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Results of search for 'su:"Sarcoglycans"', page 3 of 40
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Authors
Angelini, C
Azibi, K
Beckmann, J S
Blake, Derek J
Campbell, K P
Cossu, Giulio
Cutroneo, Giuseppina
Hoffman, E P
Kunkel, L M
Leturcq, F
McNally, E M
McNally, Elizabeth M
Nigro, V
Nigro, Vincenzo
Ozawa, E
Passos-Bueno, M R
Richard, Isabelle
Roberds, S L
Vainzof, M
Zatz, M
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Adolescent
Adult
Animals
Child
Cytoskeletal Proteins
Dystroglycans
Dystrophin
Female
Humans
Male
Membrane Glycoproteins
Mice
Muscle, Skeletal
Muscular Dystrophies
Mutation
Sarcoglycans
chemistry
deficiency
genetics
metabolism
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41.
[Anesthetic management of a child with delta sarcoglycanopathy].
[electronic resource]
by
Moro, C
Dangelser, G
Veyckemans, F
Producer:
20070516
In:
Annales francaises d'anesthesie et de reanimation
vol. 26
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42.
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex.
[electronic resource]
by
Vainzof, M
Moreira, E S
Ferraz, G
Passos-Bueno, M R
Marie, S K
Zatz, M
Producer:
19990615
In:
European journal of human genetics : EJHG
vol. 7
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43.
Gait disturbances in dystrophic hamsters.
[electronic resource]
by
Hampton, Thomas G
Kale, Ajit
Amende, Ivo
Tang, Wenlong
McCue, Scott
Bhagavan, Hemmi N
VanDongen, Case G
Producer:
20110606
In:
Journal of biomedicine & biotechnology
vol. 2011
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44.
Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay?
[electronic resource]
by
Matsumura, K
Saito, F
Yamada, H
Hase, A
Sunada, Y
Shimizu, T
Producer:
20000131
In:
Cellular and molecular biology (Noisy-le-Grand, France)
vol. 45
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45.
KCTD17 is a confirmed new gene for dystonia, but is it responsible for SGCE-negative myoclonus-dystonia?
[electronic resource]
by
Mencacci, Niccolò E
Brüggemann, Norbert
Producer:
20191114
In:
Parkinsonism & related disorders
vol. 61
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46.
Ultrastructure of diaphragm from dystrophic alpha-sarcoglycan-null mice.
[electronic resource]
by
Jakubiec-Puka, Anna
Biral, Donatella
Krawczyk, Kazimierz
Betto, Romeo
Producer:
20090820
In:
Acta biochimica Polonica
vol. 52
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47.
Sarcoglycan subcomplex in normal and pathological human muscle fibers.
[electronic resource]
by
Anastasi, G
Cutroneo, G
Rizzo, G
Favaloro, A
Producer:
20071010
In:
European journal of histochemistry : EJH
vol. 51 Suppl 1
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48.
Dystrophin-compromised sarcoglycan-δ-knockout diaphragm requires full wild-type embryonic stem cell reconstitution for correction.
[electronic resource]
by
Vitale, Joseph M
Schneider, Joel S
Beck, Amanda J
Zhao, Qingshi
Chang, Corey
Gordan, Richard
Michaels, Jennifer
Bhaumik, Mantu
Fraidenraich, Diego
Producer:
20130205
In:
Journal of cell science
vol. 125
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49.
Studying the role of dystrophin-associated proteins in influencing Becker muscular dystrophy disease severity.
[electronic resource]
by
Sewry, C A
Producer:
20151124
In:
Neuromuscular disorders : NMD
vol. 25
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50.
Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex.
[electronic resource]
by
Duggan, D J
Hoffman, E P
Producer:
19970508
In:
Neuromuscular disorders : NMD
vol. 6
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51.
[Identification of adhalin gene mutation in limb-girdle muscular dystrophy in Chinese].
[electronic resource]
by
Sun, G
Wu, Y
Zhang, K
Zhang, X
Jin, C
Sun, K
Producer:
19990128
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 15
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52.
A novel mutation of the SGCE-gene in a German family with myoclonus-dystonia syndrome.
[electronic resource]
by
Hartmann, Christian Johannes
Leube, Barbara
Wojtecki, Lars
Betz, Beate
Groiss, Stefan Jun
Bauer, Peter
Schnitzler, Alfons
Südmeyer, Martin
Producer:
20110923
In:
Journal of neurology
vol. 258
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53.
Morphofunctional compensation of masseter muscles in unilateral posterior crossbite patients.
[electronic resource]
by
Cutroneo, G
Vermiglio, G
Centofanti, A
Rizzo, G
Runci, M
Favaloro, A
Piancino, M G
Bracco, P
Ramieri, G
Bianchi, F
Speciale, F
Arco, A
Trimarchi, F
Producer:
20170213
In:
European journal of histochemistry : EJH
vol. 60
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54.
A hypertrophic and dilated cardiomyopathic sudden cardiac death case; de novo mutations in TTN and SGCD genes.
[electronic resource]
by
Baydar, Çetin Lütfi
Özen, Minel
Producer:
20181112
In:
Anatolian journal of cardiology
vol. 16
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55.
Genetic medicine and the muscular dystrophies: triumphs and tribulations.
[electronic resource]
by
Hoffman, Eric P
Chen, Yi-Wen
Producer:
20020402
In:
Developmental medicine and child neurology
vol. 44
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56.
Response to: Studying the role of dystrophin-associated proteins in influencing Becker muscular dystrophy disease severity.
[electronic resource]
by
van den Bergen, Janneke
Aartsma-Rus, Annemieke
Producer:
20151124
In:
Neuromuscular disorders : NMD
vol. 25
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57.
Myoclonus-dystonia (DYT11) with novel SGCE mutation misdiagnosed as a primary psychiatric disorder.
[electronic resource]
by
Bonello, M
Larner, A J
Alusi, S H
Producer:
20150723
In:
Journal of the neurological sciences
vol. 346
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58.
A novel mutation in alpha sarcoglycan gene in an Iranian family with limb girdle muscular dystrophy 2D.
[electronic resource]
by
Mojbafan, Marzieh
Nilipour, Yalda
Tonekaboni, Seyed Hasan
Tavakkoly-Bazzaz, Javad
Zeinali, Sirous
Producer:
20170113
In:
Neurological research
vol. 38
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59.
Pathophysiology of heart failure: more bricks in the "crumbling sarcolemmal scaffolding" paradigm?
[electronic resource]
by
Baudet, Stéphane
Producer:
20050302
In:
Cardiovascular research
vol. 65
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60.
Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscle.
[electronic resource]
by
Sunada, Y
Campbell, K P
Producer:
19960214
In:
Current opinion in neurology
vol. 8
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