D. Deyle

发表

Oncolytic Measles Virotherapy and Opposition to Measles Vaccination.

Minetta C. Liu, B. Leibovich, D. Dingli, 2019, Mayo Clinic proceedings.

Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience.

Michael J Ackerman, Eric D Wieben, Gianrico Farrugia, 2016, Mayo Clinic proceedings.

Normal collagen and bone production by gene-targeted human osteogenesis imperfecta iPSCs.

Pei-Rong Wang, D. Russell, D. Deyle, 2012, Molecular therapy : the journal of the American Society of Gene Therapy.

WNT1 for the skeleton

J. Westendorf, D. Deyle, 2013 .

Early and Late Outcomes of Cardiovascular Surgery in Patients With Ehlers-Danlos Syndrome

J. Dearani, D. Deyle, R. McBane, 2021, World journal for pediatric & congenital heart surgery.

Functional validation reveals the novel missense V419L variant in TGFBR2 associated with Loeys–Dietz syndrome (LDS) impairs canonical TGF-β signaling

Michael T. Zimmermann, Gavin R. Oliver, M. Zimmermann, 2017, Cold Spring Harbor molecular case studies.

Histone H4 Methyltransferase Suv420h2 Maintains Fidelity of Osteoblast Differentiation

G. Stein, A. V. van Wijnen, A. Dudakovic, 2017, Journal of cellular biochemistry.

A Genome-wide Map of Aav-mediated Human Gene Targeting Hhs Public Access

R. Sandstrom, J. Stamatoyannopoulos, Chia-Lin Wei, 2022 .

Spontaneous coronary artery dissection and its association with heritable connective tissue disorders

S. Kirmani, S. Hayes, D. Deyle, 2016, Heart.

Case Report: Early-Onset Behavioral Variant Frontotemporal Dementia in Patient With Retrotransposed Full-Length Transcript of Matrin-3 Variant 5

K. Vossel, B. Boeve, D. Deyle, 2020, Frontiers in Neurology.

Gene targeting of mutant COL1A2 alleles in mesenchymal stem cells from individuals with osteogenesis imperfecta.

P. Byers, D. Russell, D. Deyle, 2008, Molecular therapy : the journal of the American Society of Gene Therapy.

The effects of polymorphisms on human gene targeting

D. Russell, D. Deyle, David W. Russell, 2013, Nucleic acids research.

Nonintegrating Foamy Virus Vectors

D. Russell, D. Deyle, E. Olson, 2010, Journal of Virology.

Nonintegrating Foamy Virus Vectors (cid:1)

David W. Russell, D. Deyle, E. Olson, 2010 .

Integrin engagement-induced inhibition of human myelopoiesis is mediated by proline-rich tyrosine kinase 2 gene products.

C. Verfaillie, D. Deyle, K. Theunissen, 2004, Experimental hematology.

High‐Resolution Molecular Validation of Self‐Renewal and Spontaneous Differentiation in Clinical‐Grade Adipose‐Tissue Derived Human Mesenchymal Stem Cells

Asha A. Nair, G. Stein, A. Dietz, 2014, Journal of cellular biochemistry.

Validation of Osteogenic Properties of Cytochalasin D by High-Resolution RNA-Sequencing in Mesenchymal Stem Cells Derived from Bone Marrow and Adipose Tissues.

Asha A. Nair, A. Dietz, A. V. van Wijnen, 2018, Stem cells and development.

D. Deyle, J. Bennett, E. Conboy, 2018 .

Ehlers Danlos syndrome and gastrointestinal manifestations: a 20‐year experience at Mayo Clinic

M. Camilleri, A. Acosta, D. Deyle, 2015, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

Vitamin C epigenetically controls osteogenesis and bone mineralization

I. Kalajzic, A. V. van Wijnen, A. Dudakovic, 2020, Nature Communications.

Aortic Root Dilation: Do Patients With Marfan Syndrome Fare Worse Than Those With Marfanoid Features?

H. Schaff, D. Deyle, T. Foley, 2018, Mayo Clinic proceedings.

Lack of Genotoxicity due to Foamy Virus Vector Integration in Human iPSCs

D. Russell, D. Deyle, Iram Khan, 2013, Gene Therapy.

Epigenetic Control of Skeletal Development by the Histone Methyltransferase Ezh2*

G. Stein, A. Dietz, D. Lewallen, 2015, The Journal of Biological Chemistry.

Adeno-associated virus vector integration.

D. Russell, D. Deyle, David W Russell, 2009, Current opinion in molecular therapeutics.

Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy

S. Ellard, L. Mallin, M. McDonald, 2020, Clinical genetics.

Generation of Induced Pluripotent Stem Cells.

D. Deyle, 2020, Methods in molecular biology.

Generation of induced pluripotent stem cells.

D. Deyle, 2015, Methods in molecular biology.

F. Sim, A. Folpe, M. Yaszemski, 2017, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Impact of integrated translational research on clinical exome sequencing

Gavin R. Oliver, Tammy M. McAllister, M. Zimmermann, 2020, Genetics in Medicine.

Impact of Genetic Disorders in the Surgical Management of Congenital Heart Disease

J. Dearani, D. Deyle, H. Connolly, 2023, World journal for pediatric & congenital heart surgery.

Profiling of human epigenetic regulators using a semi-automated real-time qPCR platform validated by next generation sequencing.

G. Stein, A. Dietz, A. V. van Wijnen, 2017, Gene.

Arterial tortuosity syndrome: 40 new families and literature review

K. Devriendt, K. Prescott, H. Dietz, 2018, Genetics in Medicine.

Oncolytic measles virus as a novel therapy for malignant peripheral nerve sheath tumors.

D. Babovic‐Vuksanovic, K. Peng, D. Deyle, 2015, Gene.

Fracture incidence in Ehlers-Danlos syndrome - A population-based case-control study.

D. Deyle, J. Hand, Arne H Graff, 2019, Child abuse & neglect.

Arterial tortuosity syndrome: 40 new families and literature review

K. Devriendt, K. Prescott, H. Dietz, 2017, Genetics in Medicine.

Vascular Tumors Result from Adeno-Associated Virus-9 Angiogenic Gene Therapy of Bone Allografts

A. Folpe, D. Deyle, A. Shin, 2020 .

Functional Expression of ZNF467 and PCBP2 Supports Adipogenic Lineage Commitment in Adipose-derived Mesenchymal Stem Cells.

A. Dietz, A. V. van Wijnen, A. Dudakovic, 2020, Gene.

Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant

D. Deyle, P. Tebben, Nidhi Gupta, 2020, Journal of clinical research in pediatric endocrinology.

TRAPPC9-CDG: A novel congenital disorder of glycosylation with dysmorphic features and intellectual disability.

A. Novelli, P. Witters, B. Ghesquière, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features.

M. Schultz, B. Lanpher, E. Klee, 2018, JIMD reports.

A Genome-Wide Map of AAV-Mediated Human Gene Targeting

R. Sandstrom, Chia-Lin Wei, A. Cornea, 2014, Nature Structural &Molecular Biology.

Epigenetic Control of Skeletal Development by the Histone Methyltransferase Ezh2*

D. Lewallen, A. V. van Wijnen, M. McGee-Lawrence, 2015, The Journal of Biological Chemistry.