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84. Use of immunocytochemical analysis of a duodenal biopsy specimen to identify a carrier of ornithine transcarbamylase deficiency. Hamano Y; Kodama H; Fujikawa Y; Tanaka Y; Nishimura K; Yanagisawa M N Engl J Med; 1988 Jun; 318(23):1521-3. PubMed ID: 3367962 [No Abstract] [Full Text] [Related]
85. Import of rat ornithine transcarbamylase precursor into mitochondria: two-step processing of the leader peptide. Sztul ES; Hendrick JP; Kraus JP; Wall D; Kalousek F; Rosenberg LE J Cell Biol; 1987 Dec; 105(6 Pt 1):2631-9. PubMed ID: 3693395 [TBL] [Abstract][Full Text] [Related]
86. Increased densities of binding sites for the peripheral-type benzodiazepine receptor ligand [3H]PK 11195 in congenital ornithine transcarbamylase-deficient sparse fur mouse. Rao VL; Qureshi IA; Butterworth RF Pediatr Res; 1993 Dec; 34(6):777-80. PubMed ID: 8108192 [TBL] [Abstract][Full Text] [Related]
87. Structure of the ornithine transcarbamylase (OTC) gene and DNA diagnosis of OTC deficiency. Matsuda I; Hata A; Matsuura T; Tsuzuki T; Shimada K Clin Chim Acta; 1989 Dec; 185(3):283-9. PubMed ID: 2575934 [TBL] [Abstract][Full Text] [Related]
88. Genetic analysis of carbamoylphosphate synthetase I and ornithine transcarbamylase deficiency using fibroblasts. Rapp B; Häberle J; Linnebank M; Wermuth B; Marquardt T; Harms E; Koch HG Eur J Pediatr; 2001 May; 160(5):283-7. PubMed ID: 11388595 [TBL] [Abstract][Full Text] [Related]
89. Prenatal molecular evaluation of six fetuses in four unrelated Korean families with ornithine transcarbamylase deficiency. Yoo HW; Kim GH J Korean Med Sci; 1998 Apr; 13(2):179-85. PubMed ID: 9610619 [TBL] [Abstract][Full Text] [Related]
90. Expression of amplified DNA sequences for ornithine transcarbamylase in HeLa cells: arginine residues may be required for mitochondrial import of enzyme precursor. Horwich AL; Fenton WA; Firgaira FA; Fox JE; Kolansky D; Mellman IS; Rosenberg LE J Cell Biol; 1985 May; 100(5):1515-21. PubMed ID: 3988798 [TBL] [Abstract][Full Text] [Related]
91. Synthesis of a modified gene encoding human ornithine transcarbamylase for expression in mammalian mitochondrial and universal translation systems: a novel approach towards correction of a genetic defect. Wheeler VC; Prodromou C; Pearl LH; Williamson R; Coutelle C Gene; 1996 Mar; 169(2):251-5. PubMed ID: 8647457 [TBL] [Abstract][Full Text] [Related]
92. The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency. Maestri NE; Lord C; Glynn M; Bale A; Brusilow SW Medicine (Baltimore); 1998 Nov; 77(6):389-97. PubMed ID: 9854602 [TBL] [Abstract][Full Text] [Related]
94. Developmental study of hepatic glutamine synthetase in a mouse model of congenital hyperammonemia. Skarpetas A; Mawal Y; Qureshi IA Biochem Mol Biol Int; 1997 Sep; 43(1):133-9. PubMed ID: 9315291 [TBL] [Abstract][Full Text] [Related]
96. Mitochondrial import and processing of mutant human ornithine transcarbamylase precursors in cultured cells. Isaya G; Fenton WA; Hendrick JP; Furtak K; Kalousek F; Rosenberg LE Mol Cell Biol; 1988 Dec; 8(12):5150-8. PubMed ID: 3244350 [TBL] [Abstract][Full Text] [Related]
97. A female case of ornithine transcarbamylase deficiency with marked computed tomographic abnormalities of the brain. Takayanagi M; Ohtake A; Ogura N; Nakajima H; Hoshino M Brain Dev; 1984; 6(1):58-60. PubMed ID: 6731721 [TBL] [Abstract][Full Text] [Related]
99. Prenatal diagnosis of ornithine transcarbamylase deficiency: results in Spfash mice. Monastiri K; Rabier D; Kamoun P Prenat Diagn; 1993 Jun; 13(6):441-7. PubMed ID: 8372069 [TBL] [Abstract][Full Text] [Related]
100. Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiency. Matsuura T; Hoshide R; Komaki S; Kiwaki K; Endo F; Nakamura S; Jitosho T; Matsuda I J Inherit Metab Dis; 1995; 18(3):273-82. PubMed ID: 7474892 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]