Terkko Navigator / Genetics/ Feeds

Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis

PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly

Sets of Co-regulated Serum Lipids are Associated with Alzheimer Disease Pathophysiology

Meiotic DNA repair in the nucleolus employs a non-homologous end joining mechanism

H2A.Z-dependent and -independent recruitment of metabolic enzymes to chromatin required for histone modifications

Traces of past transposable element presence in Brassicaceae genome dark matter

Haplotype-Based Noninvasive Prenatal Diagnosis for Duchenne Muscular Dystrophy: A pilot study in South China

Micro-indentation and optical coherence tomography for the mechanical characterization of embryos: Experimental setup and measurements on fixed chicken embryos.

Gene expression noise randomizes the adaptive response to DNA alkylation damage in E. coli

Dynamic clustering regulates activity of mechanosensitive membrane channels

Comparison of SVM and Spectral Embedding in Promoter Biobricks\' Categorizing and Clustering

Neural System Identification with Cortical Information Flow

The fog of genetics: Known unknowns and unknown unknowns in the genetics of complex traits and diseases

A quantitative tri-fluorescent yeast two-hybrid system: from flow cytometry to in-cellula affinities

Lung regeneration by multipotent stem cells residing at the bronchioalveolar-duct junction

Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases

Integrated analysis of population genomics, transcriptomics and virulence provides novel insights into Streptococcus pyogenes pathogenesis

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

Experimental evidence that belowground competition can influence the evolution of root traits in two closely related morning glory species

Cancer gene therapy by NF-κB-activated cancer cell-specific expression of CRISPR/Cas9 targeting to telomere

Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairment

De novo characterization of placental transcriptome in the Eurasian beaver ( Castor fiber L.)

Motor cortex signals corresponding to the two arms are shared across hemispheres, mixed among neurons, yet partitioned within the population response

Comparison of classification methods for tissue outcome after ischemic stroke

Short-Term Plasticity Following Motor Sequence Learning Revealed by Diffusion MRI

Trait-based life-history strategies explain succession scenario for complex bacterial communities under varying disturbance

Calcium-dependent protein kinase 5 links calcium-signaling with SARD1-dependent immune memory in systemic acquired resistance

I believe, therefore I am: Effects of self-control beliefs on behavioral and electrophysiological markers of inhibitory and emotional attention control

A network supporting social influences in human decision-making

Auditory perceptual history is communicated through alpha oscillations

Evaluating Complexity of Fetal MEG Signals: A Comparison of Different Metrics and Their Applicability

Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere

The Juvenile Idiopathic Arthritis (JIA) Susceptibility Locus, IL2RA, Includes An Intronic Enhancer That Is Attenuated By JIA-Associated Genetic Variants

A functional variant alters binding of activating protein 1 regulating expression of FGF7 gene associated with chronic obstructive pulmonary disease

High-throughput phenotyping platforms enhance genomic selection for wheat grain yield across populations and cycles in early stage

The transcription factor OsbHLH138 regulates thermosensitive genic male sterility in rice via activation of TMS5

De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment

Disruption of KCNQ1 prevents methylation of the ICR2 and supports the hypothesis that its transcription is necessary for imprint establishment

A pilot eConsultation service in Eastern Ontario: bridging clinical genetics and primary care

The locomotor and predatory habits of unenlagiines (Theropoda, Paraves): inferences based on morphometric studies and comparisons with Laurasian dromaeosaurids

2-Cl-C.OXT-A Stimulates Contraction through the Suppression of Phosphodiesterase Activity in Human Induced Pluripotent Stem Cell-derived Cardiac Organoids

RecV recombinase system for spatiotemporally controlled light-inducible genomic modifications.

Serologic evidence of seasonal influenza A and B viruses in HIV patients on combined antiretroviral therapy in Lagos, Nigeria

Transcriptional Blood Signatures for Active and Amphotericin B Treated Visceral Leishmaniasis in India

The yeast Art1 arrestin domain contains disordered insertions that regulate its localization and activity

Genes, Vol. 10, Pages 156: Genome-Wide Identification and Analysis of High-Copy-Number LTR Retrotransposons in Asian Pears

Genetic Polymorphisms of CCDC26 rs891835, rs6470745, and rs55705857 in Glioma Risk: A Systematic Review and Meta-analysis

Application of seaweed organic components increases tolerance to Fe deficiency in tomato plants

Precise removal of Calm1 long 3\' UTR isoform by CRISPR-Cas9 genome editing impairs dorsal root ganglion development in mice.

Future sea-level rise drives rocky intertidal habitat loss and benthic community change