Reviews:

Jianli Dong, Juan P. Olano, Jere W. McBride, and David H. Walker

Emerging Pathogens: Challenges and Successes of Molecular Diagnostics
J Mol Diagn 2008 10: 185-197 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070063 [Abstract] [Full Text] [PDF]  

Commentaries:

Gerald Wertheim and Adam Bagg

Nucleophosmin (NPM1) Mutations in Acute Myeloid Leukemia: An Ongoing (Cytoplasmic) Tale of Dueling Mutations and Duality of Molecular Genetic Testing Methodologies
J Mol Diagn 2008 10: 198-202 First published online April 10, 2008; doi:10.2353/jmoldx.2008.080019 [Abstract] [Full Text] [PDF]  

Technical Advances:

Martina Doleshal, Amber A. Magotra, Bhavna Choudhury, Brian D. Cannon, Emmanuel Labourier, and Anna E. Szafranska

Evaluation and Validation of Total RNA Extraction Methods for MicroRNA Expression Analyses in Formalin-Fixed, Paraffin-Embedded Tissues
J Mol Diagn 2008 10: 203-211 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070153 [Abstract] [Full Text] [PDF] Supplemental Material  

Tiziana Ottone, Emanuele Ammatuna, Serena Lavorgna, Nélida I. Noguera, Francesco Buccisano, Adriano Venditti, Laura Giannì, Massimiliano Postorino, Giorgio Federici, Sergio Amadori, and Francesco Lo-Coco

An Allele-Specific RT-PCR Assay to Detect Type A Mutation of the Nucleophosmin-1 Gene in Acute Myeloid Leukemia
J Mol Diagn 2008 10: 212-216 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070166 [Abstract] [Full Text] [PDF]  

Christopher Schroeder, Michael Walter, Daniela Berg, Petra Leitner, Peter Bauer, Zacharias Kohl, Jürgen Winkler, Olaf Riess, and Michael Bonin

High-Throughput Homogeneous Mass Cleave Assay Technology for the Diagnosis of Autosomal Recessive Parkinson’s Disease
J Mol Diagn 2008 10: 217-224 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070100 [Abstract] [Full Text] [PDF] Supplemental Material  

Regular Articles:

Matthew B. Kerby, Sarah Freeman, Kristina Prachanronarong, Andrew W. Artenstein, Steven M. Opal, and Anubhav Tripathi

Direct Sequence Detection of Structured H5 Influenza Viral RNA
J Mol Diagn 2008 10: 225-235 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070094 [Abstract] [Full Text] [PDF]  

Philippe Szankasi, Mohamed Jama, and David W. Bahler

A New DNA-Based Test for Detection of Nucleophosmin Exon 12 Mutations by Capillary Electrophoresis
J Mol Diagn 2008 10: 236-241 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070167 [Abstract] [Full Text] [PDF]  

Allan R. Li, Dhananjay Chitale, Gregory J. Riely, William Pao, Vincent A. Miller, Maureen F. Zakowski, Valerie Rusch, Mark G. Kris, and Marc Ladanyi

EGFR Mutations in Lung Adenocarcinomas: Clinical Testing Experience and Relationship to EGFR Gene Copy Number and Immunohistochemical Expression
J Mol Diagn 2008 10: 242-248 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070178 [Abstract] [Full Text] [PDF]  

Daniel T. Croft, Jr, Rick M. Jordan, Heather L. Patney, Craig D. Shriver, Marina N. Vernalis, Trevor J. Orchard, and Darrell L. Ellsworth

Performance of Whole-Genome Amplified DNA Isolated from Serum and Plasma on High-Density Single Nucleotide Polymorphism Arrays
J Mol Diagn 2008 10: 249-257 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070155 [Abstract] [Full Text] [PDF]  

M. Fernanda Sábato, Anne-Marie Irani, Bonny L. Bukaveckas, Lawrence B. Schwartz, David S. Wilkinson, and Andrea Ferreira-Gonzalez

A Simple and Rapid Genotyping Assay for Simultaneous Detection of Two ADRB2 Allelic Variants Using Fluorescence Resonance Energy Transfer Probes and Melting Curve Analysis
J Mol Diagn 2008 10: 258-264 ; doi: 10.2353/jmoldx.2008.070133 [Abstract] [Full Text] [PDF]  

Caroline E. Corless, Edward Kaczmarski, Ray Borrow, and Malcolm Guiver

Molecular Characterization of Neisseria meningitidis Isolates Using a Resequencing DNA Microarray
J Mol Diagn 2008 10: 265-271 First published online March 27, 2008; doi:10.2353/jmoldx.2008.070152 [Abstract] [Full Text] [PDF] Supplemental Material  

Consultations in Molecular Diagnostics:

Massimiliano Cecconi, Francesca Forzano, Rosanna Rinaldi, Sandra Cappellacci, Paola Grammatico, Francesca Faravelli, Franca Dagna Bricarelli, Emilio Di Maria, and Marina Grasso

A Single Nucleotide Variant in the FMR1 CGG Repeat Results in a "Pseudodeletion" and Is Not Associated with the Fragile X Syndrome Phenotype
J Mol Diagn 2008 10: 272-275 First published online April 10, 2008; doi:10.2353/jmoldx.2008.070163 [Abstract] [Full Text] [PDF]  

Corrections:

Corrections
J Mol Diagn 2008 10: 276 First published online April 10, 2008; doi:10.2353/jmoldx.2008.080029 [Full Text] [PDF]  

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