Genetic control of protein secretion and localization

Peculiar nuclear clearing composed of microfilaments in papillary carcinoma of the thyroid.

Cancer·1992

Adenosine A2 receptor antagonist facilitates the reversal of long-term potentiation (depotentiation) of evoked postsynaptic potentials but inhibits that of population spikes in hippocampal CA1 neurons.

Neuroscience letters·1992

A hyperpolarizing response induced by glutamate in mouse cerebellar Purkinje cells.

Neuroscience research·1992

Studies on antiplatelet agents. I. Synthesis and platelet inhibitory activity of 5-alkyl-2-aryl-4-pyridylimidazoles.

Chemical & pharmaceutical bulletin·1992

[Interleukin 6 receptors on human bronchial epithelial cells].

Nihon Kyobu Shikkan Gakkai zasshi·1992

Manganese-mediated oxidative damage of cellular and isolated DNA by isoniazid and related hydrazines: non-Fenton-type hydroxyl radical formation.

Biochemistry·1992

Molecular mechanism of VDE-initiated intein homing in yeast nuclear genome.

Advances in biophysics·2004

Structure and function of the shufflon in plasmid R64.

Advances in biophysics·2004

Transposition mechanisms and biotechnology applications of the medaka fish Tol2 transposable element.

Advances in biophysics·2004

Genetics and epigenetics in flower pigmentation associated with transposable elements in morning glories.

Advances in biophysics·2004

Gpt delta transgenic mouse: a novel approach for molecular dissection of deletion mutations in vivo.

Advances in biophysics·2004

Cell death promoted by homologous DNA interaction from bacteria to humans.

Advances in biophysics·2004

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

Genetic control of protein secretion and localization

Related Concept Videos

Peculiar nuclear clearing composed of microfilaments in papillary carcinoma of the thyroid.

Adenosine A2 receptor antagonist facilitates the reversal of long-term potentiation (depotentiation) of evoked postsynaptic potentials but inhibits that of population spikes in hippocampal CA1 neurons.

A hyperpolarizing response induced by glutamate in mouse cerebellar Purkinje cells.

Studies on antiplatelet agents. I. Synthesis and platelet inhibitory activity of 5-alkyl-2-aryl-4-pyridylimidazoles.

[Interleukin 6 receptors on human bronchial epithelial cells].

Manganese-mediated oxidative damage of cellular and isolated DNA by isoniazid and related hydrazines: non-Fenton-type hydroxyl radical formation.

Molecular mechanism of VDE-initiated intein homing in yeast nuclear genome.

Structure and function of the shufflon in plasmid R64.

Transposition mechanisms and biotechnology applications of the medaka fish Tol2 transposable element.

Genetics and epigenetics in flower pigmentation associated with transposable elements in morning glories.

Gpt delta transgenic mouse: a novel approach for molecular dissection of deletion mutations in vivo.

Cell death promoted by homologous DNA interaction from bacteria to humans.

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

Genetic control of protein secretion and localization

Related Concept Videos

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