(Q28176853)

2

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Kazuhiro Kobayashi

3

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Kiyomi Taniguchi

4

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Masao Kawakita

5

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Tatsushi Toda

6

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Tamao Endo

Biochemical and Biophysical Research Communications

7

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language of work or name

English

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publication date

20 June 2003

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published in

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volume

306

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issue

1

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page(s)

93-7

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cites work

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Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin

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Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

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Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease

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A new beta-1,2-N-acetylglucosaminyltransferase that may play a role in the biosynthesis of mammalian O-mannosyl glycans

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X-ray crystal structure of rabbit N-acetylglucosaminyltransferase I: catalytic mechanism and a new protein superfamily

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Targeting of proteins to the Golgi apparatus

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Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

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Defective glycosylation in muscular dystrophy

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Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12788071

1 reference

Consolidated OpenCitations Corpus – April 2017