Blood phenylalanine reduction corrects CNS dopamine and serotonin deficiencies and partially improves behavioral performance in adult phenylketonuric mice.

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Tetrahydrobiopterin treatment reduces brain L-Phe but only partially improves serotonin in hyperphenylalaninemic ENU1/2 mice.

P2860

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Blood phenylalanine reduction corrects CNS dopamine and serotonin deficiencies and partially improves behavioral performance in adult phenylketonuric mice.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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Blood phenylalanine reduction ...... in adult phenylketonuric mice.

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Blood phenylalanine reduction ...... in adult phenylketonuric mice.

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type

Item

label

Blood phenylalanine reduction ...... in adult phenylketonuric mice.

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Blood phenylalanine reduction ...... in adult phenylketonuric mice.

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Blood phenylalanine reduction ...... in adult phenylketonuric mice.

@en

Blood phenylalanine reduction ...... in adult phenylketonuric mice.

@nl

P1476

Blood phenylalanine reduction ...... in adult phenylketonuric mice.

@en

P2093

Beat Thöny

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Cary O Harding

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Jacob Raber

http://www.w3.org/2001/XMLSchema#string

Ming Ying

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Shelley R Winn

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Tanja Scherer

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P2860

Amino-acid transport by heterodimers of 4F2hc/CD98 and members of a permease family

Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuria

Dwarfism and low insulin-like growth factor-1 due to dopamine depletion in Pts-/- mice rescued by feeding neurotransmitter precursors and H4-biopterin

Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase

Large Neutral Amino Acid Supplementation Exerts Its Effect through Three Synergistic Mechanisms: Proof of Principle in Phenylketonuria Mice

Expression cloning and characterization of a transporter for large neutral amino acids activated by the heavy chain of 4F2 antigen (CD98)

The Behavioral Consequence of Phenylketonuria in Mice Depends on the Genetic Background

Reduced availability of brain amines during critical phases of postnatal development in a genetic mouse model of cognitive delay.

Complete correction of hyperphenylalaninemia following liver-directed, recombinant AAV2/8 vector-mediated gene therapy in murine phenylketonuria.

Variant of dihydropteridine reductase deficiency without hyperphenylalaninaemia: effect of oral phenylalanine loading.

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6-20

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scholarly article

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10.1016/J.YMGME.2017.10.009

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P433

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P478

123

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P50

Aurora Martinez

Sydney J Weber

P577

2017-10-19T00:00:00Z

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P698

29331172

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P921

phenylketonuria

P932

5786171

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Blood phenylalanine reduction corrects CNS dopamine and serotonin deficiencies and partially improves behavioral performance in adult phenylketonuric mice.

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P2860

P2860

Blood phenylalanine reduction corrects CNS dopamine and serotonin deficiencies and partially improves behavioral performance in adult phenylketonuric mice.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932