Search

Your search keyword '"Sokolová J"' showing total 460 results

Search Constraints

Start Over You searched for: "Sokolová J" Remove constraint "Sokolová J"
460 results on '"Sokolová J"'

Search Results

1. Dietary sulfur amino acid restriction in humans with overweight and obesity: Evidence of an altered plasma and urine sulfurome, and a novel metabolic signature that correlates with loss of fat mass and adipose tissue gene expression.

2. Elevated homocysteine levels: What inborn errors of metabolism might we be missing?

Catalog

Books, media, physical & digital resources

3. High Cysteine Diet Reduces Insulin Resistance in SHR-CRP Rats

4. Cystathionine β-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis

5. Cysteine restriction-specific effects of sulfur amino acid restriction on lipid metabolism.

6. Human ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H 2 S homeostasis.

11. Royal academy of medicine in Ireland international conference on homocysteine metabolism from basic science to clinical medicine: Proceedings of meeting held at Dromoland Castle, Co. Clare on July 2nd–6th, 1995

12. Domestic Volunteer Tourism Demand in Slovakia

13. Dissecting the Role of Folr1 and Folh1 Genes in the Pathogenesis of Metabolic Syndrome in Spontaneously Hypertensive Rats

14. Cystathionine β-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis.

15. Komrower Memorial Lecture 2023. Molecular basis of phenotype expression in homocystinuria: Where are we 30 years later?

16. Metabolism of sulfur compounds in homocystinurias.

17. Biogenesis of Hydrogen Sulfide and Thioethers by Cystathionine Beta-Synthase.

18. Rapid identification of staphylococci by Raman spectroscopy.

19. Activity of the liver enzyme ornithine carbamoyltransferase (OTC) in blood: LC-MS/MS assay for non-invasive diagnosis of ornithine carbamoyltransferase deficiency.

26. Thioethers as markers of hydrogen sulfide production in homocystinurias.

27. Birth prevalence of homocystinuria in Central Europe: frequency and pathogenicity of mutation c.1105C>T (p.R369C) in the cystathionine beta-synthase gene.

30. Genetic Variation in Renal Expression of Folate Receptor 1 (Folr1) Gene Predisposes Spontaneously Hypertensive Rats to Metabolic Syndrome.

31. Insights into severe 5,10-methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patients.

32. Establishment and evaluation of a method for measuring ornithine transcarbamylase activity in micro blood of neonates.

33. Preconceptional and Periconceptional Folic Acid Supplementation in the Visegrad Group Countries for the Prevention of Neural Tube Defects.

34. Differential Impact of VNTR Polymorphism in the CBS Gene on Gastric and Breast Cancers Risk.

35. Lighting the Path: Raman Spectroscopy's Journey Through the Microbial Maze.

36. Emerging roles of hydrogen sulfide-metabolizing enzymes in cancer.

38. Metabolic syndrome, alcohol consumption and genetic factors are associated with serum uric acid concentration.

39. Folate deficiency is associated with oxidative stress, increased blood pressure, and insulin resistance in spontaneously hypertensive rats.

40. Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency.

41. Rare allelic variants determine folate status in an unsupplemented European population.

42. Cystathionine beta-synthase mutations: effect of mutation topology on folding and activity.

43. Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversion.

44. Metabolic Side Effects from Antipsychotic Treatment with Clozapine Linked to Aryl Hydrocarbon Receptor (AhR) Activation.

45. Effect of Sodium Thiosulfate Pre-Treatment on Renal Ischemia-Reperfusion Injury in Kidney Transplantation.

46. Identification and functional analysis of two novel mutations in the CBS gene in Polish patients with homocystinuria.

47. Impaired heme binding and aggregation of mutant cystathionine beta-synthase subunits in homocystinuria.

48. The human cystathionine beta-synthase (CBS) gene: complete sequence, alternative splicing, and polymorphisms.

50. Mucopolysaccharidosis Type IIIE: A Real Human Disease or a Diagnostic Pitfall?