Matches in Nanopublications for { ?s ?p "[A previously unreported case with severe bilateral microphthalmia and oesophageal atresia has a de novo missense mutation, R74P, that alters a highly evolutionarily conserved residue within the high mobility group domain, which is critical for DNA-binding of SOX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP404746.RA4IU_RAkTMFMnVvM6eoFn4GnPAKH50GdWSP_sPq54k9s130_assertion description "[A previously unreported case with severe bilateral microphthalmia and oesophageal atresia has a de novo missense mutation, R74P, that alters a highly evolutionarily conserved residue within the high mobility group domain, which is critical for DNA-binding of SOX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404746.RA4IU_RAkTMFMnVvM6eoFn4GnPAKH50GdWSP_sPq54k9s130_provenance.
- NP735971.RAu03b2CqOfCqNjkVT9GszndDWfVb1kN0GZa1g981c_q4130_assertion description "[A previously unreported case with severe bilateral microphthalmia and oesophageal atresia has a de novo missense mutation, R74P, that alters a highly evolutionarily conserved residue within the high mobility group domain, which is critical for DNA-binding of SOX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735971.RAu03b2CqOfCqNjkVT9GszndDWfVb1kN0GZa1g981c_q4130_provenance.
- NP708010.RAKRLuJMPsEy9HAnexo9ZC0BodnU6-pWIZ14pJBHdGExU130_assertion description "[A previously unreported case with severe bilateral microphthalmia and oesophageal atresia has a de novo missense mutation, R74P, that alters a highly evolutionarily conserved residue within the high mobility group domain, which is critical for DNA-binding of SOX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708010.RAKRLuJMPsEy9HAnexo9ZC0BodnU6-pWIZ14pJBHdGExU130_provenance.
- assertion description "[A previously unreported case with severe bilateral microphthalmia and oesophageal atresia has a de novo missense mutation, R74P, that alters a highly evolutionarily conserved residue within the high mobility group domain, which is critical for DNA-binding of SOX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A previously unreported case with severe bilateral microphthalmia and oesophageal atresia has a de novo missense mutation, R74P, that alters a highly evolutionarily conserved residue within the high mobility group domain, which is critical for DNA-binding of SOX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP540760.RAtc-wZwjiKncyBNBlzQqGnPd7vwSVZua1Sg-r7KepQRg130_assertion description "[A previously unreported case with severe bilateral microphthalmia and oesophageal atresia has a de novo missense mutation, R74P, that alters a highly evolutionarily conserved residue within the high mobility group domain, which is critical for DNA-binding of SOX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540760.RAtc-wZwjiKncyBNBlzQqGnPd7vwSVZua1Sg-r7KepQRg130_provenance.