BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

239 related articles for article (PubMed ID: 27600067)

  • 1. SNP Array in Hematopoietic Neoplasms: A Review.
    Song J; Shao H
    Microarrays (Basel); 2015 Dec; 5(1):. PubMed ID: 27600067
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The prognostic significance of single-nucleotide polymorphism array-based whole-genome analysis and uniparental disomy in myelodysplastic syndrome.
    Ou Y; Yang Y; Yu H; Zhang X; Liu M; Wu Y
    Int J Lab Hematol; 2021 Oct; 43(5):1062-1069. PubMed ID: 33650312
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of clonal evolution in hematopoietic malignancies by combining comparative genomic hybridization and single nucleotide polymorphism arrays.
    Hartmann L; Stephenson CF; Verkamp SR; Johnson KR; Burnworth B; Hammock K; Brodersen LE; de Baca ME; Wells DA; Loken MR; Zehentner BK
    Clin Chem; 2014 Dec; 60(12):1558-68. PubMed ID: 25320376
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Significance of genome-wide analysis of copy number alterations and UPD in myelodysplastic syndromes using combined CGH - SNP arrays.
    Ahmad A; Iqbal MA
    Curr Med Chem; 2012; 19(22):3739-47. PubMed ID: 22680919
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?
    Sato-Otsubo A; Sanada M; Ogawa S
    Semin Oncol; 2012 Feb; 39(1):13-25. PubMed ID: 22289488
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Progress of Clinical Application of SNP-A to MDS--Review].
    Chi K; Jing XY
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2018 Aug; 26(4):1244-1247. PubMed ID: 30111439
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Single-nucleotide polymorphism array (SNP-A) improves the identification of chromosomal abnormalities by metaphase cytogenetics in myelodysplastic syndrome.
    da Silva FB; Machado-Neto JA; Bertini VHLL; Velloso EDRP; Ratis CA; Calado RT; Simões BP; Rego EM; Traina F
    J Clin Pathol; 2017 May; 70(5):435-442. PubMed ID: 27836923
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The advantage of using SNP array in clinical testing for hematological malignancies--a comparative study of three genetic testing methods.
    Xu X; Johnson EB; Leverton L; Arthur A; Watson Q; Chang FL; Raca G; Laffin JJ
    Cancer Genet; 2013; 206(9-10):317-26. PubMed ID: 24269304
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Monoallelic and biallelic deletions of 13q14 in a group of CLL/SLL patients investigated by CGH Haematological Cancer and SNP array (8x60K).
    Grygalewicz B; Woroniecka R; Rygier J; Borkowska K; Rzepecka I; Łukasik M; Budziłowska A; Rymkiewicz G; Błachnio K; Nowakowska B; Bartnik M; Gos M; Pieńkowska-Grela B
    Mol Cytogenet; 2016; 9():1. PubMed ID: 26740820
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.
    Svobodova K; Zemanova Z; Lhotska H; Novakova M; Podskalska L; Belickova M; Brezinova J; Sarova I; Izakova S; Lizcova L; Berkova A; Siskova M; Jonasova A; Cermak J; Michalova K
    Leuk Res; 2016 Mar; 42():7-12. PubMed ID: 26851439
    [TBL] [Abstract][Full Text] [Related]  

  • 11. High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.
    Carr J; Bown NP; Case MC; Hall AG; Lunec J; Tweddle DA
    Cancer Genet Cytogenet; 2007 Jan; 172(2):127-38. PubMed ID: 17213021
    [TBL] [Abstract][Full Text] [Related]  

  • 12. SNP-based arrays complement classic cytogenetics in the detection of chromosomal aberrations in Wilms' tumor.
    Zin R; Pham K; Ashleigh M; Ravine D; Waring P; Charles A
    Cancer Genet; 2012 Mar; 205(3):80-93. PubMed ID: 22469507
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
    D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
    BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan.
    Ting JC; Ye Y; Thomas GH; Ruczinski I; Pevsner J
    BMC Bioinformatics; 2006 Jan; 7():25. PubMed ID: 16420694
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.
    Wang L; Fidler C; Nadig N; Giagounidis A; Della Porta MG; Malcovati L; Killick S; Gattermann N; Aul C; Boultwood J; Wainscoat JS
    Haematologica; 2008 Jul; 93(7):994-1000. PubMed ID: 18508791
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Array-Based Comparative Genomic Hybridization (aCGH).
    Zhang C; Cerveira E; Romanovitch M; Zhu Q
    Methods Mol Biol; 2017; 1541():167-179. PubMed ID: 27910023
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
    Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
    BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide Mapping of Copy Number Variations Using SNP Arrays.
    Nowak D; Hofmann WK; Koeffler HP
    Transfus Med Hemother; 2009; 36(4):246-251. PubMed ID: 21049075
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of novel genomic aberrations in anaplastic astrocytomas by GTG-banding, SKY, locus-specific FISH, and high density SNP-array.
    Holland H; Ahnert P; Koschny R; Kirsten H; Bauer M; Schober R; Meixensberger J; Fritzsch D; Krupp W
    Pathol Res Pract; 2012 Jun; 208(6):325-30. PubMed ID: 22575435
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics.
    Krupp W; Holland H; Koschny R; Bauer M; Schober R; Kirsten H; Livrea M; Meixensberger J; Ahnert P
    Cancer Genet Cytogenet; 2008 Jul; 184(2):87-93. PubMed ID: 18617056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.