Evidence that mammalian cells possess homologous recombinational repair pathways

Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN gene.

Stem cell research·2023

Outcomes and cost analysis of patients with dementia in the intensive care unit: a population-based cohort study.

BMC health services research·2023

Hydrogel oxygen reservoirs increase functional integration of neural stem cell grafts by meeting metabolic demands.

Nature communications·2023

Identifying the optimal developmental age of human pluripotent stem cell-derived midbrain dopaminergic progenitors for transplantation in a rodent model of Parkinson's disease.

Experimental neurology·2022

Homophilic binding of the neural cell adhesion molecule CHL1 regulates development of ventral midbrain dopaminergic pathways.

Scientific reports·2017

Emergency department and 'Google flu trends' data as syndromic surveillance indicators for seasonal influenza.

Epidemiology and infection·2014

A crosslinking positive control for any in vivo comet assay tissue.

Mutation research·2026

Molecular characterisation and mutational analysis of antimicrobial resistance genes in Helicobacter pylori isolates in Erbil, Iraq.

Mutation research·2026

In silico analysis of missense variants in functional domains of PWWP2A and PWWP2B proteins.

Mutation research·2026

The role of KIT mutations in oral melanoma and disease progression: A literature review on early detection and targeted therapy.

Mutation research·2026

Mothers against decapentaplegic homolog 3-activated FAT atypical cadherin 2 regulates programmed death ligand-1 to mediate immune evasion in lung squamous cell carcinoma.

Mutation research·2026

Potential targets and molecular mechanisms of curcumin in treating Laryngeal and Pharyngeal Carcinoma throat cancer based on network pharmacology and bioinformatics analysis.

Mutation research·2026

Diversity at the HYP1 locus in potato cyst nematodes does not result from developmentally-programmed somatic mutations.

PloS one·2026

Interference of Competing Beneficial Mutations on Recombining Chromosomes.

Biology·2026

The shared evolutionary capacities of plasmids and extrachromosomal DNA.

Nature reviews. Genetics·2026

Hologenomic interactions promote the higher-order evolvability of phenotypic complexity.

Trends in genetics : TIG·2026

Targeted insertion of an optimized donor DNA is effective in a humanized mouse model of dominant retinitis pigmentosa.

Cell reports. Medicine·2026

EULAR Rheumatology Open Special Issue titled 'VSI: ATT2026': the role of clonal haematopoiesis in immunological and rheumatological diseases.

EULAR rheumatology open·2026

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Evidence that mammalian cells possess homologous recombinational repair pathways

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Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN gene.

Outcomes and cost analysis of patients with dementia in the intensive care unit: a population-based cohort study.

Hydrogel oxygen reservoirs increase functional integration of neural stem cell grafts by meeting metabolic demands.

Identifying the optimal developmental age of human pluripotent stem cell-derived midbrain dopaminergic progenitors for transplantation in a rodent model of Parkinson's disease.

Homophilic binding of the neural cell adhesion molecule CHL1 regulates development of ventral midbrain dopaminergic pathways.

Emergency department and 'Google flu trends' data as syndromic surveillance indicators for seasonal influenza.

A crosslinking positive control for any in vivo comet assay tissue.

Molecular characterisation and mutational analysis of antimicrobial resistance genes in Helicobacter pylori isolates in Erbil, Iraq.

In silico analysis of missense variants in functional domains of PWWP2A and PWWP2B proteins.

The role of KIT mutations in oral melanoma and disease progression: A literature review on early detection and targeted therapy.

Mothers against decapentaplegic homolog 3-activated FAT atypical cadherin 2 regulates programmed death ligand-1 to mediate immune evasion in lung squamous cell carcinoma.

Potential targets and molecular mechanisms of curcumin in treating Laryngeal and Pharyngeal Carcinoma throat cancer based on network pharmacology and bioinformatics analysis.

Diversity at the HYP1 locus in potato cyst nematodes does not result from developmentally-programmed somatic mutations.

Interference of Competing Beneficial Mutations on Recombining Chromosomes.

The shared evolutionary capacities of plasmids and extrachromosomal DNA.

Hologenomic interactions promote the higher-order evolvability of phenotypic complexity.

Targeted insertion of an optimized donor DNA is effective in a humanized mouse model of dominant retinitis pigmentosa.

EULAR Rheumatology Open Special Issue titled 'VSI: ATT2026': the role of clonal haematopoiesis in immunological and rheumatological diseases.

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Evidence that mammalian cells possess homologous recombinational repair pathways

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