Polymorphism in the protein C gene detected by denaturing gradient gel electrophoresis

[Clinical and biological features of patients with essential thrombocythaemia according to their mutational status JAK2 or CALR: Single-center study of 40 patients and review of the literature].

Pathologie-biologie·2015

Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.

Journal of thrombosis and haemostasis : JTH·2013

Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.

Human genetics·2009

Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function.

Journal of thrombosis and haemostasis : JTH·2006

[Validation of a diagnostic kit for factor V Leiden mutation].

Annales de biologie clinique·2004

Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain.

The Biochemical journal·2001

Regulation of the histone H3K36 methyltransferase Set2 by the histone chaperone Spt6.

Nucleic acids research·2026

Mechanism of the long-B prokaryotic Argonaute-mediated nuclease activation in bacterial immunity.

Nucleic acids research·2026

The piRNA pathway mediates transcriptional silencing of LTR retrotransposons in ovaries and somatic tissues of Aedes mosquitoes.

Nucleic acids research·2026

LUCas: Light-Uncaged Cas13a using photocleavable interfering guide RNAs.

Nucleic acids research·2026

Fluorescent reporter assay reveals ribonucleotides promote mismatch correction in vivo.

Nucleic acids research·2026

Large-scale mutational analysis uncovers molecular mechanisms governing dual RNA functions in transposons.

Nucleic acids research·2026

The clinical utility of exome sequencing for risk stratification in celiac disease.

Journal of human immunity·2026

Expanding the KBG syndrome phenotype through 2D facial morphometry, clinical and molecular characterization.

Biomedical reports·2026

Non-invasive embryo assessment: Cell-free DNA-based genetic testing and amino acid metabolomics in relation to morphology: A case-control study.

International journal of reproductive biomedicine·2026

Symposium report- epigenetic inheritance: impact for biology and society 27-29 August 2025, Zurich, Switzerland.

Environmental epigenetics·2026

Severity-stratified gut microbiome dysbiosis and systemic neuroinflammation in acute traumatic brain injury: a metagenomic and cytokine profiling study.

Frontiers in microbiology·2026

Related Experiment Videos

Polymorphism in the protein C gene detected by denaturing gradient gel electrophoresis

Related Concept Videos

[Clinical and biological features of patients with essential thrombocythaemia according to their mutational status JAK2 or CALR: Single-center study of 40 patients and review of the literature].

Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant.

Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.

Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function.

[Validation of a diagnostic kit for factor V Leiden mutation].

Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain.

Regulation of the histone H3K36 methyltransferase Set2 by the histone chaperone Spt6.

Mechanism of the long-B prokaryotic Argonaute-mediated nuclease activation in bacterial immunity.

The piRNA pathway mediates transcriptional silencing of LTR retrotransposons in ovaries and somatic tissues of Aedes mosquitoes.

LUCas: Light-Uncaged Cas13a using photocleavable interfering guide RNAs.

Fluorescent reporter assay reveals ribonucleotides promote mismatch correction in vivo.

Large-scale mutational analysis uncovers molecular mechanisms governing dual RNA functions in transposons.

The clinical utility of exome sequencing for risk stratification in celiac disease.

Expanding the KBG syndrome phenotype through 2D facial morphometry, clinical and molecular characterization.

Non-invasive embryo assessment: Cell-free DNA-based genetic testing and amino acid metabolomics in relation to morphology: A case-control study.

Symposium report- epigenetic inheritance: impact for biology and society 27-29 August 2025, Zurich, Switzerland.

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Polymorphism in the protein C gene detected by denaturing gradient gel electrophoresis

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