A mouse specific polymerase chain reaction (PCR) primer: probe generation from somatic cell hybrids

Unique Genetic and Histological Signatures of Mouse Pericardial Adipose Tissue.

Nutrients·2020

Reduction of fibrillar strain-rate sensitivity in steroid-induced osteoporosis linked to changes in mineralized fibrillar nanostructure.

Bone·2019

Hepatic gene expression variations in response to high-fat diet-induced impaired glucose tolerance using RNAseq analysis in collaborative cross mouse population.

Mammalian genome : official journal of the International Mammalian Genome Society·2019

Effect of Linearization in a WNT Signaling Model.

Computational and mathematical methods in medicine·2019

Bone matrix development in steroid-induced osteoporosis is associated with a consistently reduced fibrillar stiffness linked to altered bone mineral quality.

Acta biomaterialia·2018

Multiscale alterations in bone matrix quality increased fragility in steroid induced osteoporosis.

Bone·2015

Nuclear receptor Nur77 resolves the inflammatory response of macrophages primarily by regulating expression of AP-1 transcription factors and their target genes.

Nucleic acids research·2026

When circular RNAs meet the genome: CiR-loops as chromatin regulators and disease drivers.

Nucleic acids research·2026

SpliceImpactR maps alternative RNA processing events driving protein functional diversity.

Nucleic acids research·2026

The leading region of many plasmids is adapted for translational efficiency.

Nucleic acids research·2026

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

Nucleic acids research·2026

DeepPNI: a language- and graph-based model for mutation-driven protein-nucleic acid binding energetics.

Nucleic acids research·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

Related Experiment Videos

A mouse specific polymerase chain reaction (PCR) primer: probe generation from somatic cell hybrids

Related Concept Videos

Unique Genetic and Histological Signatures of Mouse Pericardial Adipose Tissue.

Reduction of fibrillar strain-rate sensitivity in steroid-induced osteoporosis linked to changes in mineralized fibrillar nanostructure.

Hepatic gene expression variations in response to high-fat diet-induced impaired glucose tolerance using RNAseq analysis in collaborative cross mouse population.

Effect of Linearization in a WNT Signaling Model.

Bone matrix development in steroid-induced osteoporosis is associated with a consistently reduced fibrillar stiffness linked to altered bone mineral quality.

Multiscale alterations in bone matrix quality increased fragility in steroid induced osteoporosis.

Nuclear receptor Nur77 resolves the inflammatory response of macrophages primarily by regulating expression of AP-1 transcription factors and their target genes.

When circular RNAs meet the genome: CiR-loops as chromatin regulators and disease drivers.

SpliceImpactR maps alternative RNA processing events driving protein functional diversity.

The leading region of many plasmids is adapted for translational efficiency.

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

DeepPNI: a language- and graph-based model for mutation-driven protein-nucleic acid binding energetics.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

Related Experiment Videos

A mouse specific polymerase chain reaction (PCR) primer: probe generation from somatic cell hybrids

Related Concept Videos

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