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FAH encodes the last enzyme in the tyrosine catabolism pathway. Zusätzlich bieten wir Ihnen FAH Proteine (13) und FAH Kits (10) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 92 products:
Polyclonal FAH Primary Antibody für IHC (p), IP - ABIN541084
Wangensteen, Wilber, Keng, He, Matise, Wangensteen, Carson, Chen, Steer, McIvor, Largaespada, Wang, Ekker: A facile method for somatic, lifelong manipulation of multiple genes in the mouse liver. in Hepatology (Baltimore, Md.) 2008
Show all 2 Pubmed References
Cow (Bovine) Polyclonal FAH Primary Antibody für IHC, WB - ABIN2776935
Bliksrud, Brodtkorb, Andresen, van den Berg, Kvittingen: Tyrosinaemia type I--de novo mutation in liver tissue suppressing an inborn splicing defect. in Journal of molecular medicine (Berlin, Germany) 2005
Show all 3 Pubmed References
The Caenorhabditis elegans K10C2.4 gene encodes a member of the fumarylacetoacetate hydrolase family: a Caenorhabditis elegans model of type I tyrosinemia
Naked plasmid DNA transfection offers a promising alternative treatment for hereditary tyrosinemia type 1 caused by mutation of the fah gene.
Kidneys of adult Fah(-/-) mice, withdrawn from NTBC for 15 days, reveal limited characteristics of apoptosis, and have acquired resistance to a caspase-9- and caspase-3-independent form of cell death
Gene expressions in tyrosinemia type I model mice with liver failure using microarrays. Numerous genes, including amino acid metabolism and apoptosis related genes, were up- or down-regulated at the onset of liver failure.
Altogether these findings elucidate the molecular basis of HT1 caused by the frequent FAH c.1062+5G>A mutation, and demonstrate the compensatory effect of the c.1061C>A change in promoting exon definition, thus unraveling a rare mechanism leading to FAH immune-reactive mosaicism.
molecular aspects of the FAH gene and its corresponding protein and a complete listing of all the mutations identified to date; highlight of the importance of splicing mutations in hereditary tyrosinemia type 1
Results from whole exome sequencing revealed a novel homozygous missense variant in FAH causing tyrosinemia type I . This novel variant involves the catalytic pocket of the enzyme, but does not result in increased succinylacetone or tyrosine.
FAH gene mutation is associated with tyrosinemia type 1.
Four splicing mutations affecting exonic or intronic nucleotides of the FAH gene were identified in two hereditary tyrosinemia type I patients.
Two siblings have been described with tyrosinemia type 1 complicated by reversible hypertrophic cardiomyopathy in infancy due to a FAH homozygous mutation.
Compound mutations (R237X and L375P) in the fumarylacetoacetate hydrolase gene causing tyrosinemia type I in a Chinese patient.
Identification of novel mutations in the fumarylacetoacetase gene in Hereditary tyrosinaemia type I.
We detected 11 novel and 6 previously described pathogenic mutations in the fumarylacetoacetase gene in a cohort of 43 patients originating from the Middle East with the acute form hereditary tyrosinemia type I
A missense mutation in the fumarylacetoacetate hydrolase gene, responsible for hereditary tyrosinemia, acts as a splicing mutation.
Data describe the metabolism of fumarylacetoacetate hydrolase mRNA harboring a nonsense mutation, W262X, in lymphoblastoid cell lines derived from hereditary tyrosinemia type I patients.
identification of an alternative nonsense transcript of the fah gene, which despite being subjected to nonsense-mediated mRNA decay, produces a protein in different human tissues
An immunopositive liver nodule was found in a patient with tyrosinemia having a mosaic pattern of FAH.
This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT).
, hypothetical protein