All Stories

  1. EZH2 Cooperates with DNA Methylation to Downregulate Key Tumor Suppressors and IFN Gene Signatures in Melanoma
  2. A MicroRNA Cluster in the DLK1-DIO3 Imprinted Region on Chromosome 14q32.2 Is Dysregulated in Metastatic Hepatoblastomas
  3. Genomic and signalling pathway characterization of the NZM panel of melanoma cell lines: A valuable model for studying the impact of genetic diversity in melanoma
  4. Lipid and Polymer-Based Nanoparticle siRNA Delivery Systems for Cancer Therapy
  5. Reawakening the Developmental Origins of Cancer Through Transposable Elements
  6. Promoter DNA Hypermethylation and Paradoxical Gene Activation
  7. Extensive Inter-Cyst DNA Methylation Variation in Autosomal Dominant Polycystic Kidney Disease Revealed by Genome Scale Sequencing
  8. Designing phantoms to accurately replicate circular depolarization in biological scattering media
  9. Targeted Therapies for Autosomal Dominant Polycystic Kidney Disease
  10. Characterisation of DNA methylation changes in EBF3 and TBC1D16 associated with tumour progression and metastasis in multiple cancer types
  11. Genome-wide miRNA methylome analysis in oral cancer: possible biomarkers associated with patient survival
  12. Targeting DNA Methylation and EZH2 Activity to Overcome Melanoma Resistance to Immunotherapy
  13. MIS416 as a siRNA Delivery System with the Ability to Target Antigen-Presenting Cells
  14. Marked Global DNA Hypomethylation Is Associated with Constitutive PD-L1 Expression in Melanoma
  15. SMAD proteins directly suppressPAX2transcription downstream of transforming growth factor-beta 1 (TGF-β1) signalling in renal cell carcinoma
  16. Genome-Scale Single Nucleotide Resolution Analysis of DNA Methylation in Human Autosomal Dominant Polycystic Kidney Disease
  17. A Guide for Designing and Analyzing RNA-Seq Data
  18. The Genes of Life and Death: A Potential Role for Placental-Specific Genes in Cancer
  19. Identifying drivers of metastasis; towards a systematic approach
  20. A streamlined method for analysing genome-wide DNA methylation patterns from low amounts of FFPE DNA
  21. Epigenetic drivers of tumourigenesis and cancer metastasis
  22. Comparative assessment of DNA methylation patterns between reduced representation bisulfite sequencing and Sequenom EpiTyper methylation analysis
  23. The Slow Cycling Phenotype: A Growing Problem for Treatment Resistance in Melanoma
  24. An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations
  25. PAX2 (Paired box gene 2)
  26. MicroRNA expression patterns and signalling pathways in the development and progression of childhood solid tumours
  27. Genome-wide methylation sequencing of paired primary and metastatic cell lines identifies common DNA methylation changes and a role for EBF3 as a candidate epigenetic driver of melanoma metastasis
  28. Tools and Strategies for Analysis of Genome-Wide and Gene-Specific DNA Methylation Patterns
  29. Repression of CMIP transcription by WT1 is relevant to podocyte health
  30. scan_tcga tools for integrated epigenomic and transcriptomic analysis of tumor subgroups
  31. The Paired Box (PAX) Gene Family: Introduction to Paired Box Genes
  32. PAX2 and the Renal-Coloboma Syndrome
  33. Faculty of 1000 evaluation for Primary cilia are not calcium-responsive mechanosensors.
  34. NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand
  35. Bridging Small Molecules to Modified Bacterial Microparticles Using a Disulphide Linkage: MIS416 as a Cargo Delivery System
  36. Multi-platform microRNA profiling of hepatoblastoma patients using formalin fixed paraffin embedded archival samples
  37. Erratum: A cross comparison of technologies for the detection of microRNAs in clinical FFPE samples of hepatoblastoma patients
  38. Large animal models of rare genetic disorders: sheep as phenotypically relevant models of human genetic disease
  39. A cross comparison of technologies for the detection of microRNAs in clinical FFPE samples of hepatoblastoma patients
  40. DNA methylation and epigenomics: new technologies and emerging concepts
  41. Correction: G-Quadruplex Structures and CpG Methylation Cause Drop-Out of the Maternal Allele in Polymerase Chain Reaction Amplification of the Imprinted MEST Gene Promoter
  42. G-Quadruplex Structures and CpG Methylation Cause Drop-Out of the Maternal Allele in Polymerase Chain Reaction Amplification of the Imprinted MEST Gene Promoter
  43. Application of circularly polarized light for non-invasive diagnosis of cancerous tissues and turbid tissue-like scattering media
  44. Polycystic kidney disease – where gene dosage counts
  45. Diffusing-wave polarimetry for tissue diagnostics
  46. Faculty Opinions recommendation of Multilocus polycystic disease.
  47. Melanoma genetics/genomics
  48. Increased paired box transcription factor 8 has a survival function in Glioma
  49. Biallelic DICER1 mutations occur in Wilms tumours
  50. Screening Cancer Aggressiveness by Using Circularly Polarized Light
  51. Melanoma Genetics/Genomics
  52. Targeted Therapy; From Advanced Melanoma to the Adjuvant Setting
  53. MITF and PAX3 Play Distinct Roles in Melanoma Cell Migration; Outline of a “Genetic Switch” Theory Involving MITF and PAX3 in Proliferative and Invasive Phenotypes of Melanoma
  54. Cohesin Is Required for Activation of MYC by Estradiol
  55. Primary cilia defects in the polycystic kidneys from an ovine model of Meckel Gruber syndrome
  56. Feasibility of preventing of renal cyst formation in utero studied in mice
  57. PAX2 is an antiapoptotic molecule with deregulated expression in medulloblastoma
  58. Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database
  59. The Mapping of Tissues Scattering Properties on the Poincaré Sphere
  60. Senescence Associated �-galactosidase Staining
  61. PAX Genes in Cancer; Friends or Foes?
  62. Somatic Reactivation of Expression of the Silent Maternal Mest Allele and Acquisition of Normal Reproductive Behaviour in a Colony of Peg1/Mest Mutant Mice
  63. PAX8 promotes tumor cell growth by transcriptionally regulating E2F1 and stabilizing RB protein
  64. Abstract 2940: A role for PAX8 in promoting tumor cell type-specific proliferation through positively regulating E2F1 transcription and stabilizing RB protein
  65. Clinical utility gene card for: renal coloboma (Papillorenal) syndrome
  66. PAX3 knockdown in metastatic melanoma cell lines does not reduce MITF expression
  67. PAX3 Is Extensively Expressed in Benign and Malignant Tissues of the Melanocytic Lineage in Humans
  68. A Gene Expression Signature of Invasive Potential in Metastatic Melanoma Cells
  69. Expression of cohesin and condensin genes during zebrafish development supports a non-proliferative role for cohesin
  70. PAX3 is Expressed in the Stromal Compartment of the Developing Kidney and in Wilms Tumors with Myogenic Phenotype
  71. Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease
  72. PAX8 Regulates Telomerase Reverse Transcriptase and Telomerase RNA Component in Glioma
  73. Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies
  74. In vivo validation of PAX2 as a target for renal cancer therapy
  75. Self-RegulatedPaxGene Expression and Modulation by the TGFβ Superfamily
  76. Disruption of ROBO2 Is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux
  77. A novel Cys1638Tyr NC1 domain substitution in  5(IV) collagen causes Alport syndrome with late onset renal failure without hearing loss or eye abnormalities
  78. Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease
  79. Correction to "PAX2 inactivation enhances cisplatin-induced apoptosis in renal carcinoma cells"
  80. Neuronal apoptosis inhibitory protein is expressed in developing kidney and is regulated by PAX2
  81. Suppression of Ureteric Bud Apoptosis Rescues Nephron Endowment and Adult Renal Function inPax2Mutant Mice
  82. PAX2 inactivation enhances cisplatin-induced apoptosis in renal carcinoma cells
  83. A PANorama of PAX genes in cancer and development
  84. Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome
  85. Congenital polycystic kidney disease in lambs
  86. Corrigendum to: Conjugate for efficient delivery of short interfering RNA (siRNA) into mammalian cells (FEBS 28019) [FEBS Letters 558 (2004) 63-68]
  87. Conjugate for efficient delivery of short interfering RNA (siRNA) into mammalian cells
  88. Delivery of antisense peptide nucleic acids (PNAs) to the cytosol by disulphide conjugation to a lipophilic cation
  89. Paired-Box genes are frequently expressed in cancer and often required for cancer cell survival
  90. PAX2 and Renal-Coloboma Syndrome
  91. Embryonal hyperplasia of Bowman's capsular epithelium in patients with WT1 mutations
  92. PAX2 mutations in renal–coloboma syndrome: mutational hotspot and germline mosaicism
  93. PAX2 Suppresses Apoptosis in Renal Collecting Duct Cells
  94. Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutations
  95. The role of PAX2 in normal and abnormal development of the urinary tract
  96. Cloning and Characterization of the HumanPAX2Promoter
  97. Unravelling the genetics of vesicoureteric reflux: a common familial disorder
  98. Genomic Structure of the HumanPAX2Gene
  99. Erratum: Corrigendum: Mutation of the gene in a family with optic nerve colobomas, renal anomolies and vesicoureteral reflux
  100. Mutation of PAX2 in two siblings with renal-coloboma syndrome
  101. Erratum: Corrigendum: Jackson–Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
  102. Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
  103. Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
  104. Genes encoding the platelet-derived growth factor (PDGF) receptor and colony-stimulating factor 1 (CSF-1) receptor are physically associated in mice as in humans
  105. Studies of Secondary Transforming Events in Murine c-myc Retrovirus-Induced Monocyte Tumors
  106. Expression of insulin-like growth factor-II transcripts in Wilms' tumour
  107. Harvey-ras allele deletion detected by in situ hybridization to Wilms' tumor chromosomes