Standard
Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis. / Ranea-Robles, P; Violante, S; Argmann, C; Dodatko, T; Bhattacharya, D; Chen, H; Yu, C; Friedman, SL; Puchowicz, M; Houten, SM.
I:
Cellular and molecular life sciences : CMLS, 06.2021.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Ranea-Robles, P, Violante, S, Argmann, C, Dodatko, T, Bhattacharya, D, Chen, H, Yu, C, Friedman, SL, Puchowicz, M & Houten, SM 2021, '
Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis.',
Cellular and molecular life sciences : CMLS.
https://doi.org/10.1007/s00018-021-03869-9
APA
Ranea-Robles, P., Violante, S., Argmann, C., Dodatko, T., Bhattacharya, D., Chen, H., Yu, C., Friedman, SL., Puchowicz, M., & Houten, SM. (2021).
Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis. Cellular and molecular life sciences : CMLS.
https://doi.org/10.1007/s00018-021-03869-9
Vancouver
Ranea-Robles P, Violante S, Argmann C, Dodatko T, Bhattacharya D, Chen H o.a.
Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis. Cellular and molecular life sciences : CMLS. 2021 jun.
https://doi.org/10.1007/s00018-021-03869-9
Author
Ranea-Robles, P ; Violante, S ; Argmann, C ; Dodatko, T ; Bhattacharya, D ; Chen, H ; Yu, C ; Friedman, SL ; Puchowicz, M ; Houten, SM. / Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis. I: Cellular and molecular life sciences : CMLS. 2021.
Bibtex
@article{15584a23f8ef43d1a9542f18a53283ef,
title = "Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis.",
author = "P Ranea-Robles and S Violante and C Argmann and T Dodatko and D Bhattacharya and H Chen and C Yu and SL Friedman and M Puchowicz and SM Houten",
year = "2021",
month = jun,
doi = "10.1007/s00018-021-03869-9",
language = "English",
journal = "Cellular and Molecular Life Sciences",
issn = "1420-682X",
publisher = "Birkhauser Verlag Basel",
}
RIS
TY - JOUR
T1 - Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis.
AU - Ranea-Robles, P
AU - Violante, S
AU - Argmann, C
AU - Dodatko, T
AU - Bhattacharya, D
AU - Chen, H
AU - Yu, C
AU - Friedman, SL
AU - Puchowicz, M
AU - Houten, SM
PY - 2021/6
Y1 - 2021/6
UR - http://europepmc.org/abstract/med/34110423
U2 - 10.1007/s00018-021-03869-9
DO - 10.1007/s00018-021-03869-9
M3 - Journal article
C2 - 34110423
JO - Cellular and Molecular Life Sciences
JF - Cellular and Molecular Life Sciences
SN - 1420-682X
ER -
