All Stories

  1. The Society for Craniofacial Genetics and Developmental Biology 40th annual meeting

    Article • American Journal of Medical Genetics Part A, April 2018, Wiley

    Timothy Cox

  2. Loss of PiT-2 results in abnormal bone development and decreased bone mineral density and length in mice

    Article • Biochemical and Biophysical Research Communications, January 2018, Elsevier

    Timothy Cox

  3. Rapamycin treatment attenuates age-associated periodontitis in mice

    Article • GeroScience, August 2017, Springer Science + Business Media

    Timothy Cox

  4. Isl1 Controls Patterning and Mineralization of Enamel in the Continuously Renewing Mouse Incisor

    Article • Journal of Bone and Mineral Research, July 2017, Wiley

    Timothy Cox

  5. Differences in Oral Structure and Tissue Interactions during Mouse vs. Human Palatogenesis: Implications for the Translation of Findings from Mice

    Article • Frontiers in Physiology, March 2017, Frontiers

    Timothy Cox

  6. Retreatability of two endodontic sealers, EndoSequence BC Sealer and AH Plus: a micro-computed tomographic comparison

    Article • Restorative Dentistry & Endodontics, January 2017, The Korean Academy of Conservative Dentistry (KAMJE)

    Timothy Cox

  7. Massively Increased Caries Susceptibility in an Irf6 Cleft Lip/Palate Model

    Article • Journal of Dental Research, December 2016, SAGE Publications

    Timothy Cox

  8. Assessment of Disease-Associated Sequence Variants and Considerations for Functional Validation using Mouse Models

    Article • August 2016, Wiley

    Timothy Cox

  9. Full Spectrum of Postnatal Tooth Phenotypes in a Novel Irf6 Cleft Lip Model

    Article • Journal of Dental Research, July 2016, SAGE Publications

    Timothy Cox

  10. Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology

    Article • Developmental Biology, July 2016, Elsevier

    Timothy Cox

  11. A distal 594 bp ECR specifiesHmx1expression in pinna and lateral facial morphogenesis and is regulated by the Hox-Pbx-Meis complex

    Article • Development, June 2016, The Company of Biologists

    Timothy Cox

  12. SLC20A2 Deficiency in Mice Leads to Elevated Phosphate Levels in Cerbrospinal Fluid and Glymphatic Pathway-Associated Arteriolar Calcification, and Recapitulates Human Idiopathic Basal Ganglia Calcification

    Article • Brain Pathology, May 2016, Wiley

    Timothy Cox

  13. Postnatal Ontogeny of the Cranial Base and Craniofacial Skeleton in Male C57BL/6J Mice: A Reference Standard for Quantitative Analysis

    Article • Frontiers in Physiology, January 2016, Frontiers

    Timothy Cox

  14. Inhibition of Notch Signaling During Mouse Incisor Renewal Leads to Enamel Defects

    Article • Journal of Bone and Mineral Research, August 2015, Wiley

    Timothy Cox

  15. Utility and limitations of animal models for the functional validation of human sequence variants

    Article • Molecular Genetics & Genomic Medicine, August 2015, Wiley

    Timothy Cox

  16. Digging adaptation in insectivorous subterranean eutherians. The enigma ofMesoscalops montanensisunveiled by geometric morphometrics and finite element analysis

    Article • Journal of Morphology, June 2015, Wiley

    Timothy Cox

  17. Automated Detection of 3D Landmarks for the Elimination of Non-Biological Variation in Geometric Morphometric Analyses

    Article • June 2015, Institute of Electrical & Electronics Engineers (IEEE)

    Timothy Cox

  18. Quantitative trait loci affecting the 3D skull shape and size in mouse and prioritization of candidate genes in-silico

    Article • Frontiers in Physiology, March 2015, Frontiers

    Timothy Cox

  19. Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate

    Article • PLoS Genetics, March 2015, PLOS

    Timothy Cox

  20. Impaired myocardial development resulting in neonatal cardiac hypoplasia alters postnatal growth and stress response in the heart

    Article • Cardiovascular Research, February 2015, European Society of Cardiology

    Dr Jörg-Detlef Drenckhahn, Timothy Cox

  21. Molecular Genetics and Biology of Craniofacial Craniosynostoses

    Article • January 2015, Elsevier

    Timothy Cox

  22. The genetics of auricular development and malformation: New findings in model systems driving future directions for microtia research

    Article • European Journal of Medical Genetics, August 2014, Elsevier

    Timothy Cox

  23. Perspectives and challenges in advancing research into craniofacial anomalies

    Article • American Journal of Medical Genetics Part C Seminars in Medical Genetics, October 2013, Wiley

    Timothy Cox

  24. The MID1 E3 Ligase Catalyzes the Polyubiquitination of Alpha4 (α4), a Regulatory Subunit of Protein Phosphatase 2A (PP2A)

    Article • Journal of Biological Chemistry, June 2013, American Society for Biochemistry & Molecular Biology (ASBMB)

    Timothy Cox

  25. The Microtubule-Associated C-I Subfamily of TRIM Proteins and the Regulation of Polarized Cell Responses

    Article • January 2012, Springer Science + Business Media

    Timothy Cox

  26. Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice

    Article • PLoS Genetics, September 2011, PLOS

    Timothy Cox

  27. A landmark-free framework for the detection and description of shape differences in embryos

    Article • August 2011, Institute of Electrical & Electronics Engineers (IEEE)

    Timothy Cox

  28. Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1

    Article • Journal of Medical Genetics, April 2011, BMJ

    Timothy Cox

  29. Mutation discovery in mice by whole exome sequencing

    Article • Genome Biology, January 2011, Springer Science + Business Media

    Timothy Cox

  30. Vascular remodeling of the vitelline artery initiates extravascular emergence of hematopoietic clusters

    Article • Blood, August 2010, American Society of Hematology

    Timothy Cox

  31. Maternal Ethanol Consumption Alters the Epigenotype and the Phenotype of Offspring in a Mouse Model

    Article • PLoS Genetics, January 2010, PLOS

    Nina Kaminen-Ahola, Timothy Cox

  32. Purifying natively folded proteins from inclusion bodies using sarkosyl, Triton X-100, and CHAPS

    Article • BioTechniques, January 2010, Future Science

    Timothy Cox

  33. Compensatory Growth of Healthy Cardiac Cells in the Presence of Diseased Cells Restores Tissue Homeostasis during Heart Development

    Article • Developmental Cell, October 2008, Elsevier

    Dr Jörg-Detlef Drenckhahn, Timothy Cox

  34. Structure of the MID1 tandem B-boxes reveals an interaction reminiscent of intermolecular RING heterodimers

    Article • March 2008, Protein Data Bank, Rutgers University

    Timothy Cox

  35. Structure of the MID1 Tandem B-Boxes Reveals an Interaction Reminiscent of Intermolecular Ring Heterodimers†,‡

    Article • Biochemistry, February 2008, American Chemical Society (ACS)

    Timothy Cox

  36. A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development

    Article • Genome Biology, January 2008, Springer Science + Business Media

    Timothy Cox

  37. Solution Structure of the MID1 B-box2 CHC(D/C)C2H2 Zinc-binding Domain: Insights into an Evolutionarily Conserved RING Fold

    Article • Journal of Molecular Biology, May 2007, Elsevier

    Timothy Cox

  38. solution structure of the Mid1 B Box2 Chc(D/C)C2H2 Zinc-Binding Domain: insights into an evolutionary conserved ring fold

    Article • April 2007, Protein Data Bank, Rutgers University

    Timothy Cox

  39. Somatic FGFR and TWIST Mutations are not a Common Cause of Isolated Nonsyndromic Single Suture Craniosynostosis

    Article • Journal of Craniofacial Surgery, March 2007, Wolters Kluwer Health

    Timothy Cox

  40. Solution structure of the RBCC/TRIM B-box1 domain of human MID1: B-box with a RING

    Article • May 2006, Protein Data Bank, Rutgers University

    Timothy Cox

  41. Solution Structure of the RBCC/TRIM B-box1 Domain of Human MID1: B-box with a RING

    Article • Journal of Molecular Biology, April 2006, Elsevier

    Timothy Cox

  42. A case of Beare???Stevenson syndrome with a broad spectrum of features and a review of the FGFR2 Y375C mutation phenotype

    Article • Clinical Dysmorphology, April 2006, Wolters Kluwer Health

    Timothy Cox

  43. Subclassification of the RBCC/TRIM Superfamily Reveals a Novel Motif Necessary for Microtubule Binding

    Article • Journal of Biological Chemistry, January 2006, American Society for Biochemistry & Molecular Biology (ASBMB)

    Timothy Cox

  44. Do Craniosynostosis Syndrome Phenotypes with Both FGFR2 and TWIST Mutations have a Worse Clinical Outcome?

    Article • Journal of Craniofacial Surgery, January 2006, Wolters Kluwer Health

    Timothy Cox

  45. The major splice variant of human 5-aminolevulinate synthase-2 contributes significantly to erythroid heme biosynthesis

    Article • The International Journal of Biochemistry & Cell Biology, February 2004, Elsevier

    Timothy Cox

  46. Analysis of Intracranial Volume in Apert Syndrome Genotypes

    Article • Pediatric Neurosurgery, January 2004, Karger Publishers

    Timothy Cox

  47. 3-D Imaging of Biomedical Samples

    Article • Wiley

    Dr Jörg-Detlef Drenckhahn, Timothy Cox