Matches in Nanopublications for { ?s ?p "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP321316.RAtvuP6LwypbZ7WURpRuNmChJuX-Pz75Tm4p0CuUb8_EQ130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321316.RAtvuP6LwypbZ7WURpRuNmChJuX-Pz75Tm4p0CuUb8_EQ130_provenance.
- NP603698.RAfVgQh_jSk89qN_2C4qNC7VzxJk2U2WZK3qMdqywyYlY130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603698.RAfVgQh_jSk89qN_2C4qNC7VzxJk2U2WZK3qMdqywyYlY130_provenance.
- assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP355363.RAjqmQS3m2IJPuaiKxnywUZ7Ql5PoToh8L6s92gUUd1yQ130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355363.RAjqmQS3m2IJPuaiKxnywUZ7Ql5PoToh8L6s92gUUd1yQ130_provenance.
- NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_provenance.
- NP1357050.RAAW9a0w1TqStq8hkjPP4wKYjT3RzpBVSX81V36WWTpOg130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357050.RAAW9a0w1TqStq8hkjPP4wKYjT3RzpBVSX81V36WWTpOg130_provenance.
- NP1357045.RAmNzEAxwlZPGvOxKR9yO1F_YTMqvsKQxJwBZF10Mf7cE130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357045.RAmNzEAxwlZPGvOxKR9yO1F_YTMqvsKQxJwBZF10Mf7cE130_provenance.
- NP355543.RAKxTOuDdoL2FzrdpwChT9DtyOKgU8bMvD4yW7GE-EQXk130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355543.RAKxTOuDdoL2FzrdpwChT9DtyOKgU8bMvD4yW7GE-EQXk130_provenance.
- NP1357047.RA8NwxDBMtFC9vy68vsZDh5F7WrOaEzGlIvYr-YtrsaZM130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357047.RA8NwxDBMtFC9vy68vsZDh5F7WrOaEzGlIvYr-YtrsaZM130_provenance.
- NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357048.RA0biAuJ0Z0lJ1ZN6v_8yBN4qSIOOyKBSFlbIxr8Zfcwc130_provenance.
- NP1357051.RA_QwXNnmgr6zAj0jm6yBw4xeo33UAsqXYwbMkraYPvCQ130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1357051.RA_QwXNnmgr6zAj0jm6yBw4xeo33UAsqXYwbMkraYPvCQ130_provenance.