Eosinophilic leukaemia--eosinophilic collagen disease; a diagnostic dilemma

Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element.

Molecular and cellular probes·2003

Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction.

European journal of obstetrics, gynecology, and reproductive biology·2001

Familial adenomatous polyposis coli in South Africa--molecular basis and diagnosis.

South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde·2000

Lipoprotein(a) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemia.

South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde·2000

Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia.

Journal of medical genetics·2000

Mutation -59c-->t in repeat 2 of the LDL receptor promoter: reduction in transcriptional activity and possible allelic interaction in a South African family with familial hypercholesterolaemia.

Human molecular genetics·1999

Heterozygous germline deletion in Hif3a exacerbates esophageal squamous cell carcinoma development.

The Journal of pathology·2026

Network based approach identifies miR-145-3p as a central regulatory hub associated to the progression from localized to metastatic medullary thyroid carcinoma.

The Journal of pathology·2026

Differential FGFR1 copy number status displays unique tumour immune microenvironment in triple-negative breast cancer.

The Journal of pathology·2026

Spatial transcriptomics reveals club cell features and strong CLDN18 expression along the mucinous pathway to invasive mucinous adenocarcinoma.

The Journal of pathology·2026

DUCK-Net: automated deep learning segmentation of ductular reactions in murine liver injury captures multicellular niche dynamics from H&E morphology.

The Journal of pathology·2026

CAFs-mediated histone lactylation reprograms cholesterol metabolism in colorectal cancer to drive CD8+ T cell immunosuppression.

The Journal of pathology·2026

Monocytic Cell Variations in Postallotransplant Environment: Balancing Graft Versus Host Disease and Graft-Versus-Leukemia Effect.

Journal of immunology research·2026

Early antithrombin depletion after trauma is associated with biomarkers of endotheliopathy and systemic protein loss: a retrospective observational study.

Shock (Augusta, Ga.)·2026

Establishment of Reference Intervals for Thrombus Biomarkers in a Single-Center Chinese Population Using Indirect Methods.

Journal of clinical laboratory analysis·2026

Re-evaluating haemolysis rejection criteria for PT, aPTT, and D-dimer testing: evidence from paired clinical samples on the CN-3000 analyser.

Advances in laboratory medicine·2026

Diagnostic Utility of Platelet Indices in Differentiating Hypoproductive and Hyperdestructive Thrombocytopenia: A Cross-Sectional Study From North India.

Cureus·2026

Medium-term biological variation of sodium, potassium and chloride in whole blood in cohorts of healthy individuals and hemodialysis patients.

Advances in laboratory medicine·2026

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Eosinophilic leukaemia--eosinophilic collagen disease; a diagnostic dilemma

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Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element.

Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction.

Familial adenomatous polyposis coli in South Africa--molecular basis and diagnosis.

Lipoprotein(a) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemia.

Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia.

Mutation -59c-->t in repeat 2 of the LDL receptor promoter: reduction in transcriptional activity and possible allelic interaction in a South African family with familial hypercholesterolaemia.

Heterozygous germline deletion in Hif3a exacerbates esophageal squamous cell carcinoma development.

Network based approach identifies miR-145-3p as a central regulatory hub associated to the progression from localized to metastatic medullary thyroid carcinoma.

Differential FGFR1 copy number status displays unique tumour immune microenvironment in triple-negative breast cancer.

Spatial transcriptomics reveals club cell features and strong CLDN18 expression along the mucinous pathway to invasive mucinous adenocarcinoma.

DUCK-Net: automated deep learning segmentation of ductular reactions in murine liver injury captures multicellular niche dynamics from H&E morphology.

CAFs-mediated histone lactylation reprograms cholesterol metabolism in colorectal cancer to drive CD8+ T cell immunosuppression.

Monocytic Cell Variations in Postallotransplant Environment: Balancing Graft Versus Host Disease and Graft-Versus-Leukemia Effect.

Early antithrombin depletion after trauma is associated with biomarkers of endotheliopathy and systemic protein loss: a retrospective observational study.

Establishment of Reference Intervals for Thrombus Biomarkers in a Single-Center Chinese Population Using Indirect Methods.

Re-evaluating haemolysis rejection criteria for PT, aPTT, and D-dimer testing: evidence from paired clinical samples on the CN-3000 analyser.

Diagnostic Utility of Platelet Indices in Differentiating Hypoproductive and Hyperdestructive Thrombocytopenia: A Cross-Sectional Study From North India.

Medium-term biological variation of sodium, potassium and chloride in whole blood in cohorts of healthy individuals and hemodialysis patients.

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Eosinophilic leukaemia--eosinophilic collagen disease; a diagnostic dilemma

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