Molecular & Medical Genetics

Phone503 494-7703, 503 494-6886
Emailmedgen@ohsu.edu
Websitehttp://www.ohsu.edu/xd/education/schools/school-of-medicine/departments/basic-science-departments/molecular-and-medical-genetics/

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Novel roles for USP36 in ribosome biogenesis
Dai, M.
Project: Research project
Augmented Phenylalanine Clearance by Muscles as Novel Therapy for Phenylketonuria
Harding, C.
Project: Research project
Stem Cell-Mediated Liver Repopulation for Murine PKU
Harding, C.
Project: Research project
Intravenous non-viral gene therapy for phenylketonuria (PKU)
Harding, C.
Project: Research project
HYPOHIDROTIC ECTODERMAL DYSPLASIA--A GENETIC ANALYSIS
Zonana, J. (.
Project: Research project
Translational Opportunities for the Heritable Disorders of Connective Tissue
Sakai, L.
Project: Research project
27th Annual Conference of the National Marfan Foundation
Sakai, L.
Project: Research project
6th Pan Pacific Connective Tissue Societies Symposium
Sakai, L.
Project: Research project
The Role of Hepatic Copper Accumulation in Wilson Disease
Ralle, M.
Project: Research project
Development of novel markers to contextualize X-ray fluorescence microscopy
Ralle, M.
Project: Research project
MOLECULAR BASIS OF SYNDROMIC RETINITIS PIGMENTOSA
Hayflick, S.
Project: Research project
FIRST SCIENTIFIC WORKSHOP ON HALLERVORDEN-SPATZ SYNDROME
Hayflick, S.
Project: Research project
Pathophysiology and Treatment of Fanconi Anemia
Moses, R. & Grompe, M.
Project: Research project
DeSUMOylation regulation of c-Myc
Dai, M., Sears, R., Dai, M. & Sears, R.
Project: Research project
CYP2D6 gene variants and effectiveness of adjuvant tamoxifen in breast cancer
Richards, C. (.
Project: Research project
Inductively Coupled Plasma Mass Spectrometer for High Sensitivity Elemental Analysis
Ralle, M.
Project: Research project
Hyperphenylalaninemia Disorders Consortium of the Rare Disease Clinical Research Network
Harding, C.
Project: Research project
Screening for Chemicals that Potentiate TRAIL-Induced Apoptosis of Cancer Cells
Rozanov, D.
Project: Research project
Genome analysis to elucidate molecular mechanisms for peripheral neuropathies
Wiszniewski, W.
Project: Research project
ECTODERMAL DYSPLASIAS A MOLECULAR GENETIC ANALYSIS
Zonana, J. (.
Project: Research project
Role of Fatty Acid Oxidation Defects in Insulin Sensitivity
Gillingham, M., Purnell, J. & Purnell, J.
Project: Research project
The Natural History of LCHAD Retinopathy
Gillingham, M.
Project: Research project
KDM5B Mediates Cell Survival in MYC-Dependent T-ALL
Liefwalker, D.
Project: Research project
Dissection of the feedback inhibition of c-Myc by L11
Dai, M.
Project: Research project
HETEROLOGOUS GENE THERAPY FOR METABOLISM
Harding, C.
Project: Research project
Novel roles for USP36 in ribosome biogenesis
Dai, M.
Project: Research project
AAV-MEDIATED GENE THERAPY--INBORN ERRORS OF METABOLISM
Harding, C.
Project: Research project
Gordon Research Conference on Elastin &Elastic Fibers
Sakai, L.
Project: Research project
Characterizing patient-specific TBR1 mutations: Understanding a master regulator of autism risk.
O'Roak, B.
Project: Research project
Microfibril Fragments: Biomarkers of Aortic Disease
Sakai, L.
Project: Research project
27th Annual Conference of the National Marfan Foundation
Sakai, L.
Project: Research project
6th Pan Pacific Connective Tissue Societies Symposium
Sakai, L.
Project: Research project
PATHOGENESIS OF MARFAN SYNDROME AND RELATED DISORDERS
Sakai, L.
Project: Research project
Consortium for Translational Research in Marfan Syndrome
Sakai, L.
Project: Research project
Epigenetic tools and resources for cell-type and spatial analysis of individual mammalian non-neuronal cells
Adey, A.
Project: Research project
Development of novel markers to contextualize X-ray fluorescence microscopy
Ralle, M.
Project: Research project
ICP-MS to Measure Elemental Concentrations
Ralle, M.
Project: Research project
MOLECULAR BASIS OF SYNDROMIC RETINITIS PIGMENTOSA
Hayflick, S.
Project: Research project
The Molecular Basis of Syndromic Retinitis Pigmentosa
Hayflick, S.
Project: Research project
The Molecular Basis of Infantile Neuroaxonal Dystrophy
Hayflick, S.
Project: Research project
An international scientific conference on NBIA disorders
Hayflick, S.
Project: Research project
Exploring the pathophysiology and treatment of LCHADD retinopathy
Gillingham, M.
Project: Research project
High-content single-cell epigenetic technologies scalable to the human brain
Adey, A.
Project: Research project
The Natural History of LCHAD Retinopathy
Gillingham, M.
Project: Research project
Diet-Induced Insulin Resistance in a Murine Fatty Acid Oxidation Disorder
Gillingham, M.
Project: Research project
HYPOHIDROTIC ECTODERMAL DYSPLASIA GENE
Zonana, J. (.
Project: Research project
Fatty Acid Oxidation Disorders &Body Weight Regulation
Gillingham, M.
Project: Research project
Diet Therapy of Long-Chain Fatty Acid Oxidation Defects
Gillingham, M.
Project: Research project
Development and Characterization of a Swine Model of Phenylketonuria
Harding, C.
Project: Research project
AAV2/8 vector-mediated liver gene therapy for phenylketonuria (PKU)
Harding, C.
Project: Research project