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Academic Journal

CNV-mediated dysregulation of the ceRNA network mechanism revealed heterogeneity in diffuse and intestinal gastric cancers.

  • Authors : Xu R; College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China.; He D

Subjects: Stomach Neoplasms*/Stomach Neoplasms*/Stomach Neoplasms*/genetics ; Stomach Neoplasms*/Stomach Neoplasms*/Stomach Neoplasms*/pathology ; DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics

  • Source: Journal of translational medicine [J Transl Med] 2025 Mar 11; Vol. 23 (1), pp. 308. Date of Electronic Publication: 2025 Mar 11.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

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Academic Journal

High copy number variations, particular transcription factors, and low immunity contribute to the stemness of prostate cancer cells.

  • Authors : Dai Z; College of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.; Liu P

Subjects: DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics ; Prostatic Neoplasms*/Prostatic Neoplasms*/Prostatic Neoplasms*/genetics; Gene Expression Profiling

  • Source: Journal of translational medicine [J Transl Med] 2021 May 13; Vol. 19 (1), pp. 206. Date of Electronic Publication: 2021 May 13.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

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Academic Journal

High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases.

  • Authors : Zeng Y; Medical Genetics Center, Guangdong Women and Children Hospital, Xingnan Road 521, Guangzhou, 510010, Guangdong, China.; Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, China.

Subjects: DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics ; Exome Sequencing* ; Genetic Diseases, Inborn*/Genetic Diseases, Inborn*/Genetic Diseases, Inborn*/diagnosis

  • Source: Journal of translational medicine [J Transl Med] 2024 Jul 09; Vol. 22 (1), pp. 644. Date of Electronic Publication: 2024 Jul 09.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

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