2.9.1.2 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26115735&form=6&db=m Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate. causal interaction,unassigned 3,0 2.9.1.2 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26805434&form=6&db=m Pontocerebellar hypoplasia type 2D and optic nerve atrophy further expand the spectrum associated with selenoprotein biosynthesis deficiency. causal interaction,unassigned 4,0 2.9.1.2 Cerebellar Ataxia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29464431&form=6&db=m A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxia. causal interaction,ongoing research,unassigned 2,1,0 2.9.1.2 Hepatitis B, Chronic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17456317&form=6&db=m [The significance of anti-soluble liver antigen/liver-pancreas in diagnosing and typing autoimmune hepatitis] diagnostic usage,unassigned 1,0 2.9.1.2 Hepatitis, Autoimmune http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10801173&form=6&db=m Identification of target antigen for SLA/LP autoantibodies in autoimmune hepatitis. causal interaction,diagnostic usage,ongoing research,unassigned 2,4,1,0 2.9.1.2 Hepatitis, Autoimmune http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11360449&form=6&db=m [Presence of SLA/LP autoantibodies in patients with primary biliary cirrhosis as a marker for secondary autoimmune hepatitis (overlap syndrome)] causal interaction,diagnostic usage,unassigned 1,4,0 2.9.1.2 Hepatitis, Autoimmune http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12117891&form=6&db=m Establishment of standardised SLA/LP immunoassays: specificity for autoimmune hepatitis, worldwide occurrence, and clinical characteristics. diagnostic usage,therapeutic application,unassigned 2,1,0 2.9.1.2 Hepatitis, Autoimmune http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16521218&form=6&db=m Characterization of human gene encoding SLA/LP autoantigen and its conserved homologs in mouse, fish, fly, and worm. unassigned - 2.9.1.2 Hepatitis, Autoimmune http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20623998&form=6&db=m Human SepSecS or SLA/LP: selenocysteine formation and autoimmune hepatitis. causal interaction,ongoing research,therapeutic application,unassigned 4,4,1,0 2.9.1.2 Hepatitis, Autoimmune http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23575112&form=6&db=m Structural mimicry between SLA/LP and Rickettsia surface antigens as a driver of autoimmune hepatitis: insights from an in silico study. diagnostic usage,ongoing research,unassigned 3,1,0 2.9.1.2 Hepatitis, Autoimmune http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28690845&form=6&db=m Diagnostic autoantibodies for autoimmune liver diseases. causal interaction,unassigned 1,0 2.9.1.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26975431&form=6&db=m Selenoproteins of African trypanosomes are dispensable for parasite survival in a mammalian host. ongoing research,therapeutic application,unassigned 3,1,0 2.9.1.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28810614&form=6&db=m Evolution of correlation between Helicobacter pylori infection and autoimmune liver disease. diagnostic usage,unassigned 2,0 2.9.1.2 Liver Cirrhosis, Biliary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11360449&form=6&db=m [Presence of SLA/LP autoantibodies in patients with primary biliary cirrhosis as a marker for secondary autoimmune hepatitis (overlap syndrome)] causal interaction,diagnostic usage,unassigned 1,4,0 2.9.1.2 Liver Cirrhosis, Biliary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17456317&form=6&db=m [The significance of anti-soluble liver antigen/liver-pancreas in diagnosing and typing autoimmune hepatitis] diagnostic usage,unassigned 1,0 2.9.1.2 Liver Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11826415&form=6&db=m Fine specificity of autoantibodies to soluble liver antigen and liver/pancreas. causal interaction,diagnostic usage,unassigned 4,4,0 2.9.1.2 Microcephaly http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29464431&form=6&db=m A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxia. causal interaction,ongoing research,unassigned 2,1,0 2.9.1.2 Neurodegenerative Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29709707&form=6&db=m Consequences of mutations and inborn errors of selenoprotein biosynthesis and functions. causal interaction,unassigned 4,0