Isoleucine
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Subject Areas on Research
- 2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolism.
- A past mutation at isoleucine 397 is now a common cause of moderate/mild haemophilia B.
- An inner activation gate controls TMEM16F phospholipid scrambling.
- Calmodulin supports both inactivation and facilitation of L-type calcium channels.
- Clinical comparison of Alzheimer's disease in pedigrees with the codon 717 Val-->Ile mutation in the amyloid precursor protein gene.
- Cytocidal amino acid starvation of Saccharomyces cerevisiae and Candida albicans acetolactate synthase (ilv2{Delta}) mutants is influenced by the carbon source and rapamycin.
- Force-induced prolyl cis-trans isomerization in elastin-like polypeptides.
- Mutational analysis of the function of Met137 and Ile197, two amino acids implicated in sequence-specific DNA recognition by the EcoRI endonuclease.
- Myotilin is mutated in limb girdle muscular dystrophy 1A.
- Myotilin overexpression enhances myopathology in the LGMD1A mouse model.
- Rapid diagnosis of homocystinuria and other hypermethioninemias from newborns' blood spots by tandem mass spectrometry.
- Rapid diagnosis of maple syrup urine disease in blood spots from newborns by tandem mass spectrometry.
- Silencing of the constitutive activity of the dopamine D1B receptor. Reciprocal mutations between D1 receptor subtypes delineate residues underlying activation properties.
- Thrombin-catalyzed activation of recombinant human factor V.
- Transport interactions of cystine and dibasic amino acids in isolated rat renal tubules.
- Two PDGF-B chain residues, arginine 27 and isoleucine 30, mediate receptor binding and activation.
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Keywords of People
- Pitt, Geoffrey Stuart, Adjunct Professor in the Department of Medicine, Medicine, Cardiology