Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37DK020503-19
Application #
2137474
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1977-09-01
Project End
1998-03-31
Budget Start
1996-04-01
Budget End
1997-03-31
Support Year
19
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Utah
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Piel 3rd, Robert B; Shiferaw, Mesafint T; Vashisht, Ajay A et al. (2016) A Novel Role for Progesterone Receptor Membrane Component 1 (PGRMC1): A Partner and Regulator of Ferrochelatase. Biochemistry 55:5204-17
Hanson, W Miachel; Chen, Zhe; Jackson, Laurie K et al. (2016) Reversible Oligonucleotide Chain Blocking Enables Bead Capture and Amplification of T-Cell Receptor ? and ? Chain mRNAs. J Am Chem Soc 138:11073-6
Dailey, Harry A; Gerdes, Svetlana; Dailey, Tamara A et al. (2015) Noncanonical coproporphyrin-dependent bacterial heme biosynthesis pathway that does not use protoporphyrin. Proc Natl Acad Sci U S A 112:2210-5
Medlock, Amy E; Shiferaw, Mesafint T; Marcero, Jason R et al. (2015) Identification of the Mitochondrial Heme Metabolism Complex. PLoS One 10:e0135896
Yien, Yvette Y; Robledo, Raymond F; Schultz, Iman J et al. (2014) TMEM14C is required for erythroid mitochondrial heme metabolism. J Clin Invest 124:4294-304
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Phillips, John D; Kushner, James P; Bergonia, Hector A et al. (2011) Uroporphyria in the Cyp1a2-/- mouse. Blood Cells Mol Dis 47:249-54
To-Figueras, J; Phillips, J D; Gonzalez-López, J M et al. (2011) Hepatoerythropoietic porphyria due to a novel mutation in the uroporphyrinogen decarboxylase gene. Br J Dermatol 165:499-505
Ajioka, Richard S; Phillips, John D; Weiss, Robert B et al. (2008) Down-regulation of hepcidin in porphyria cutanea tarda. Blood 112:4723-8
Akagi, Reiko; Inoue, Rikako; Muranaka, Shikibu et al. (2006) Dual gene defects involving delta-aminolaevulinate dehydratase and coproporphyrinogen oxidase in a porphyria patient. Br J Haematol 132:237-43

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