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Deletion mutation

Calcification in dermal fibroblasts from a patient with GGCX syndrome accompanied by upregulation of osteogenic molecules

Yumi Okubo, Ritsuko Masuyama, [ ... ], Atsushi Utani

Various mutations compensate for a deleterious lacZα insert in the replication enhancer of M13 bacteriophage

Emily M. Zygiel, Karen A. Noren, [ ... ], Marilena Fitzsimons Hall

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease

Nancy J. Butcher, Daniele Merico, [ ... ], Anne S. Bassett

Computational prediction of the tolerance to amino-acid deletion in green-fluorescent protein

Eleisha L. Jackson, Stephanie J. Spielman, Claus O. Wilke

High-throughput transformation of Saccharomyces cerevisiae using liquid handling robots

Guangbo Liu, Clayton Lanham, J. Ross Buchan, Matthew E. Kaplan

Chromosome 19q13 disruption alters expressions of CYP2A7, MIA and MIA-RAB4B lncRNA and contributes to FAP-like phenotype in APC mutation-negative familial colorectal cancer patients

Lai Fun Thean, Yu Hui Wong, [ ... ], Peh Yean Cheah

Histidine-rich protein 2 (pfhrp2) and pfhrp3 gene deletions in Plasmodium falciparum isolates from select sites in Brazil and Bolivia

Giselle Maria Rachid Viana, Sheila Akinyi Okoth, [ ... ], John W. Barnwell

Risk for molecular contamination of tissue samples evaluated for targeted anti-cancer therapy

Eyal Asor, Michael Y. Stav, [ ... ], Dov Hershkovitz

Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome

Alejandro García Castaño, Gustavo Pérez de Nanclares, [ ... ], Gema Ariceta

Growth condition dependency is the major cause of non-responsiveness upon genetic perturbation

Saman Amini, Frank C. P. Holstege, Patrick Kemmeren

An outbreak of acute respiratory disease caused by a virus associated RNA II gene mutation strain of human adenovirus 7 in China, 2015

Xiaoxia Yang, Qiongshu Wang, [ ... ], Hongbin Song

No Evidence for Pathogenic Role of UBQLN2 Mutations in Sporadic Amyotrophic Lateral Sclerosis in the Mainland Chinese Population

Xiao Huang, Shen Shen, Dongsheng Fan

Superior Multiplexing Capacity of PlexPrimers Enables Sensitive and Specific Detection of SNPs and Clustered Mutations in qPCR

Lit Yeen Tan, Samantha Michelle Walker, [ ... ], Elisa Mokany

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