BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 33487542)

  • 1. Methionine dependence in tumor cells: The potential role of cobalamin and MMACHC.
    Sorin M; Watkins D; Gilfix BM; Rosenblatt DS
    Mol Genet Metab; 2021 Mar; 132(3):155-161. PubMed ID: 33487542
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epigenetic modification of the gene for the vitamin B(12) chaperone MMACHC can result in increased tumorigenicity and methionine dependence.
    Loewy AD; Niles KM; Anastasio N; Watkins D; Lavoie J; Lerner-Ellis JP; Pastinen T; Trasler JM; Rosenblatt DS
    Mol Genet Metab; 2009 Apr; 96(4):261-7. PubMed ID: 19200761
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Growth requirement for methionine in human melanoma-derived cell lines with different levels of MMACHC expression and methylation.
    Bauer WG; Watkins D; Zacharias C; Gilfix BM; Rosenblatt DS
    Mol Genet Metab; 2024 Jan; 141(1):108111. PubMed ID: 38103461
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cobalamin metabolism in methionine-dependent human tumour and leukemia cell lines.
    Watkins D
    Clin Invest Med; 1998 Jun; 21(3):151-8. PubMed ID: 9627769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations.
    Cavicchi C; Oussalah A; Falliano S; Ferri L; Gozzini A; Gasperini S; Motta S; Rigoldi M; Parenti G; Tummolo A; Meli C; Menni F; Furlan F; Daniotti M; Malvagia S; la Marca G; Chery C; Morange PE; Tregouet D; Donati MA; Guerrini R; Guéant JL; Morrone A
    Clin Epigenetics; 2021 Jul; 13(1):137. PubMed ID: 34215320
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A high frequency and geographical distribution of MMACHC R132* mutation in children with cobalamin C defect.
    Kaur R; Attri SV; Saini AG; Sankhyan N
    Amino Acids; 2021 Feb; 53(2):253-264. PubMed ID: 33515116
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic, epigenetic and genomic mechanisms of methionine dependency of cancer and tumor-initiating cells: What could we learn from folate and methionine cycles.
    Guéant JL; Oussalah A; Zgheib R; Siblini Y; Hsu SB; Namour F
    Biochimie; 2020 Jun; 173():123-128. PubMed ID: 32289469
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHC.
    Bassila C; Ghemrawi R; Flayac J; Froese DS; Baumgartner MR; Guéant JL; Coelho D
    Biochim Biophys Acta Mol Basis Dis; 2017 Jan; 1863(1):103-112. PubMed ID: 27771510
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B
    Oussalah A; Siblini Y; Hergalant S; Chéry C; Rouyer P; Cavicchi C; Guerrini R; Morange PE; Trégouët D; Pupavac M; Watkins D; Pastinen T; Chung WK; Ficicioglu C; Feillet F; Froese DS; Baumgartner MR; Benoist JF; Majewski J; Morrone A; Rosenblatt DS; Guéant JL
    Clin Epigenetics; 2022 Apr; 14(1):52. PubMed ID: 35440018
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epimutation of MMACHC compound to a genetic mutation in cblC cases.
    Zhang X; Chen Q; Song Y; Guo P; Wang Y; Luo S; Zhang Y; Zhou C; Li D; Chen Y; Wei H
    Mol Genet Genomic Med; 2021 Jun; 9(6):e1625. PubMed ID: 33982424
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1.
    Yu HC; Sloan JL; Scharer G; Brebner A; Quintana AM; Achilly NP; Manoli I; Coughlin CR; Geiger EA; Schneck U; Watkins D; Suormala T; Van Hove JL; Fowler B; Baumgartner MR; Rosenblatt DS; Venditti CP; Shaikh TH
    Am J Hum Genet; 2013 Sep; 93(3):506-14. PubMed ID: 24011988
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Changes in cobalamin metabolism are associated with the altered methionine auxotrophy of highly growth autonomous human melanoma cells.
    Liteplo RG; Hipwell SE; Rosenblatt DS; Sillaots S; Lue-Shing H
    J Cell Physiol; 1991 Nov; 149(2):332-8. PubMed ID: 1748723
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Methionine auxotrophy in inborn errors of cobalamin metabolism.
    Garovic-Kocic V; Rosenblatt DS
    Clin Invest Med; 1992 Aug; 15(4):395-400. PubMed ID: 1516297
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Development and reversion of methionine dependence in a human glioma cell line: relation to homocysteine remethylation and cobalamin status.
    Fiskerstrand T; Christensen B; Tysnes OB; Ueland PM; Refsum H
    Cancer Res; 1994 Sep; 54(18):4899-906. PubMed ID: 8069855
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mechanism of vitamin B12-responsiveness in cblC methylmalonic aciduria with homocystinuria.
    Froese DS; Zhang J; Healy S; Gravel RA
    Mol Genet Metab; 2009 Dec; 98(4):338-43. PubMed ID: 19700356
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mouse models to study the pathophysiology of combined methylmalonic acidemia and homocystinuria, cblC type.
    Chern T; Achilleos A; Tong X; Hsu CW; Wong L; Poché RA
    Dev Biol; 2020 Dec; 468(1-2):1-13. PubMed ID: 32941884
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Abnormal chondrocyte intercalation in a zebrafish model of
    Paz D; Pinales BE; Castellanos BS; Perez I; Gil CB; Madrigal LJ; Reyes-Nava NG; Castro VL; Sloan JL; Quintana AM
    bioRxiv; 2023 Jan; ():. PubMed ID: 36711998
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia.
    Fofou-Caillierez MB; Mrabet NT; Chéry C; Dreumont N; Flayac J; Pupavac M; Paoli J; Alberto JM; Coelho D; Camadro JM; Feillet F; Watkins D; Fowler B; Rosenblatt DS; Guéant JL
    Hum Mol Genet; 2013 Nov; 22(22):4591-601. PubMed ID: 23825108
    [TBL] [Abstract][Full Text] [Related]  

  • 19. THAP11F80L cobalamin disorder-associated mutation reveals normal and pathogenic THAP11 functions in gene expression and cell proliferation.
    Dehaene H; Praz V; Lhôte P; Lopes M; Herr W
    PLoS One; 2020; 15(1):e0224646. PubMed ID: 31905202
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation spectrum of MMACHC in Chinese pediatric patients with cobalamin C disease: A case series and literature review.
    Wang C; Li D; Cai F; Zhang X; Xu X; Liu X; Zhang C; Wang D; Liu X; Lin S; Zhang Y; Shu J
    Eur J Med Genet; 2019 Oct; 62(10):103713. PubMed ID: 31279840
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.