Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08DK002574-05
Application #
6380081
Study Section
Special Emphasis Panel (SRC)
Program Officer
Hyde, James F
Project Start
1997-09-12
Project End
2002-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
5
Fiscal Year
2001
Total Cost
$120,420
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
937727907
City
Winston-Salem
State
NC
Country
United States
Zip Code
27157
Yang, Zi; Lantz, Patrick E; Ibdah, Jamal A (2007) Post-mortem analysis for two prevalent beta-oxidation mutations in sudden infant death. Pediatr Int 49:883-7
Angdisen, J; Moore, V D G; Cline, J M et al. (2005) Mitochondrial trifunctional protein defects: molecular basis and novel therapeutic approaches. Curr Drug Targets Immune Endocr Metabol Disord 5:27-40
Shekhawat, Prem; Bennett, Michael J; Sadovsky, Yoel et al. (2003) Human placenta metabolizes fatty acids: implications for fetal fatty acid oxidation disorders and maternal liver diseases. Am J Physiol Endocrinol Metab 284:E1098-105
Yang, Zi; Zhao, Yiwen; Bennett, Michael J et al. (2002) Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations. Am J Obstet Gynecol 187:715-20
Yang, Zi; Yamada, Jennifer; Zhao, Yiwen et al. (2002) Prospective screening for pediatric mitochondrial trifunctional protein defects in pregnancies complicated by liver disease. JAMA 288:2163-6
Ibdah, J A; Paul, H; Zhao, Y et al. (2001) Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death. J Clin Invest 107:1403-9
Ibdah, J A; Zhao, Y; Viola, J et al. (2001) Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutations. J Pediatr 138:396-9
Vitkute, J; Stankevicius, K; Tamulaitiene, G et al. (2001) Specificities of eleven different DNA methyltransferases of Helicobacter pylori strain 26695. J Bacteriol 183:443-50
Blaser, M J; Berg, D E (2001) Helicobacter pylori genetic diversity and risk of human disease. J Clin Invest 107:767-73
Ibdah, J A; Yang, Z; Bennett, M J (2000) Liver disease in pregnancy and fetal fatty acid oxidation defects. Mol Genet Metab 71:182-9

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