saito F ; Sunada Y ; Shimizu T | 1997

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American journal of human genetics (The), 40, 3. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency : molecular genetic evidence for deletions

Francke U ; Harper JF ; Darras BT ; Cowan JM ; McCabe ERB ; Kohlschütter A ; Seltzer WK ; Saito F ; Goto J ; Harpey JP ; Wise JE | 1987

Accès au résumé PubMed / to PubMed abstract

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Article

eLife, 12. N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy

Okuma H ; Hord JM ; Chandel I ; Venzke D ; Anderson ME ; Walimbe AS ; Joseph S ; Gastel Z ; Hara Y ; Saito F ; Matsumura K ; Campbell KP | England | 0102/2023

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Auteur Saito F

Documents disponibles écrits par cet auteur (17)

FASEB bioAdvances, 5, 11. Antioxidants restore store-operated Ca2+ entry in patient-iPSC-derived myotubes with tubular aggregate myopathy-associated Ile484ArgfsX21 STIM1 mutation via upregulation of binding immunoglobulin protein

Molecular therapy. Methods & clinical development, 18. Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach

Proceedings of the national Academy of sciences of the United States of America, 113, 39. Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle

Human molecular genetics, 23, 17. Overexpression of LARGE suppresses muscle regeneration via down-regulation of insulin-like growth factor 1 and aggravates muscular dystrophy in mice.

Neuromuscular disorders : NMD, 18, 9-10. Glycosylation of alpha-dystroglycan in cultured cells and its restoration by glycosyltransferase (Poster)

Journal of neurochemistry, 101, 6. Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice

FEBS Letters, 579, 11. Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy

Cell, 117, 7. Molecular recognition by LARGE is essential for expression of functional dystroglycan

Neuromuscular disorders : NMD, 14, 2. A Japanese patient with distal myopathy with rimmed vacuoles : missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins

Nature, 418. Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

Cell, 110. Disruption of Dag1 in differentiated skeletal muscle reveals a role of dystroglycan in muscle regeneration

Journal of biological chemistry (The), 274, 12. Characterization of the transmembrane molecular architecture of the Dystroglycan complex in Schwann cells

Muscle & Nerve A 180-KDA protein is deficient in Fukuyama-type congenital muscular dystrophy skeletal muscle

Histology and histopathology, 12. The role of dystroglycan, a novel receptor of laminin and agrin, in cell differentiation

Neuromuscular disorders : NMD, 7, 1. Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

American journal of human genetics (The), 40, 3. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency : molecular genetic evidence for deletions

eLife, 12. N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy