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Items: 1 to 20 of 81

1.

Identification and functional characterization of mutations within HADHB associated with mitochondrial trifunctional protein deficiency.

Liu ZR, Dong HL, Ma Y, Wu ZY.

Mitochondrion. 2019 Sep 12. pii: S1567-7249(19)30028-5. doi: 10.1016/j.mito.2019.09.004. [Epub ahead of print]

PMID:
31521624
2.

Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability.

Li J, Suda K, Ueoka I, Tanaka R, Yoshida H, Okada Y, Okamoto Y, Hiramatsu Y, Takashima H, Yamaguchi M.

Exp Cell Res. 2019 Jun 15;379(2):150-158. doi: 10.1016/j.yexcr.2019.03.040. Epub 2019 Apr 3.

PMID:
30953623
3.

Analysis of Liver Proteome and Identification of Critical Proteins Affecting Milk Fat, Protein, and Lactose Metabolism in Dariy Cattle with iTRAQ.

Xu L, Shi L, Liu L, Liang R, Li Q, Li J, Han B, Sun D.

Proteomics. 2019 Jun;19(12):e1800387. doi: 10.1002/pmic.201800387. Epub 2019 May 28.

PMID:
30903674
4.

Expression of miR-33 from an SREBP2 intron inhibits the expression of the fatty acid oxidation-regulatory genes CROT and HADHB in chicken liver.

Shao F, Wang X, Yu J, Shen K, Qi C, Gu Z.

Br Poult Sci. 2019 Apr;60(2):115-124. doi: 10.1080/00071668.2018.1564242. Epub 2019 Jan 30.

PMID:
30698464
5.

HADHA and HADHB gene associated phenotypes - Identification of rare variants in a patient cohort by Next Generation Sequencing.

Diebold I, Schön U, Horvath R, Schwartz O, Holinski-Feder E, Kölbel H, Abicht A.

Mol Cell Probes. 2019 Apr;44:14-20. doi: 10.1016/j.mcp.2019.01.003. Epub 2019 Jan 22.

PMID:
30682426
6.

Posttranscriptional Regulation of 14q32 MicroRNAs by the CIRBP and HADHB during Vascular Regeneration after Ischemia.

Downie Ruiz Velasco A, Welten SMJ, Goossens EAC, Quax PHA, Rappsilber J, Michlewski G, Nossent AY.

Mol Ther Nucleic Acids. 2019 Mar 1;14:329-338. doi: 10.1016/j.omtn.2018.11.017. Epub 2018 Dec 6.

7.

PKCζ Phosphorylates SIRT6 to Mediate Fatty Acid β-Oxidation in Colon Cancer Cells.

Gao T, Li M, Mu G, Hou T, Zhu WG, Yang Y.

Neoplasia. 2019 Jan;21(1):61-73. doi: 10.1016/j.neo.2018.11.008. Epub 2018 Nov 30.

8.

Genetic Basis of Severe Childhood-Onset Cardiomyopathies.

Vasilescu C, Ojala TH, Brilhante V, Ojanen S, Hinterding HM, Palin E, Alastalo TP, Koskenvuo J, Hiippala A, Jokinen E, Jahnukainen T, Lohi J, Pihkala J, Tyni TA, Carroll CJ, Suomalainen A.

J Am Coll Cardiol. 2018 Nov 6;72(19):2324-2338. doi: 10.1016/j.jacc.2018.08.2171.

PMID:
30384889
9.

HADHB mutations cause infantile-onset axonal Charcot-Marie-Tooth disease: A report of two cases.

Lu Y, Wu R, Meng L, Lv H, Liu J, Zuo Y, Zhang W, Yuan Y, Wang Z.

Clin Neuropathol. 2018 Sep/Oct;37(5):232-238. doi: 10.5414/NP301097.

PMID:
29956646
10.

The whole transcriptome effects of the PPARα agonist fenofibrate on livers of hepatocyte humanized mice.

de la Rosa Rodriguez MA, Sugahara G, Hooiveld GJEJ, Ishida Y, Tateno C, Kersten S.

BMC Genomics. 2018 Jun 7;19(1):443. doi: 10.1186/s12864-018-4834-3.

11.

Fatty Acid β-Oxidation Is Essential in Leptin-Mediated Oocytes Maturation of Yellow Catfish Pelteobagrus fulvidraco.

Song YF, Tan XY, Pan YX, Zhang LH, Chen QL.

Int J Mol Sci. 2018 May 14;19(5). pii: E1457. doi: 10.3390/ijms19051457.

12.

Trifunctional Protein Deficiency Due to HADHB Mutations Is a Multisystem, β-Oxidation Disorder.

Finsterer J, Zarrouk-Mahjoub S.

Arch Iran Med. 2017 Dec 1;20(12):767-769. No abstract available.

13.

Integrated analyses of multi-omics reveal global patterns of methylation and hydroxymethylation and screen the tumor suppressive roles of HADHB in colorectal cancer.

Zhu Y, Lu H, Zhang D, Li M, Sun X, Wan L, Yu D, Tian Y, Jin H, Lin A, Gao F, Lai M.

Clin Epigenetics. 2018 Mar 2;10:30. doi: 10.1186/s13148-018-0458-3. eCollection 2018.

14.

Metabolomics Based Identification of SIRT5 and Protein Kinase C Epsilon Regulated Pathways in Brain.

Koronowski KB, Khoury N, Morris-Blanco KC, Stradecki-Cohan HM, Garrett TJ, Perez-Pinzon MA.

Front Neurosci. 2018 Jan 30;12:32. doi: 10.3389/fnins.2018.00032. eCollection 2018.

15.

The key genes underlying pathophysiology association between the type 2-diabetic and colorectal cancer.

Peng WF, Bai F, Shao K, Shen LS, Li HH, Huang S.

J Cell Physiol. 2018 Nov;233(11):8551-8557. doi: 10.1002/jcp.26440. Epub 2018 Jun 15.

PMID:
29319171
16.

Fish Oil Suppresses Body Fat Accumulation in Zebrafish.

Meguro S, Hasumura T.

Zebrafish. 2018 Feb;15(1):27-32. doi: 10.1089/zeb.2017.1475. Epub 2017 Nov 29.

PMID:
29185886
17.

High prevalence of carriers of variant c.1528G>C of HADHA gene causing long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) in the population of adult Kashubians from North Poland.

Nedoszytko B, Siemińska A, Strapagiel D, Dąbrowski S, Słomka M, Sobalska-Kwapis M, Marciniak B, Wierzba J, Skokowski J, Fijałkowski M, Nowicki R, Kalinowski L.

PLoS One. 2017 Nov 2;12(11):e0187365. doi: 10.1371/journal.pone.0187365. eCollection 2017.

18.

Genetic Dissection of the Impact of miR-33a and miR-33b during the Progression of Atherosclerosis.

Price NL, Rotllan N, Canfrán-Duque A, Zhang X, Pati P, Arias N, Moen J, Mayr M, Ford DA, Baldán Á, Suárez Y, Fernández-Hernando C.

Cell Rep. 2017 Oct 31;21(5):1317-1330. doi: 10.1016/j.celrep.2017.10.023.

19.

Uncovering the embryonic development-related proteome and metabolome signatures in breast muscle and intramuscular fat of fast-and slow-growing chickens.

Liu R, Wang H, Liu J, Wang J, Zheng M, Tan X, Xing S, Cui H, Li Q, Zhao G, Wen J.

BMC Genomics. 2017 Oct 23;18(1):816. doi: 10.1186/s12864-017-4150-3.

20.

Peripheral Neuropathy, Episodic Rhabdomyolysis, and Hypoparathyroidism in a Patient with Mitochondrial Trifunctional Protein Deficiency.

van Vliet P, Berden AE, van Schie MKM, Bakker JA, Heringhaus C, de Coo IFM, Langeveld M, Schroijen MA, Arbous MS.

JIMD Rep. 2018;38:101-105. doi: 10.1007/8904_2017_37. Epub 2017 Jul 7.

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