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Items: 1 to 20 of 41

1.

Hyperammonemia in review: pathophysiology, diagnosis, and treatment.

Auron A, Brophy PD.

Pediatr Nephrol. 2012 Feb;27(2):207-22. doi: 10.1007/s00467-011-1838-5. Review.

PMID:
21431427
2.

Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyond.

Erez A, Nagamani SC, Lee B.

Am J Med Genet C Semin Med Genet. 2011 Feb 15;157C(1):45-53. doi: 10.1002/ajmg.c.30289. Review.

3.

Functional complementation in yeast allows molecular characterization of missense argininosuccinate lyase mutations.

Trevisson E, Burlina A, Doimo M, Pertegato V, Casarin A, Cesaro L, Navas P, Basso G, Sartori G, Salviati L.

J Biol Chem. 2009 Oct 16;284(42):28926-34. doi: 10.1074/jbc.M109.050195.

4.

Systemic hypertension in two patients with ASL deficiency: a result of nitric oxide deficiency?

Brunetti-Pierri N, Erez A, Shchelochkov O, Craigen W, Lee B.

Mol Genet Metab. 2009 Sep-Oct;98(1-2):195-7. doi: 10.1016/j.ymgme.2009.06.006.

5.

Intellectual, adaptive, and behavioral functioning in children with urea cycle disorders.

Krivitzky L, Babikian T, Lee HS, Thomas NH, Burk-Paull KL, Batshaw ML.

Pediatr Res. 2009 Jul;66(1):96-101. doi: 10.1203/PDR.0b013e3181a27a16.

6.

Evaluation of endogenous nitric oxide synthesis in congenital urea cycle enzyme defects.

Nagasaka H, Tsukahara H, Yorifuji T, Miida T, Murayama K, Tsuruoka T, Takatani T, Kanazawa M, Kobayashi K, Okano Y, Takayanagi M.

Metabolism. 2009 Mar;58(3):278-82. doi: 10.1016/j.metabol.2008.09.025.

PMID:
19217439
7.

Methods to detect nitric oxide and its metabolites in biological samples.

Bryan NS, Grisham MB.

Free Radic Biol Med. 2007 Sep 1;43(5):645-57. Review.

8.

Arginine metabolism: boundaries of our knowledge.

Morris SM Jr.

J Nutr. 2007 Jun;137(6 Suppl 2):1602S-1609S. Review.

9.

The L-arginine paradox: Importance of the L-arginine/asymmetrical dimethylarginine ratio.

Bode-Böger SM, Scalera F, Ignarro LJ.

Pharmacol Ther. 2007 Jun;114(3):295-306. Review.

PMID:
17482266
10.

Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novel ASL pseudogene.

Trevisson E, Salviati L, Baldoin MC, Toldo I, Casarin A, Sacconi S, Cesaro L, Basso G, Burlina AB.

Hum Mutat. 2007 Jul;28(7):694-702.

PMID:
17326097
11.

CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.

Morello R, Bertin TK, Chen Y, Hicks J, Tonachini L, Monticone M, Castagnola P, Rauch F, Glorieux FH, Vranka J, Bächinger HP, Pace JM, Schwarze U, Byers PH, Weis M, Fernandes RJ, Eyre DR, Yao Z, Boyce BF, Lee B.

Cell. 2006 Oct 20;127(2):291-304.

12.

Measurement of nitric oxide levels in the red cell: validation of tri-iodide-based chemiluminescence with acid-sulfanilamide pretreatment.

Wang X, Bryan NS, MacArthur PH, Rodriguez J, Gladwin MT, Feelisch M.

J Biol Chem. 2006 Sep 15;281(37):26994-7002.

13.

Role of macula densa neuronal nitric oxide synthase in renal diseases.

Tojo A, Onozato ML, Fujita T.

Med Mol Morphol. 2006 Mar;39(1):2-7. Review.

PMID:
16575507
15.
16.

The role of nitric oxide in cardiovascular diseases.

Naseem KM.

Mol Aspects Med. 2005 Feb-Apr;26(1-2):33-65. Review.

PMID:
15722114
17.

Arginine metabolic enzymes, nitric oxide and infection.

Mori M, Gotoh T.

J Nutr. 2004 Oct;134(10 Suppl):2820S-2825S; discussion 2853S. Review.

18.

Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolism.

Scaglia F, Brunetti-Pierri N, Kleppe S, Marini J, Carter S, Garlick P, Jahoor F, O'Brien W, Lee B.

J Nutr. 2004 Oct;134(10 Suppl):2775S-2782S; discussion 2796S-2797S. Review.

19.

Nitric oxide function in the skin.

Cals-Grierson MM, Ormerod AD.

Nitric Oxide. 2004 Jun;10(4):179-93. Review.

PMID:
15275864
20.

Cellular targets and mechanisms of nitros(yl)ation: an insight into their nature and kinetics in vivo.

Bryan NS, Rassaf T, Maloney RE, Rodriguez CM, Saijo F, Rodriguez JR, Feelisch M.

Proc Natl Acad Sci U S A. 2004 Mar 23;101(12):4308-13.

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