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  1. Holocarboxylase synthetase knockout is embryonic lethal in mice
  2. Nutrition, microRNAs, and Human Health
  3. Biological Activities of Extracellular Vesicles and Their Cargos from Bovine and Human Milk in Humans and Implications for Infants
  4. Gene regulation by dietary microRNAs 1
  5. The Intestinal Transport of Bovine Milk Exosomes Is Mediated by Endocytosis in Human Colon Carcinoma Caco-2 Cells and Rat Small Intestinal IEC-6 Cells1–3
  6. Loss of miRNAs during Processing and Storage of Cow’s ( Bos taurus ) Milk
  7. β-Keto and β-hydroxyphosphonate analogs of biotin-5′-AMP are inhibitors of holocarboxylase synthetase
  8. Reply to Witwer1,2
  9. Low activity of LSD1 elicits a pro-inflammatory gene expression profile in riboflavin-deficient human T Lymphoma Jurkat cells
  10. Holocarboxylase synthetase interacts physically with nuclear receptor co-repressor, histone deacetylase 1 and a novel splicing variant of histone deacetylase 1 to repress repeats
  11. Off-target effects of sulforaphane include the derepression of long terminal repeats through histone acetylation events
  12. Lysine biotinylation and methionine oxidation in the heat shock protein HSP60 synergize in the elimination of reactive oxygen species in human cell cultures
  13. Novel roles of holocarboxylase synthetase in gene regulation and intermediary metabolism
  14. Three promoters regulate the transcriptional activity of the human holocarboxylase synthetase gene
  15. Holocarboxylase synthetase interacts physically with euchromatic histone-lysine N-methyltransferase, linking histone biotinylation with methylation events
  16. Handbook of Vitamins, Fifth Edition
  17. Vitamins, Bioactive Food Compounds, and Histone Modifications
  18. Mechanisms of Gene Transcriptional Regulation through Biotin and Biotin-Binding Proteins in Mammals
  19. Holocarboxylase synthetase synergizes with methyl CpG binding protein 2 and DNA methyltransferase 1 in the transcriptional repression of long-terminal repeats
  20. Enrichment of meiotic recombination hotspot sequences by avidin capture technology
  21. Identification and assessment of markers of biotin status in healthy adults
  22. Nutrition, Histone Epigenetic Marks, and Disease
  23. Biotinylation of lysine 16 in histone H4 contributes toward nucleosome condensation
  24. K16-biotinylated histone H4 is overrepresented in repeat regions and participates in the repression of transcriptionally competent genes in human Jurkat lymphoid cells
  25. Biotin
  26. Cytosine methylation in miR-153 gene promoters increases the expression of holocarboxylase synthetase, thereby increasing the abundance of histone H4 biotinylation marks in HEK-293 human kidney cells
  27. Biotin requirements for DNA damage prevention
  28. CHAPTER 10. Biochemistry of Biotin
  29. Biotinylation is a natural, albeit rare, modification of human histones
  30. Development of an internet based system for modeling biotin metabolism using Bayesian networks
  31. Effects of single-nucleotide polymorphisms in the human holocarboxylase synthetase gene on enzyme catalysis
  32. Human holocarboxylase synthetase with a start site at methionine-58 is the predominant nuclear variant of this protein and has catalytic activity
  33. The role of holocarboxylase synthetase in genome stability is mediated partly by epigenomic synergies between methylation and biotinylation events
  34. Identification of holocarboxylase synthetase chromatin binding sites in human mammary cell lines using the DNA adenine methyltransferase identification technology
  35. Holocarboxylase synthetase is a chromatin protein and interacts directly with histone H3 to mediate biotinylation of K9 and K18
  36. A 96-well plate assay for high-throughput analysis of holocarboxylase synthetase activity
  37. Novel histone biotinylation marks are enriched in repeat regions and participate in repression of transcriptionally competent genes
  38. The Role of Histone H4 Biotinylation in the Structure of Nucleosomes
  39. Molecular Aspects of Physical Performance and Nutritional Assessment
  40. K12-biotinylated histone H4 is enriched in telomeric repeats from human lung IMR-90 fibroblasts
  41. The polypeptide Syn67 interacts physically with human holocarboxylase synthetase, but is not a target for biotinylation
  42. Overview to Symposium “Nutrients and Epigenetic Regulation of Gene Expression”1
  43. N- and C-terminal domains in human holocarboxylase synthetase participate in substrate recognition
  44. Nitric Oxide Signaling Depends on Biotin in Jurkat Human Lymphoma Cells
  45. Biotin
  46. Biotinyl-methyl 4-(amidomethyl)benzoate is a competitive inhibitor of human biotinidase
  47. Handbook of Vitamins,: 4th ed, edited by Janos Zempleni, Robert B Rucker, Donald B McCormick, and John W Suttie, 2007, 593 pages, hardcover, $107.96. CRC Press, New York.
  48. A novel, enigmatic histone modification: biotinylation of histones by holocarboxylase synthetase
  49. Biotin and biotinidase deficiency
  50. Epigenetic regulation of chromatin structure and gene function by biotin: are biotin requirements being met?
  51. Proliferation of Peripheral Blood Mononuclear Cells Increases Riboflavin Influx
  52. Marginal Biotin Deficiency Is Teratogenic
  53. Holocarboxylase synthetase regulates expression of biotin transporters by chromatin remodeling events at the SMVT locus
  54. Use of Synthetic Peptides for Identifying Biotinylation Sites in Human Histones
  55. K12-biotinylated histone H4 marks heterochromatin in human lymphoblastoma cells
  56. An avidin-based assay for histone debiotinylase activity in human cell nuclei
  57. Genomic Implications of H2O2 for Cell Proliferation and Growth of Caco-2 Cells
  58. Handbook of Vitamins, Fourth Edition
  59. Vitamin-Dependent Modifications of Chromatin
  60. Lysine residues in N-terminal and C-terminal regions of human histone H2A are targets for biotinylation by biotinidase
  61. Riboflavin deficiency causes protein and DNA damage in HepG2 cells, triggering arrest in G1 phase of the cell cycle
  62. Biotin supplementation decreases the expression of the SERCA3 gene (ATP2A3) in Jurkat cells, thus, triggering unfolded protein response
  63. The expression of genes encoding ribosomal subunits and eukaryotic translation initiation factor 5A depends on biotin and bisnorbiotin in HepG2 cells
  64. Pantothenic Acid and Biotin
  65. HepG2 cells develop signs of riboflavin deficiency within 4 days of culture in riboflavin-deficient medium
  66. UPTAKE, LOCALIZATION, AND NONCARBOXYLASE ROLES OF BIOTIN*
  67. K4, K9 and K18 in human histone H3 are targets for biotinylation by biotinidase
  68. Biotin availability regulates expression of the sodium-dependent multivitamin transporter and the rate of biotin uptake in HepG2 cells
  69. Biological functions of biotinylated histones
  70. Nutrients and Cell Signaling
  71. Roles for Biotinylation of Histones in Chromatin Structure
  72. Biotin deficiency stimulates survival pathways in human lymphoma cells exposed to antineoplastic drugs
  73. Roles for nutrients in epigenetic events
  74. Biotin deficiency decreases life span and fertility but increases stress resistance in Drosophila melanogaster
  75. Clusters of biotin-responsive genes in human peripheral blood mononuclear cells
  76. K8 and K12 are biotinylated in human histone H4
  77. Biotin supply affects rates of cell proliferation, biotinylation of carboxylases and histones, and expression of the gene encoding the sodium-dependent multivitamin transporter in JAr choriocarcinoma cells
  78. Regulation of gene expression by biotin☆ (review)
  79. Molecular nutrition
  80. BIOTIN | Physiology
  81. Synthesis of a Rabbit Polyclonal Antibody to the Human Sodium-Dependent Multivitamin Transporter
  82. Biotin dependency due to a defect in biotin transport
  83. Biotin dependency due to a defect in biotin transport
  84. Biotin dependency due to a defect in biotin transport
  85. Biotinidase catalyzes debiotinylation of histones
  86. Biotinylation of histones in human cells
  87. Proliferation of peripheral blood mononuclear cells causes increased expression of the sodium-dependent multivitamin transporter gene and increased uptake of pantothenic acid☆ ☆This work was supported by National Institutes of Health grant DK 36823, US...
  88. Proliferation of Peripheral Blood Mononuclear Cells Increases Riboflavin Influx
  89. Marginal Biotin Deficiency Is Teratogenic
  90. Chemical Synthesis of Biotinylated Histones and Analysis by Sodium Dodecyl Sulfate–Polyacrylamide Gel Electrophoresis/Streptavidin–Peroxidase
  91. Biotin biochemistry and human requirements
  92. Biokinetic analysis of vitamin absorption and disposition in humans
  93. Utilization of intravenously infused thiamin hydrochloride in healthy adult males
  94. Lipoic acid (thioctic acid) analogs, tryptophan analogs, and urea do not interfere with the assay of biotin and biotin metabolites by high-performance liquid chromatography/avidin-binding assay
  95. Intrauterine Vitamin B2 Uptake of Preterm and Full-Term Infants
  96. Metabolism of vitamin B6 by human kidney
  97. Determination of Riboflavin and Flavocoenzymes in Human Blood Plasma by High-Performance Liquid Chromatography
  98. The utilization of intravenously infused pyridoxine in humans
  99. Use of Synthetic Peptides for Identifying Biotinylation Sites in Human Histones
  100. Nutrient homeostasis in proliferating cells.
  101. Biotinylation of histones in human cells.