BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Ovarian cancer AND NBN, AT-V2, 4683, ENSG00000104320, ATV, FLJ10155, NBS, AT-V1, MGC87362, NBS1
114 results:

  • 1. HIF-2α-dependent TGFBI promotes ovarian cancer chemoresistance by activating PI3K/Akt pathway to inhibit apoptosis and facilitate DNA repair process.
    Ma S; Wang J; Cui Z; Yang X; Cui X; Li X; Zhao L
    Sci Rep; 2024 Feb; 14(1):3870. PubMed ID: 38365849
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Suppression of nbs1 Upregulates CyclinB to Induce Olaparib Sensitivity in ovarian cancer.
    Zhong A; Cheng CS; Lu RQ; Guo L
    Technol Cancer Res Treat; 2024; 23():15330338231212085. PubMed ID: 38192153
    [No Abstract]    [Full Text] [Related]  

  • 3. Pathogenic germline variants in non-BRCA1/2 homologous recombination genes in ovarian cancer: Analysis of tumor phenotype and survival.
    Kahn RM; Selenica P; Boerner T; Roche KL; Xiao Y; Sia TY; Maio A; Kemel Y; Sheehan M; Salo-Mullen E; Breen KE; Zhou Q; Iasonos A; Grisham RN; O'Cearbhaill RE; Chi DS; Berger MF; Kundra R; Schultz N; Ellenson LH; Stadler ZK; Offit K; Mandelker D; Aghajanian C; Zamarin D; Sabbatini P; Weigelt B; Liu YL
    Gynecol Oncol; 2024 Jan; 180():35-43. PubMed ID: 38041901
    [TBL] [Abstract] [Full Text] [Related]  

  • 4.
    Ramos CRN; Oliveira RJS; Rosa MN; Pereira AS; de Abreu RBV; van Helvoort Lengert A; Reis RM; Silva VAO; Palmero EI; Melendez ME
    Curr Cancer Drug Targets; 2023; 23(11):900-909. PubMed ID: 37076963
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Targeted next-generation sequencing of 21 candidate genes in hereditary ovarian cancer patients from the Republic of Bashkortostan.
    Prokofyeva DS; Mingazheva ET; Valova YV; Sakaeva DD; Faishanova RR; Nurgalieva AK; Valiev RR; Bogdanova N; Dörk T; Khusnutdinova EK
    J Ovarian Res; 2023 Apr; 16(1):66. PubMed ID: 37013556
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception.
    Bychkovsky BL; Lo MT; Yussuf A; Horton C; Hemyari P; LaDuca H; Garber JE; Scheib R; Rana HQ
    Breast Cancer Res Treat; 2023 Jul; 200(1):63-72. PubMed ID: 36856935
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Beyond BRCA: Patterns of risk-reducing surgery for non-BRCA, homologous recombination repair pathway gene variant carriers.
    Lee SS; Karpel HC; Oh C; Smith J; Pothuri B
    Gynecol Oncol; 2023 Mar; 170():234-240. PubMed ID: 36724586
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. OWL: an optimized and independently validated machine learning prediction model for lung cancer screening based on the UK Biobank, PLCO, and NLST populations.
    Pan Z; Zhang R; Shen S; Lin Y; Zhang L; Wang X; Ye Q; Wang X; Chen J; Zhao Y; Christiani DC; Li Y; Chen F; Wei Y
    EBioMedicine; 2023 Feb; 88():104443. PubMed ID: 36701900
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. Patient uptake of updated genetic testing following uninformative BRCA1 and BRCA2 results.
    Macklin-Mantia SK; Clift KE; Maimone S; Hodge DO; Riegert-Johnson D; Hines SL
    J Genet Couns; 2023 Jun; 32(3):598-606. PubMed ID: 36478495
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Interdisciplinary risk counseling for hereditary breast and ovarian cancer: real-world data from a specialized center.
    Zang B; Helms M; Besch L; Kalmbach N; Stegen S; Blohmer JU; Speiser D
    Arch Gynecol Obstet; 2023 May; 307(5):1585-1592. PubMed ID: 36307613
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. Overlapping gene dependencies for PARP inhibitors and carboplatin response identified by functional CRISPR-Cas9 screening in ovarian cancer.
    Coelho R; Tozzi A; Disler M; Lombardo F; Fedier A; López MN; Freuler F; Jacob F; Heinzelmann-Schwarz V
    Cell Death Dis; 2022 Oct; 13(10):909. PubMed ID: 36307400
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. Moderate-Risk Genes for Hereditary ovarian cancers Involved in the Homologous Recombination Repair Pathway.
    Abe A; Imoto I; Ueki A; Nomura H; Kanao H
    Int J Mol Sci; 2022 Oct; 23(19):. PubMed ID: 36233090
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. Pancreatic cancer with Mutation in BRCA1/2, MLH1, and APC Genes: Phenotype Correlation and Detection of a Novel Germline BRCA2 Mutation.
    Vietri MT; D'Elia G; Caliendo G; Albanese L; Signoriello G; Napoli C; Molinari AM
    Genes (Basel); 2022 Feb; 13(2):. PubMed ID: 35205366
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. Hereditary ovarian Carcinoma: cancer Pathogenesis Looking beyond
    Samuel D; Diaz-Barbe A; Pinto A; Schlumbrecht M; George S
    Cells; 2022 Feb; 11(3):. PubMed ID: 35159349
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. Clinical significance of gene polymorphisms for hereditary predisposition to breast and ovarian cancer (review of literature).
    Vodolazhsky DI; Mayakovskaya AV; Kubyshkin AV; Aliev KA; Fomochkina II
    Klin Lab Diagn; 2021 Dec; 66(12):760-767. PubMed ID: 35020290
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. Pan-cancer Analysis of Homologous Recombination Repair-associated Gene Alterations and Genome-wide Loss-of-Heterozygosity Score.
    Westphalen CB; Fine AD; André F; Ganesan S; Heinemann V; Rouleau E; Turnbull C; Garcia Palacios L; Lopez JA; Sokol ES; Mateo J
    Clin Cancer Res; 2022 Apr; 28(7):1412-1421. PubMed ID: 34740923
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Rad50 promotes ovarian cancer progression through NF-κB activation.
    Li Y; Wang S; Li P; Li Y; Liu Y; Fang H; Zhang X; Liu Z; Kong B
    J Cell Mol Med; 2021 Dec; 25(23):10961-10972. PubMed ID: 34734468
    [TBL] [Abstract] [Full Text] [Related]  

  • 18. nbs1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations.
    Tomioka K; Miyamoto T; Akutsu SN; Yanagihara H; Fujita K; Royba E; Tauchi H; Yamamoto T; Koh I; Hirata E; Kudo Y; Kobayashi M; Okada S; Matsuura S
    Sci Rep; 2021 Oct; 11(1):19661. PubMed ID: 34608183
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. Bilateral ovarian Germ Cell Tumor in a 46,XX Female with Nijmegen Breakage Syndrome and Hypergonadotropic Hypogonadism.
    Krawczyk MA; Styczewska M; Birkholz-Walerzak D; Iliszko M; Lipska-Zietkiewicz BS; Kosiak W; Irga-Jaworska N; Izycka-Swieszewska E; Bien E
    J Clin Res Pediatr Endocrinol; 2022 Jun; 14(2):251-257. PubMed ID: 34544220
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. Detection of Germline Variants in 450 Breast/ovarian cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions.
    Guglielmi C; Scarpitta R; Gambino G; Conti E; Bellè F; Tancredi M; Cervelli T; Falaschi E; Cosini C; Aretini P; Congregati C; Marino M; Patruno M; Pilato B; Spina F; Balestrino L; Tenedini E; Carnevali I; Cortesi L; Tagliafico E; Tibiletti MG; Tommasi S; Ghilli M; Vivanet C; Galli A; Caligo MA
    Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34299313
    [TBL] [Abstract] [Full Text] [Related]  


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