Literature DB >> 13520699

The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria.

W E KNOX, E C MESSINGER.   

Abstract

Entities:  

Keywords:  PHENYLPYRUVIC OLIGOPHRENIA/heredity

Mesh：

Year:  1958        PMID： 13520699      PMCID： PMC1931862     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  9 in total

1.  Pathogenetic problems in phenylketonuria.

Authors:  W E KNOX; D Y HSIA
Journal:  Am J Med       Date:  1957-05       Impact factor: 4.965

2.  A case of phenylketonuria with borderline intelligence.

Authors:  D Y HSIA; W E KNOX; R S PAINE
Journal:  AMA J Dis Child       Date:  1957-07

3.  The excretion of amino acids by the human; a quantitative study with ion-exchange chromatography.

Authors:  D F EVERED
Journal:  Biochem J       Date:  1956-03       Impact factor: 3.857

4.  Detection of the heterozygous carriers of phenylketonuria.

Authors:  K W DRISCOLL; D Y HSIA
Journal:  Lancet       Date:  1956-12-29       Impact factor: 79.321

5.  Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria.

Authors:  K W DRISCOLL; D Y HSIA; W E KNOX; W TROLL
Journal:  Nature       Date:  1956-12-01       Impact factor: 49.962

6.  The amino acid content of the blood and urine in Wilson's disease.

Authors:  W H STEIN; A G BEARN; S MOORE
Journal:  J Clin Invest       Date:  1954-03       Impact factor: 14.808

7.  Assay of L-phenylalanine as phenylethylamine after enzymatic decarboxylation; application to isotopic studies.

Authors:  S UDENFRIEND; J R COOPER
Journal:  J Biol Chem       Date:  1953-08       Impact factor: 5.157

8.  The hydroxylation of phenylalanine and antipyrine in phenylpyruvic oligophrenia.

Authors:  S UDENFRIEND; S P BESSMAN
Journal:  J Biol Chem       Date:  1953-08       Impact factor: 5.157

9.  Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system.

Authors:  G A JERVIS
Journal:  Proc Soc Exp Biol Med       Date:  1953-03
  9 in total
  12 in total

1.  The high frequency of phenylketonuria in Ireland and Western Scotland.

Authors:  L I Woolf
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

2.  Increased reliability for the determination of the carrier state in phenylketonuria.

Authors:  H L WANG; N E MORTON; H A WAISMAN
Journal:  Am J Hum Genet       Date:  1961-06       Impact factor: 11.025

3.  Discrimination of genetic entities in muscular dystrophy.

Authors:  C S CHUNG; N E MORTON
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

4.  Phenylketonuria: a linkage study using phenylalanine tolerance tests.

Authors:  J H RENWICK; S D LAWLER; V A COWIE
Journal:  Am J Hum Genet       Date:  1960-09       Impact factor: 11.025

5.  [Advances in the recognition of heterozygous characteristics in hereditary enzymopathies].

Authors:  F LINNEWEH
Journal:  Klin Wochenschr       Date:  1962-06-01

6.  Dominance, pleiotropy and metabolic structure.

Authors:  P D Keightley; H Kacser
Journal:  Genetics       Date:  1987-10       Impact factor: 4.562

7.  Classic phenylketonuria: heterozygote detection during pregnancy.

Authors:  R F Griffin; M E Humienny; E C Hall; L J Elsas
Journal:  Am J Hum Genet       Date:  1973-11       Impact factor: 11.025

8.  The molecular basis of dominance.

Authors:  H Kacser; J A Burns
Journal:  Genetics       Date:  1981 Mar-Apr       Impact factor: 4.562

9.  Detection of phenylketonuria carriers.

Authors:  S Kelly; F Rose
Journal:  Public Health Rep       Date:  1969-02       Impact factor: 2.792

10.  Phenylketonuria heterozygote detection in families with affected children.

Authors:  T D Paul; I K Brandt; L J Elsas; C E Jackson; P Mamunes; C S Nance; W E Nance
Journal:  Am J Hum Genet       Date:  1978-05       Impact factor: 11.025
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.