All Stories

  1. Different TP53 mutations are associated with specific chromosomal rearrangements, telomere length changes, and remodeling of the nuclear architecture of telomeres
  2. Evaluation of the impact of density gradient centrifugation on fetal cell loss during enrichment from maternal peripheral blood
  3. Validation of automatic scanning of microscope slides in recovering rare cellular events: application for detection of fetal cells in maternal blood
  4. Strengths and pitfalls of Canadian gamete and embryo donor registries: searching for beneficent solutions
  5. Gender Eugenics Between Medicine, Culture, and Society
  6. A new der(1;7)(q10;p10) leading to a singular 1p loss in a case of glioblastoma with oligodendroglioma component
  7. Cytosine containing dipyrimidine sites can be hotspots of cyclobutane pyrimidine dimer formation after UVB exposure
  8. Differences between selective termination of pregnancy and fetal reduction in multiple pregnancy: a narrative review
  9. Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database
  10. Efficiency of Manual Scanning in Recovering Rare Cellular Events Identified by FluorescenceIn SituHybridization: Simulation of the Detection of Fetal Cells in Maternal Blood
  11. A survey of APC mutations in Quebec
  12. Neurofibromatosis Type 1 and the “Elephant Man's” Disease: The Confusion Persists: An Ethnographic Study
  13. Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22
  14. DNAc: A Clustering Method for Identifying Kinship Relations Between DNA Profiles Using a Novel Similarity Measure*
  15. The Sunscreen Agent 2-Phenylbenzimidazole-5-Sulfonic Acid Photosensitizes the Formation of Oxidized Guanines In Cellulo after UV-A or UV-B Exposure
  16. Sizing the ends: Normal length of human telomeres
  17. p53 functions and cell lines: Have we learned the lessons from the past?
  18. Comprendre la mutagenèse somatique grâce à la cartographie des dommages à l’ADN
  19. 11. Marked variability in urinary Gb3/creatinine excretion in healthy infants
  20. EGF receptor inhibitors in the treatment of glioblastoma multiform: Old clinical allies and newly emerging therapeutic concepts
  21. Fetal–maternal exchange of multipotent stem/progenitor cells: microchimerism in diagnosis and disease
  22. Is the 1p/19q deletion a diagnostic marker of oligodendrogliomas?
  23. Fabry disease urinary globotriaosylceramide/creatinine biomarker evaluation by liquid chromatography–tandem mass spectrometry in healthy infants from birth to 6months
  24. Influence of cytosine methylation on ultraviolet-induced cyclobutane pyrimidine dimer formation in genomic DNA
  25. P53 transcriptional activities: A general overview and some thoughts
  26. In Cellulo DNA Analysis (LMPCR Footprinting)
  27. Postprandial free fatty acids metabolism early in the natural history of type 2 diabetes mellitus
  28. Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord
  29. Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry disease
  30. High-resolution R-banding at the 1250-band level
  31. Application of Multi-PRINS to Simultaneously Identify Chromosomes 18, X, and Y in Prenatal Diagnosis
  32. Postprandial Free Fatty Acids (FFA) Metabolism Early in the Natural History of Type 2 Diabetes Mellitus (DM2)
  33. 74 Development of a filter paper method applicable to a mass urinary screening for Fabry disease
  34. Repair kinetics of specific types of nitroso-induced DNA damage using the comet assay in human cells
  35. In vivo footprinting analysis of the Glypican 3 (GPC3) promoter region in neuroblastoma cells
  36. Pyrimidine (6–4) Pyrimidone Photoproduct Mapping After Sublethal UVC Doses: Nucleotide Resolution Using Terminal Transferase‐dependent PCR
  37. Formamidopyrimidine adducts are detected using the comet assay in human cells treated with reactive metabolites of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)
  38. Activité dominante négative des protéines p53 mutées
  39. A GC/MS validated method for the nanomolar range determination of succinylacetone in amniotic fluid and plasma: An analytical tool for tyrosinemia type I
  40. From DNA Photolesions to Mutations, Skin Cancer and Cell Death
  41. SW480, a p53 Double-mutant Cell Line Retains Proficiency for Some p53 Functions
  42. In vivo DNase I-mediated footprinting analysis along the human bradykinin B1 receptor ( BDKRB1 ) gene promoter: evidence for cell-specific regulation
  43. Optimal conditions and specific characteristics ofVentexo– DNA polymerase in ligation-mediated polymerase chain reaction protocols
  44. Characterization of the survival motor neuron (SMN) promoter provides evidence for complex combinatorial regulation in undifferentiated and differentiated P19 cells
  45. Increased frequency of multiradial chromosome structures in mouse embryonic fibroblasts lacking functional Werner syndrome protein and poly(ADP-ribose) polymerase-1
  46. Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniques
  47. An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22
  48. De la conception du PRINS à son couronnement
  49. Genetic Cooperation between the Werner Syndrome Protein and Poly(ADP-Ribose) Polymerase-1 in Preventing Chromatid Breaks, Complex Chromosomal Rearrangements, and Cancer in Mice
  50. Mouse telomere analysis using an optimized primed in situ (PRINS) labeling technique
  51. A unique clone involving multiple structural chromosome rearrangements in a myelodysplastic syndrome case
  52. Evidence that extrachromosomal double-strand break repair can be coupled to the repair of chromosomal double-strand breaks in mammalian cells
  53. Human cells bearing homozygous mutations in the DNA mismatch repair genes hMLH1 or hMSH2 are fully proficient in transcription-coupled nucleotide excision repair
  54. A physical sunscreen protects engineered human skin against artificial solar ultraviolet radiation-induced tissue and DNA damage
  55. Characterization and mapping of DNA damage induced by reactive metabolites of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) at nucleotide resolution in human genomic DNA
  56. Repeated exposures of human skin equivalent to low doses of ultraviolet-B radiation lead to changes in cellular functions and accumulation of cyclobutane pyrimidine dimers
  57. Alkylating agent and chromatin structure determine sequence context-dependent formation of alkylpurines11Edited by I. Tinoco
  58. Tetrasomy 8 is associated with a major cellular proliferative advantage and a poor prognosis
  59. Creating a new color by omission of 3′ end blocking step for simultaneous detection of different chromosomes in multi-PRINS technique
  60. Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling, fluorescence in situ hybridization, and conventional cytogenetic analyses.
  61. Establishment and Characterization of a New Cell Line Derived from a Human Primary Breast Carcinoma
  62. Treatment of Human Cells with N-Nitroso(acetoxymethyl)methylamine:  Distribution Patterns of Piperidine-Sensitive DNA Damage at the Nucleotide Level of Resolution Are Related to the Sequence Context
  63. Physiological and Cytogenetic Characterization of Immortalized Human Endometriotic Cells Containing Episomal Simian Virus 40 DNA
  64. Mapping Reactive Oxygen-Induced DNA Damage at Nucleotide Resolution
  65. ABC50, a Novel Human ATP-Binding Cassette Protein Found in Tumor Necrosis Factor-α-Stimulated Synoviocytes
  66. Chemical inactivators as sterilization agents for bovine collagen materials
  67. UVB‐induced Cyclobutane Pyrimidine Dimer Frequency Correlates with Skin Cancer Mutational Hotspots in p53
  68. A Hot Spot for Hydrogen Peroxide-Induced Damage in the Human Hypoxia-Inducible Factor 1 Binding Site of thePGK 1Gene
  69. Agarose Gel Electrophoresis for DNA Damage Analysis
  70. Ligation-Mediated PCR for Analysis of Oxidative DNA Damage
  71. Cupric ion/ascorbate/hydrogen peroxide-induced DNA damage: DNA-bound copper ion primarily induces base modifications
  72. High-Resolution Replication Bands Compared with Morphologic G- and R-bands
  73. Detection of DNA adducts at the DNA sequence level by ligation-mediated PCR
  74. Detection by electron microscopy of a small subband 13q14.11 deletion in an hereditary retinoblastoma
  75. Analysis of DNA replication during S-phase by means of dynamic chromosome banding at high resolution
  76. High-resolution R-banding at the 1250-band level. II. Schematic representation and nomenclature of human RBG-banded chromosomes
  77. Idiograms of horse chromosomes at prometaphase, early metaphase, and midmetaphase after R-banding by BrdU incorporation followed by the fluorochrome–photolysis–Giemsa technique
  78. In Vivo DNA Analysis
  79. New Rapid Multicolor PRINS Protocol
  80. Dual-Color PRINS for <i>In Situ</i> Detection of Fetal Cells in Maternal Blood