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1. The origin of long-chain fatty acids required for de novo ether lipid/plasmalogen synthesis

2. Autophagy Inhibitors Do Not Restore Peroxisomal Functions in Cells With the Most Common Peroxisome Biogenesis Defect

3. A Functional SMAD2/3 Binding Site in the PEX11β Promoter Identifies a Role for TGFβ in Peroxisome Proliferation in Humans

4. Phosphomevalonate kinase is a cytosolic protein in humans

5. Assessing Science Inquiry using MDP Goal Detectors

6. Modifying Cognitive Load Component Survey for K-12 STEM Testing

7. <scp>3‐Hydroxyisobutyric</scp> acid dehydrogenase deficiency: Expanding the clinical spectrum and quantitation of D‐ and <scp>L‐3‐Hydroxyisobutyric</scp> acid by an <scp>LC–MS</scp> / <scp>MS</scp> method

10. Glutaminase deficiency caused by short tandem repeat expansion in GLS

11. Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy

12. A novel case of ACOX2 deficiency leads to recognition of a third human peroxisomal acyl-CoA oxidase

13. A Functional SMAD2/3 Binding Site in the PEX11β Promoter Identifies a Role for TGFβ in Peroxisome Proliferation in Humans

14. Deciphering the potential involvement of PXMP2 and PEX11B in hydrogen peroxide permeation across the peroxisomal membrane reveals a role for PEX11B in protein sorting

15. Peroxisomal abnormalities in the immortalized human hepatocyte (IHH) cell line

16. Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis

17. Sodium Taurocholate Cotransporting Polypeptide (SLC10A1) Deficiency

18. Transfection of Primary Human Skin Fibroblasts for Peroxisomal Studies

19. A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3

20. An unusual phenotype of X-linked developmental delay and extreme behavioral difficulties associated with a mutation in the EBP gene

21. ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism

22. Substrate specificity of human carnitine acetyltransferase: Implications for fatty acid and branched-chain amino acid metabolism

23. Transfection of Primary Human Skin Fibroblasts for Peroxisomal Studies

24. ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism

25. Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficient

26. Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum Disorder

27. Desmosterolosis-phenotypic and molecular characterization of a third case and review of the literature

28. HMG-CoA reductase inhibition induces IL-1 beta release through Rac1/PI3K/PKB-dependent caspase-1 activation

29. A Lethal Defect of Mitochondrial and Peroxisomal Fission

30. Mevalonate kinase is a cytosolic enzyme in humans

31. Human mevalonate pyrophosphate decarboxylase is localized in the cytosol

32. Phosphomevalonate kinase is a cytosolic protein in humans

33. A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform

34. A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene

35. Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder

36. Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines

37. 12.2 Mevalonate kinase deficiency: Impaired isoprenoid synthesis induces IL-1beta production via activation of Rac1

38. Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency

39. Mutational spectrum and genotype-phenotype correlations in mevalonate kinase deficiency

40. Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

41. Mutations in the 3beta-hydroxysterol Delta24-reductase gene cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesis

42. Identification and characterization of three novel missense mutations in'mevalonate kinase cDNA causing mevalonic aciduria, a disorder of isoprene biosynthesis

43. Erratum: Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

45. Autosomal Recessive HEM/Greenberg Skeletal Dysplasia Is Caused by 3β-Hydroxysterol Δ14-Reductase Deficiency Due to Mutations in the Lamin B Receptor Gene

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