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Journal Abstract Search

1091 related items for PubMed ID: 29159707

  • 1. Propionyl-CoA carboxylase pcca-1 and pccb-1 gene deletions in Caenorhabditis elegans globally impair mitochondrial energy metabolism.
    Chapman KA, Ostrovsky J, Rao M, Dingley SD, Polyak E, Yudkoff M, Xiao R, Bennett MJ, Falk MJ.
    J Inherit Metab Dis; 2018 Mar; 41(2):157-168. PubMed ID: 29159707
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  • 6. Pathophysiological mechanisms of complications associated with propionic acidemia.
    Marchuk H, Wang Y, Ladd ZA, Chen X, Zhang GF.
    Pharmacol Ther; 2023 Sep; 249():108501. PubMed ID: 37482098
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  • 10. Propionic acidemia in the Arab World.
    Zayed H.
    Gene; 2015 Jun 15; 564(2):119-24. PubMed ID: 25865301
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  • 11. Propionyl-CoA carboxylase - A review.
    Wongkittichote P, Ah Mew N, Chapman KA.
    Mol Genet Metab; 2017 Dec 15; 122(4):145-152. PubMed ID: 29033250
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  • 12. Seventeen Novel Mutations in PCCA and PCCB Genes in Indian Propionic Acidemia Patients, and Their Outcomes.
    Gupta D, Bijarnia-Mahay S, Kohli S, Saxena R, Puri RD, Shigematsu Y, Yamaguchi S, Sakamoto O, Gupta N, Kabra M, Thakur S, Deb R, Verma IC.
    Genet Test Mol Biomarkers; 2016 Jul 15; 20(7):373-82. PubMed ID: 27227689
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  • 15. Propionic acidemia: identification of twenty-four novel mutations in Europe and North America.
    Pérez B, Desviat LR, Rodríguez-Pombo P, Clavero S, Navarrete R, Perez-Cerdá C, Ugarte M.
    Mol Genet Metab; 2003 Jan 15; 78(1):59-67. PubMed ID: 12559849
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  • 16. Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations.
    Kör D, Şeker-Yılmaz B, Bulut FD, Kılavuz S, Öktem M, Ceylaner S, Yıldızdaş D, Önenli-Mungan N.
    Turk J Pediatr; 2019 Jan 15; 61(3):330-336. PubMed ID: 31916709
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  • 18. [Analysis of PCCA and PCCB gene mutations in patients with propionic acidemia].
    Chen Z, Wen P, Wang G, Hu Y, Liu X, Chen L, Chen S, Wan L, Cui D, Shang Y, Li C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Feb 15; 32(1):26-30. PubMed ID: 25636094
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  • 19. Biochemical and anaplerotic applications of in vitro models of propionic acidemia and methylmalonic acidemia using patient-derived primary hepatocytes.
    Collado MS, Armstrong AJ, Olson M, Hoang SA, Day N, Summar M, Chapman KA, Reardon J, Figler RA, Wamhoff BR.
    Mol Genet Metab; 2020 Jul 15; 130(3):183-196. PubMed ID: 32451238
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