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Academic Journal

New plasma protein C and protein S concentrate: A synergy for therapeutic purposes.

Subjects: PROTEIN C; BLOOD proteins; PROTEIN S

  • Source: Vox Sanguinis; Mar2024, Vol. 119 Issue 3, p193-202, 10p

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Academic Journal

Genetic polymorphisms in vitamin E transport genes as determinants for risk of equine neuroaxonal dystrophy.

Subjects: VITAMIN E; GENETIC polymorphisms; WHOLE genome sequencing

  • Source: Journal of Veterinary Internal Medicine; Jan/Feb2024, Vol. 38 Issue 1, p417-423, 7p

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Academic Journal

A large single‐center cohort of bare lymphocyte syndrome: Immunological and genetic features in Turkey.

Subjects: SEVERE combined immunodeficiency; HEMATOPOIETIC stem cell transplantation; MAJOR histocompatibility complexTURKEY

  • Source: Scandinavian Journal of Immunology; Jan2024, Vol. 99 Issue 1, p1-11, 11p

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Academic Journal

A young boy with rash, arthritis, and developmental delay: Monogenic lupus due to DNASE2 gene defect.

Subjects: DEVELOPMENTAL delay; MAGNETIC resonance imaging; ANTINUCLEAR factors

  • Source: International Journal of Rheumatic Diseases; Dec2023, Vol. 26 Issue 12, p2599-2602, 4p

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Academic Journal

Complement, complosome, and complotype: A perspective.

Subjects: COMPLEMENT activation; CELL physiology; NATURAL immunity

  • Source: European Journal of Immunology; Dec2023, Vol. 53 Issue 12, p1-11, 11p

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Academic Journal

Sensitivity to change and minimal clinically important difference of the angioedema control test.

Subjects: ANGIONEUROTIC edema; PREVENTIVE medicine; BLOOD coagulation factor XIII

  • Source: Clinical & Translational Allergy; Sep2023, Vol. 13 Issue 9, p1-10, 10p

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Academic Journal

Iatrogenic copper deficiency: Risks and cautions with zinc prescribing.

Subjects: COPPER; ZINC; TRACE elements

  • Source: British Journal of Clinical Pharmacology; Sep2023, Vol. 89 Issue 9, p2825-2829, 5p

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Academic Journal

Genetic variants causing G6PD deficiency: Clinical and biochemical data support new WHO classification.

Subjects: GLUCOSE-6-phosphate dehydrogenase deficiency; GENETIC variation; GLUCOSE-6-phosphate dehydrogenase

  • Source: British Journal of Haematology; Sep2023, Vol. 202 Issue 5, p1024-1032, 9p

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Academic Journal

Identification of an α‐l‐iduronidase (IDUA) M1T mutation in a Chinese family with autosomal recessive mucopolysaccharidosis I.

Subjects: MUCOPOLYSACCHARIDOSIS I; ARACHIDONIC acid; GENE expression

  • Source: Annals of the New York Academy of Sciences; Aug2023, Vol. 1526 Issue 1, p114-125, 12p, 5 Color Photographs, 1 Black and White Photograph, 1 Diagram, 1 Graph

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Academic Journal

Structural and functional characterization of novel F7 mutations identified in Chinese factor VII‐deficient patients.

Subjects: BLOOD coagulation factor XIII; GENETIC mutation; MISSENSE mutation

  • Source: British Journal of Haematology; Aug2023, Vol. 202 Issue 3, p623-635, 13p

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  • 1-10 of  464 results for ""BLOOD coagulation factor XIII""