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1. Full Text Generation of Human Induced Pluripotent Stem Cells from Dermal Fibroblasts
by W. E. Lowry and L. Richter and R. Yachechko and A. D. Pyle and J. Tchieu and R. Sridharan and A. T. Clark and K. Plath
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2008, Volume 105, Issue 8, pp. 2883 - 2888
The generation of patient-specific pluripotent stem cells has the potential to accelerate the implementation of stem cells for clinical treatment of... 
Induced pluripotent stem cells | Somatic cells | Genes | Stem cells | Cell lines | Fibroblasts | Viruses | Mice | Embryonic stem cells | Cells | OCT4 | SOX2 | Reprogramming | Stem cell | reprogramming | DEFINED FACTORS | stem cell | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | DIFFERENTIATION | INDUCTION | LINES | Pluripotent Stem Cells - cytology | Tissue Engineering - methods | Fibroblasts - physiology | Humans | Pluripotent Stem Cells - physiology | DNA, Complementary - genetics | Gene Expression Profiling | Cell Culture Techniques - methods | Genetic Vectors - genetics | Pluripotent Stem Cells - metabolism | Transcription Factors - metabolism | Microarray Analysis | Fibroblasts - cytology | Dermis - cytology | Cell Differentiation - physiology | Fibroblasts - metabolism | Properties | Stem cell research | Biological Sciences
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2. Full Text Deep dermal fibroblasts contribute to hypertrophic scarring
by Wang, Jianfei and Dodd, Carole and Shankowsky, Heather A and Scott, Paul G and Tredget, Edward E and Wound Healing Research Grp and Wound Healing Research Group
Laboratory Investigation, ISSN 0023-6837, 12/2008, Volume 88, Issue 12, pp. 1278 - 1290
Hypertrophic scar (HTS) following thermal injury is a dermal fibroproliferative disorder that leads to considerable morbidity. The development of HTS involves... 
Proteoglycan | TGF-β1 | Dermal depth | Fibroblast | Collagen | HTS | MEDICINE, RESEARCH & EXPERIMENTAL | TGF-beta 1 | THERMAL-INJURY | PIG MODEL | collagen | FACTOR-I | PATHOLOGY | BLOOD MONONUCLEAR-CELLS | proteoglycan | fibroblast | TISSUE GROWTH-FACTOR | MESSENGER-RNA | TRANSFORMING GROWTH-FACTOR-BETA-1 | NORMAL SKIN | RETICULAR DERMIS | BURN PATIENTS | dermal depth | Cell Proliferation | Enzyme-Linked Immunosorbent Assay | Cell Separation | Skin - metabolism | Cicatrix, Hypertrophic - metabolism | Humans | Middle Aged | Child, Preschool | Cell Size | Male | Cicatrix, Hypertrophic - pathology | DNA Primers | Reverse Transcriptase Polymerase Chain Reaction | Case-Control Studies | Flow Cytometry | Base Sequence | Adolescent | Adult | Female | Fibroblasts - cytology | Collagenases - metabolism | Skin - pathology | Transforming Growth Factor beta1 - biosynthesis | Fibroblasts - metabolism
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3. Full Text Human dermal fibroblasts in psychiatry research
by Kálmán, S and Garbett, K.A and Janka, Z and Mirnics, K
Neuroscience, ISSN 0306-4522, 2016, Volume 320, pp. 105 - 121
Graphical abstract 
Neurology | in vitro model | geneenvironment interaction | dermal fibroblasts | bipolar disorder | schizophrenia | major depression | Dermal fibroblasts | Gene | Major depression | In vitro model | Schizophrenia | Bipolar disorder | environment interaction | AMINO-ACID-TRANSPORT | CULTURED SKIN FIBROBLASTS | IMPAIRED GLUTATHIONE SYNTHESIS | DEPENDENT PROTEIN-KINASE | NEUROSCIENCES | PLURIPOTENT STEM-CELLS | CATECHOL-O-METHYLTRANSFERASE | DECREASED TYROSINE TRANSPORT | MAJOR DEPRESSIVE DISORDER | NAIVE 1ST-EPISODE SCHIZOPHRENIA | CIRCADIAN GENE-EXPRESSION | Models, Biological | Humans | Mental Disorders | Cells, Cultured | Fibroblasts | Biomedical Research - methods | Psychiatry - methods | Skin
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4. Full Text Effect of fiber diameter, pore size and seeding method on growth of human dermal fibroblasts in electrospun poly(ε-caprolactone) fibrous mats
by Lowery, Joseph L and Datta, Néha and Rutledge, Gregory C
Biomaterials, ISSN 0142-9612, 2009, Volume 31, Issue 3, pp. 491 - 504
Abstract Nonwoven fiber mats of poly(ε-caprolactone) (PCL) and PCL blended with poly(ethylene oxide) (PEO) were generated by electrospinning. Differential... 
Advanced Basic Science | Dentistry | Electrospinning | Tissue scaffold | Porosity | Perfusion | MATRIX | MATERIALS SCIENCE, BIOMATERIALS | MESHES | TISSUE ENGINEERING SCAFFOLDS | NANOFIBERS | ENGINEERING, BIOMEDICAL | MECHANICAL-PROPERTIES | IN-VITRO | CELLULAR INFILTRATION | POLYMER | PERFUSION BIOREACTOR | MICROFIBER | Microscopy, Electron, Scanning | Skin - cytology | Fibroblasts - physiology | Biocompatible Materials - chemistry | Humans | Cells, Cultured | Materials Testing | Caproates - chemistry | Electrochemical Techniques - instrumentation | Tissue Scaffolds - chemistry | Surface Properties | Calorimetry, Differential Scanning | Electrochemical Techniques - methods | Fibroblasts - cytology | Cell Culture Techniques | Lactones - chemistry
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5. Full Text Isolation and culture of human dermal fibroblasts
by Kisiel, Marta A and Klar, Agnes S
Methods in Molecular Biology, ISSN 1064-3745, 2019, Volume 1993, pp. 71 - 78
Dermal fibroblasts are the main cell type present in skin connective tissue (dermis). Fibroblasts interact with epidermal cells during hair development and in... 
Regenerative medicine | Tissue engineering | Collagen | Skin equivalent | Organotypic culture | Dermis | Fibroblasts | Skin
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6. Full Text Specific age-associated DNA methylation changes in human dermal fibroblasts
by Koch, Carmen M and Suschek, Christoph V and Lin, Qiong and Bork, Simone and Goergens, Maria and Joussen, Sylvia and Pallua, Norbert and Ho, Anthony D and Zenke, Martin and Wagner, Wolfgang
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 2, p. e16679
Epigenetic modifications of cytosine residues in the DNA play a critical role for cellular differentiation and potentially also for aging. In mesenchymal... 
5-METHYLCYTOSINE | MULTIDISCIPLINARY SCIENCES | TISSUE | GENE-EXPRESSION | DIFFERENTIATION | SKIN | STROMAL CELLS | CULTURE | CANCER | MESENCHYMAL STEM-CELLS | REPLICATIVE SENESCENCE | Epigenetic inheritance | Analysis | Genes | DNA | Stem cells | Methylation | Cell differentiation | Elderly people | Cell culture | Senescence | Mesenchyme | Genomes | Medical schools | Engineering | Biomedical materials | Mineralization | DNA methylation | Bone marrow | Fibroblasts | Aging | Biocompatibility | Cytosine | Cyclin-dependent kinase inhibitors | Bioinformatics | Age | Deoxyribonucleic acid--DNA | Biomedical engineering | CpG islands | Aging (artificial) | INK4 protein | Gene expression | Stromal cells | Epigenetics | Skin | Hand surgery | Bayesian analysis | Elderly | Geriatrics | Deoxyribonucleic acid
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7. Full Text Transcription factors ETS2 and MESP1 transdifferentiate human dermal fibroblasts into cardiac progenitors
by Jose Francisco Islas and Yu Liu and Kuo-Chan Weng and Matthew J. Robertson and Shuxing Zhang and Allan Prejusa and John Harger and Dariya Tikhomirova and Mani Chopra and Dinakar Iyer and Mark Mercola and Robert G. Oshima and James T. Willerson and Vladimir N. Potaman and Robert J. Schwartz
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2012, Volume 109, Issue 32, pp. 13016 - 13021
Unique insights for the reprograming of cell lineages have come from embryonic development in the ascidian Ciona, which is dependent upon the transcription... 
Transcription factors | Delta cells | Genes | Stem cells | Cell lines | Fibroblasts | Embryonic stem cells | Progenitor cells | Cells | Endothelial cells | Kinetic imaging | Fibroblast reprograming | Cardiogenesis | Protein transduction | HEART PRECURSOR CELLS | cardiogenesis | DEFINED FACTORS | protein transduction | MULTIDISCIPLINARY SCIENCES | DIRECT CONVERSION | fibroblast reprograming | CARDIOMYOCYTES | MOUSE EMBRYO | PLURIPOTENT STEM-CELLS | LINEAGE COMMITMENT | TROPHOBLAST | kinetic imaging | GENE | DIFFERENTIATION | Myoblasts, Cardiac - cytology | Skin - cytology | Basic Helix-Loop-Helix Transcription Factors - genetics | Humans | Cell Transdifferentiation - genetics | Gene Knockout Techniques | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Animals | Cell Transdifferentiation - physiology | Flow Cytometry | Basic Helix-Loop-Helix Transcription Factors - metabolism | Fluorescent Antibody Technique | Polymerase Chain Reaction | Proto-Oncogene Protein c-ets-2 - genetics | Fibroblasts - cytology | Mice | Myoblasts, Cardiac - physiology | Proto-Oncogene Protein c-ets-2 - metabolism | Growth | Transdifferentiation | Heart cells | Genetic aspects | Properties | Biological Sciences
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8. Full Text Altered Dermal Fibroblasts in Systemic Sclerosis Display Podoplanin and CD90
by Nazari, Banafsheh and Rice, Lisa M and Stifano, Giuseppina and Barron, Alexander M.S and Wang, Yu Mei and Korndorf, Tess and Lee, Jungeun and Bhawan, Jag and Lafyatis, Robert and Browning, Jeffrey L
American Journal of Pathology, The, ISSN 0002-9440, 2016, Volume 186, Issue 10, pp. 2650 - 2664
Tissue injury triggers the activation and differentiation of multiple cell types to minimize damage and initiate repair processes. In systemic sclerosis, these... 
Pathology | GROWTH-FACTOR-BETA | IN-VITRO | TGF-BETA | DENDRITIC CELLS | CD34 EXPRESSION | LYMPH-NODES | GENE-EXPRESSION | SKIN-DISEASE | PATHOLOGY | IMMUNOHISTOCHEMICAL MARKER | RETICULAR CELLS | Tumor Necrosis Factor-alpha - metabolism | Membrane Glycoproteins - metabolism | Humans | Middle Aged | Scleroderma, Systemic - pathology | Male | Interleukin-1beta - metabolism | Fibrosis - immunology | Aged, 80 and over | Adult | Female | Cell Differentiation | Skin - pathology | Skin - immunology | Interleukin-1beta - immunology | Scleroderma, Systemic - immunology | Fibroblasts - pathology | Dermis - immunology | Thy-1 Antigens - metabolism | Animals | Dermis - pathology | Fibroblasts - immunology | Aged | Mice | Fibrosis - pathology | Regular
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9. Full Text TGF-β-mediated downregulation of microRNA-196a contributes to the constitutive upregulated type I collagen expression in scleroderma dermal fibroblasts
by Honda, Noritoshi and Jinnin, Masatoshi and Kajihara, Ikko and Makino, Takamitsu and Makino, Katsunari and Masuguchi, Shinichi and Fukushima, Satoshi and Okamoto, Yoshinobu and Hasegawa, Minoru and Fujimoto, Manabu and Ihn, Hironobu
Journal of Immunology, ISSN 0022-1767, 04/2012, Volume 188, Issue 7, pp. 3323 - 3331
Previous reports indicated the significance of the TGF-beta signaling in the pathogenesis of systemic sclerosis. We tried to evaluate the possibility that... 
PATHOGENESIS | FIBROSIS | SYSTEMIC-SCLEROSIS FIBROBLASTS | GROWTH-FACTOR-BETA | TRANSCRIPTIONAL ACTIVATION | GENES | TARGETS | GERANYLGERANYL TRANSFERASE I | IMMUNOLOGY | TGF-BETA-1 STIMULATION | SKIN FIBROBLASTS | Cells, Cultured - drug effects | MicroRNAs - antagonists & inhibitors | Humans | Middle Aged | Scleroderma, Systemic - genetics | Scleroderma, Systemic - pathology | 3' Untranslated Regions - genetics | Male | MicroRNAs - metabolism | Fibroblasts - pathology | Gene Expression Regulation - drug effects | Transforming Growth Factor beta - pharmacology | Collagen Type I - biosynthesis | Phenotype | Collagen Type I - genetics | Transfection | Fibroblasts - drug effects | Dermis - pathology | Female | Aged | Cells, Cultured - metabolism | MicroRNAs - genetics | Binding Sites | Fibroblasts - metabolism
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