The Journal of molecular diagnostics

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  Año 2006, Vol. 8, Número 4

  • JAK2 V617F in myeloid disorders: Molecular diagnostic techniques and their clinical utility - A paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology

    D. P. Steensma

    pág. 397

    

  • Molecular diagnosis of mast cell disorders - A paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology

    C. Akin

    pág. 412

    

  • Phenotypic heterogeneity in patients with homozygous prothrombin 20210AA genotype - A paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology

    D. Bosler, J. Mattson, D. Crisan

    pág. 420

    

  • Immunoglobulin and T-Cell receptor gene rearrangements: Minding your B's and T's in assessing lineage and clonality in neoplastic lymphoproliferative disorders

    Adam Bagg

    pág. 426

    

  • Sensitivity of the ViroSeq HIV-1 genotyping system for detection of the K103N resistance mutation in HIV-1 subtypes A, C, and D

    D. Hoover, N. Marlowe, Shu Chen, Ch. Shi, James R. Eshleman, L. A. Guay, J. B. Jackson, N. Kumwenda, T. E. Taha, Susan H. Eshleman, J. D. Church, Dan Jones, T. Flys

    pág. 430

    

  • Multiplex ligation-dependent probe amplification - A diagnostic tool for simultaneous identification of different genetic markers in glial tumors

    S. Gijsen, P. Wesseling, J. Jeuken, S. Cornelissen, S. Boots Sprenger

    pág. 433

    

  • Multiplex pyrosequencing of two polymorphisms in DNA repair gene XRCC1

    J. Bogaartz, Henk Jan Guchelaar, Tahar van der Straaten, D. Kweekel, M. Tiller

    pág. 444

    

  • Defining ploidy-specific thresholds in array comparative genomic hybridization to improve the sensitivity of detection of single copy alterations in cell lines

    N. Coleman, G. Ng, Jingxiang Huang, I. Roberts

    pág. 449

    

  • Fluorescence in situ hybridization analysis of immunoglobulin heavy chain translocations in plasma cell myeloma using intact paraffin sections and simultaneous CD138 immunofluorescence

    R. R. Tubbs, J. R. Cook, M. Hartke, J. Pettay

    pág. 459

    

  • The frequency of B- and T-Cell gene rearrangements and Epstein-Barr virus in T-Cell lymphomas - A comparison between angioimmunoblastic T-Cell lymphoma and peripheral T-Cell Lymphoma, Unspecified With and Without Associated B-Cell Proliferations

    Brent T. Tan, Roger A. Warnke, Daniel A. Arber

    pág. 466

    

  • An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome

    G. C. Kennedy, D. Sidransky, A. Maitra, J. Califano, S. Zhou, K. Kassauei, D. J. Cutler

    pág. 476

    

  • Detection of mutations in genes associated with hearing loss using a microarray-based approach

    D. du Sart, D. Phelan, H. H. M. Dahl, K. Siemering, S. S. M. Manji, W. M. Hutchison

    pág. 483

    

  • Microarray analysis of thyroid nodule fine-needle aspirates accurately classifies benign and malignant lesions

    B. Zhu, T. Scognamiglio, Yao Tseng Chen, T. J. Fahey, C. C. Lubitz, S. K. Ugras, J. J. Kazam

    pág. 490

    

  • A new insertion/deletion of the cystic fibrosis transmembrane conductance regulator gene accounts for 3.4% of cystic fibrosis mutations in Sardinia: Implications for population screening

    M. Zanda, V. Ferri, Antonio Cao, Maria Cristina Rosatelli, Valeria Faa, P. P. Bettoli, M. Demurtas

    pág. 499

    

  • Rapid and simple detection of hot spot point mutations of epidermal growth factor receptor, BRAF, and NRAS in cancers using the loop-hybrid mobility shift assay

    A. Kato, A. Yoshida, M. Akaike, O. Kobayashi, H. Nakayama, Y. Sakuma, T. Yoshida, Y. Kameda, E. Tsuchiya, Y. Miyagi, S. Matsukuma, M. Yoshihara, F. Kasai

    pág. 504

    

  • Analytical characteristics of cleavable isotope-coded affinity tag-LC-tandem mass spectrometry for quantitative proteomic studies

    Kojo S. J. Elenitoba Johnson, Cecily P. Vaughn, D. K. Crockett, Megan S. Lim

    pág. 513

    

  • Application of multicolor banding for identification of complex chromosome 18 rearrangements

    U. Surti, J. Hu, M. Sathanoori, S. J. Kochmar

    pág. 521

    

  • JMD CME Program in Molecular Diagnostics

    pág. 526