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There are 9160 results for: content related to: Zinc supplementation reduces blood ammonia and increases liver ornithine transcarbamylase activity in experimental cirrhosis

  1. Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene

    Human Mutation

    Volume 27, Issue 7, July 2006, Pages: 626–632, Saori Yamaguchi, Lisa L. Brailey, Hiroki Morizono, Allen E. Bale and Mendel Tuchman

    Version of Record online : 19 JUN 2006, DOI: 10.1002/humu.20339

  2. Living donor liver transplantation from an asymptomatic mother who was a carrier for ornithine transcarbamylase deficiency

    Pediatric Transplantation

    Volume 16, Issue 6, September 2012, Pages: E196–E200, T. Wakiya, Y. Sanada, T. Urahashi, Y. Ihara, N. Yamada, N. Okada, S. Egami, K. Sakamoto, K. Murayama, K. Hakamada, Y. Yasuda and K. Mizuta

    Version of Record online : 14 MAY 2012, DOI: 10.1111/j.1399-3046.2012.01716.x

  3. Mutations and polymorphisms in the human ornithine transcarbamylase gene

    Human Mutation

    Volume 19, Issue 2, February 2002, Pages: 93–107, Mendel Tuchman, Naser Jaleel, Hiroki Morizono, Lisa Sheehy and Michael G. Lynch

    Version of Record online : 7 JAN 2002, DOI: 10.1002/humu.10035

  4. Mutations and polymorphisms in the human ornithine transcarbamylase gene

    Human Mutation

    Volume 2, Issue 3, 1993, Pages: 174–178, Mendel Tuchman

    Version of Record online : 1 JUN 2005, DOI: 10.1002/humu.1380020304

  5. You have free access to this content
    The role of orthotopic liver transplantation in the treatment of ornithine transcarbamylase deficiency

    Liver Transplantation and Surgery

    Volume 4, Issue 5, September 1998, Pages: 350–354, Ashley A. Busuttil, John A. Goss, Philip Seu, Tom S. Dulkanchainun, George S. Yanni, Sue V. McDiarmid and Ronald W. Busuttil

    Version of Record online : 30 DEC 2003, DOI: 10.1002/lt.500040504

  6. Genotype spectrum of ornithine transcarbamylase deficiency: Correlation with the clinical and biochemical phenotype

    American Journal of Medical Genetics

    Volume 93, Issue 4, 14 August 2000, Pages: 313–319, Beth A. McCullough, Marc Yudkoff, Mark L. Batshaw, James M. Wilson, Steven E. Raper and Mendel Tuchman

    Version of Record online : 11 AUG 2000, DOI: 10.1002/1096-8628(20000814)93:4<313::AID-AJMG11>3.0.CO;2-M

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    A single mutation in the active site swaps the substrate specificity of N-acetyl-L-ornithine transcarbamylase and N-succinyl-L-ornithine transcarbamylase

    Protein Science

    Volume 16, Issue 8, August 2007, Pages: 1689–1699, Dashuang Shi, Xiaolin Yu, Juan Cabrera-Luque, Tony Y. Chen, Lauren Roth, Hiroki Morizono, Norma M. Allewell and Mendel Tuchman

    Version of Record online : 2 JAN 2009, DOI: 10.1110/ps.072919907

  8. Living donor liver transplantation for ornithine transcarbamylase deficiency

    Pediatric Transplantation

    Volume 15, Issue 4, June 2011, Pages: 390–395, T. Wakiya, Y. Sanada, K. Mizuta, M. Umehara, T. Urahasi, S. Egami, S. Hishikawa, T. Fujiwara, Y. Sakuma, M. Hyodo, K. Murayama, K. Hakamada, Y. Yasuda and H. Kawarasaki

    Version of Record online : 9 MAR 2011, DOI: 10.1111/j.1399-3046.2011.01494.x

  9. Enzymes of Arginine and Urea Systhesis

    Advances in Enzymology and Related Areas of Molecular Biology, Volume 39

    Alton Meister, Pages: 1–90, 2006

    Published Online : 22 NOV 2006, DOI: 10.1002/9780470122846.ch1

  10. Clinical and biochemical heterogeneity in females of a large pedigree with ornithine transcarbamylase deficiency due to the R141Q mutation

    American Journal of Medical Genetics

    Volume 66, Issue 3, 18 December 1996, Pages: 311–315, Mary J. Ahrens, Susan A. Berry, Chester B. Whitley, Dorothy J. Markowitz, Robert J. Plante and Mendel Tuchman

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19961218)66:3<311::AID-AJMG14>3.0.CO;2-P

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    Mutations Affecting the Repressibility of Arginine Biosynthetic Enzymes in Sacchromyces cerevisiae

    European Journal of Biochemistry

    Volume 12, Issue 1, January 1970, Pages: 31–39, J. Bechet, M. Grenson and J. M. Wiame

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1432-1033.1970.tb00817.x

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    Effect of the Transition-State Analogue, δ-N-(Phosphonacetyl)-l-ornithine on Citrulline Synthesis in Isolated Rat-Liver Mitochondria and on Urea Synthesis in Isolated Rat Hepatocytes

    European Journal of Biochemistry

    Volume 100, Issue 1, October 1979, Pages: 309–315, Nicholas J. HOOGENRAAD, Teresa M. SUTHERLAND and Geoffrey J. HOWLETT

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1432-1033.1979.tb02062.x

  13. Identification of novel mutations in the human ornithine transcarbamylase (OTC) gene of Korean patients with OTC deficiency and transient expression of the mutant proteins in vitro

    Human Mutation

    Volume 27, Issue 11, November 2006, Page: 1159, Gu-Hwan Kim, Jin-Ho Choi, Hyung-Haon Lee, Sangwook Park, Sung-Su Kim and Han-Wook Yoo

    Version of Record online : 13 OCT 2006, DOI: 10.1002/humu.9465

  14. Effects of Protein Size on the Rate of Import of the Precursors of Aldehyde Dehydrogenase and Ornithine Transcarbamylase into Rat Liver Mitochondria

    Alcoholism: Clinical and Experimental Research

    Volume 15, Issue 2, April 1991, Pages: 286–290, Thomas T. Y. Wang, Yi Wang and Henry Weiner

    Version of Record online : 11 APR 2006, DOI: 10.1111/j.1530-0277.1991.tb01870.x

  15. Apparent segregation of null alleles ascribed to deletions of the ornithine transcarbamylase gene in congenital hyperammonaemia

    Prenatal Diagnosis

    Volume 15, Issue 8, August 1995, Pages: 757–761, Bertrand Segues, Jean-Michel Rozet, Brigitte Gilbert, Pascale Saugier-Veber, Daniel Rabier, Jean-Marie Saudubray, Mireille Carré, Françoise Parrot Rouleau, Alain Menget, Jean-Michel Bonardi, Stanislas Lyonnet, Jean-Paul Bonnefont and Arnold Munnich

    Version of Record online : 14 DEC 2005, DOI: 10.1002/pd.1970150812

  16. Molecular mechanisms underlying large genomic deletions in ornithine transcarbamylase (OTC) gene

    Clinical Genetics

    Volume 75, Issue 5, May 2009, Pages: 457–464, R Quental, L Azevedo, V Rubio, L Diogo and A Amorim

    Version of Record online : 21 APR 2009, DOI: 10.1111/j.1399-0004.2009.01172.x

  17. Ornithine transcarbamylase deficiency: long-term survival

    Clinical Genetics

    Volume 22, Issue 4, October 1982, Pages: 211–214, Virginia V. Michels, Elaine Potts, Mackenzie Walser and Arthur L. Beaudet

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1982.tb01435.x

  18. Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensorium

    Clinical Genetics

    Volume 25, Issue 6, June 1984, Pages: 538–542, Jun Oizumi, Won G. Ng, Richard Koch, Kenneth N. F. Shaw, Lawrence Sweetman, Antonio Velazquez and George N. Donnell

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1984.tb00498.x

  19. Treatment of a Patient with Ornithine Transcarbamylase Deficiency with Essential Amino Acids and Sodium Benzoate

    Pediatrics International

    Volume 25, Issue 1, March 1983, Pages: 70–73, Hiroko Kodama, Osamu Nose, Hitoshi Tajiri, Ichiro Maki and Hyakuji Yabuuchi

    Version of Record online : 9 OCT 2007, DOI: 10.1111/j.1442-200X.1983.tb00590.x

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    H intragenic polymorphisms and haplotype analysis in the ornithine transcarbamylase (OTC) gene and their relevance for tracking the inheritance of OTC deficiency

    Human Mutation

    Volume 20, Issue 5, November 2002, Pages: 407–408, Consuelo Climent and Vicente Rubio

    Version of Record online : 25 OCT 2002, DOI: 10.1002/humu.9076