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1. Full Text Predicting the Risk of Pathologic Fracture for Enchondromas of the Hand Using Reproducible Clinical Criteria
by Riester, Scott M., MD and Kakar, Sanjeev, MD, MBA and van Wijnen, Andre, PhD and Wenger, Doris, MD and Ramaesh, Rishi, MD
Journal of Hand Surgery, ISSN 0363-5023, 2013, Volume 38, Issue 10, pp. e30 - e31
Orthopedics
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2. Full Text The histone H3.3K36M mutation reprograms the epigenome of chondroblastomas
by Fang, Dong and Gan, Haiyun and Lee, Jeong-Heon and Han, Jing and Wang, Zhiquan and Riester, Scott M and Jin, Long and Chen, Jianji and Zhou, Hui and Wang, Jinglong and Zhang, Honglian and Yang, Na and Bradley, Elizabeth W and Ho, Thai H and Rubin, Brian P and Bridge, Julia A and Thibodeau, Stephen N and Ordog, Tamas and Chen, Yue and Van Wijnen, Andre J and Oliveira, Andre M and Xu, Rui-Ming and Westendorf, Jennifer J and Zhang, Zhiguo
Science, ISSN 0036-8075, 06/2016, Volume 352, Issue 6291, pp. 1344 - 1348
More than 90% of chondroblastomas contain a heterozygous mutation replacing lysine-36 with methionine-36 (K36M) in the histone H3 variant H3.3. Here we show... 
H3K36 METHYLATION | REPAIR | ACTIVATION | MULTIDISCIPLINARY SCIENCES | REGIONS | BONE | VARIANT H3.3 | EXPRESSION | Epigenesis, Genetic | Genes, Neoplasm | Humans | Carcinogenesis - genetics | Lysine - genetics | Histones - genetics | Chondroblastoma - genetics | Histone-Lysine N-Methyltransferase - metabolism | Bone Neoplasms - genetics | Mutation | Methylation | Repressor Proteins - metabolism | Amino Acid Substitution | Epigenetic inheritance | Gene mutations | Histones | Physiological aspects | Genetic aspects | Observations | Cancer | Proteins | Pediatrics | Residues | Mutations | Genes | Gene expression
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3. Full Text MicroRNA and mRNA cargo of extracellular vesicles from porcine adipose tissue-derived mesenchymal stem cells
by Eirin, Alfonso and Riester, Scott M and Zhu, Xiang-Yang and Tang, Hui and Evans, Jared M and O'Brien, Daniel and van Wijnen, Andre J and Lerman, Lilach O
Gene, ISSN 0378-1119, 11/2014, Volume 551, Issue 1, pp. 55 - 64
Mesenchymal stromal/stem cells (MSCs) are clinically useful for cell-based therapy, but concerns regarding their ability to replicate limit their human... 
Next generation sequencing (NGS) | Extracellular vesicles | miRNA | Microvesicles | Exosomes | Gene expression | RNASeq | Mesenchymal stem cells | MiRNA | MARROW | ENHANCER-BINDING-PROTEIN | HEPATOCYTE GROWTH-FACTOR | LARGE GENE LISTS | BETA | THERAPY | ANALYSIS PIPELINE | DISEASE | GENETICS & HEREDITY | EXPRESSION | RENAL-ARTERY STENOSIS | Cells, Cultured | Gene Expression Regulation | Adipose Tissue - cytology | Exosomes - genetics | MicroRNAs - metabolism | Transcription Factors - genetics | RNA, Messenger - metabolism | Transcription Factors - metabolism | Animals | Swine | High-Throughput Nucleotide Sequencing | MicroRNAs - genetics | Gene Ontology | Mesenchymal Stromal Cells - physiology | Adipose tissues | Messenger RNA | MicroRNA | Proteolysis | Analysis | Stem cells | Bone morphogenetic proteins | Transforming growth factors | extracellular vesicles | exosomes | next generation sequencing (NGS) | microvesicles | gene expression
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4. Full Text High‐Resolution Molecular Validation of Self‐Renewal and Spontaneous Differentiation in Clinical‐Grade Adipose‐Tissue Derived Human Mesenchymal Stem Cells
by Dudakovic, Amel and Camilleri, Emily and Riester, Scott M and Lewallen, Eric A and Kvasha, Sergiy and Chen, Xiaoyue and Radel, Darcie J and Anderson, Jarett M and Nair, Asha A and Evans, Jared M and Krych, Aaron J and Smith, Jay and Deyle, David R and Stein, Janet L and Stein, Gary S and Im, Hee‐Jeong and Cool, Simon M and Westendorf, Jennifer J and Kakar, Sanjeev and Dietz, Allan B and van Wijnen, Andre J
Journal of Cellular Biochemistry, ISSN 0730-2312, 10/2014, Volume 115, Issue 10, pp. 1816 - 1828
Improving the effectiveness of adipose‐tissue derived human mesenchymal stromal/stem cells (AMSCs) for skeletal therapies requires a detailed characterization... 
WNT2A | ECM2 | FIBROBLAST | PLURIPOTENT | WISP2 | OCT4 | CCND1 | CYCLIN | WNT5B | ADIPOSE‐TISSUE DERIVED STROMAL CELLS | CD90 | WNT5A | OSTEOGENESIS | POU5F1 | ASPN | ACTA2 | SFRP4 | SFRP2 | TNNT3 | CHI3L1 | EXTRACELLULAR MATRIX | CD105 | CHONDROGENESIS | CD44 | ENG | MULTIPOTENT | ADH1B | THY1 | ADIPOGENESIS | HIST2H4A | CCNB2 | NPAT | NT5E | HIST2H4B | E2F1 | CELL CYCLE | HIST1H3H | WNT2 | E2F7 | E2F8 | CD73 | WNT7B | RARRES2 | KLF4 | PODN | MESENCHYMAL STEM CELL | HISTONE | HINFP | H19 | HIST1H4A | OGN | NANOG | FMOD | LINEAGE‐COMMITMENT | NES | LINEAGE-COMMITMENT | ADIPOSE-TISSUE DERIVED STROMAL CELLS | CELL BIOLOGY | ALTERNATIVES | SCAFFOLDS | STROMAL CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CULTURE | EXPANSION | HUMAN PLATELET LYSATE | FETAL BOVINE SERUM | BONE | CARTILAGE | EXPRESSION | Cell Proliferation - genetics | Chondrogenesis - genetics | Humans | Adipose Tissue - cytology | Immunophenotyping | Cell Communication - genetics | Cell- and Tissue-Based Therapy | Mitosis - genetics | Extracellular Matrix - genetics | Mesenchymal Stromal Cells - cytology | Flow Cytometry | Sequence Analysis, RNA | Base Sequence | DNA Replication - genetics | Thy-1 Antigens - biosynthesis | Cell Cycle Checkpoints - genetics | Cell Differentiation | High-Throughput Nucleotide Sequencing | Membrane Proteins - metabolism | Adipogenesis - genetics | Osteogenesis - genetics | Adipose tissues | DNA replication | RNA | Stem cells
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5. Full Text Erratum to: RNA sequencing reveals a depletion of collagen targeting microRNAs in Dupuytren’s disease
by Riester, Scott M and Arsoy, Diren and Camilleri, Emily T and Dudakovic, Amel and Paradise, Christopher R and Evans, Jared M and Torres-Mora, Jorge and Rizzo, Marco and Kloen, Peter and Kruithof-de Julio, Marianna and van Wijnen, Andre J and Kakar, Sanjeev
BMC Medical Genomics, ISSN 1755-8794, 12/2016, Volume 9, Issue 1
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6. Full Text Mapping molecular landmarks of human skeletal ontogeny and pluripotent stem cell-derived articular chondrocytes
by Ferguson, Gabriel B and Van Handel, Ben and Bay, Maxwell and Fiziev, Petko and Org, Tonis and Lee, Siyoung and Shkhyan, Ruzanna and Banks, Nicholas W and Scheinberg, Mila and Wu, Ling and Saitta, Biagio and Elphingstone, Joseph and Larson, A. Noelle and Riester, Scott M and Pyle, April D and Bernthal, Nicholas M and Mikkola, Hanna Ka and Ernst, Jason and van Wijnen, Andre J and Bonaguidi, Michael and Evseenko, Denis
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 3634 - 16
Tissue-specific gene expression defines cellular identity and function, but knowledge of early human development is limited, hampering application of... 
MYOGENIC CELLS | PROGENITOR-CELL | ADHESION MOLECULE | INTEGRATIVE ANALYSIS | BONE-FORMATION | INTEGRIN | MULTIDISCIPLINARY SCIENCES | ANIMAL-MODELS | CARTILAGE REGENERATION | GROWTH-PLATE | LARGE GENE LISTS | Biomarkers - metabolism | Epigenesis, Genetic | Humans | Transcriptome | Fetal Development | Gene Expression Profiling | Tenocytes - metabolism | Myoblasts - metabolism | Animals | Sequence Analysis, RNA | Swine | Histone Code | Transcription, Genetic | Mice | Chondrogenesis | Osteoblasts - metabolism | Chondrocytes - metabolism | Chromatin | Tissue engineering | Modules | Fetuses | Muscles | Ontogeny | Gene expression | Kinases | Regeneration (physiology) | Cartilage | Regeneration | Biomedical materials | Network analysis | Stem cells | Chondrocytes | Biocompatibility | Pluripotency
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7. Full Text Enhancer of zeste homolog 2 inhibition stimulates bone formation and mitigates bone loss caused by ovariectomy in skeletally mature mice
by Dudakovic, Amel and Camilleri, Emily T and Riester, Scott M and Paradise, Christopher R and Gluscevic, Martina and O'Toole, Thomas M and Thaler, Roman and Evans, Jared M and Yan, Huihuang and Subramaniam, Malayannan and Hawse, John R and Stein, Gary S and Montecino, Martin A and McGee-Lawrence, Meghan E and Westendorf, Jennifer J and Van Wijnen, Andre J
Journal of Biological Chemistry, ISSN 0021-9258, 11/2016, Volume 291, Issue 47, pp. 24594 - 24606
Perturbations in skeletal development and bone degeneration may result in reduced bone mass and quality, leading to greater fracture risk. Bone loss is... 
CHIP-SEQ DATA | MUSCLE DIFFERENTIATION | INTEGRATIVE ANALYSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | TARGETING EZH2 | SELF-RENEWAL | DEVELOPMENTAL GENES | HISTONE METHYLTRANSFERASE EZH2 | MESENCHYMAL STEM-CELLS | DNA-METHYLATION | OSTEOPOROSIS | Cell Line | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Ovariectomy | Paracrine Communication | RNA, Small Interfering - pharmacology | Wnt Proteins - metabolism | Receptor, Parathyroid Hormone, Type 1 | Osteoblasts - pathology | Animals | Wnt Proteins - genetics | Methylation - drug effects | Osteoporosis - metabolism | Osteoporosis - pathology | Smad5 Protein - metabolism | Smad1 Protein - genetics | Smad1 Protein - metabolism | Female | Mice | Smad5 Protein - genetics | Osteoblasts - metabolism | Osteogenesis | Gene Regulation | histone methylation | skeleton | methyltransferase | histone | osteoblast | osteoporosis | epigenetics
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8. Full Text Histone Deacetylase 3 Deletion in Mesenchymal Progenitor Cells Hinders Long Bone Development
by Feigenson, Marina and Shull, Lomeli Carpio and Taylor, Earnest L and Camilleri, Emily T and Riester, Scott M and van Wijnen, Andre J and Bradley, Elizabeth W and Westendorf, Jennifer J
Journal of Bone and Mineral Research, ISSN 0884-0431, 12/2017, Volume 32, Issue 12, pp. 2453 - 2465
ABSTRACT Long bone formation is a complex process that requires precise transcriptional control of gene expression programs in mesenchymal progenitor cells.... 
HDAC3 | LIMB DEVELOPMENT | MMP3 | RGFP966 | CHONDROGENESIS | MMP10 | VORINOSTAT | FGF21 | PHYSIOLOGY | CHROMATIN-STRUCTURE | ACETYLATION | MAINTENANCE | THERAPY | DISEASE | ENDOCRINOLOGY & METABOLISM | INHIBITORS | EXPRESSION | GROWTH-FACTOR 21 | SKELETAL DEVELOPMENT | Enzymes | Analysis | Stem cells | Histones | DNA binding proteins | Gene expression | Cell differentiation | Osteoprogenitor cells | Histone deacetylase | Chromatin | Stromelysin 2 | Mesenchyme | Transcription | Bone (intramembranous) | Lethality | Gene deletion | Bone growth | Osteoblastogenesis | Mood | Clonal deletion | Teratogenicity | Bone (long) | Skeleton | Chondrogenesis | Bone (endochondral) | Osteogenesis | Index Medicus | Hdac3 | limb development | vorinostat | Mmp3 | chondrogenesis | Fgf21 | Mmp10
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9. Full Text Biological Strategies for Improved Osseointegration and Osteoinduction of Porous Metal Orthopedic Implants
by Lewallen, Eric Alexander and Riester, Scott M and Bonin, Carolina A and Kremers, Hilal Maradit and Dudakovic, Amel and Kakar, Sanjeev and Cohen, Robert C and Westendorf, Jennifer J and Lewallen, David G and van Wijnen, Andre J
Tissue Engineering Part B: Reviews, ISSN 1937-3368, 04/2015, Volume 21, Issue 2, pp. 218 - 230
The biological interface between an orthopedic implant and the surrounding host tissue may have a dramatic effect upon clinical outcome. Desired effects... 
Review Articles | REVISION HIP-ARTHROPLASTY | OSTEOGENIC DIFFERENTIATION | MECHANICAL-PROPERTIES | MESENCHYMAL STEM-CELLS | TOTAL KNEE ARTHROPLASTY | CELL & TISSUE ENGINEERING | CELL BIOLOGY | IN-VITRO | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | SHOCK-WAVE THERAPY | BONE REGENERATION | TITANIUM SCAFFOLDS | LOW-INTENSITY ULTRASOUND | Osseointegration | Animals | Orthopedics - methods | Models, Biological | Humans | Bone Substitutes | Prostheses and Implants | Porosity | Orthopedic apparatus | Biology | Transplants & implants | Metals | Review
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10. Full Text Wnt/-Catenin Signaling Activates Expression of the Bone-Related Transcription Factor RUNX2 in Select Human Osteosarcoma Cell Types
by Vega, OA and Lucero, CMJ and Araya, HF and Jerez, S and Tapia, JC and Antonelli, M and Salazar-Onfray, F and Heras, FL and Thaler, R and Riester, SM and Stein, GS and van Wijnen, AJ and Galindo, MA
JOURNAL OF CELLULAR BIOCHEMISTRY, ISSN 0730-2312, 11/2017, Volume 118, Issue 11, pp. 3662 - 3674
Osteosarcoma is the most common malignant bone tumor in children and adolescents. Metastasis and poor responsiveness to chemotherapy in osteosarcoma correlates... 
MULTIPLE PATHWAYS | OSTEOBLAST DIFFERENTIATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CATENIN | MALIGNANT-MELANOMA | BETA-CATENIN | CANCER | CELL BIOLOGY | NUCLEAR ACCUMULATION | BREAST-CANCER CELLS | RUNX2 TRANSCRIPTION FACTOR | ONCOGENE | CASEIN KINASE-I | GENE-EXPRESSION | OSTEOSARCOMA | TUMOR-SUPPRESSOR | INHIBITORY FACTOR-1 | Wnt | Chemotherapy | Osteosarcoma | Analysis | Development and progression | B cells | Metastasis | Gene expression | Cancer | Adolescence | Biotechnology | Transcription factors | Wnt protein | Nuclei | Metastases | Proteins | Signal transduction | Bone growth | Biocompatibility | Children | Adolescents | Localization | Catenin | Cbfa-1 protein | siRNA | Ribonucleic acid--RNA | Bone cancer | Overexpression | Osteoblastogenesis | Cell lines | Nuclei (cytology) | Bone | Differentiation | Osteogenesis | Cytoplasm
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11. Full Text Epigenetic control of skeletal development by the histone methyltransferase Ezh2
by Dudakovic, Amel and Camilleri, Emily T and Xu, Fuhua and Riester, Scott M and McGee-Lawrence, Meghan E and Bradley, Elizabeth W and Paradise, Christopher R and Lewallen, Eric A and Thaler, Roman and Deyle, David R and Larson, A. Noelle and Lewallen, David G and Dietz, Allan B and Stein, Gary S and Montecino, Martin A and Westendorf, Jennifer J and Van Wijnen, Andre J
Journal of Biological Chemistry, ISSN 0021-9258, 11/2015, Volume 290, Issue 46, pp. 27604 - 27617
Epigenetic control of gene expression is critical for normal fetal development. However, chromatin-related mechanisms that activate bone-specific programs... 
TRANSCRIPTIONAL ACTIVATION | METHYLATION | OSTEOBLAST DIFFERENTIATION | GENE | CHROMATIN | VERTEBRAL FRACTURE RISK | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEACETYLASE INHIBITORS | POSTMENOPAUSAL WOMEN | MESENCHYMAL STEM-CELLS | RUNX2 | Polycomb Repressive Complex 2 - antagonists & inhibitors | Cell Line | RNA, Small Interfering - genetics | Histone-Lysine N-Methyltransferase - genetics | Polycomb Repressive Complex 2 - genetics | Epigenesis, Genetic | Humans | Adipose Tissue - cytology | Enhancer of Zeste Homolog 2 Protein | Growth Plate - abnormalities | Cell Differentiation - genetics | Mesenchymal Stromal Cells - cytology | Animals | Histone-Lysine N-Methyltransferase - metabolism | Mice | Histones - metabolism | Osteoblasts - cytology | Bone and Bones - embryology | Polycomb Repressive Complex 2 - metabolism | Body Patterning - genetics | Osteogenesis - genetics | Gene Regulation | histone methylation | adipogenesis | mesenchymal stem cells (MSCs) | bone | osteoblast | osteogenesis | epigenetics | Ezh2
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12. Full Text Expression of the ectodomain‐releasing protease ADAM17 is directly regulated by the osteosarcoma and bone‐related transcription factor RUNX2
by Araya, Héctor F and Sepulveda, Hugo and Lizama, Carlos O and Vega, Oscar A and Jerez, Sofia and Briceño, Pedro F and Thaler, Roman and Riester, Scott M and Antonelli, Marcelo and Salazar‐Onfray, Flavio and Rodríguez, Juan Pablo and Moreno, Ricardo D and Montecino, Martin and Charbonneau, Martine and Dubois, Claire M and Stein, Gary S and van Wijnen, Andre J and Galindo, Mario A
Journal of Cellular Biochemistry, ISSN 0730-2312, 10/2018, Volume 119, Issue 10, pp. 8204 - 8219
Osteoblast differentiation is controlled by transcription factor RUNX2 which temporally activates or represses several bone‐related genes, including those... 
ADAM genes | ADAM17 | osteoblast differentiation | transcriptional regulation | RUNX2 | CONVERTING-ENZYME TACE | ENDOCHONDRAL OSSIFICATION | STEM-CELLS | LINEAGE PROGRESSION | SIGNALING PATHWAYS | BIOCHEMISTRY & MOLECULAR BIOLOGY | NECROSIS-FACTOR-ALPHA | OSTEOBLAST-LIKE CELLS | CELL BIOLOGY | FACTOR BINDING PROTEIN-5 | GENE-EXPRESSION | PARATHYROID-HORMONE | Genetic research | Bone morphogenetic proteins | Promoters (Genetics) | Proteases | Analysis | Shedding | Transcription factors | Genes | Differentiation (biology) | Paracrine signalling | Feedback loops | Cell interactions | Osteoblasts | Cell surface | Gene sequencing | Proteins | Signal transduction | Negative feedback | Proteolysis | Osteosarcoma | Extracellular matrix | Biocompatibility | Growth factors | Binding | Translocation | Cbfa-1 protein | Bone morphogenetic protein 2 | Secretion | Cell membranes | Tumor necrosis factor-α | Ribonucleic acid--RNA | Nuclear transport | Osteoblastogenesis | DNA microarrays | Regulatory mechanisms (biology) | Bone | Control theory | Niches | Osteoblast differentiation
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13. Full Text Enhancer of zeste homolog 2 (Ezh2) controls bone formation and cell cycle progression during osteogenesis in mice
by Dudakovic, Amel and Camilleri, Emily T and Paradise, Christopher R and Samsonraj, Rebekah M and Gluscevic, Martina and Paggi, Carlo Alberto and Begun, Dana L and Khani, Farzaneh and Pichurin, Oksana and Ahmed, Farah S and Elsayed, Ranya and Elsalanty, Mohammed and McGee-Lawrence, Meghan E and Karperien, Marcel and Riester, Scott M and Thaler, Roman and Westendorf, Jennifer J and van Wijnen, Ane J
Journal of biological chemistry, ISSN 0021-9258, 08/2018, Volume 293, Issue 33, pp. 12894 - 12907
Epigenetic mechanisms control skeletal development and osteoblast differentiation. Pharmacological inhibition of the histone 3 Lys-27 (H3K27) methyltransferase... 
Molecular Biology | Biochemistry | Cell Biology | methyltransferase | OSTEOBLAST DIFFERENTIATION | EPIGENETIC CONTROL | CHROMATIN | enhancer of zeste homolog | BIOCHEMISTRY & MOLECULAR BIOLOGY | bone | osteoblast | osteogenesis | LINEAGE SPECIFICATION | epigenetics | MESENCHYMAL STEM-CELLS | histone methylation | skeleton | OSTEOCALCIN GENE | SKELETAL GROWTH | chromatin regulation | bone development | INTEGRATIVE GENOMICS VIEWER | histone | HISTONE MODIFICATIONS | METHYLTRANSFERASE EZH2 | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Osteogenesis - physiology | Animals | Cell Cycle - physiology | Female | Male | Mice, Transgenic | Mice | Osteoblasts - cytology | Sex Characteristics | Osteoblasts - metabolism
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