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Journal of Molecular Diagnostics
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2006, v. 8, n. 4
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Página 397-411(15)
Autor/es: Steensma, David P.
Título: JAK2 V617F in Myeloid Disorders: Molecular Diagnostic Techniques and Their Clinical Utility - A Paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology
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Página 412-419(8)
Autor/es: Akin, Cem
Título: Molecular Diagnosis of Mast Cell Disorders - A Paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology
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Página 420-425(6)
Autor/es: Bosler, David - Mattson, Joan - Crisan, Domnita
Título: Phenotypic Heterogeneity in Patients with Homozygous Prothrombin 20210AA Genotype - A Paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology
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Página 426-429(4)
Autor/es: Bagg, Adam
Título: Immunoglobulin and T-Cell Receptor Gene Rearrangements: Minding Your Bs and Ts in Assessing Lineage and Clonality in Neoplastic Lymphoproliferative Disorders
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Página 430-432(3)
Autor/es: Church, Jessica D. - Jones, Dana - Flys, Tamara - Hoover, Donald - Marlowe,
Título: Sensitivity of the ViroSeq HIV-1 Genotyping System for Detection of the K103N Resistance Mutation in HIV-1 Subtypes A, C, and D
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Página 433-443(11)
Autor/es: Jeuken, Judith - Cornelissen, Sandra - Boots-Sprenger, Sandra - Gijsen, Sabin
Título: Multiplex Ligation-Dependent Probe Amplification - A Diagnostic Tool for Simultaneous Identification of Different Genetic Markers in Glial Tumors
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Página 444-448(5)
Autor/es: van der Straaten, Tahar - Kweekel, Dinemarie - Tiller, Marco - Bogaartz, Judi
Título: Multiplex Pyrosequencing of Two Polymorphisms in DNA Repair Gene XRCC1
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Página 449-458(10)
Autor/es: Ng, Grace - Huang, Jingxiang - Roberts, Ian - Coleman, Nicholas
Título: Defining Ploidy-Specific Thresholds in Array Comparative Genomic Hybridization to Improve the Sensitivity of Detection of Single Copy Alterations in Cell Lines
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Página 459-465(7)
Autor/es: Cook, James R. - Hartke, Marybeth - Pettay, James - Tubbs, Raymond R.
Título: Fluorescence in Situ Hybridization Analysis of Immunoglobulin Heavy Chain Translocations in Plasma Cell Myeloma Using Intact Paraffin Sections and Simultaneous CD138 Immunofluorescence
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Página 466-475(10)
Autor/es: Tan, Brenton T. - Warnke, Roger A. - Arber, Daniel A.
Título: 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
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Página 476-482(7)
Autor/es: Zhou, Shaoyu - Kassauei, Keyaunoosh - Cutler, David J. - Kennedy, Giulia C. -
Título: An Oligonucleotide Microarray for High-Throughput Sequencing of the Mitochondrial Genome
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Página 483-489(7)
Autor/es: Siemering, Kirby - Manji, Shehnaaz S.M. - Hutchison, Wendy M. - Du Sart, Desi
Título: Detection of Mutations in Genes Associated with Hearing Loss Using a Microarray-Based Approach
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Página 490-498(9)
Autor/es: Lubitz, Carrie C. - Ugras, Stacy K. - Kazam, J. Jacob - Zhu, Biaxin - Scogna
Título: Microarray Analysis of Thyroid Nodule Fine-Needle Aspirates Accurately Classifies Benign and Malignant Lesions
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Página 499-503(5)
Autor/es: Faa, Valeria - Bettoli, Pietro Pellegrini - Demurtas, Maria - Zanda, Maurizio
Título: 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
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Página 504-512(9)
Autor/es: Matsukuma, Shoichi - Yoshihara, Mitsuyo - Kasai, Fumio - Kato, Akinori - Yos
Título: 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
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Página 513-520(8)
Autor/es: Vaughn, Cecily P. - Crockett, David K. - Lim, Megan S. - Elenitoba-Johnson, K
Título: Analytical Characteristics of Cleavable Isotope-Coded Affinity Tag-LC-Tandem Mass Spectrometry for Quantitative Proteomic Studies
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Página 521-525(5)
Autor/es: Hu, Jie - Sathanoori, Malini - Kochmar, Sally J. - Surti, Urvashi
Título: Application of Multicolor Banding for Identification of Complex Chromosome 18 Rearrangements
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