All Stories

  1. BMP4 and Temozolomide Synergize in the Majority of Patient-Derived Glioblastoma Cultures
  2. Butyrate selectively targets super-enhancers and transcriptional networks associated with human mast cell function
  3. Human Pluripotent Stem Cell-Derived Astrocyte Functionality Compares Favorably with Primary Rat Astrocytes
  4. Genome-wide methylation analysis in patients with proximal hypospadias – a pilot study and review of the literature
  5. A cellular reporter system to evaluate endogenous fetal hemoglobin induction and screen for therapeutic compounds
  6. The Cellular Origin of the Pulmonary Pericyte
  7. DNA methylation database for gynecological cancer detection, classification and assay development
  8. Epigenomic partitioning of a polygenic risk score for asthma reveals distinct genetically driven disease pathways
  9. Unraveling the impact of AXIN1 mutations on HCC development: Insights from CRISPR/Cas9 repaired AXIN1-mutant liver cancer cell lines
  10. Epigenetic and Genomic Hallmarks of PARP-Inhibitor Resistance in Ovarian Cancer Patients
  11. Split Pool Ligation-based Single-cell Transcriptome sequencing (SPLiT-seq) data processing pipeline comparison
  12. Species-specific responses during Seoul orthohantavirus infection in human and rat lung microvascular endothelial cells
  13. Distinctive cell‐free DNA methylation characterizes presymptomatic genetic frontotemporal dementia
  14. Runx1+ vascular smooth muscle cells are essential for hematopoietic stem and progenitor cell development in vivo
  15. A three-dimensional vessel-on-chip model to study Puumala orthohantavirus pathogenesis
  16. Comparison of Single Cell Transcriptome Sequencing Methods: Of Mice and Men
  17. Single-Cell RNA Sequencing of Donor-Reactive T Cells Reveals Role of Apoptosis in Donor-Specific Hyporesponsiveness of Kidney Transplant Recipients
  18. Liquid Biopsies for Colorectal Cancer and Advanced Adenoma Screening and Surveillance: What to Measure?
  19. Phenotypic differences in resistance to thyroid hormone alpha: differential recruitment of cofactors by thyroid hormone receptor alpha 1 mutants
  20. Mutation Analysis of Pancreatic Juice and Plasma for the Detection of Pancreatic Cancer
  21. 3D chromatin reprogramming primes human memory T H 2 cells for rapid recall and pathogenic dysfunction
  22. Targeted Genomic Sequencing of TSC1 and TSC2 Reveals Causal Variants in Individuals for Whom Previous Genetic Testing for Tuberous Sclerosis Complex Was Normal
  23. Machine learning-based somatic variant calling in cell-free DNA of metastatic breast cancer patients using large NGS panels
  24. PD-L1 checkpoint blockade promotes regulatory T cell activity that underlies therapy resistance
  25. Genome-wide analysis toward the epigenetic aetiology of myelodysplastic syndrome disease progression and pharmacoepigenomic basis of hypomethylating agents drug treatment response
  26. Zeb2 DNA-Binding Sites in Neuroprogenitor Cells Reveal Autoregulation and Affirm Neurodevelopmental Defects, Including in Mowat-Wilson Syndrome
  27. Retrospective analysis of enhancer activity and transcriptome history
  28. Exploring the Interspecific Interactions and the Metabolome of the Soil Isolate Hylemonella gracilis
  29. Rabies virus uniquely reprograms the transcriptome of human monocyte-derived macrophages
  30. CABA-V7: a prospective biomarker selected trial of cabazitaxel treatment in AR-V7 positive prostate cancer patients
  31. USP7 regulates the ncPRC1 Polycomb axis to stimulate genomic H2AK119ub1 deposition uncoupled from H3K27me3
  32. A kinase inhibitor screen reveals MEK1/2 as a novel therapeutic target to antagonize IGF1R-mediated antiestrogen resistance in ERα-positive luminal breast cancer
  33. Bio-distribution and longevity of mesenchymal stromal cell derived membrane particles
  34. Molecular and behavioral consequences of Ube3a gene overdosage in mice
  35. Effect of bovine milk fat-based infant formulae on microbiota, metabolites and stool parameters in healthy term infants in a randomized, crossover, placebo-controlled trial
  36. Rapid specification of human pluripotent stem cells to functional astrocytes
  37. Identification of candidate enhancers controlling the transcriptome during the formation of interphalangeal joints
  38. A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson’s disease with dementia
  39. PDGFRβ+ cells play a dual role as hematopoietic precursors and niche cells during mouse ontogeny
  40. Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophy
  41. JMJD3 intrinsically disordered region links the 3D-genome structure to TGFβ-dependent transcription activation
  42. Comparative single-cell RNA-sequencing profiling of BMP4-treated primary glioma cultures reveals therapeutic markers
  43. CRISPRs in the human genome are differentially expressed between malignant and normal adjacent to tumor tissue
  44. Temozolomide and Radiotherapy versus Radiotherapy Alone in Patients with Glioblastoma, IDH-wildtype: Post Hoc Analysis of the EORTC Randomized Phase III CATNON Trial
  45. Genetic and epigenetic determinants of reactivation of Mecp2 and the inactive X chromosome in neural stem cells
  46. Kidney Organoids Are Capable of Forming Tumors, but Not Teratomas
  47. NOXA expression drives synthetic lethality to RUNX1 inhibition in pancreatic cancer
  48. Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge
  49. Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts
  50. Genome-wide aberrant methylation in primary metastatic UM and their matched metastases
  51. Combined Analysis of Transcriptome and T-Cell Receptor Alpha and Beta (TRA/TRB) Repertoire in Paucicellular Samples at the Single-Cell Level
  52. Multi-Omics Profiling in Marfan Syndrome: Further Insights into the Molecular Mechanisms Involved in Aortic Disease
  53. SPEN is required for Xist upregulation during initiation of X chromosome inactivation
  54. The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a Model
  55. The tumor suppressor MIR139 is silenced by POLR2M to promote AML oncogenesis
  56. RMplex: An efficient method for analyzing 30 Y-STRs with high mutation rates
  57. High-throughput and affordable genome-wide methylation profiling of circulating cell-free DNA by methylated DNA sequencing (MeD-seq) of LpnPI digested fragments
  58. Heritability and De Novo Mutations in Oesophageal Atresia and Tracheoesophageal Fistula Aetiology
  59. Enhancer-associated H3K4 methylation safeguards in vitro germline competence
  60. Identification of SPRY4 as a Novel Candidate Susceptibility Gene for Familial Nonmedullary Thyroid Cancer
  61. CTCF chromatin residence time controls three-dimensional genome organization, gene expression and DNA methylation in pluripotent cells
  62. Genome wide DNA methylation analysis of alveolar capillary dysplasia lung tissue reveals aberrant methylation of genes involved in development including the FOXF1 locus
  63. High throughput and affordable genome-wide methylation profiling of circulating cell-free DNA by Methylated DNA sequencing (MeD-seq) of LpnPI digested fragments
  64. Zeb2 DNA-binding sites in neuroprogenitor cells reveal autoregulation and affirm neurodevelopmental defects, including in Mowat-Wilson Syndrome
  65. Orphan CpG islands amplify poised enhancer regulatory activity and determine target gene responsiveness
  66. Molecular analysis of the erythroid phenotype of a patient with BCL11A haploinsufficiency
  67. Selective cell death in HIV-1-infected cells by DDX3 inhibitors leads to depletion of the inducible reservoir
  68. Prognostic significance of genome-wide DNA methylation profiles within the randomized, phase 3, EORTC CATNON trial on non-1p/19q deleted anaplastic glioma
  69. Endothelial Zeb2 preserves the hepatic angioarchitecture and protects against liver fibrosis
  70. Forkhead Box F1 as a mediator of Wnt signaling in human lung endothelial cells
  71. Interplay between FLI-1 and the LDB1 complex in murine erythroleukemia cells and during megakaryopoiesis
  72. Genetic and epigenetic determinants of reactivation of Mecp2 and the inactive X chromosome in neural stem cells
  73. Exploring the interspecific interactions and the metabolome of the soil isolateHylemonella gracilis
  74. Steroid-resistant human inflammatory ILC2s are marked by CD45RO and elevated in type 2 respiratory diseases
  75. CirculatingTP53mutations are associated with early tumor progression and poor survival in pancreatic cancer patients treated with FOLFIRINOX
  76. Low Input Targeted Chromatin Capture (Low-T2C)
  77. SPEN is Required forXistUpregulation during Initiation of X Chromosome Inactivation
  78. Comparison of the PU.1 transcriptional regulome and interactome in human and mouse inflammatory dendritic cells
  79. The Bone-Forming Properties of Periosteum-Derived Cells Differ Between Harvest Sites
  80. Histological, immunohistochemical and transcriptomic characterization of human tracheoesophageal fistulas
  81. Alveolar barrier disruption in varicella pneumonia is associated with neutrophil extracellular trap formation
  82. Differentially Methylated Regions in Desmoid-Type Fibromatosis: A Comparison Between CTNNB1 S45F and T41A Tumors
  83. Validation of a Combined Transcriptome and T Cell Receptor Alpha/Beta (TRA/TRB) Repertoire Assay at the Single Cell Level for Paucicellular Samples
  84. Induction of selective cell death in HIV-1-infected cells by DDX3 inhibitors leads to depletion of the inducible reservoir
  85. Gliotoxin, identified from a screen of fungal metabolites, disrupts 7SK snRNP, releases P-TEFb, and reverses HIV-1 latency
  86. Hemolysis in the spleen drives erythrocyte turnover
  87. Orphan CpG islands boost the regulatory activity of poised enhancers and dictate the responsiveness of their target genes
  88. Targeted chromatin conformation analysis identifies novel distal neural enhancers of ZEB2 in pluripotent stem cell differentiation
  89. p53 drives premature neuronal differentiation in response to radiation-induced DNA damage during early neurogenesis
  90. Rapid in vitro generation of bona fide exhausted CD8+ T cells is accompanied by Tcf7 promotor methylation
  91. In vitro capture and characterization of embryonic rosette-stage pluripotency between naive and primed states
  92. MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange Syndrome
  93. Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length
  94. Butyrate inhibits human mast cell activation via epigenetic regulation of FcεRI‐mediated signaling
  95. Infantile hypertrophic pyloric stenosis in patients with esophageal atresia
  96. Notch signaling licenses allergic airway inflammation by promoting Th2 cell lymph node egress
  97. Redundant and specific roles of cohesin STAG subunits in chromatin looping and transcriptional control
  98. Cystic renal-epithelial derived induced pluripotent stem cells from polycystic kidney disease patients
  99. MicroRNA expression and DNA methylation profiles do not distinguish between primary and recurrent well-differentiated liposarcoma
  100. Multifaceted actions of Zeb2 in postnatal neurogenesis from the ventricular-subventricular zone to the olfactory bulb
  101. CREPT Promotes Melanoma Progression Through Accelerated Proliferation and Enhanced Migration by RhoA-Mediated Actin Filaments and Focal Adhesion Formation
  102. Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
  103. Characterization of the ferret TRB locus guided by V, D, J, and C gene expression analysis
  104. G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population
  105. Gliotoxin, identified from a screen of fungal metabolites, disrupts 7SK snRNP, releases P-TEFb and reverses HIV-1 latency
  106. Hemolysis in the Spleen Drives Erythrocyte Turnover
  107. Distinct IL‐1α‐responsive enhancers promote acute and coordinated changes in chromatin topology in a hierarchical manner
  108. Pathogen-induced activation of disease-suppressive functions in the endophytic root microbiome
  109. Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform specific start-loss mutations of essential genes can cause genetic diseases
  110. Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family
  111. The presence of CLL-associated stereotypic B cell receptors in the normal BCR repertoire from healthy individuals increases with age
  112. A functional variant in the miR‐142 promoter modulating its expression and conferring risk of Alzheimer disease
  113. PDGFRB SIGNALING IS REQUIRED TO GENERATE AORTIC HAEMATOPOIETIC CELLS IN VIVO
  114. Publisher Correction: Mediator complex interaction partners organize the transcriptional network that defines neural stem cells
  115. Lewy pathology in Parkinson’s disease consists of crowded organelles and lipid membranes
  116. Mediator complex interaction partners organize the transcriptional network that defines neural stem cells
  117. Engram-specific transcriptome profiling of contextual memory consolidation
  118. Redundant and specific roles of cohesin STAG subunits in chromatin looping and transcription control
  119. Models for infantile hypertrophic pyloric stenosis development in patients with esophageal atresia
  120. Modeling the Pathological Long-Range Regulatory Effects of Human Structural Variation with Patient-Specific hiPSCs
  121. The mouse KLF1 Nan variant impairs nuclear condensation and erythroid maturation
  122. Distinct Functions for Mammalian CLASP1 and -2 During Neurite and Axon Elongation
  123. MAU2 and NIPBL variants in Cornelia de Lange syndrome reveal MAU2-independent loading of cohesin and uncover a protective mechanism against early truncating mutations in NIPBL
  124. Epigenome analysis links gene regulatory elements in group 2 innate lymphocytes to asthma susceptibility
  125. The mouse Klf1 Nan variant impairs nuclear condensation and erythroid maturation
  126. PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability
  127. Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness
  128. Progression of ductal carcinoma in situ to invasive breast cancer: comparative genomic sequencing
  129. Mitotic progression, arrest, exit or death relies on centromere structural integrity, rather than de novo transcription
  130. LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
  131. Colony-Stimulating Factor 1 Receptor (CSF1R) Regulates Microglia Density and Distribution, but Not Microglia Differentiation In Vivo
  132. Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease
  133. Large-Scale Expansion of Human iPSC-Derived Skeletal Muscle Cells for Disease Modeling and Cell-Based Therapeutic Strategies
  134. Employed family-based genetic discovery combining linkage analysis and exome sequencing to identify RCL1 as a novel candidate gene for depression, with independent replication in a population-based cohort
  135. Mitotic progression, arrest, exit or death is determined by centromere integrity and independent of de novo transcription
  136. ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia
  137. Analysis of Mouse Brain Transcriptome After Experimental Duvenhage Virus Infection Shows Activation of Innate Immune Response and Pyroptotic Cell Death Pathway
  138. Nimbus: a design-driven analyses suite for amplicon-based NGS data
  139. SNPitty
  140. Investigation of the spatial structure and interactions of the genome at sub-kilobase-pair resolution using T2C
  141. Sensitive detection of mitochondrial DNA variants for analysis of mitochondrial DNA-enriched extracts from frozen tumor tissue
  142. Allele-specific long-distance regulation dictates IL-32 isoform switching and mediates susceptibility to HIV-1
  143. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome
  144. UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia
  145. Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer element
  146. Genome-wide DNA methylation profiling using the methylation-dependent restriction enzyme LpnPI
  147. Group 2 Innate Lymphoid Cells Exhibit a Dynamic Phenotype in Allergic Airway Inflammation
  148. Germline variant in MSX1 identified in a Dutch family with clustering of Barrett’s esophagus and esophageal adenocarcinoma
  149. Thyroid State Regulates Gene Expression in Human Whole Blood
  150. Exome-Wide Meta-Analysis Identifies Rare 3′-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea
  151. Immune Repertoire after Immunization As Seen by Next-Generation Sequencing and Proteomics
  152. Transcriptomic Analyses Reveal Differential Gene Expression of Immune and Cell Death Pathways in the Brains of Mice Infected with West Nile Virus and Chikungunya Virus
  153. DOC1-Dependent Recruitment of NURD Reveals Antagonism with SWI/SNF during Epithelial-Mesenchymal Transition in Oral Cancer Cells
  154. Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
  155. The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies
  156. Cell lines generated from a chronic lymphocytic leukemia mouse model exhibit constitutive Btk and Akt signaling
  157. Lewy pathology in Parkinson’s disease consists of a crowded organellar, membranous medley
  158. PRC2 Facilitates the Regulatory Topology Required for Poised Enhancer Function during Pluripotent Stem Cell Differentiation
  159. Fungal volatile compounds induce production of the secondary metabolite Sodorifen in Serratia plymuthica PRI-2C
  160. An interaction network of mental disorder proteins in neural stem cells
  161. Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations
  162. A rare missense variant in RCL1 segregates with depression in extended families
  163. Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice
  164. Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes
  165. Targeted Apoptosis of Senescent Cells Restores Tissue Homeostasis in Response to Chemotoxicity and Aging
  166. Exploiting native forces to capture chromosome conformation in mammalian cell nuclei
  167. The detailed 3D multi-loop aggregate/rosette chromatin architecture and functional dynamic organization of the human and mouse genomes
  168. Unbiased Interrogation of 3D Genome Topology Using Chromosome Conformation Capture Coupled to High-Throughput Sequencing (4C-Seq)
  169. Transcriptome assists prognosis of disease severity in respiratory syncytial virus infected infants
  170. Zeb2 Regulates Cell Fate at the Exit from Epiblast State in Mouse Embryonic Stem Cells
  171. GATA1-Deficient Dendritic Cells Display Impaired CCL21-Dependent Migration toward Lymph Nodes Due to Reduced Levels of Polysialic Acid
  172. Comparison of Mycoplasma pneumoniae Genome Sequences from Strains Isolated from Symptomatic and Asymptomatic Patients
  173. Decreased IL7Rα and TdT expression underlie the skewed immunoglobulin repertoire of human B-cell precursors from fetal origin
  174. Binding of nuclear factor κB to noncanonical consensus sites reveals its multimodal role during the early inflammatory response
  175. Human age estimation from blood using mRNA, DNA methylation, DNA rearrangement, and telomere length
  176. Overexpression of LMO2 causes aberrant human T-Cell development in vivo by three potentially distinct cellular mechanisms
  177. Genomes of Ellobius species provide insight into the evolutionary dynamics of mammalian sex chromosomes
  178. Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms
  179. Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
  180. Genetic variants in RBFOX3 are associated with sleep latency
  181. Inefficient DNA Repair Is an Aging-Related Modifier of Parkinson’s Disease
  182. Paroxysmal exercise-induced dystonia within the phenotypic spectrum ofECHS1deficiency
  183. Effects of Freeze–Thawing and Intravenous Infusion on Mesenchymal Stromal Cell Gene Expression
  184. BMP and Hedgehog Regulate Distinct AGM Hematopoietic Stem Cells Ex Vivo
  185. Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis
  186. Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy
  187. ACTG2variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
  188. Control of developmentally primed erythroid genes by combinatorial co-repressor actions
  189. miR-634 restores drug sensitivity in resistant ovarian cancer cells by targeting the Ras-MAPK pathway
  190. Erratum: Corrigendum: BMP signalling differentially regulates distinct haematopoietic stem cell types
  191. Nuclear positioning rather than contraction controls ordered rearrangements of immunoglobulin loci
  192. Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects
  193. The Isl1/Ldb1 Complex Orchestrates Genome-wide Chromatin Organization to Instruct Differentiation of Multipotent Cardiac Progenitors
  194. BMP signalling differentially regulates distinct haematopoietic stem cell types
  195. The core spliceosome as target and effector of non-canonical ATM signalling
  196. DC immunotherapy in HIV-1 infection induces a major blood transcriptome shift
  197. Proteins that bind regulatory regions identified by histone modification chromatin immunoprecipitations and mass spectrometry
  198. Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up
  199. Allogeneic Mature Human Dendritic Cells Generate Superior Alloreactive Regulatory T Cells in the Presence of IL-15
  200. A New CRB1 Rat Mutation Links Müller Glial Cells to Retinal Telangiectasia
  201. Incomplete meiotic sex chromosome inactivation in the domestic dog
  202. PLD3 variants in population studies
  203. Correction: Hypoxia Inducible Factor 3α Plays a Critical Role in Alveolarization and Distal Epithelial Cell Differentiation during Mouse Lung Development
  204. Time since Onset of Disease and Individual Clinical Markers Associate with Transcriptional Changes in Uncomplicated Dengue
  205. Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations
  206. Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects
  207. Global quantitative proteomics reveals novel factors in the ecdysone signaling pathway inDrosophila melanogaster
  208. Deciphering the RNA landscape by RNAome sequencing
  209. Endogenous WNT Signals Mediate BMP-Induced and Spontaneous Differentiation of Epiblast Stem Cells and Human Embryonic Stem Cells
  210. Whole-transcriptome analysis of endothelial to hematopoietic stem cell transition reveals a requirement for Gpr56 in HSC generation
  211. Sp1/Sp3 transcription factors regulate hallmarks of megakaryocyte maturation and platelet formation and function
  212. Gene reprogramming in exercise-induced cardiac hypertrophy in swine: A transcriptional genomics approach
  213. Regulated genes in psoriatic skin during treatment with fumaric acid esters
  214. The dystrophin gene and cognitive function in the general population
  215. Identification of microRNAs in Human Plasma
  216. Ovarian Cancer Cell Line Panel (OCCP): Clinical Importance of In Vitro Morphological Subtypes
  217. Analysis of the transcriptome and immune function of monocytes during IFNα-based therapy in chronic HCV revealed induction of TLR7 responsiveness
  218. SF3B1 and EIF1AX mutations in uveal melanoma: a protective factor, or not?
  219. Gene Expression Profiling To Predict and Assess the Consequences of Therapy-Induced Virus Eradication in Chronic Hepatitis C Virus Infection
  220. MicroRNA response to hypoxic stress in soft tissue sarcoma cells: microRNA mediated regulation of HIF3α
  221. Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma
  222. HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers
  223. Pre-B Cell Receptor Signaling Induces Immunoglobulin κ Locus Accessibility by Functional Redistribution of Enhancer-Mediated Chromatin Interactions
  224. Two independent transcription initiation codes overlap on vertebrate core promoters
  225. A Cohesin-Independent Role for NIPBL at Promoters Provides Insights in CdLS
  226. MicroRNA expression profiles distinguish liposarcoma subtypes and implicate miR-145 and miR-451 as tumor suppressors
  227. In vivo murine hepatic microRNA and mRNA expression signatures predicting the (non-)genotoxic carcinogenic potential of chemicals
  228. Gene Expression Analysis Reveals Inhibition of Radiation-Induced TGFβ-Signaling by Hyperbaric Oxygen Therapy in Mouse Salivary Glands
  229. Targeted Chromatin Capture (T2C): a novel high resolution high throughput method to detect genomic interactions and regulatory elements
  230. DNA damage responsive microRNAs misexpressed in human cancer modulate therapy sensitivity
  231. Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells
  232. Gene Expression Analysis of Peripheral Cells for Subclassification of Pediatric Inflammatory Bowel Disease in Remission
  233. BACH2: A marker of DNA damage and ageing
  234. Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation–differentiation balance early in life and optic nerve degeneration at old age
  235. Developmental and Activity-Dependent miRNA Expression Profiling in Primary Hippocampal Neuron Cultures
  236. Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model
  237. Histone Chaperone NAP1 Mediates Sister Chromatid Resolution by Counteracting Protein Phosphatase 2A
  238. Dynamic regulation of the transcription initiation landscape at single nucleotide resolution during vertebrate embryogenesis
  239. MiR-17-92 and miR-221/222 cluster members target KIT and ETV1 in human gastrointestinal stromal tumours
  240. Genome-wide, whole mount in situ analysis of transcriptional regulators in zebrafish embryos
  241. Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia
  242. Balancing of Histone H3K4 Methylation States by the Kdm5c/SMCX Histone Demethylase Modulates Promoter and Enhancer Function
  243. In vivo live imaging of RNA polymerase II transcription factories in primary cells
  244. Canonical Wnt Signaling Induces a Primitive Endoderm Metastable State in Mouse Embryonic Stem Cells
  245. Small Hydrophobic Protein of Human Metapneumovirus Does Not Affect Virus Replication and Host Gene Expression In Vitro
  246. Early divergence of Th1 and Th2 transcriptomes involves a small core response and sets of transiently expressed genes
  247. Hypoxia Inducible Factor 3α Plays a Critical Role in Alveolarization and Distal Epithelial Cell Differentiation during Mouse Lung Development
  248. Multiplexed chromosome conformation capture sequencing for rapid genome-scale high-resolution detection of long-range chromatin interactions
  249. Genome-wide analysis shows that Ldb1 controls essential hematopoietic genes/pathways in mouse early development and reveals novel players in hematopoiesis
  250. MicroRNA-133 Controls Brown Adipose Determination in Skeletal Muscle Satellite Cells by Targeting Prdm16
  251. Genome Instability in Lactobacillus rhamnosus GG
  252. Directed Migration of Cortical Interneurons Depends on the Cell-Autonomous Action of Sip1
  253. MicroRNA-Mediated Down-Regulation of M-CSF Receptor Contributes to Maturation of Mouse Monocyte-Derived Dendritic Cells
  254. Hydroxyurea responsiveness in  -thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity
  255. miR-141 regulates KEAP1 and modulates cisplatin sensitivity in ovarian cancer cells
  256. KLF10gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients
  257. The Microtubule Plus-End Tracking Protein CLASP2 Is Required for Hematopoiesis and Hematopoietic Stem Cell Maintenance
  258. Snail Regulates MyoD Binding-Site Occupancy to Direct Enhancer Switching and Differentiation-Specific Transcription in Myogenesis
  259. A Novel Complex, RUNX1-MYEF2, Represses Hematopoietic Genes in Erythroid Cells
  260. Metabolic Enzyme IMPDH Is Also a Transcription Factor Regulated by Cellular State
  261. The male germ cell gene regulator CTCFL is functionally different from CTCF and binds CTCF-like consensus sites in a nucleosome composition-dependent manner
  262. Transcriptional Dominance of Pax7 in Adult Myogenesis Is Due to High-Affinity Recognition of Homeodomain Motifs
  263. RNF12 initiates X-chromosome inactivation by targeting REX1 for degradation
  264. A new function of ROD1 in nonsense-mediated mRNA decay
  265. Hypoxia-Inducible Factor 2α Plays a Critical Role in the Formation of Alveoli and Surfactant
  266. Progesterone Inhibits Epithelial-to-Mesenchymal Transition in Endometrial Cancer
  267. Genome-wide DNA methylation profiling of non-small cell lung carcinomas
  268. Dynamic long-range chromatin interactions controlMybproto-oncogene transcription during erythroid development
  269. Remodelers Organize Cellular Chromatin by Counteracting Intrinsic Histone-DNA Sequence Preferences in a Class-Specific Manner
  270. NARWHAL, a primary analysis pipeline for NGS data
  271. Left ventricular remodeling in swine after myocardial infarction: a transcriptional genomics approach
  272. The DNA-Binding Protein CTCF Limits Proximal Vκ Recombination and Restricts κ Enhancer Interactions to the Immunoglobulin κ Light Chain Locus
  273. Modulation of Androgen Receptor Signaling in Hormonal Therapy-Resistant Prostate Cancer Cell Lines
  274. Absence of Common Somatic Alterations in Genes on 1p and 19q in Oligodendrogliomas
  275. Chronic IFN-  production in mice induces anemia by reducing erythrocyte life span and inhibiting erythropoiesis through an IRF-1/PU.1 axis
  276. Effective Treatment of Psoriasis with Narrow-Band UVB Phototherapy Is Linked to Suppression of the IFN and Th17 Pathways
  277. The inactive X chromosome adopts a unique three-dimensional conformation that is dependent on Xist RNA
  278. Gene expression profiling assigns CHEK2 1100delC breast cancers to the luminal intrinsic subtypes
  279. Discovery of new microRNAs by small RNAome deep sequencing in childhood acute lymphoblastic leukemia
  280. The DNA binding factor Hmg20b is a repressor of erythroid differentiation
  281. Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes
  282. Mobilization of hepatic mesenchymal stem cells from human liver grafts
  283. Distinct Severe Acute Respiratory Syndrome Coronavirus-Induced Acute Lung Injury Pathways in Two Different Nonhuman Primate Species
  284. A systems approach to analyze transcription factors in mammalian cells
  285. Inflammatory conditions affect gene expression and function of human adipose tissue-derived mesenchymal stem cells
  286. Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome
  287. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
  288. Unacylated Ghrelin Rapidly Modulates Lipogenic and Insulin Signaling Pathway Gene Expression in Metabolically Active Tissues of GHSR Deleted Mice
  289. Pandemic 2009 H1N1 Influenza Virus Causes Diffuse Alveolar Damage in Cynomolgus Macaques
  290. FUNCTION OF HUMAN MESENCHYMAL STEM CELLS UNDER INFLAMMATORY CONDITIONS
  291. Gene Expression-Based Classification of Non-Small Cell Lung Carcinomas and Survival Prediction
  292. Exacerbated Innate Host Response to SARS-CoV in Aged Non-Human Primates
  293. Short-term dietary restriction and fasting precondition against ischemia reperfusion injury in mice
  294. The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation
  295. Cell-specific occupancy of an extended repertoire of CREM and CREB binding loci in male germ cells
  296. The ubiquitin-conjugating enzyme HR6B is required for maintenance of X chromosome silencing in mouse spermatocytes and spermatids
  297. CITED2 and NCOR2 in anti-oestrogen resistance and progression of breast cancer
  298. Monitoring of the Immunomodulatory Effect of CP-690,550 by Analysis of the JAK/STAT Pathway in Kidney Transplant Patients
  299. The FOXF2 pathway in the human prostate stroma
  300. Physiological Thyroid Hormone Levels Regulate Numerous Skeletal Muscle Transcripts
  301. MicroRNA-mediated gene silencing modulates the UV-induced DNA-damage response
  302. Persistent transcription-blocking DNA lesions trigger somatic growth attenuation associated with longevity
  303. Gene Expression Profiling in Uveal Melanoma: Two Regions on 3p Related to Prognosis
  304. Delayed and Accelerated Aging Share Common Longevity Assurance Mechanisms
  305. MN1 affects expression of genes involved in hematopoiesis and can enhance as well as inhibit RAR/RXR-induced gene expression
  306. Transcription and Chromatin Organization of a Housekeeping Gene Cluster Containing an Integrated β-Globin Locus Control Region
  307. Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene
  308. Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene
  309. Difference in signalling between various hormone therapies in endometrium, myometrium and upper part of the vagina
  310. Genomic and Nongenomic Effects of Estrogen Signaling in Human Endometrial Cells: Involvement of the Growth Factor Receptor Signaling Downstream AKT Pathway
  311. Stable RNA markers for identification of blood and saliva stains revealed from whole genome expression analysis of time-wise degraded samples
  312. HPV related VIN: Highly proliferative and diminished responsiveness to extracellular signals
  313. The hormone replacement therapy drug tibolone acts very similar to medroxyprogesterone acetate in an estrogen-and progesterone-responsive endometrial cancer cell line
  314. Functional Differentiation of SWI/SNF Remodelers in Transcription and Cell Cycle Control
  315. Characterization of Spodoptera exigua multicapsid nucleopolyhedrovirus ORF17/18, a homologue of Xestia c-nigrum granulovirus ORF129
  316. Furin Is Involved in Baculovirus Envelope Fusion Protein Activation
  317. Identification of a Novel Occlusion Derived Virus-Specific Protein in Spodoptera exigua Multicapsid Nucleopolyhedrovirus
  318. The sequence of the Helicoverpa armigera single nucleocapsid nucleopolyhedrovirus genome
  319. Characteristics of the transactivator gene ie1 of Spodoptera exigua multiple nucleopolyhedrovirus
  320. Isolation of a Spodoptera exigua baculovirus recombinant with a 10·6 kbp genome deletion that retains biological activity
  321. A Novel Baculovirus Envelope Fusion Protein with a Proprotein Convertase Cleavage Site
  322. Identification, sequence analysis and phylogeny of the lef-2 gene of Helicoverpa armigera single-nucleocapsid baculovirus
  323. Sequence and organization of the Spodoptera exigua multicapsid nucleopolyhedrovirus genome