Congenital muscular dystrophies involving the O-mannose pathway.
about
Tumor suppressor function of laminin-binding alpha-dystroglycan requires a distinct beta3-N-acetylglucosaminyltransferaseMammalian O-mannosylation: unsolved questions of structure/functionMetabolic manipulation of glycosylation disorders in humans and animal modelsEfficacy of Gene Therapy Is Dependent on Disease Progression in Dystrophic Mice with Mutations in the FKRP GeneSite mapping and characterization of O-glycan structures on alpha-dystroglycan isolated from rabbit skeletal muscle.Glycomic analyses of mouse models of congenital muscular dystrophyGlycosylated synaptomatrix regulation of trans-synaptic signaling.Identification of cell surface molecules involved in dystroglycan-independent Lassa virus cell entryCongenital protein hypoglycosylation diseases.Expression pattern in retinal photoreceptors of POMGnT1, a protein involved in muscle-eye-brain disease.Muscular dystrophies due to defective glycosylation of dystroglycan.Adeno-associated virus 9 mediated FKRP gene therapy restores functional glycosylation of α-dystroglycan and improves muscle functionsMuscular dystrophies due to glycosylation defects.Glycosylation diseases: quo vadis?The neurobiology of the dystrophin-associated glycoprotein complex.A developmental and genetic classification for midbrain-hindbrain malformations.Congenital muscular dystrophy. Part II: a review of pathogenesis and therapeutic perspectives.Protein O-mannosylation in animal development and physiology: from human disorders to Drosophila phenotypesGolgi glycosylation and human inherited diseases.Solving glycosylation disorders: fundamental approaches reveal complicated pathways.Mammalian O-mannosylation pathway: glycan structures, enzymes, and protein substrates.Drosophila Dystroglycan is a target of O-mannosyltransferase activity of two protein O-mannosyltransferases, Rotated Abdomen and TwistedMass spectrometric analysis of hepatitis C viral envelope protein E2 reveals extended microheterogeneity of mucin-type O-linked glycosylation.Protein O-mannosyltransferases affect sensory axon wiring and dynamic chirality of body posture in the Drosophila embryo.Sexually dimorphic skeletal muscle and cardiac dysfunction in a mouse model of limb girdle muscular dystrophy 2i.Skeletal muscle contractile properties in a novel murine model for limb girdle muscular dystrophy 2i.Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies.Distinct expression of functionally glycosylated alpha-dystroglycan in muscle and non-muscle tissues of FKRP mutant mice.Expression in retinal neurons of fukutin and FKRP, the protein products of two dystroglycanopathy-causative genes.Second international workshop for glycosylation defects in muscular dystrophies, 11-12 November, 2010, Charlotte, USA.Overexpression of Mutant FKRP Restores Functional Glycosylation and Improves Dystrophic Phenotype in FKRP Mutant Mice.
P2860
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P2860
Congenital muscular dystrophies involving the O-mannose pathway.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Congenital muscular dystrophies involving the O-mannose pathway.
@en
type
label
Congenital muscular dystrophies involving the O-mannose pathway.
@en
prefLabel
Congenital muscular dystrophies involving the O-mannose pathway.
@en
P2860
P1476
Congenital muscular dystrophies involving the O-mannose pathway.
@en
P2093
Paul T Martin
P2860
P304
P356
10.2174/156652407780831601
P577
2007-06-01T00:00:00Z