|1.||Converse, Paul J: 1 article (03/2008)|
|2.||Cao, Hua: 1 article (03/2008)|
|3.||Hotha, Srinivas: 1 article (03/2008)|
|4.||Nathan, Carl: 1 article (03/2008)|
|5.||Vandal, Omar: 1 article (03/2008)|
|6.||Gold, Benjamin: 1 article (03/2008)|
|7.||Samy, Raghu: 1 article (03/2008)|
|8.||Ly, Lan: 1 article (03/2008)|
|9.||Gurney, Mark: 1 article (03/2008)|
|10.||Cherian, Joseph: 1 article (03/2008)|
|1.||Biliary Liver Cirrhosis (Primary Biliary Cirrhosis)
06/01/2003 - "Characterization of a lipoyl domain-independent B-cell autoepitope on the human branched-chain acyltransferase in primary biliary cirrhosis and overlap syndrome with autoimmune hepatitis."
08/01/1995 - "Autoantibodies to BCOADC-E2 in patients with primary biliary cirrhosis recognize a conformational epitope."
05/01/2003 - "To develope a new enzyme immune assay (ELISA) for detection of M2 antibody specific for primary biliary cirrhosis (PBC) by using a triple hybrid clone as antigen, which coexpresses the three immunodominant lipoyl domains of PDC-E2, BCOADC-E2 and OGDC-E2 from human sources. "
07/01/1999 - "In situ nucleic acid detection of PDC-E2, BCOADC-E2, OGDC-E2, PDC-E1alpha, BCOADC-E1alpha, OGDC-E1, and the E3 binding protein (protein X) in primary biliary cirrhosis."
06/01/1989 - "Antimitochondrial antibodies of primary biliary cirrhosis recognize dihydrolipoamide acyltransferase and inhibit enzyme function of the branched chain alpha-ketoacid dehydrogenase complex."
|2.||Maple Syrup Urine Disease
02/01/2004 - "A novel deletion creating a new terminal exon of the dihydrolipoyl transacylase gene is a founder mutation of Filipino maple syrup urine disease."
08/01/1997 - "E2 transacylase-deficient (type II) maple syrup urine disease. "
06/01/1993 - "Thiamin-responsive maple syrup urine disease in a patient antigenically missing dihydrolipoamide acyltransferase."
03/20/1992 - "Branched chain acyltransferase absence due to an Alu-based genomic deletion allele and an exon skipping allele in a compound heterozygote proband expressing maple syrup urine disease."
02/01/1991 - "Molecular genetic basis of maple syrup urine disease in a family with two defective alleles for branched chain acyltransferase and localization of the gene to human chromosome 1."
|3.||Chronic Hepatitis C
|2.||3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide) (Alpha-Keto Acid Dehydrogenase)
|5.||Mitochondrial Proteins (Mitochondrial Protein)
|6.||Complementary DNA (cDNA)
|7.||Messenger RNA (mRNA)
|10.||Nitric Oxide (Nitrogen Monoxide)