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129 related items for PubMed ID: 3617058
1. Immunoenzymatic studies of ornithine transcarbamylase (OTC) in liver of patients with OTC deficiency by enzyme linked immunosorbent assay (ELISA). Oyanagi K, Tsubakihara K, Itakura Y, Nagao M, Takayanagi N, Tsuchiyama A, Nakao T, Inoue I, Saheki T. Tohoku J Exp Med; 1987 May; 152(1):15-21. PubMed ID: 3617058 [Abstract] [Full Text] [Related]
2. Expression of ornithine transcarbamylase deficiency in the small intestine and colon of sparse-fur mutant mice. Qureshi IA, Letarte J, Ouellet R. J Pediatr Gastroenterol Nutr; 1985 Feb; 4(1):118-24. PubMed ID: 3981356 [Abstract] [Full Text] [Related]
3. Activity of the liver enzyme ornithine carbamoyltransferase (OTC) in blood: LC-MS/MS assay for non-invasive diagnosis of ornithine carbamoyltransferase deficiency. Krijt J, Sokolová J, Ješina P, Dvořáková L, Řeboun M, Brennerová K, Mistrík M, Zeman J, Honzík T, Kožich V. Clin Chem Lab Med; 2017 Jul 26; 55(8):1168-1177. PubMed ID: 28107167 [Abstract] [Full Text] [Related]
4. Increase of ornithine transcarbamylase protein in sparse-fur mice with ornithine transcarbamylase deficiency. Briand P, Cathelineau L, Kamoun P, Gigot D, Penninckx M. FEBS Lett; 1981 Jul 20; 130(1):65-8. PubMed ID: 6793393 [No Abstract] [Full Text] [Related]
6. Molecular basis of ornithine transcarbamylase deficiency lacking enzyme protein. Saheki T, Imamura Y, Inoue I, Miura S, Mori M, Ohtake A, Tatibana M, Katsumata N, Ohno T. J Inherit Metab Dis; 1984 Jul 20; 7(1):2-8. PubMed ID: 6429436 [Abstract] [Full Text] [Related]
7. Missense mutations in codon 225 of ornithine transcarbamylase (OTC) result in decreased amounts of OTC protein: a hypothesis on the molecular mechanism of the OTC deficiency. García-Pérez MA, Climent C, Briones P, Vilaseca MA, Rodés M, Rubio V. J Inherit Metab Dis; 1997 Nov 20; 20(6):769-77. PubMed ID: 9427144 [Abstract] [Full Text] [Related]
8. Carbamyl phosphate synthetase and ornithine transcarbamylase activities in enzyme-deficient human liver measured by radiochromatography and correlated with outcome. Tuchman M, Tsai MY, Holzknecht RA, Brusilow SW. Pediatr Res; 1989 Jul 20; 26(1):77-82. PubMed ID: 2771513 [Abstract] [Full Text] [Related]
9. Correction of ornithine transcarbamylase deficiency in adult spf(ash) mice and in OTC-deficient human hepatocytes with recombinant adenoviruses bearing the CAG promoter. Kiwaki K, Kanegae Y, Saito I, Komaki S, Nakamura K, Miyazaki JI, Endo F, Matsuda I. Hum Gene Ther; 1996 May 01; 7(7):821-30. PubMed ID: 8860834 [Abstract] [Full Text] [Related]
10. The R40H mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients. Nishiyori A, Yoshino M, Kato H, Matsuura T, Hoshide R, Matsuda I, Kuno T, Miyazaki S, Hirose S, Kuromaru R, Mori M. Hum Genet; 1997 Feb 01; 99(2):171-6. PubMed ID: 9048915 [Abstract] [Full Text] [Related]
11. Ornithine transcarbamylase deficiencies in human males. Kinetic and immunochemical classification. Briand P, Francois B, Rabier D, Cathelineau L. Biochim Biophys Acta; 1982 May 21; 704(1):100-6. PubMed ID: 7093283 [Abstract] [Full Text] [Related]
12. Long-term correction of ammonia metabolism and prolonged survival in ornithine transcarbamylase-deficient mice following liver-directed treatment with adeno-associated viral vectors. Moscioni D, Morizono H, McCarter RJ, Stern A, Cabrera-Luque J, Hoang A, Sanmiguel J, Wu D, Bell P, Gao GP, Raper SE, Wilson JM, Batshaw ML. Mol Ther; 2006 Jul 21; 14(1):25-33. PubMed ID: 16677864 [Abstract] [Full Text] [Related]
13. Compared expression levels of ornithine transcarbamylase and carbamylphosphate synthetase in liver and small intestine of normal and mutant mice. Dubois N, Cavard C, Chasse JF, Kamoun P, Briand P. Biochim Biophys Acta; 1988 Sep 07; 950(3):321-8. PubMed ID: 3167057 [Abstract] [Full Text] [Related]
14. Ornithine transcarbamylase (OTC) in white blood cells. Nagata N, Akaboshi I, Yamamoto J, Matsuda I, Ohtsuka H, Katsuki T. Pediatr Res; 1980 Dec 07; 14(12):1370-3. PubMed ID: 7208155 [Abstract] [Full Text] [Related]
15. Ornithine transcarbamylase deficiency: a case with a truncated enzyme precursor and a case with undetectable mRNA activity. Kodama H, Ohtake A, Mori M, Okabe I, Tatibana M, Kamoshita S. J Inherit Metab Dis; 1986 Dec 07; 9(2):175-85. PubMed ID: 3091923 [Abstract] [Full Text] [Related]