insertions and deletions
Genome Wide Spectra of Transcription Insertions and Deletions Reveal That Slippage Depends on RNA:DNA Hybrid Complementarity
13
Exploring insertions and deletions (indels) of MSRB3 gene and their association with growth traits in four Chinese indigenous cattle breeds
11
Linear-time protein 3-D structure searching with insertions and deletions
8
The role of small in-frame insertions/deletions in inherited eye disorders and how structural modelling can help estimate their pathogenicity
8
The association of insertions/deletions (INDELs) and variable number tandem repeats (VNTRs) with obesity and its related traits and complications
17
Chemogenomic Screen for Imipenem Resistance in Gram-Negative Bacteria
17
Variation of the Mycobacterium tuberculosis PE PGRS33 Gene among Clinical Isolates
7
LoRTE: Detecting transposon-induced genomic variants using low coverage PacBio long read sequences
6
Evaluating the Pairwise String Alignment of Pronunciations
9
Diversification of the Ig Variable Region Gene Repertoire of Synovial B Lymphocytes by Nucleotide Insertion and Deletion
9
Spontaneous Mutations Occur Near Dam Recognition Sites in a dam-Escherichia coli Host
5
Length Requirements for Membrane Fusion of Influenza Virus Hemagglutinin Peptide Linkers to Transmembrane or Fusion Peptide Domains
12
Unique Pattern of Convergent Envelope Evolution in Simian Immunodeficiency Virus-Infected Rapid Progressor Macaques: Association with CD4-Independent Usage of CCR5
14
DCJ-Indel sorting revisited
9
High Frequency and Diversity of Rearrangements in Polyomavirus BK Noncoding Regulatory Regions Cloned from Urine and Plasma of Israeli Renal Transplant Patients and Evidence for a New Genetic Subtype
10
Neutral genomic microevolution of a recently emerged pathogen, salmonella enterica serovar agona
20
Extensive Mutagenesis of the Hepatitis B Virus Core Gene and Mapping of Mutations That Allow Capsid Formation
8
SRC TN 1997 021 pdf
19
Host range mutants of v-src: alterations in kinase activity and substrate interactions.
10
X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males
11