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 #
7R37DK026466-17
Application #
2137867
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1979-07-01
Project End
1998-12-31
Budget Start
1996-01-01
Budget End
1996-12-31
Support Year
17
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Bloomer, Joseph R; Wang, Yongming; Singhal, Anuj et al. (2006) Biochemical abnormality in erythropoietic protoporphyria: cause and consequences. J Pediatr Gastroenterol Nutr 43 Suppl 1:S36-40
Rand, Elizabeth B; Bunin, Nancy; Cochran, William et al. (2006) Sequential liver and bone marrow transplantation for treatment of erythropoietic protoporphyria. Pediatrics 118:e1896-9
McGuire, Brendan M; Bonkovsky, Herbert L; Carithers Jr, Robert L et al. (2005) Liver transplantation for erythropoietic protoporphyria liver disease. Liver Transpl 11:1590-6
Bloomer, Joseph; Wang, Yongming; Singhal, Anuj et al. (2005) Molecular studies of liver disease in erythropoietic protoporphyria. J Clin Gastroenterol 39:S167-75
Liu, Yunying L; Ang, Sonny O; Weigent, Douglas A et al. (2004) Regulation of ferrochelatase gene expression by hypoxia. Life Sci 75:2035-43
Risheg, Hiba; Chen, Fu-Ping; Bloomer, Joseph R (2003) Genotypic determinants of phenotype in North American patients with erythropoietic protoporphyria. Mol Genet Metab 80:196-206
Chen, Fu-Ping; Risheg, Hiba; Liu, Yunying et al. (2002) Ferrochelatase gene mutations in erythropoietic protoporphyria: focus on liver disease. Cell Mol Biol (Noisy-le-grand) 48:83-9
Bloomer, J R; Poh-Fitzpatrick, M B (2000) Theodore Woodward Award. Pathogenesis of biochemical abnormalities in protoporphyria. Trans Am Clin Climatol Assoc 111:245-56; discussion 256-7
Wang, X; Yang, L; Kurtz, L et al. (1999) Haplotype analysis of families with erythropoietic protoporphyria and novel mutations of the ferrochelatase gene. J Invest Dermatol 113:87-92
Jenkins, M M; LeBoeuf, R D; Ruth, G R et al. (1998) A novel stop codon mutation (X417L) of the ferrochelatase gene in bovine protoporphyria, a natural animal model of the human disease. Biochim Biophys Acta 1408:18-24

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