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          <dc:title>&lt;p&gt;Genetic Variants of the CDH1 Gene from ClinVar Database.&lt;/p&gt;</dc:title>
          <dc:creator>Faria Ferdouse Mim (25038563)</dc:creator>
          <dc:creator>Taslima Akter Sumiya (25038566)</dc:creator>
          <dc:creator>Roksana Khanam (25038569)</dc:creator>
          <dc:creator>Jannati Akter (25038572)</dc:creator>
          <dc:creator>Farhana Arzu (25038575)</dc:creator>
          <dc:creator>Samia Haque (25038578)</dc:creator>
          <dc:creator>Md. Roman Miah (25038581)</dc:creator>
          <dc:creator>K.M. Tanjida Islam (23142024)</dc:creator>
          <dc:creator>Shahin Mahmud (13993958)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Information Systems not elsewhere classified</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>transcription factor ezh2</dc:subject>
          <dc:subject>prominent hub gene</dc:subject>
          <dc:subject>precise therapeutic decisions</dc:subject>
          <dc:subject>patient survival data</dc:subject>
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          <dc:subject>identify critical genes</dc:subject>
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          <dc:subject>conformational change detection</dc:subject>
          <dc:subject>biophysical energetics assessment</dc:subject>
          <dc:subject>altered patient survival</dc:subject>
          <dc:subject>886 genes exhibiting</dc:subject>
          <dc:subject>60 nonsense snps</dc:subject>
          <dc:subject>36 missense snps</dc:subject>
          <dc:subject>pathogenic variations disrupting</dc:subject>
          <dc:subject>unsupervised machine learning</dc:subject>
          <dc:subject>molecular framework demonstrating</dc:subject>
          <dc:subject>depth computational analyses</dc:subject>
          <dc:subject>three tumor suppressors</dc:subject>
          <dc:subject>multiple common oncogenes</dc:subject>
          <dc:subject>common cancer globally</dc:subject>
          <dc:subject>oncogenic genetic variations</dc:subject>
          <dc:subject>mutations trigger dysregulation</dc:subject>
          <dc:subject>level analysis provides</dc:subject>
          <dc:subject>high mutation propensity</dc:subject>
          <dc:subject>tumor suppressor pathways</dc:subject>
          <dc:subject>8 %), cdh1</dc:subject>
          <dc:subject>mutation propensity</dc:subject>
          <dc:subject>level analysis</dc:subject>
          <dc:subject>genetic variations</dc:subject>
          <dc:subject>molecular components</dc:subject>
          <dc:subject>deep learning</dc:subject>
          <dc:subject>computational screening</dc:subject>
          <dc:subject>translational modification</dc:subject>
          <dc:subject>suppressive capacity</dc:subject>
          <dc:subject>study aimed</dc:subject>
          <dc:subject>significantly upregulated</dc:subject>
          <dc:subject>potential biomarkers</dc:subject>
          <dc:subject>often driven</dc:subject>
          <dc:subject>mirna mir</dc:subject>
          <dc:subject>individual studies</dc:subject>
          <dc:subject>including ccne1</dc:subject>
          <dc:subject>genetic variants</dc:subject>
          <dc:subject>gc pathways</dc:subject>
          <dc:subject>expression dysregulation</dc:subject>
          <dc:subject>dysregulated expression</dc:subject>
          <dc:subject>differential expression</dc:subject>
          <dc:subject>cbioportal database</dc:subject>
          <dc:subject>cbioportal confirmed</dc:subject>
          <dc:subject>2 %),</dc:subject>
          <dc:subject>05 ).</dc:subject>
          <dc:description>&lt;p&gt;Genetic Variants of the CDH1 Gene from ClinVar Database.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-17T17:37:42Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1371/journal.pone.0358440.s012</dc:identifier>
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