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Mammalian O-mannosylation: unsolved questions of structure/function
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title
Mammalian O-mannosylation: unsolved questions of structure/function
(English)
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PubMed
author name string
Stephanie H Stalnaker
series ordinal
1
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Crossref
Ryan Stuart
series ordinal
2
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Crossref
Lance Wells
series ordinal
3
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language of work or name
English
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PubMed
publication date
October 2011
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published in
Current Opinion in Structural Biology
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PubMed
volume
21
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PubMed
issue
5
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PubMed
page(s)
603-9
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PubMed
cites work
Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity
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PubMed Central
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21 March 2017
Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome
1 reference
stated in
PubMed Central
reference URL
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retrieved
21 March 2017
Cloning and expression of a novel UDP-GlcNAc:alpha-D-mannoside beta1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
21 March 2017
Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
21 March 2017
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
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
A stoichiometric complex of neurexins and dystroglycan in brain
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PubMed Central
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21 March 2017
Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
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PubMed Central
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21 March 2017
Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease
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PubMed Central
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21 March 2017
LARGE2 facilitates the maturation of alpha-dystroglycan more effectively than LARGE
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Fukutin-related protein associates with the sarcolemmal dystrophin-glycoprotein complex
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Glycosylation defects: a new mechanism for muscular dystrophy?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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21 March 2017
Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse
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PubMed Central
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21 March 2017
Dystrophin: the protein product of the Duchenne muscular dystrophy locus
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PubMed Central
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7 April 2017
Membrane organization of the dystrophin-glycoprotein complex
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PubMed Central
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7 April 2017
Glycomic analyses of mouse models of congenital muscular dystrophy
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PubMed Central
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28 September 2017
Genetic defects in muscular dystrophy
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PubMed Central
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28 September 2017
Site mapping and characterization of O-glycan structures on alpha-dystroglycan isolated from rabbit skeletal muscle.
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PubMed Central
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28 September 2017
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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28 September 2017
Mucin-type O-glycosylation--putting the pieces together.
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PubMed Central
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28 September 2017
Comprehensive classification of nucleotidyltransferase fold proteins: identification of novel families and their representatives in human
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28 September 2017
Adaptive regulation at the cell surface by N-glycosylation.
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PubMed Central
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28 September 2017
Mutational and functional analysis of Large in a novel CHO glycosylation mutant
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28 September 2017
Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE.
1 reference
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PubMed Central
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28 September 2017
Muscular dystrophies due to glycosylation defects
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PubMed Central
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28 September 2017
Congenital muscular dystrophies involving the O-mannose pathway
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PubMed Central
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28 September 2017
Regulation of mammalian protein O-mannosylation: preferential amino acid sequence for O-mannose modification
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PubMed Central
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28 September 2017
Diagnosis and cell-based therapy for Duchenne muscular dystrophy in humans, mice, and zebrafish
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28 September 2017
Dystroglycan: from biosynthesis to pathogenesis of human disease.
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28 September 2017
Posttranslational modification of alpha-dystroglycan, the cellular receptor for arenaviruses, by the glycosyltransferase LARGE is critical for virus binding.
1 reference
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PubMed Central
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28 September 2017
Mouse large can modify complex N- and mucin O-glycans on alpha-dystroglycan to induce laminin binding
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28 September 2017
Role of glycosylation in development
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28 September 2017
Defective glycosylation in congenital muscular dystrophies
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28 September 2017
N-Acetylglucosaminyltransferase IX acts on the GlcNAc beta 1,2-Man alpha 1-Ser/Thr moiety, forming a 2,6-branched structure in brain O-mannosyl glycan.
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PubMed Central
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28 September 2017
Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatids
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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28 September 2017
Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.
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28 September 2017
Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice
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PubMed Central
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28 September 2017
Muscular dystrophy--reason for optimism?
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28 September 2017
O-mannosyl glycans in mammals
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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28 September 2017
Detection of O-mannosyl glycans in rabbit skeletal muscle alpha-dystroglycan
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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28 September 2017
The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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28 September 2017
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
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
28 September 2017
Novel mannitol-containing oligosaccharides obtained by mild alkaline borohydride treatment of a chondroitin sulfate proteoglycan from brain
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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28 September 2017
Structural analysis of sequences O-linked to mannose reveals a novel Lewis X structure in cranin (dystroglycan) purified from sheep brain.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
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31 May 2018
Characterization of site-specific O-glycan structures within the mucin-like domain of alpha-dystroglycan from human skeletal muscle
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
28 November 2018
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
28 November 2018
Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
28 November 2018
High prevalence of 2-mono- and 2,6-di-substituted manol-terminating sequences among O-glycans released from brain glycopeptides by reductive alkaline hydrolysis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
28 November 2018
Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
28 November 2018
Brain contains HNK-1 immunoreactive O-glycans of the sulfoglucuronyl lactosamine series that terminate in 2-linked or 2,6-linked hexose (mannose).
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356693
retrieved
28 November 2018
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21945038
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cloning and expression of a novel UDP-GlcNAc:α-d-mannoside β1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:α-3-d-mannoside β1,2-N-acetylglucosaminyltransferase I
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21945038
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.SBI.2011.09.001
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1985608
OpenCitations bibliographic resource ID
1985608
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1985608
PMCID
3356693
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1985608
PubMed ID
21945038
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1985608
ResearchGate publication ID
51672126
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