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Items: 10

1.
A longitudinal study of urea cycle disorders
Mark L. Batshaw, Mendel Tuchman, Marshall Summar, Jennifer Seminara, the Members of the Urea Cycle Disorders Consortium
Mol Genet Metab. Author manuscript; available in PMC 2015 Sep 1.
Published in final edited form as: Mol Genet Metab. 2014 Sep-Oct; 113(0): 127–130. Published online 2014 Aug 10. doi: 10.1016/j.ymgme.2014.08.001
PMCID:
PMC4178008
AbstractArticlePDF–46K
2.
INDUCTION OF ARGINASE ACTIVITY WITH THE SHOPE PAPILLOMA VIRUS IN TISSUE CULTURE CELLS FROM AN ARGININEMIC PATIENT
Stanfield Rogers, A. Lowenthal, H. G. Terheggen, J. P. Columbo
J Exp Med. 1973 Mar 31; 137(4): 1091–1096. doi: 10.1084/jem.137.4.1091
PMCID:
PMC2139227
SummaryPDF–293K
3.
Properties of fetal and adult red blood cell arginase: a possible prenatal diagnostic test for arginase deficiency.
E B Spector, M Kiernan, B Bernard, S D Cederbaum
Am J Hum Genet. 1980 Jan; 32(1): 79–87.
PMCID:
PMC1685933
SummaryPage BrowsePDF–754K
4.
Human hyperargininemia: a mutation not expressed in skin fibroblasts?
A F Van Elsen, J G Leroy
Am J Hum Genet. 1977 Jul; 29(4): 350–355.
PMCID:
PMC1685390
SummaryPage BrowsePDF–517K
5.
Three novel mutations in the liver-type arginase gene in three unrelated Japanese patients with argininemia.
T Uchino, Y Haraguchi, J M Aparicio, N Mizutani, M Higashikawa, H Naitoh, M Mori, I Matsuda
Am J Hum Genet. 1992 Dec; 51(6): 1406–1412.
PMCID:
PMC1682900
SummaryPage BrowsePDF–1.1M
6.
Molecular genetic study of human arginase deficiency
Wayne W. Grody, Deborah Klein, Amy E. Dodson, Rita M. Kern, Paul B. Wissmann, Barbara K. Goodman, Patrick Bassand, Bert Marescau, Soo-Sang Kang, James V. Leonard, Stephen D. Cederbaum
Am J Hum Genet. 1992 Jun; 50(6): 1281–1290.
PMCID:
PMC1682550
SummaryPage BrowsePDF–2.0M
7.
Familial hyperargininaemia.
H G Terheggen, A Lowenthal, F Lavinha, J P Colombo
Arch Dis Child. 1975 Jan; 50(1): 57–62. doi: 10.1136/adc.50.1.57
PMCID:
PMC1544492
SummaryPage BrowsePDF–787K
8.
Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysis.
W W Grody, C Argyle, R M Kern, G J Dizikes, E B Spector, A D Strickland, D Klein, S D Cederbaum
J Clin Invest. 1989 Feb; 83(2): 602–609. doi: 10.1172/JCI113923
PMCID:
PMC303720
SummaryPage BrowsePDF–2.3M
9.
Molecular basis of argininemia. Identification of two discrete frame-shift deletions in the liver-type arginase gene.
Y Haraguchi, J M Aparicio, M Takiguchi, I Akaboshi, M Yoshino, M Mori, I Matsuda
J Clin Invest. 1990 Jul; 86(1): 347–350. doi: 10.1172/JCI114707
PMCID:
PMC296728
SummaryPage BrowsePDF–1.0M
10.
Mouse Model for Human Arginase Deficiency
Ramaswamy K. Iyer, Paul K. Yoo, Rita M. Kern, Nora Rozengurt, Rosemarie Tsoa, William E. O'Brien, Hong Yu, Wayne W. Grody, Stephen D. Cederbaum
Mol Cell Biol. 2002 Jul; 22(13): 4491–4498. doi: 10.1128/MCB.22.13.4491-4498.2002
PMCID:
PMC133904
AbstractArticlePDF–374K

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