These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 35362222)

  • 1. S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome.
    Chen F; Ni C; Wang X; Cheng R; Pan C; Wang Y; Liang J; Zhang J; Cheng J; Chin YE; Zhou Y; Wang Z; Guo Y; Chen S; Htun S; Mathes EF; de Alba Campomanes AG; Slavotinek AM; Zhang S; Li M; Yao Z
    EMBO Mol Med; 2022 May; 14(5):e14904. PubMed ID: 35362222
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Coenzyme Q10 serves to couple mitochondrial oxidative phosphorylation and fatty acid β-oxidation, and attenuates NLRP3 inflammasome activation.
    Chokchaiwong S; Kuo YT; Lin SH; Hsu YC; Hsu SP; Liu YT; Chou AJ; Kao SH
    Free Radic Res; 2018 Dec; 52(11-12):1445-1455. PubMed ID: 30003820
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Riboflavin in Neurological Diseases: A Narrative Review.
    Plantone D; Pardini M; Rinaldi G
    Clin Drug Investig; 2021 Jun; 41(6):513-527. PubMed ID: 33886098
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Law LK; Tang NL; Hui J; Fung SL; Ruiter J; Wanders RJ; Fok TF; Lam CW
    Clin Chim Acta; 2009 Jun; 404(2):95-9. PubMed ID: 19265687
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Electron transfer flavoprotein and its role in mitochondrial energy metabolism in health and disease.
    Henriques BJ; Katrine Jentoft Olsen R; Gomes CM; Bross P
    Gene; 2021 Apr; 776():145407. PubMed ID: 33450351
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular and Clinical Investigations on Portuguese Patients with Multiple acyl-CoA Dehydrogenase Deficiency.
    Henriques BJ; Lucas TG; Martins E; Gaspar A; Bandeira A; Nogueira C; Brandão O; Rocha H; Vilarinho L; Gomes CM
    Curr Mol Med; 2019; 19(7):487-493. PubMed ID: 31418342
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Electron transfer flavoprotein deficiency: functional and molecular aspects.
    Schiff M; Froissart R; Olsen RK; Acquaviva C; Vianey-Saban C
    Mol Genet Metab; 2006 Jun; 88(2):153-8. PubMed ID: 16510302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ETF-QO Mutants Uncoupled Fatty Acid β-Oxidation and Mitochondrial Bioenergetics Leading to Lipid Pathology.
    Chokchaiwong S; Kuo YT; Hsu SP; Hsu YC; Lin SH; Zhong WB; Lin YF; Kao SH
    Cells; 2019 Jan; 8(2):. PubMed ID: 30709034
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional characterization of electron-transferring flavoprotein and its dehydrogenase required for fungal development and plant infection by the rice blast fungus.
    Li Y; Zhu J; Hu J; Meng X; Zhang Q; Zhu K; Chen X; Chen X; Li G; Wang Z; Lu G
    Sci Rep; 2016 Apr; 6():24911. PubMed ID: 27113712
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hepatic neddylation targets and stabilizes electron transfer flavoproteins to facilitate fatty acid β-oxidation.
    Zhang X; Zhang YL; Qiu G; Pian L; Guo L; Cao H; Liu J; Zhao Y; Li X; Xu Z; Huang X; Huang J; Dong J; Shen B; Wang HX; Ying X; Zhang WJ; Cao X; Zhang J
    Proc Natl Acad Sci U S A; 2020 Feb; 117(5):2473-2483. PubMed ID: 31941714
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Case Report: Recombinant human growth hormone therapy in a patient with spondyloepiphyseal dysplasia, Kondo-Fu type.
    Chen C; Wu J; Liu Y
    Front Pediatr; 2023; 11():1068718. PubMed ID: 36816387
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Flavin Adenine Dinucleotide Depletion Caused by
    Park KH; Gooz M; Ye ZW; Zhang J; Beeson GC; Rockey DC; Kim SH
    Hepatol Commun; 2021 Jun; 5(6):976-991. PubMed ID: 34141984
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA gene.
    Chautard R; Laroche-Raynaud C; Lia AS; Chazelas P; Derouault P; Sturtz F; Baaj Y; Veauville-Merllié A; Acquaviva C; Favreau F; Faye PA
    BMC Med Genomics; 2020 Jan; 13(1):12. PubMed ID: 31996215
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report.
    Yamada K; Ito M; Kobayashi H; Hasegawa Y; Fukuda S; Yamaguchi S; Taketani T
    Brain Dev; 2019 Aug; 41(7):638-642. PubMed ID: 30982706
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect.
    Cotelli MS; Vielmi V; Rimoldi M; Rizzetto M; Castellotti B; Bertasi V; Todeschini A; Gregorelli V; Baronchelli C; Gellera C; Padovani A; Filosto M
    Neurol Sci; 2012 Dec; 33(6):1383-7. PubMed ID: 22190129
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ATP5B and ETFB metabolic markers in children with congenital hydronephrosis.
    Zhao Q; Yang Y; Wang C; Hou Y; Chen H
    Mol Med Rep; 2016 Dec; 14(6):5111-5115. PubMed ID: 27840937
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2.
    Xiao C; Astiazaran-Symonds E; Basu S; Kisling M; Scaglia F; Chapman KA; Wang Y; Vockley J; Ferreira CR
    Am J Med Genet A; 2020 Oct; 182(10):2426-2431. PubMed ID: 32804429
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency.
    Cornelius N; Byron C; Hargreaves I; Guerra PF; Furdek AK; Land J; Radford WW; Frerman F; Corydon TJ; Gregersen N; Olsen RK
    Hum Mol Genet; 2013 Oct; 22(19):3819-27. PubMed ID: 23727839
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A.
    Wang ZQ; Chen XJ; Murong SX; Wang N; Wu ZY
    J Mol Med (Berl); 2011 Jun; 89(6):569-76. PubMed ID: 21347544
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
    Olsen RK; Olpin SE; Andresen BS; Miedzybrodzka ZH; Pourfarzam M; Merinero B; Frerman FE; Beresford MW; Dean JC; Cornelius N; Andersen O; Oldfors A; Holme E; Gregersen N; Turnbull DM; Morris AA
    Brain; 2007 Aug; 130(Pt 8):2045-54. PubMed ID: 17584774
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.