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Items: 1 to 20 of 131

1.

Genetic variation in the urea cycle: a model resource for investigating key candidate genes for common diseases.

Mitchell S, Ellingson C, Coyne T, Hall L, Neill M, Christian N, Higham C, Dobrowolski SF, Tuchman M, Summar M; Urea Cycle Disorder Consortium.

Hum Mutat. 2009 Jan;30(1):56-60. doi: 10.1002/humu.20813.

PMID:
18666241
2.

[Molecular basis of urea cycle disorders].

Matsuda I, Matsuura T, Hoshide R, Uchino T, Matsubasa T.

Nihon Rinsho. 1993 Feb;51(2):520-4. Review. Japanese.

PMID:
8464164
3.

[Molecular genetics of urea cycle diseases].

Ohtake A, Mori M.

Seikagaku. 1990 Sep;62(9):1170-7. Japanese. No abstract available.

PMID:
2258657
4.

Contrasting features of urea cycle disorders in human patients and knockout mouse models.

Deignan JL, Cederbaum SD, Grody WW.

Mol Genet Metab. 2008 Jan;93(1):7-14. Epub 2007 Oct 22. Review.

5.

Evolutionary aspects of urea cycle enzyme genes.

Takiguchi M, Matsubasa T, Amaya Y, Mori M.

Bioessays. 1989 May;10(5):163-6. Review.

PMID:
2662961
6.

[Prenatal diagnosis of enzymopathies of the urea cycle].

Chadefaux B, Rabier D, Kamoun P.

Ann Biol Clin (Paris). 1988;46(7):471-6. Review. French.

PMID:
3056128
7.

Double deficiencies of urea cycle enzymes in human liver.

Raijman L.

Biochem Med. 1979 Apr;21(2):226-33. No abstract available.

PMID:
465019
8.
9.

[Regulatory mechanisms for liver-selective transcription of ornithine cycle enzyme genes].

Takiguchi M.

Seikagaku. 1994 Oct;66(10):1293-303. Review. Japanese. No abstract available.

PMID:
7829923
10.

Genetic approach to prenatal diagnosis in urea cycle defects.

Häberle J, Koch HG.

Prenat Diagn. 2004 May;24(5):378-83.

PMID:
15164414
11.

Leukocyte urea cycle enzymes in hyperammonemia.

Wolfe DM, Gatfield PD.

Pediatr Res. 1975 Jun;9(6):531-5.

PMID:
1161340
12.

[Hereditary diseases related to a disorder of the enzymatic activity of the urea formation cycle].

Kazanskaia NS, Alekseenko LP.

Vopr Med Khim. 1976 Jul-Aug;22(4):435-43. Review. Russian. No abstract available.

PMID:
800301
13.

[Urea cycle disorders].

Tazawa Y.

Ryoikibetsu Shokogun Shirizu. 1995;(8):367-9. Review. Japanese. No abstract available.

PMID:
8581654
14.

Regulation of genes for inducible nitric oxide synthase and urea cycle enzymes in rat liver in endotoxin shock.

Tabuchi S, Gotoh T, Miyanaka K, Tomita K, Mori M.

Biochem Biophys Res Commun. 2000 Feb 5;268(1):221-4.

PMID:
10652239
15.

Changes of activity and mRNA expression of urea cycle enzymes in the liver of developing Holstein calves.

Takagi M, Yonezawa T, Haga S, Shingu H, Kobayashi Y, Takahashi T, Ohtani Y, Obara Y, Katoh K.

J Anim Sci. 2008 Jul;86(7):1526-32. doi: 10.2527/jas.2007-0799. Epub 2008 Mar 14.

16.

Disorders of the urea cycle.

Brusilow SW.

Hosp Pract (Off Ed). 1985 Oct 15;20(10):65-72. No abstract available.

PMID:
3930543
17.

Congenital hyperammonemic syndromes.

Shih VE.

Clin Perinatol. 1976 Mar;3(1):3-14.

PMID:
954343
18.

Urea biosynthesis II. Normal and abnormal regulation.

Shambaugh GE 3rd.

Am J Clin Nutr. 1978 Jan;31(1):126-33. Review. No abstract available.

19.

Transcriptional regulation of genes for ornithine cycle enzymes.

Takiguchi M, Mori M.

Biochem J. 1995 Dec 15;312 ( Pt 3):649-59. Review. No abstract available.

20.

Prospective treatment of urea cycle disorders.

Maestri NE, Hauser ER, Bartholomew D, Brusilow SW.

J Pediatr. 1991 Dec;119(6):923-8.

PMID:
1720458
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