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There are 7398371 results for: content related to: Tryptophan Overload in the Pregnant Rat: Effect on Brain Amino Acid Levels and In Vitro Protein Synthesis

  1. Fetal Heart Malformations in Experimental Hyperphenylalaninemia in Pregnant Rats

    Congenital Anomalies

    Volume 29, Issue 1, March 1989, Pages: 15–29, Itsujin SUYAMA, Mayumi TANI, Masahiro MATSUMURA, Gen ISSHIKI, Yoshiyuki OKANO, Toshiaki OURA and Kouichi NISHI-MURA

    Version of Record online : 2 MAY 2008, DOI: 10.1111/j.1741-4520.1989.tb00732.x

  2. Experimental maternal hyperphenylalaninemia: Biochemical effects and offspring development

    Developmental Psychobiology

    Volume 7, Issue 2, March 1974, Pages: 175–184, Dr. J. H. Copenhaver, M. J. Carver and R. L. Schalock

    Version of Record online : 13 OCT 2004, DOI: 10.1002/dev.420070211

  3. REFERENCES

    Monographs of the Society for Research in Child Development

    Volume 62, Issue 3, June 1997, Pages: 194–205,

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1540-5834.1997.tb02563.x

  4. Heterozygote detection in phenylketonuria

    Clinical Genetics

    Volume 11, Issue 2, February 1977, Pages: 137–146, Flemming Güttler and Gert Hansen

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1977.tb01291.x

  5. VIII. HETEROZYGOUS HETEROGENEITY

    Acta Paediatrica

    Volume 69, Issue S280, April 1980, Pages: 62–65,

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1980.tb06207.x

  6. Chronic Hyperphenylalaninemia Produces Cerebral Hyperglycinemia in Immature Rats

    Journal of Neurochemistry

    Volume 36, Issue 1, January 1981, Pages: 34–43, Gerald A. Dienel

    Version of Record online : 5 OCT 2006, DOI: 10.1111/j.1471-4159.1981.tb02374.x

  7. Biochemical Studies on the Effect of Maternal Hyperphenyl-alaninemia on Fetal Brain Maturation of Mice

    Congenital Anomalies

    Volume 28, Issue 2, June 1988, Pages: 79–83, Yasushi YAMAWAKI, Noriaki OHYA and Morimi SHIMADA

    Version of Record online : 2 MAY 2008, DOI: 10.1111/j.1741-4520.1988.tb00580.x

  8. You have free access to this content
    Molecular analysis of phenylketonuria (PKU) in newborns from Texas

    Human Mutation

    Volume 17, Issue 6, June 2001, Page: 523, Y. Yang, M. Drummond-Borg and J. Garcia-Heras

    Version of Record online : 25 MAY 2001, DOI: 10.1002/humu.1141

  9. Comparative developmental toxicity study of indium in rats and mice

    Teratogenesis, Carcinogenesis, and Mutagenesis

    Volume 20, Issue 4, 2000, Pages: 219–227, Mikio Nakajima, Hiroki Takahashi, Masanori Sasaki, Youshiro Kobayashi, Yasuo Ohno and Makoto Usami

    Version of Record online : 19 JUL 2000, DOI: 10.1002/1520-6866(2000)20:4<219::AID-TCM4>3.0.CO;2-Q

  10. You have free access to this content
    Modulation of body fluids and angiotensin II receptors in a rat model of intra-uterine growth restriction

    The Journal of Physiology

    Volume 562, Issue 3, February 2005, Pages: 937–950, Sophie Bédard, Benoit Sicotte, Jean St-Louis and Michèle Brochu

    Version of Record online : 20 JAN 2005, DOI: 10.1113/jphysiol.2004.064683

  11. Generation n + 1: Projected numbers of babies born to women with PKU compared to babies with PKU in the United States in 2009

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Pages: 1118–1123, Robert Resta

    Version of Record online : 11 APR 2012, DOI: 10.1002/ajmg.a.35312

  12. SEROTONIN DEFICIENCY IN EXPERIMENTAL HYPERPHENYLALANINEMIA

    Journal of Neurochemistry

    Volume 23, Issue 1, July 1974, Pages: 139–147, Y. H. Loo

    Version of Record online : 4 OCT 2006, DOI: 10.1111/j.1471-4159.1974.tb06928.x

  13. Regulation of the First Step of the Initiation of Brain Protein Synthesis by Guanosine Diphosphate

    Journal of Neurochemistry

    Volume 34, Issue 6, June 1980, Pages: 1639–1647, Barney Dwyer and Claude G. Wasterlain

    Version of Record online : 5 OCT 2006, DOI: 10.1111/j.1471-4159.1980.tb11255.x

  14. Mutation analysis of the 6-pyruvoyl-tetrahydropterin synthase gene in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiency

    Human Mutation

    Volume 11, Issue 1, 1998, Pages: 76–83, Tze-Tze Liu, Kwang-Jen Hsiao, Sheng-Feng Lu, Sheu-Jen Wu, Kuei-Fen Wu, Szu-Hui Chiang, Xiao-Quing Liu, Rui-Guan Chen and Wei-Min Yu

    Version of Record online : 7 JAN 1999, DOI: 10.1002/(SICI)1098-1004(1998)11:1<76::AID-HUMU12>3.0.CO;2-W

  15. IV. THE GENETIC BASIS FOR THE VARIOUS TYPES OF PHENYLALANINE HYDROXYLASE DEFICIENCY

    Acta Paediatrica

    Volume 69, Issue S280, April 1980, Pages: 37–43,

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1980.tb06203.x

  16. Loss of neurotransmitter receptors by hyperphenylalaninemia in the HPH-5 mouse brain

    Acta Paediatrica

    Volume 83, Issue s407, December 1994, Pages: 120–121, FA Hommes

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1994.tb13469.x

  17. The acute toxicity and teratogenicity of cadmium in the pregnant rat

    Journal of Applied Toxicology

    Volume 1, Issue 5, October 1981, Pages: 264–269, G. P. Samarawickrama and M. Webb

    Version of Record online : 11 JAN 2006, DOI: 10.1002/jat.2550010506

  18. Reticulocyte Ripening Substances in Pregnant Rats and their Fetuses.

    Acta Physiologica Scandinavica

    Volume 8, Issue 4, December 1944, Pages: 365–368, CLAUS MUNK PLUM

    Version of Record online : 8 DEC 2008, DOI: 10.1111/j.1748-1716.1944.tb03076.x

  19. Treatment of Inborn Errors of Metabolism

    Pediatrics International

    Volume 24, Issue 1, March 1980, Pages: 95–100, Keiya Tada

    Version of Record online : 9 OCT 2007, DOI: 10.1111/j.1442-200X.1980.tb00487.x

  20. The frequency of PKU and hyperphenylalaninemia in Sweden - a study in institutions for the mentally retarded as well as in neonates

    Clinical Genetics

    Volume 10, Issue 5, November 1976, Pages: 313–318, Gösta Holmgren, Agne Larsson, Hans Palmstierna and Jan Alm

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1976.tb00054.x