[1] CRISPR/Cas9-Mediated Immunity in Plants Against Pathogens

[2] Genetically determined susceptibility to mycobacterial infection

[3] Application of a mathematical model to prevent in vivo amplification of antibiotic-resistant bacterial populations during therapy

[4] Prognostic impact of low allelic ratio FLT3- ITD and NPM1 mutation in acute myeloid leukemia

[5] Biological function of unannotated transcription during the early development of Drosophila melanogaster

[6] Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid-activated transcription factor

[7] A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation

[8] Recurrent CCND3 mutations in MLL-rearranged acute myeloid leukemia

[9] The evolutionary fate and consequences of duplicate genes

[10] The genetics of obesity. Lessons for polycystic ovary syndrome

[11] Molecular Patterns of Resistance Among Helicobacter pylori Strains in South-Western Poland

[12] Evaluation of two live, cold-passaged, temperature-sensitive respiratory syncytial virus vaccines in chimpanzees and in human adults, infants, and children

[13] Effects of hypergravity on the photosynthetic flagellate, Euglena gracilis

[14] Initial sequencing and analysis of the human genome

[15] Emergence of teicoplanin resistance during therapy of Staphylococcus aureus endocarditis

[16] TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa

[17] Investigation into the selection frequency of resistant mutants and the bacterial kill rate by levofloxacin and ciprofloxacin in non-mucoid Pseudomonas aeruginosa isolates from cystic fibrosis patients

[18] Heterogeneity in the substitution process of amino acid sites of proteins coded for by mitochondrial DNA

[19] a comparative study of the evolution of real incomes of pensioners and unemployed using genetic algorithms

[20] Enhancement of Peroxidase Activity in Artificial Mimochrome VI Catalysts through Rational Design

[21] Sterol-dependent repression of low density lipoprotein receptor promoter mediated by 16-base pair sequence adjacent to binding site for transcription factor Sp1

[22] Transcription factor-specific requirements for coactivators and their acetyltransferase functions

[23] A role for the Smc3 hinge domain in the maintenance of sister chromatid cohesion

[24] Characterization of gtf, a glucosyltransferase gene in the genomes of Pediococcus parvulus and Oenococcus oeni, two bacterial species commonly found in wine

[25] Pseudomonas aeruginosa defends against phages through type IV pilus glycosylation

[26] Evolution, population structure, and phylogeography of genetically monomorphic bacterial pathogens

[27] Signature-tagged mutagenesis in a chicken infection model leads to the identification of a novel avian pathogenic Escherichia coli fimbrial adhesin

[28] Myc signaling via the ARF tumor suppressor regulates p53-dependent apoptosis and immortalization

[29] Positional cloning of the nude locus: genetic, physical, and transcription maps of the region and mutations in the mouse and rat

[30] Genetic analysis of T-DNA transcripts in nopaline crown galls

[31] MAPK interacts with XGef and is required for CPEB activation during meiosis in Xenopus oocytes

[32] A xenograft model for venous malformation

[33] Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage

[34] Disruption of the ARF-Mdm2-p53 tumor suppressor pathway in Myc-induced lymphomagenesis

[35] Oseltamivir-resistant influenza A pandemic (H1N1) 2009 virus, Hong Kong, China

[36] Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

[37] Regulation of p53 stability by Mdm2

[38] In vivo analysis of chromosome condensation in Saccharomyces cerevisiae

[39] Establishment of left-right asymmetry in vertebrate development: the node in mouse embryos

[40] The real life of pseudogenes

[41] Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity

[42] Physical Association of Saccharomyces cerevisiae Polo-like Kinase Cdc5 with Chromosomal Cohesin Facilitates DNA Damage Response

[43] Genetic interaction between Wnt/beta-catenin and BMP receptor signaling during formation of the AER and the dorsal-ventral axis in the limb

[44] Enforced proximity in the function of a famous scaffold

[45] Eco1-dependent cohesin acetylation during establishment of sister chromatid cohesion

[46] A direct link between sister chromatid cohesion and chromosome condensation revealed through the analysis of MCD1 in S. cerevisiae

[47] Cdkn2a encodes functional variation of p16INK4a but not p19ARF, which confers selection in mouse lung tumorigenesis

[48] Genetic, biochemical, and clinical features of chronic granulomatous disease

[49] Functional diversity and mutational analysis of Agrobacterium 6B oncoproteins

[50] Effect of fasting and leptin deficiency on hypothalamic neuropeptide Y gene transcription in vivo revealed by expression of a lacZ reporter gene

[51] The nature and character of the transition state for the ADP-ribosyltransferase reaction

[52] Cohesins: chromosomal proteins that prevent premature separation of sister chromatids

[53] Group A streptococcal infections in injection drug users in Barcelona, Spain: epidemiologic, clinical, and microbiologic analysis of 3 clusters of cases from 2000 to 2003

[54] p53 and microRNA-34 are suppressors of canonical Wnt signaling

[55] Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin

[56] Genetic incorporation of histidine derivatives using an engineered pyrrolysyl-tRNA synthetase

[57] Novel mutations associated with inherited human calcium-sensing receptor disorders: a clinical genetic study.

[58] Robustness of coalescent estimators to between-lineage mutation rate variation.

[59] PRISMOID: a comprehensive 3D structure database for post-translational modifications and mutations with functional impact.

[60] Security mutation testing of the FileZilla FTP server

[61] Improving test adequacy assessment by novel JavaScript mutation operators

[62] The creation and selection of mutations resistant to a gene drive over multiple generations in the malaria mosquito.

[63] High BRAFV600E mutation frequency in Chinese patients with papillary thyroid carcinoma increases diagnostic efficacy in cytologically indeterminate thyroid nodules.

[64] Acute pulmonary thromboembolism caused by factor V Leiden mutation in South Korea: A case report.

[65] In search for genetic explanation for LDLc variabily in an FH family: Common SNPs and a rare mutation in microsomal triglyceride transfer protein explain only part of LDL variability in an FH family.

[66] Frequent mutations in EGFR, KRAS and TP53 genes in human lung cancer tumors detected by ion torrent DNA sequencing.

[67] Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.

[68] Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH.

[69] Antiretroviral drug resistance mutations among patients failing first-line treatment in Hanoi, Vietnam

[70] Characterization of the most common embCAB gene mutations associated with ethambutol resistance in Mycobacterium tuberculosis isolates from Iran

[71] Evaluation of the accuracy of molecular assays targeting the mutation A2059G for detecting high-level azithromycin resistance in Neisseria gonorrhoeae: a systematic review and meta-analysis

[72] Characterization of hepatitis C virus resistance to grazoprevir reveals complex patterns of mutations following on-treatment breakthrough that are not observed at relapse

[73] Patterns of emergent resistance-associated mutations after initiation of non-nucleoside reverse-transcriptase inhibitor-containing antiretroviral regimens in Taiwan: a multicenter cohort study

[74] The clinical significance of silent mutations with respect to ciprofloxacin resistance in MRSA

[75] Interaction between rpsL and gyrA mutations affects the fitness and dual resistance of Mycobacterium tuberculosis clinical isolates against streptomycin and fluoroquinolones

[76] Enriched whole genome sequencing identified compensatory mutations in the RNA polymerase gene of rifampicin-resistant Mycobacterium leprae strains

[77] Molecular analysis of multidrug resistance in clinical isolates of Shigella spp. from 2001–2010 in Kolkata, India: role of integrons, plasmids, and topoisomerase mutations

[78] Naturally occurring genotypic drug-resistant mutations of HBV in Huzhou, China: a single-center study

[79] Genotyping of HBV and tracking of resistance mutations in treatment-naïve patients with chronic hepatitis B

[80] Mycoplasma genitalium infection: current treatment options, therapeutic failure, and resistance-associated mutations

[81] Detection of epidermal growth factor receptor mutation in lung cancer by droplet digital polymerase chain reaction

[82] First Report of Diabetes Phenotype due to a Loss-of-Function ABCC8 Mutation Previously Known to Cause Congenital Hyperinsulinism

[83] Acute Myeloid Leukemia with Concomitant BCR-ABL and NPM1 Mutations

[84] Antiretroviral drug resistance mutations among patients failing first-line treatment in Hanoi, Vietnam

[85] Characterization of the most common embCAB gene mutations associated with ethambutol resistance in Mycobacterium tuberculosis isolates from Iran

[86] Evaluation of the accuracy of molecular assays targeting the mutation A2059G for detecting high-level azithromycin resistance in Neisseria gonorrhoeae: a systematic review and meta-analysis

[87] Characterization of hepatitis C virus resistance to grazoprevir reveals complex patterns of mutations following on-treatment breakthrough that are not observed at relapse

[88] Patterns of emergent resistance-associated mutations after initiation of non-nucleoside reverse-transcriptase inhibitor-containing antiretroviral regimens in Taiwan: a multicenter cohort study

[89] The clinical significance of silent mutations with respect to ciprofloxacin resistance in MRSA

[90] Interaction between rpsL and gyrA mutations affects the fitness and dual resistance of Mycobacterium tuberculosis clinical isolates against streptomycin and fluoroquinolones

[91] Enriched whole genome sequencing identified compensatory mutations in the RNA polymerase gene of rifampicin-resistant Mycobacterium leprae strains

[92] Molecular analysis of multidrug resistance in clinical isolates of Shigella spp. from 2001–2010 in Kolkata, India: role of integrons, plasmids, and topoisomerase mutations

[93] Naturally occurring genotypic drug-resistant mutations of HBV in Huzhou, China: a single-center study

[94] Genotyping of HBV and tracking of resistance mutations in treatment-naïve patients with chronic hepatitis B

[95] Mycoplasma genitalium infection: current treatment options, therapeutic failure, and resistance-associated mutations

[96] Detection of epidermal growth factor receptor mutation in lung cancer by droplet digital polymerase chain reaction

[97] Proof of Principle that Molecular Modeling Followed by a Biophysical Experiment Can Develop Small Molecules that Restore Function to the Cardiac Thin Filament in the Presence of Cardiomyopathic Mutations.

[98] Detection of genetic mutations associated with macrolide resistance of Mycoplasma pneumoniae

[99] Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome.

[100] Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome.

[101] Where phonology meets morphology in the context of rapid language change and universal bilingualism: Irish initial mutations in child language