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  <titleInfo>
    <title>Genetic profiling of cell free circulating tumor DNA in breast cancer patients</title>
  </titleInfo>
  <titleInfo type="alternative">
    <title>النمط الجيني للحمض النووي الديوكسي ريبوسي المتحرر من خلايا مرضى سرطان الثدي</title>
  </titleInfo>
  <name type="personal">
    <namePart>Mai Mohamed Elsayed Lotfy</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Abdelrahman Nabawy Zekri</namePart>
    <role>
      <roleTerm type="text">Supervisor</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Amany Abdelhhameed Aboubakr</namePart>
    <role>
      <roleTerm type="text">Supervisor</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Zeinab Korany M. Hassan</namePart>
    <role>
      <roleTerm type="text">Supervisor</roleTerm>
    </role>
  </name>
  <typeOfResource>text</typeOfResource>
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  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">ua</placeTerm>
    </place>
    <place>
      <placeTerm type="text">Cairo</placeTerm>
    </place>
    <publisher>Mai Mohamed Elsayed Lotfy</publisher>
    <dateIssued>2021</dateIssued>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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    <extent>138 P. :  charts , facsimiles ;  25cm </extent>
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  <abstract>detected pathogenic variants (PVs) and likely pathogenic variants (LPVs). These genes were found to be involved in DNA repair mechanisms and WNT/Ý-catenin signalling pathways that will ultimately lead to cancer development. Also, it was revealed that 27.2% of the tissue-derived PVs/LPVs could be detected in ctDNAs, and 35.7% of ctDNA-derived PVs/LPVs could be found in paired tissues. The overall concordance rates for all of the identified somatic variants, PVs/LPVs only and genes carrying PVs/LPVs between both assays across all patients are 85.48%, 82.46% and 76.10%, respectively. According to their Cohen{u2019}s Kappa values, they have a statistically significant slight to fair agreement in both biopsies. While, the positive concordance rates for all of the identified somatic variants, PVs/LPVs only and the genes carrying PVs/LPVs in both assays across all patients are 28.77%, 7.79% and 11.56%, respectively. The level of agreement between the 2 assays -confined to the presence of concordant variants only- was represented by the negative values of Cohen{u2019}s Kappa which implies a statistically significant disagreement between the two platforms</abstract>
  <targetAudience authority="marctarget">specialized</targetAudience>
  <note type="statement of responsibility">Mai Mohamed Elsayed Lotfy ; Supervised Abd Elrahman N. Zekri , Amany Abd Elhameed Aboubakr , Zeinab Korany M. Hassan</note>
  <note>Thesis (Ph.D.) - Cairo University - National Cancer Institute - Department of Cancer Biology</note>
  <note>Issued also as CD</note>
  <subject>
    <topic>Breast cancer patients </topic>
  </subject>
  <subject>
    <topic>Circulating tumor </topic>
  </subject>
  <subject>
    <topic>DNA </topic>
  </subject>
  <identifier type="uri">http://172.23.153.220/th.pdf</identifier>
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    <recordCreationDate encoding="marc">210913</recordCreationDate>
    <recordChangeDate encoding="iso8601">20250223032814.0</recordChangeDate>
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