نتایج جستجو برای: phenylalanine phe

تعداد نتایج: 18602  

Journal: :Langmuir : the ACS journal of surfaces and colloids 2011
Yi Liu Yi Cheng Hsuan-Chen Wu Eunkyoung Kim Rein V Ulijn Gary W Rubloff William E Bentley Gregory F Payne

Electroaddressing, the use of imposed electrical stimuli to guide assembly, is attractive because electrical stimuli can be conveniently applied with high spatial and temporal resolution. Several electroaddressing mechanisms have been reported in which electrode-induced pH gradients trigger stimuli-responsive materials to undergo localized sol-gel transitions to form hydrogel matrices. A common...

Journal: :Journal of bacteriology 1998
J Gowrishankar A J Pittard

Osmotic regulation of proU expression in the enterobacteria is achieved, at least in part, by a repression mechanism involving the histone-like nucleoid protein H-NS. By the creation of binding sites for the TyrR regulator protein in the vicinity of the sigma70-controlled promoter of proU in Escherichia coli, we were able to demonstrate a superposed TyrR-mediated activation by L-phenylalanine (...

Journal: :Surface and interface analysis : SIA 2013
Jordan O Lerach Nicholas Winograd

A novel approach to elucidate the ionization mechanism for the [M + H]+ molecular ion of organic molecules is investigated by molecular depth profiling of isotopically enriched thin films. Using a model bi-layer film of phenylalanine (PHE) and PHE-D8, the results show formation of an [M + D]+ molecular ion for the non-enriched PHE molecule attributed to rearrangements of chemical damage due to ...

Journal: :American journal of physiology. Endocrinology and metabolism 2003
Paolo Tessari Edward Kiwanuka Michela Zanetti Rocco Barazzoni

Whether phenylalanine-tyrosine (Phe-Tyr) tracers yield estimates of postprandial protein synthesis comparable to those of the widely used leucine (Leu) tracer is unclear. We measured Leu oxidation (Ox), Phe hydroxylation (Hy), and their disposal into whole body protein synthesis before and after the administration of a mixed meal (62 kJ/kg body wt, 22% of energy as protein), over 4 h in healthy...

Journal: :American journal of physiology. Endocrinology and metabolism 2012
Patrick Solverson Sangita G Murali Adam S Brinkman David W Nelson Murray K Clayton Chi-Liang Eric Yen Denise M Ney

Phenylketonuria (PKU) is caused by a mutation in the phenylalanine (phe) hydroxylase gene and requires a low-phe diet plus amino acid (AA) formula to prevent cognitive impairment. Glycomacropeptide (GMP) contains minimal phe and provides a palatable alternative to AA formula. Our objective was to compare growth, body composition, and energy balance in Pah(enu2) (PKU) and wild-type mice fed low-...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2008
Paolo Tessari Edward Kiwanuka Monica Vettore Rocco Barazzoni Michela Zanetti Diego Cecchet Rocco Orlando

We explored the mechanism(s) of increased aromatic amino acids concentrations in liver cirrhosis using phenylalanine (Phe) and tyrosine (Tyr) isotope infusions in male patients with compensated cirrhosis (five in Child Class A, three in B) and in eight matched healthy controls, in both postabsorptive and fed states. After a baseline period, a standard liquid mixed meal was fed continuously over...

Journal: :Jornal de pediatria 2007
Viviane C Kanufre Ana L P Starling Ennio Leão Marcos J B Aguiar Jacqueline S Santos Rosângelis D L Soares Adriana M Silveira

OBJECTIVE To evaluate the effect of breastmilk as a source of phenylalanine (phe) on levels of this amino acid and on growth in phenylketonuric infants. METHODS The study recruited 35 breastfed phenylketonuric infants and compared their results with those of 35 infants fed on commercial, milk-based formula. The groups were paired for sex and age at weaning from breastfeeding. Data were analyz...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1994
A Diamond V Ciaramitaro E Donner S Djali M B Robinson

Phenylketonuria (PKU) is a genetic disorder in which the hydroxylation of phenylalanine (Phe) to tyrosine is severely disrupted. If PKU is left untreated, severe mental retardation results. The accepted treatment is to restrict dietary intake of Phe. It has generally been thought that cognitive impairments are prevented if levels of Phe in plasma are maintained at or below five times the normal...

Journal: :JIMD reports 2017
Ana Claudia Marquim F Araújo Wilma M C Araújo Ursula M Lanfer Marquez Rita Akutsu Eduardo Y Nakano

BACKGROUND Knowing the phenylalanine (Phe) content of foods is essential for managing the diet of patients with phenylketonuria. Data on the Phe content of foods are scarce and sometimes vary between different Food Composition Tables (FCT). Brazil created its own table of the Phe contents of fruits and vegetables based exclusively on the chemical analysis of protein content, considering that pr...

Carnation (Dianthus caryophyllus L.) is one of the most important cut flowers in the world. This experiment was carried out to evaluate the effects of pre-harvest application of some amino acids and organic acids on enzymatic traits and longevity of carnation flowers (Dianthus caryophyllus cv. Tessino) based on completely randomized design with 13 treatments and three...

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