OpenAlex 393 eser 2 yazar konusu
Çalışmalar
393 eser
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 99.5%
As a result of ischemia or hemorrhage, blood supply to neurons is disrupted which subsequently promotes a cascade of pathophysiological responses resulting in cell loss. Many mechanisms are involved solely or in combination in this disorder including excitotoxicity, mitochondrial death pathways, and the release of fre…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 99.5%
Dystroglycan, which serves as a major extracellular matrix receptor in muscle and the central nervous system, requires extensive O-glycosylation to function.We identified a dystroglycan missense mutation (Thr192→Met) in a woman with limb-girdle muscular dystrophy and cognitive impairment.A mouse model harboring this m…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 99.5%
Dystroglycan, which serves as a major extracellular matrix receptor in muscle and the central nervous system, requires extensive O-glycosylation to function.We identified a dystroglycan missense mutation (Thr192→Met) in a woman with limb-girdle muscular dystrophy and cognitive impairment.A mouse model harboring this m…
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OpenAlex üst %1
OpenAlex 99.4%
Dystroglycan, which serves as a major extracellular matrix receptor in muscle and the central nervous system, requires extensive O-glycosylation to function.We identified a dystroglycan missense mutation (Thr192→Met) in a woman with limb-girdle muscular dystrophy and cognitive impairment.A mouse model harboring this m…
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OpenAlex üst %10
OpenAlex 97.0%
Özet henüz yok.
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Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of Dystroglycan 2013YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.3%
Özet henüz yok.
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Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of Dystroglycan 2013YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.2%
Özet henüz yok.
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %10
OpenAlex 97.5%
Hypoglycosylation of alpha-dystroglycan underpins a subgroup of muscular dystrophies ranging from congenital onset of weakness, severe brain malformations and death in the perinatal period to mild weakness in adulthood without brain involvement. Mutations in six genes have been identified in a proportion of patients.…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %10
OpenAlex 93.0%
Autosomal recessive limb girdle muscular dystrophy (LGMD2) is a clinically and genetically heterogenous group of diseases involving at least six different loci. Five genes have already been identified: calpain-3 at LGMD2A (15q15), and four members of the sarcoglycan (SG) complex, alpha-SG at LGMD2D (17q21), beta-SG at…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %10
OpenAlex 91.9%
BACKGROUND AND PURPOSE: Matrix metalloproteinases (MMPs) and cysteine proteases (calpain and cathepsin B) play an important role in cell death and are upregulated after focal cerebral ischemia. Because there is a significant interaction between MMP-9 with calpain and cathepsin B, we investigated the role of E64d (a ca…
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YÖKSİS
SJR Q1
JCR Q3
OpenAlex üst %10
OpenAlex 92.9%
Deficiency in the vasorelaxant capacity is a result of an oxidative stress in diabetic animals and seems to be an etiological factor of vascular complications of diabetes. The present study was designed to examine whether resveratrol (RSV), a polyphenolic compound which is naturally present in grape and red wine, has…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %10
OpenAlex 92.6%
Hexamethylenebisacetamide (HMBA) is a potent inducer of murine erythroleukemia (MEL) cell differentiation. The mechanism of action of HMBA is not known. In this study we provide evidence that protein kinase C has a role in inducer-mediated MEL cell differentiation: (i) HMBA induces the formation of a soluble, proteoly…
Akademisyenler
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