Intron/exon structure of the human gene for the muscle isozyme of glycogen phosphorylase

No abstract is available for this paper.

• Publication year

  1987

• Venue

  Proteins: Structure, Function, and Bioinformatics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/prot.340020303PMID 3447177
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Convergent and divergent evolution of regulatory sites in eukaryotic phosphorylases

  1986cited by this paper
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  1986cited by this paper
• The complete amino acid sequence of potato alpha-glucan phosphorylase.

  1986cited by this paper
• Complete cDNA sequence for rabbit muscle glycogen phosphorylase

  1986cited by this paper
• Interactive program for visualization and modelling of proteins, nucleic acids and small molecules

  1986cited by this paper
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  1986cited by this paper
• The Triosephosphate lsomerase Gene from Maize: lntrons Antedate the Plant-Animal Divergence

  1986cited by this paper
• Compact units in proteins.

  1986cited by this paper
• Sequence analysis of the cDNA encoding human liver glycogen phosphorylase reveals tissue-specific codon usage.

  1986cited by this paper
• Loops in globular proteins: a novel category of secondary structure.

  1986cited by this paper
• Comparative sequence analysis of rat, rabbit, and human muscle glycogen phosphorylase cDNAs.

  1985cited by this paper
• Evolution of catalytic and regulatory sites in phosphorylases

  1985cited by this paper
• Intron-dependent evolution of chicken glyceraldehyde phosphate dehydrogenase gene

  1985cited by this paper
• Response of global deep-water circulation to Earth's climatic change 135,000–107,000 years ago

  1985cited by this paper
• Structure of the human phosphoglycerate kinase gene and the intron-mediated evolution and dispersal of the nucleotide-binding domain.

  1985cited by this paper
• Protein structure and gene organization of mouse lactate dehydrogenase-A isozyme.

  1985cited by this paper
• Exons and the evolution of proteins.

  1985cited by this paper
• Intron/exon structure of the chicken pyruvate kinase gene.

  1985cited by this paper
• Correlation of exons with structural domains in alcohol dehydrogenase.

  1984cited by this paper
• Splice junctions: association with variation in protein structure.

  1983cited by this paper
• Comparison of AMP and NADH binding to glycogen phosphorylase b.

  1983cited by this paper
• Structure of maltoheptaose by difference Fourier methods and a model for glycogen.

  1982cited by this paper
• Intron–exon splice junctions map at protein surfaces

  1982cited by this paper
• Catalytic site of glycogen phosphorylase: structure of the T state and specificity for alpha-D-glucose.

  1982cited by this paper
• Relationship between the total size of exons and introns in protein-coding genes of higher eukaryotes.

  1982cited by this paper
• THE RELATIONSHIP OF GENE STRUCTURE TO PROTEIN STRUCTURE

  1982cited by this paper
• Glycogen phosphorylase structures and function

  1982cited by this paper
• Correlation of DNA exonic regions with protein structural units in haemoglobin

  1981cited by this paper
• Organization and expression of eucaryotic split genes coding for proteins.

  1981cited by this paper
• Structural aspects of the catalytic and regulatory function of glycogen phosphorylase.

  1981cited by this paper
• Subunit interactions and the allosteric response in phosphorylase.

  1980cited by this paper
• The structures and related functions of phosphorylase a.

  1980cited by this paper
• The structure of glycogen phosphorylase alpha at 2.5 A resolution.

  1979cited by this paper
• The structure of glycogen phosphorylase a at 2.5 Å resolution

  1979cited by this paper
• Analysis of the surface topography of glycogen phosphorylase a: implications for metabolic interconversion and regulatory mechanisms.

  1979cited by this paper
• Crystal structure of cat muscle pyruvate kinase at a resolution of 2.6 A.

  1979cited by this paper
• Solvent accessibility properties of complex proteins

  1979cited by this paper
• Sequence, structure and activity of phosphoglycerate kinase: a possible hinge-bending enzyme

  1979cited by this paper
• Why genes in pieces?

  1978cited by this paper
• Assignment of the amino acid sequence to the crystal structure of glycogen phosphorylase b.

  1978cited by this paper
• The Isolation and Characterization of Linked δ- and β-Globin Genes from a Cloned Library of Human DNA

  1978cited by this paper
• The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA.

  1978cited by this paper
• Synergistic regulation of phosphorylase a by glucose and caffeine.

  1978cited by this paper
• DNA sequencing with chain-terminating inhibitors.

  1977cited by this paper
• Complete amino acid sequence of rabbit muscle glycogen phosphorylase.

  1977cited by this paper
• Screening lambdagt recombinant clones by hybridization to single plaques in situ.

  1977cited by this paper
• Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

  1977cited by this paper
• Structural patterns in globular proteins

  1976cited by this paper
• Structure of glycogen phosphorylase a at 3.0 A resolution and its ligand binding sites at 6 A.

  1976cited by this paper
• Detection of specific sequences among DNA fragments separated by gel electrophoresis.

  1975cited by this paper
• Chemical and biological evolution of a nucleotide-binding protein

  1974cited by this paper
• The interpretation of protein structures: estimation of static accessibility.

  1971cited by this paper

• Fatigue and associated factors in 172 patients with McArdle disease: An international web-based survey.

  2023cites this paper
• Discovery and Biotechnological Exploitation of Glycoside-Phosphorylases

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• Preclinical Gene Therapy Studies for Metabolic Myopathy

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• Thermostable alpha-glucan phosphorylases: characteristics and industrial applications

  2018cites this paper
• Novel myophosphorylase mutation (p.Arg94Pro) with progressive exercise intolerance

  2018cites this paper
• McArdle Disease and Exercise Physiology

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• Molecular and clinical study of McArdle's disease in a cohort of 123 European patients. Identification of 20 novel mutations.

  2011cites this paper
• Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: identification of 10 new mutations. Absence of genotype-phenotype correlation.

  2007cites this paper
• Patients with Myophosphorylase Deficiency (McArdle Disease)

  2007influential citation
• A novel mutation in the PYGM gene in a family with pseudo-dominant transmission of McArdle disease.

  2005cites this paper
• The location of exon boundaries in the multimeric iron-storage protein ferritin

  2005cites this paper
• A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle disease.

  2004cites this paper
• Two novel mutations in the myophosphorylase gene in a patient with McArdle disease

  2003cites this paper
• A novel nonsense mutation (R269X) in the myophosphorylase gene in a patient with McArdle disease.

  2001cites this paper
• Molecular heterogeneity of myophosphorylase deficiency (Mcardle's disease): A genotype‐phenotype correlation study

  2001cites this paper
• A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's disease.

  2000cites this paper
• A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's disease.

  2000cites this paper
• The molecular diagnosis of metabolic myopathies.

  2000cites this paper
• A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle disease.

  2000cites this paper
• A missense mutation W797R in the myophosphorylase gene in a Spanish patient with McArdle's disease

  2000cites this paper
• McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patient.

  1999cites this paper
• Structural and functional characterization of the Drosophila glycogen phosphorylase gene.

  1999cites this paper
• The Molecular Background of Glycogen Metabolism Disorders

  1999cites this paper
• The enigma of intron origins

  1999cites this paper
• Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chain.

  1998cites this paper
• Molecular diagnosis of McArdle disease: revised genomic structure of the myophosphorylase gene and identification of a novel mutation.

  1998cites this paper
• Molecular diagnosis of McArdle disease: Revised genomic structure of the myophosphorylase gene and identification of a novel mutation

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  1998influential citation
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  1997cites this paper
• Expression of glycogen phosphorylase isozymes in developing rat lung.

  1997cites this paper
• Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'.

  1997cites this paper
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• Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.

  1997cites this paper
• [McArdle's disease in adults: clinical and genetic study].

  1997cites this paper
• A splice-site mutation causing ovine McArdle's disease.

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• Diagnosis of McArdle's disease by molecular genetic analysis of blood

  1996cites this paper
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• The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)

  1995cites this paper
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  1995cites this paper
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  1995cites this paper
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  1995cites this paper
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  1995cites this paper
• Methods for evaluating exon-protein correspondences

  1995cites this paper
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  1994cites this paper
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  1994cites this paper
• Two mutations, one novel and one frequently observed, in Japanese patients with McArdle's disease.

  1994cites this paper
• Testing the exon theory of genes: the evidence from protein structure.

  1994cites this paper
• Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease).

  1993cites this paper
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  1993cites this paper
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  1993cites this paper
• Evolution of allosteric control in glycogen phosphorylase.

  1993cites this paper
• McArdle's disease: a nonsense mutation in exon 1 of the muscle glycogen phosphorylase gene explains some but not all cases.

  1993cites this paper
• Characterization of the 5' flanking region of the gene encoding rat liver glycogen phosphorylase.

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• Glycogen phosphorylase: control by phosphorylation and allosteric effectors

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  1992cites this paper
• The nucleotide sequence of rat liver glycogen phosphorylase cDNA.

  1992cites this paper
• Adenovirus-mediated transfer of the muscle glycogen phosphorylase gene into hepatocytes confers altered regulation of glycogen metabolism.

  1992cites this paper
• Identification of a tissue-specific regulatory element within the human muscle glycogen phosphorylase gene.

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  1991cites this paper
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• An engineered liver glycogen phosphorylase with AMP allosteric activation.

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• Developmental expression of glycogenolytic enzymes in rabbit tissues: possible relationship to fetal lung maturation.

  1991cites this paper
• Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence

  1990cites this paper
• Molecular heterogeneity in McArdle's disease.

  1990cites this paper
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  1990cites this paper
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  1990influential citation
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  1989cites this paper
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  1989cites this paper
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  1989cites this paper
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  1988cites this paper
• Do exons code for structural or functional units in proteins?

  1988cites this paper
• Isolation and mapping of a polymorphic DNA sequence for human muscle glycogen phosphorylase (pMCMP1) on chromosome II [PYGM].

  1988cites this paper
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  1988cites this paper
• Modeling the biochemical differences between rabbit muscle and human liver phosphorylase

  1987cites this paper