Works about COENZYME A


Results: 364
    1

    Tratamiento de urgencia de la acidemia metilmalónica.

    Published in:
    Acta Pediatrica de Mexico, 2012, v. 33, n. 1, p. 48
    By:
    • Santillán-Aguayo, Enrique;
    • Revilla-Estivil, Nuria;
    • Belmont-Martínez, Leticia;
    • Fernández-Lainez, Q. F. B. Cynthia;
    • Guillén-López, L. N. C. P. Sara;
    • Ibarra-González, M en C. Isabel;
    • Monroy-Santoyo, Susana;
    • Rodríguez-Schmidt, L. N. Romina;
    • Vela-Amieva, Marcela
    Publication type:
    Article
    2
    3
    4
    5
    6

    Metabolism of β-valine via a CoA-dependent ammonia lyase pathway.

    Published in:
    Applied Microbiology & Biotechnology, 2015, v. 99, n. 21, p. 8987, doi. 10.1007/s00253-015-6551-z
    By:
    • Otzen, Marleen;
    • Crismaru, Ciprian;
    • Postema, Christiaan;
    • Wijma, Hein;
    • Heberling, Matthew;
    • Szymanski, Wiktor;
    • Wildeman, Stefaan;
    • Janssen, Dick
    Publication type:
    Article
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24

    Exclusive neuronal expression of SUCLA2 in the human brain.

    Published in:
    Brain Structure & Function, 2015, v. 220, n. 1, p. 135, doi. 10.1007/s00429-013-0643-2
    By:
    • Dobolyi, Arpád;
    • Ostergaard, Elsebet;
    • Bagó, Attila;
    • Dóczi, Tamás;
    • Palkovits, Miklós;
    • Gál, Aniko;
    • Molnár, Mária;
    • Adam-Vizi, Vera;
    • Chinopoulos, Christos
    Publication type:
    Article
    25
    26
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37
    38
    39
    40
    41
    42

    Statins stabilize the renal function of IgA nephropathy.

    Published in:
    Renal Failure, 2014, v. 36, n. 3, p. 356, doi. 10.3109/0886022X.2013.866512
    By:
    • Moriyama, Takahito;
    • Oshima, Yasuko;
    • Tanaka, Kayu;
    • Iwasaki, Chihiro;
    • Ochi, Ayami;
    • Itabashi, Mitsuyo;
    • Takei, Takashi;
    • Uchida, Keiko;
    • Nitta, Kosaku
    Publication type:
    Article
    43
    44
    45
    46
    47

    The first case in Asia of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (HSD10 disease) with atypical presentation.

    Published in:
    Journal of Human Genetics, 2014, v. 59, n. 11, p. 609, doi. 10.1038/jhg.2014.79
    By:
    • Fukao, Toshiyuki;
    • Akiba, Kazuhisa;
    • Goto, Masahiro;
    • Kuwayama, Nobuki;
    • Morita, Mikiko;
    • Hori, Tomohiro;
    • Aoyama, Yuka;
    • Venkatesan, Rajaram;
    • Wierenga, Rik;
    • Moriyama, Yohsuke;
    • Hashimoto, Takashi;
    • Usuda, Nobuteru;
    • Murayama, Kei;
    • Ohtake, Akira;
    • Hasegawa, Yuki;
    • Shigematsu, Yosuke;
    • Hasegawa, Yukihiro
    Publication type:
    Article
    48
    49
    50