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145 related items for PubMed ID: 15234340
1. Congenic mapping and genotyping of the tetrahydrobiopterin-deficient hph-1 mouse. Khoo JP, Nicoli T, Alp NJ, Fullerton J, Flint J, Channon KM. Mol Genet Metab; 2004 Jul; 82(3):251-4. PubMed ID: 15234340 [Abstract] [Full Text] [Related]
2. Linkage analysis of the hph-1 mutation and the GTP cyclohydrolase I structural gene. Montañez CS, McDonald JD. Mol Genet Metab; 1999 Sep; 68(1):91-2. PubMed ID: 10479487 [Abstract] [Full Text] [Related]
3. Molecular characterization of HPH-1: a mouse mutant deficient in GTP cyclohydrolase I activity. Gütlich M, Ziegler I, Witter K, Hemmens B, Hültner L, McDonald JD, Werner T, Rödl W, Bacher A. Biochem Biophys Res Commun; 1994 Sep 30; 203(3):1675-81. PubMed ID: 7524491 [Abstract] [Full Text] [Related]
4. Pulmonary hypertension in a GTP-cyclohydrolase 1-deficient mouse. Nandi M, Miller A, Stidwill R, Jacques TS, Lam AA, Haworth S, Heales S, Vallance P. Circulation; 2005 Apr 26; 111(16):2086-90. PubMed ID: 15824199 [Abstract] [Full Text] [Related]
15. GTP cyclohydrolase I gene expression in the brains of male and female hph-1 mice. Shimoji M, Hirayama K, Hyland K, Kapatos G. J Neurochem; 1999 Feb 19; 72(2):757-64. PubMed ID: 9930750 [Abstract] [Full Text] [Related]
19. GTP-cyclohydrolase deficiency induced peripheral and deep microcirculation dysfunction with age. Simonet S, Gosgnach W, Billou L, Lucats L, Royere E, Crespo C, Lapret I, Ragonnet L, Moreau K, Vayssettes-Courchay C, Berson P, Bourguignon MP. Microvasc Res; 2021 Jan 19; 133():104078. PubMed ID: 32980388 [Abstract] [Full Text] [Related]
20. [Studies on neonatal screening, clinical and gene analysis for tetrahydrobiopterin deficiency in Southern Chinese]. Ye J, Liu X, Ma X, Huang X, Zhang Y, Gu X, Chen R. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr 19; 18(2):92-5. PubMed ID: 11295124 [Abstract] [Full Text] [Related] Page: [Next] [New Search]