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Mutation

Somaclonal Variation Is Induced De Novo via the Tissue Culture Process: A Study Quantifying Mutated Cells in Saintpaulia

Mitsuru Sato, Munetaka Hosokawa, Motoaki Doi

Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population

Lotte N. Moens, Peter De Rijk, [ ... ], Jurgen Del-Favero

Frequent Alteration of MLL3 Frameshift Mutations in Microsatellite Deficient Colorectal Cancer

Yoshiyuki Watanabe, Ryan J. Castoro, [ ... ], Jean-Pierre J. Issa

Multimodal Pyrethroid Resistance in Malaria Vectors, Anopheles gambiae s.s., Anopheles arabiensis, and Anopheles funestus s.s. in Western Kenya

Hitoshi Kawada, Gabriel O. Dida, [ ... ], Masahiro Takagi

Including Total EGFR Staining in Scoring Improves EGFR Mutations Detection by Mutation-Specific Antibodies and EGFR TKIs Response Prediction

Shang-Gin Wu, Yih-Leong Chang, [ ... ], Jin-Yuan Shih

Predicting Transcriptional Activity of Multiple Site p53 Mutants Based on Hybrid Properties

Tao Huang, Shen Niu, [ ... ], Kuo-Chen Chou

Molecular Analysis of the Retinoic Acid Induced 1 Gene (RAI1) in Patients with Suspected Smith-Magenis Syndrome without the 17p11.2 Deletion

Thierry Vilboux, Carla Ciccone, [ ... ], Marjan Huizing

Role of Heterozygous APC Mutation in Niche Succession and Initiation of Colorectal Cancer – A Computational Study

Roschen Sasikumar, John Raji Rejitha, Ponthananiyil Kumaran Binumon, Muraleedharan Manoj

Analysis of the IDS Gene in 38 Patients with Hunter Syndrome: The c.879G>A (p.Gln293Gln) Synonymous Variation in a Female Create Exonic Splicing

Huiwen Zhang, Jing Li, [ ... ], Xuefan Gu

p53 Interacts with RNA Polymerase II through Its Core Domain and Impairs Pol II Processivity In Vivo

Sunyoung Kim, Sri Kripa Balakrishnan, David S. Gross

Persistence of Escherichia coli O157:H7 and Its Mutants in Soils

Jincai Ma, A. Mark Ibekwe, [ ... ], Ching-Hong Yang

A Twin Study of Mitochondrial DNA Polymorphisms Shows that Heteroplasmy at Multiple Sites Is Associated with mtDNA Variant 16093 but Not with Zygosity

Toby Andrew, Cassandra D. Calloway, [ ... ], Ana M. Valdes

Determination of the Loss of Function Complement C4 Exon 29 CT Insertion Using a Novel Paralog-Specific Assay in Healthy UK and Spanish Populations

Lora Boteva, IMAGEN , [ ... ], Michelle M. A. Fernando

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