STRUCTURE/FUNCTION RELATIONSHIP STUDIES ON VERY LONG-CHAIN ACYL-COA DEHYDROGENASE (VLCAD)

被引：0
|
作者：
Kang, H. [1 ]
Wang, Y. [1 ]
Mohsen, A-W [1 ]
Vockley, J. [1 ]
机构：
[1] Univ Pittsburgh, Pittsburgh, PA USA
来源：
MOLECULAR GENETICS AND METABOLISM | 2009年 / 98卷 / 1-2期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
324
引用
收藏
页码：55 / 55
页数：1
相关论文
共 50 条
  • [1] PRENATAL-DIAGNOSIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE (VLCAD) DEFICIENCY
    BIALER, MG
    NADA, MA
    VIANEYSABAN, C
    ROE, CR
    MATHIEU, M
    MCGLYNN, JA
    DING, JH
    MANDON, G
    SLONIM, AE
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 1600 - 1600
  • [2] Cardiac hypertrophy in mice with long-chain acyl-CoA dehydrogenase or very long-chain acyl-CoA dehydrogenase deficiency
    Cox, Keith B.
    Liu, Jian
    Tian, Liqun
    Barnes, Stephen
    Yang, Qinglin
    Wood, Philip A.
    LABORATORY INVESTIGATION, 2009, 89 (12) : 1348 - 1354
  • [3] Defining plasma acylcarnitine ranges for very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency
    Hall, Patricia
    Gavrilov, Dimitar
    Oglesbee, Devin
    Raymond, Kimiyo
    Rinaldo, Piero
    Tortorelli, Silvia
    Matern, Dietrich
    MOLECULAR GENETICS AND METABOLISM, 2012, 105 (03) : 322 - 322
  • [4] Energy expenditure and lipid metabolism in very long-chain Acyl-CoA dehydrogenase (VLCAD) deficiency
    Haglind, Charlotte Bieneck
    Ask, Sara
    von Dobeln, Ulrika
    Engvall, Martin
    Ekblom, Orjan
    Stenlid, Maria Halldin
    Nordenstrom, Anna
    MOLECULAR GENETICS AND METABOLISM, 2015, 114 (03) : 333 - 333
  • [5] Development and pathomechanisms of cardiomyopathy in very long-chain acyl-CoA dehydrogenase deficient (VLCAD-/-) mice
    Tucci, Sara
    Floegel, Ulrich
    Hermann, Sven
    Sturm, Marga
    Schaefers, Michael
    Spiekerkoetter, Ute
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2014, 1842 (05): : 677 - 685
  • [6] The Pathogenesis of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
    Sharma, Shashwat
    Mckenzie, Matthew
    BIOMOLECULES, 2025, 15 (03)
  • [7] AAV-Mediated Phenotypic Correction of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency in Mice
    Stone, Michele
    Tutto, Amanda
    Tang, Qiushi
    Leu, Jiewu
    Shen, Weiran
    Mallory, Jason
    Keeler-Klunk, Allison
    MOLECULAR THERAPY, 2022, 30 (04) : 250 - 250
  • [8] Expression and characterization of patient mutations in very long-chain acyl-CoA dehydrogenase (VLCAD) using a prokaryotic system
    Goetzman, E. S.
    Wang, Y.
    Mohsen, A-W
    He, M.
    Ninness, B. K.
    Vockley, J.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 : 56 - 56
  • [9] Management and Outcomes of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD Deficiency): A Retrospective Chart Review
    Al Bandari, Maria
    Nagy, Laura
    Cruz, Vivian
    Hewson, Stacy
    Hossain, Alomgir
    Inbar-Feigenberg, Michal
    INTERNATIONAL JOURNAL OF NEONATAL SCREENING, 2024, 10 (02)
  • [10] Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse
    Cox, KB
    Hamm, DA
    Millington, DS
    Matern, D
    Vockley, J
    Rinaldo, P
    Pinkert, CA
    Rhead, WJ
    Lindsey, JR
    Wood, PA
    HUMAN MOLECULAR GENETICS, 2001, 10 (19) : 2069 - 2077
12345