Pages that link to "Q36493686"
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The following pages link to Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells (Q36493686):
Displaying 50 items.
- Single cell genomics: advances and future perspectives (Q21563353) (← links)
- The Use of Stem Cells to Model Amyotrophic Lateral Sclerosis and Frontotemporal Dementia: From Basic Research to Regenerative Medicine (Q26766372) (← links)
- Somatic mosaicism in the human genome (Q26823199) (← links)
- Proceedings: consideration of genetics in the design of induced pluripotent stem cell-based models of complex disease (Q26999033) (← links)
- Human pluripotent stem cells for modelling human liver diseases and cell therapy (Q27005360) (← links)
- Multifocal epithelial tumors and field cancerization: stroma as a primary determinant (Q27005678) (← links)
- Cell-based screening: extracting meaning from complex data (Q27305816) (← links)
- Long-term culture of genome-stable bipotent stem cells from adult human liver (Q28254408) (← links)
- Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation (Q28263098) (← links)
- Automated, high-throughput derivation, characterization and differentiation of induced pluripotent stem cells (Q28265816) (← links)
- Variations in brain DNA (Q28383011) (← links)
- Concise review: carbon nanotechnology: perspectives in stem cell research (Q28383608) (← links)
- Ultra-fast local-haplotype variant calling using paired-end DNA-sequencing data reveals somatic mosaicism in tumor and normal blood samples (Q28387263) (← links)
- The landscape of somatic mutations in protein coding genes in apparently benign human tissues carries signatures of relaxed purifying selection (Q28389979) (← links)
- The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement (Q28390462) (← links)
- Patterns of somatically acquired amplifications and deletions in apparently normal tissues of ovarian cancer patients (Q28390831) (← links)
- Abnormal dosage of ultraconserved elements is highly disfavored in healthy cells but not cancer cells (Q28396411) (← links)
- Genetic heterogeneity of induced pluripotent stem cells: results from 24 clones derived from a single C57BL/6 mouse (Q28544903) (← links)
- Integrated Genomic Analysis of Diverse Induced Pluripotent Stem Cells from the Progenitor Cell Biology Consortium (Q28596287) (← links)
- Properties and rates of germline mutations in humans (Q28678675) (← links)
- Multiple mechanisms determine the sensitivity of human-induced pluripotent stem cells to the inducible caspase-9 safety switch (Q28828176) (← links)
- FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders (Q28973611) (← links)
- Creating Patient-Specific Neural Cells for the In Vitro Study of Brain Disorders (Q30278015) (← links)
- Functional analysis of a chromosomal deletion associated with myelodysplastic syndromes using isogenic human induced pluripotent stem cells (Q30397539) (← links)
- Mosaic copy number variation in human neurons (Q30409886) (← links)
- Perspectives of gene combinations in phenotype presentation (Q30450809) (← links)
- Comparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome (Q30453156) (← links)
- Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons (Q30543660) (← links)
- Somatic alpha-synuclein mutations in Parkinson's disease: hypothesis and preliminary data (Q30626337) (← links)
- Kv3.3 Channels Bind Hax-1 and Arp2/3 to Assemble a Stable Local Actin Network that Regulates Channel Gating (Q30740155) (← links)
- Copy number variation is a fundamental aspect of the placental genome. (Q31159938) (← links)
- iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types (Q33559864) (← links)
- Transposable elements in cancer as a by-product of stress-induced evolvability (Q33687526) (← links)
- X Chromosome of female cells shows dynamic changes in status during human somatic cell reprogramming (Q33729692) (← links)
- Single Cell-Based Vector Tracing in Patients with ADA-SCID Treated with Stem Cell Gene Therapy (Q33784306) (← links)
- Coherent somatic mutation in autoimmune disease (Q33837769) (← links)
- Influence of donor age on induced pluripotent stem cells (Q33893730) (← links)
- Measurement of absolute copy number variation reveals association with essential hypertension (Q33937543) (← links)
- Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome (Q34038853) (← links)
- An Inducible Caspase-9 Suicide Gene to Improve the Safety of Therapy Using Human Induced Pluripotent Stem Cells (Q34044130) (← links)
- A comparison of genetically matched cell lines reveals the equivalence of human iPSCs and ESCs (Q34045234) (← links)
- Passage number is a major contributor to genomic structural variations in mouse iPSCs (Q34195138) (← links)
- Whole-genome sequencing identifies genetic variances in culture-expanded human mesenchymal stem cells (Q34250405) (← links)
- Identification of male-specific amh duplication, sexually differentially expressed genes and microRNAs at early embryonic development of Nile tilapia (Oreochromis niloticus) (Q34250772) (← links)
- Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations. (Q34310903) (← links)
- A genomic view of mosaicism and human disease (Q34339935) (← links)
- Mechanisms and models of somatic cell reprogramming (Q34345169) (← links)
- Genetics. Genome mosaicism--one human, multiple genomes (Q34359951) (← links)
- Aging genomes: a necessary evil in the logic of life (Q34400145) (← links)
- Role of non-coding sequence variants in cancer (Q34509633) (← links)