ARUP Scientific Resource for Research and Education

This site is hosted by ARUP Laboratories and the University of Utah Department of Pathology as a scientific and educational resource for pathologists and professionals in laboratory medicine. ARUP is an enterprise of the University of Utah and its Department of Pathology.

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Click on the menu items below to see the latest content additions:

spacer Mutation Databases

The University of Utah Department of Pathology and ARUP Laboratories hosts a growing number of human gene variant-disease database collections. Each database relies on both medical and molecular expertise, and uniquely displays sequence variation and clinical information together.

  • ALPORT (COL4A5)
  • Biotinidase Deficiency (BTD)
  • BRCA (BRCA1 and BRCA2)
  • Galactosemia (GALT)
  • Hereditary Hemorrhagic Telangiectasia (ACVRL1 and ENG)
  • Juvenile Polyposis Syndrome (SMAD4)
  • Legius Syndrome (SPRED1)
  • Multiple Endocrine Neoplasia type 1 (MEN1)
  • Multiple Endocrine Neoplasia type 2 (RET)
  • Primary Carnitine Deficiency (SLC22A5)
  • Pulmonary Arterial Hypertension (BMPR2)
  • RASA1-related disorders

spacer Video Lectures

  • Online Credits:    CME | SAM | PACE Implementing a Test Utilization Management Program: Combining Medicine and Management by Casey Leavitt, MBA
  • Online Credits:    PACE | Florida Blood Bank vs Piggy Bank: Keys to Harmonizing Margin and Mission by Kent Gordon, CPA, MAcc
  • Online Credits:    CME | SAM | PACE Carrier detection for Tay-Sachs disease: A model for genetic disease prevention by Irene De Biase, MD, PhD
  • Online Credits:    CME | SAM | PACE | Florida A Hippocratic Oath for the Diagnostics Industry by Brian R. Jackson, MD, MS
  • Online Credits:    PACE | Florida Are You a Customer Service “Have” or “Have Not”? by Chérie V. Petersen, BA

More video lectures

spacer Short Topics

  • Spotlight on Testing Technologies:
    An Overview of Time of Flight Mass Spectrometry by Frederick Strathmann, PhD, DABCC (CC,TC)
  • Spotlight on Testing:
    Utility of Genetic Testing for Mutations in the EIF2AK4 Gene in the Diagnosis of pulmonary capillary hemangiomatosis and pulmonary veno-occlusive disease by Hunter Best, PhD
  • AACC 2014 Booth Presentation:
    How to Estimate the Impact of Changing Laboratory Methods by Robert Schmidt, MD, PhD, MBA
  • AACC 2014 Booth Presentation:
    Extreme Makeover: Lab Edition by Brian R. Jackson, MD, MS

More short topics

spacer Case Reports

  • Online Credits:    spacer spacer Cytopathology Case 16: FNA and Core Biopsy Diagnosis of a Retroperitoneal Mass
  • Online Credits:    spacer spacer Hematopathology Case 3: 2-Year Old Male with Numerous Infections, Persistent Leukocytosis and Monocytosis
  • Online Credits:    spacer spacer Hematopathology Case 2: CD15 positive diffuse large B-cell lymphoma
  • Online Credits:    spacer spacer Cytopathology Case 15: Fine Needle Aspirate of Parotid Gland Mass in a 53 year-old Woman

More case reports

spacer Collaborate with ARUP

  • Contacts by Disease or Technology
  • Academic Collaborations Information
  • Industry Collaborations Information

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