检索结果 - Brian Fowler

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  1. 1
    The folate cycle and disease in humans

    The folate cycle and disease in humans 由 Brian Fowler

    出版 2001
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  2. 2
    Causes of and diagnostic approach to methylmalonic acidurias

    Causes of and diagnostic approach to methylmalonic acidurias 由 Brian Fowler, James V. Leonard, Matthias R. Baumgartner

    出版 2008
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  3. 3
    Vitamin B<sub>12</sub>, folate, and the methionine remethylation cycle—biochemistry, pathways, and regulation

    Vitamin B<sub>12</sub>, folate, and the methionine remethylation cycle—biochemistry, pathways, and regulation 由 D. Sean Froese, Brian Fowler, Matthias R. Baumgartner

    出版 2019
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  4. 4
    Purification and properties of cystathionine beta-synthase from human liver. Evidence for identical subunits.

    Purification and properties of cystathionine beta-synthase from human liver. Evidence for identical subunits. 由 Jan P. Kraus, Seymour Packman, Brian Fowler, Leah Rosenberg

    出版 1978
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  5. 5
    Homocystinuria

    Homocystinuria 由 Brian Fowler, Jan P. Kraus, Seymour Packman, León E. Rosenberg

    出版 1978
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  6. 6
    The TOR-controlled transcription activators GLN3, RTG1, and RTG3 are regulated in response to intracellular levels of glutamine

    The TOR-controlled transcription activators GLN3, RTG1, and RTG3 are regulated in response to intracellular levels of glutamine 由 José L. Crespo, Ted Powers, Brian Fowler, Michael N. Hall

    出版 2002
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  7. 7
    Adjustments of lipid pathways in plant adaptation to temperature stress

    Adjustments of lipid pathways in plant adaptation to temperature stress 由 Qiang Li, Wenyun Shen, Qian Zheng, Brian Fowler, Jitao Zou

    出版 2016
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  8. 8
    Detection of heterozygotes for homocystinuria: Study of sulphur-containing amino acids in plasma and urine after L-methionine loading

    Detection of heterozygotes for homocystinuria: Study of sulphur-containing amino acids in plasma and urine after L-methionine loading 由 I. B. Sardharwalla, Brian Fowler, A. J. Robins, G. M. Komrower

    出版 1974
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  9. 9
    Evidence for disturbed S-adenosylmethionine: S-adenosylhomocysteine ratio in patients with end-stage renal failure: a cause for disturbed methylation reactions?

    Evidence for disturbed S-adenosylmethionine: S-adenosylhomocysteine ratio in patients with end-stage renal failure: a cause for disturbed methylation reactions? 由 F. Loehrer, Christof Angst, Felix Brunner, Walter E. Haefeli, Brian Fowler

    出版 1998
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  10. 10
    Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism

    Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism 由 Martin Stucki, David Coelho, Terttu Suormala, Patricie Burda, Brian Fowler, Matthias R. Baumgartner

    出版 2011
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  11. 11
    Understanding the Biochemical Basis of Temperature-Induced Lipid Pathway Adjustments in Plants

    Understanding the Biochemical Basis of Temperature-Induced Lipid Pathway Adjustments in Plants 由 Qiang Li, Qian Zheng, Wenyun Shen, Dustin Cram, Brian Fowler, Yangdou Wei, Jitao Zou

    出版 2015
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  12. 12
    Hyperhomocysteinemia: An Independent Risk Factor for Vascular Disease

    Hyperhomocysteinemia: An Independent Risk Factor for Vascular Disease 由 Robert Clarke, Leslie Daly, Killian Robinson, E. R. Naughten, S. F. Cahalane, Brian Fowler, Ian Graham

    出版 1991
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  13. 13
    Neonatal hepatic steatosis by disruption of the adenosine kinase gene

    Neonatal hepatic steatosis by disruption of the adenosine kinase gene 由 Detlev Boison, Louis Scheurer, Valérie Zumsteg, Thomas Rülicke, Piotr Litynski, Brian Fowler, Sebastian Brandner, Hanns Möhler

    出版 2002
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  14. 14
    Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis

    Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis 由 Hanna Mandel, Benjamin Brenner, Moshe Berant, Nurith Rosenberg, Naomi Lanir, Cornelis Jakobs, Brian Fowler, Uri Seligsohn

    出版 1996
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  15. 15
    Homocysteine, folate and vitamin B<sub>12</sub>in neuropsychiatric diseases: review and treatment recommendations

    Homocysteine, folate and vitamin B<sub>12</sub>in neuropsychiatric diseases: review and treatment recommendations 由 Olaf Stanger, Brian Fowler, Klaus Piertzik, Martina Huemer, Elisabeth Haschke‐Becher, Alexander Semmler, Stefan Lorenzl, Michael Linnebank

    出版 2009
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  16. 16
    Molecular Genetic Characterization of 151<i>Mut</i>-Type Methylmalonic Aciduria Patients and Identification of 41 Novel Mutations in<i>MUT</i>

    Molecular Genetic Characterization of 151<i>Mut</i>-Type Methylmalonic Aciduria Patients and Identification of 41 Novel Mutations in<i>MUT</i> 由 Patrick Forny, Anne-Sophie Schnellmann, Celine Buerer, Seraina Lutz, Brian Fowler, D. Sean Froese, Matthias R. Baumgartner

    出版 2016
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  17. 17
    Gene Identification for the cblD Defect of Vitamin B<sub>12</sub>Metabolism

    Gene Identification for the cblD Defect of Vitamin B<sub>12</sub>Metabolism 由 David Coelho, Terttu Suormala, Martin Stucki, Jordan Lerner‐Ellis, David S. Rosenblatt, Robert F. Newbold, Matthias R. Baumgartner, Brian Fowler

    出版 2008
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  18. 18
    Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancy

    Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancy 由 Martina Huemer, Sabine Scholl‐Bürgi, Karine Hadaya, Ilse Kern, Ronny Beer, Klaus Seppi, Brian Fowler, Matthias R. Baumgartner, Daniela Karall

    出版 2014
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  19. 19
    Long-Term Outcome in Methylmalonic Acidurias Is Influenced by the Underlying Defect (mut0, mut−, cblA, cblB)

    Long-Term Outcome in Methylmalonic Acidurias Is Influenced by the Underlying Defect (mut0, mut−, cblA, cblB) 由 Friederike Hörster, Matthias R. Baumgartner, Caroline Viardot, Terttu Suormala, Peter Burgard, Brian Fowler, Georg F. Hoffmann, Sven F. Garbade, Stefan Kölker, E. R. Baumgartner

    出版 2007
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  20. 20
    Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency

    Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency 由 D. Sean Froese, Martina Huemer, Terttu Suormala, Patricie Burda, David Coelho, Jean‐Louis Guéant, Markus A. Landolt, Viktor Kožich, Brian Fowler, Matthias R. Baumgartner

    出版 2016
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