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  1. 521
    “…The presence of the m(6)A modification in mammalian mRNAs is proposed to promote mRNA recruitment to stress granules through the interaction with YTHDF proteins. …”
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    Limited effects of m(6)A modification on mRNA partitioning into stress granules
  2. 522
    “…SIMPLE SUMMARY: N(6)-methyladenosine (m(6)A) modification and m(6)A regulators play important roles in the occurrence and development of various cancers. …”
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    The Role of m(6)A Modification and m(6)A Regulators in Esophageal Cancer
  3. 523
    “…The aim of this study was to understand possible status of M1 and M2 type macrophages in the pathogenesis of keloid. …”
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    Macrophages of the M1 and M2 types play a role in keloids pathogenesis
  4. 524
    “…We used high-performance liquid chromatography tandem high-resolution mass spectrometry (HPLC-HRMS) to investigate the toxin profile of Gambierdiscus balechii 1123M1M10, which was obtained from Marakei Island (2°01′N, 173°15′E), Republic of Kiribati, located in the central Pacific Ocean. …”
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    Characterization of New Gambierones Produced by Gambierdiscus balechii 1123M1M10
  5. 525
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    Who uses mHealth apps? Identifying user archetypes of mHealth apps
  6. 526
    Publicado 1795
    Libro
    Real Cédula de S. M. para la Erección del Consulado de la M. N. M. L. Ciudad de Veracruz 1795.
  7. 527
    por Moran Gárcia, Edmundo
    Publicado 1979
    Libro
    Métodos de la mediana y de la transformación M.M.M. Por calcular el agua disponible de un río
  8. 528
    por Phan, Thi Hong Ngoc
    Publicado 2013
    “…Three different variables: m_T2, m_T2perp and m_lb are used in this study. …”
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    Measurement of the top quark mass in the $t\bar{t} \to $ dilepton decay channel using the $m_{T2}, m_{T2\perp}$ and $m_{lb}$ variables with ATLAS data
  9. 529
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    $^{204m}$Pb: a new probe for TDPAC experiments in biology complementing the well established probes $^{111m}$Cd and $^{199m}$Hg
  10. 530
    “…PURPOSE: To investigate the prognostic value of N6-methyladenosine (m6A)-, 5-methylcytosine (m5C)-, and N1-methyladenosine (m1A)-related genes in cervical cancer (CESC) and predicting immunotherapy response. …”
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    RNA methylation-related genes of m6A, m5C, and m1A predict prognosis and immunotherapy response in cervical cancer
  11. 531
    “…BACKGROUND: RNA methylation is a crucial in many biological functions, and its aberrant regulation is associated with cancer progression. N6-Methyladenosine (m6A), 5-Methylcytosine (m5C), N1-methyladenosine (m1A) are common modifications of RNA methylation. …”
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    The m6A/m5C/m1A regulator genes signature reveals the prognosis and is related with immune microenvironment for hepatocellular carcinoma
  12. 532
    “…Internal modifications of mRNA have emerged as widespread and versatile regulatory mechanism to control gene expression at the post-transcriptional level. …”
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    MePMe-seq: antibody-free simultaneous m(6)A and m(5)C mapping in mRNA by metabolic propargyl labeling and sequencing
  13. 533
    “…Ribonucleotide reductase subunits M1 (RRM1) and M2 (RRM2) are involved in the metabolism of gemcitabine (2′,2′-difluorodeoxycytidine), which is used for the treatment of nonsmall cell lung cancer. …”
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    Ribonucleotide reductase subunits M1 and M2 mRNA expression levels and clinical outcome of lung adenocarcinoma patients treated with docetaxel/gemcitabine
  14. 534
    “…mTOR has emerged as an important regulator of T helper cell differentiation. …”
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    The mammalian Target of Rapamycin (mTOR) regulates T helper cell differentiation through the selective activation of mTORC1 and mTORC2 signaling
  15. 535
    “…Mammalian target of rapamycin complex 1 and 2 (mTORC1/2) are overactive in colorectal carcinomas; however, the first generation of mTOR inhibitors such as rapamycin have failed to show clinical benefits in treating colorectal carcinoma in part due to their effects only on mTORC1. …”
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    Combination of mTOR and EGFR Kinase Inhibitors Blocks mTORC1 and mTORC2 Kinase Activity and Suppresses the Progression of Colorectal Carcinoma
  16. 536
    “…TAMs display a continuum of different polarization states between antitumorigenic M1 and protumorigenic M2 phenotypes, with a lower M1/M2 ratio correlating with worse prognosis. …”
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    Anti-CD47 Treatment Stimulates Phagocytosis of Glioblastoma by M1 and M2 Polarized Macrophages and Promotes M1 Polarized Macrophages In Vivo
  17. 537
    por Weinberg, Mark A.
    Publicado 2016
    “…RES-529 (previously named Palomid 529, P529) is a phosphoinositide 3-kinase (PI3K)/AKT/mechanistic target of rapamycin (mTOR) pathway inhibitor that interferes with the pathway through both mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2) dissociation. …”
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    RES-529: a PI3K/AKT/mTOR pathway inhibitor that dissociates the mTORC1 and mTORC2 complexes
  18. 538
    “…mSin1 is a unique component within the mammalian target of rapamycin (mTOR) complex 2 (mTORC2), which is responsible for cellular morphology and glucose metabolism. …”
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    Association of mSin1 with mTORC2 Ras and Akt reveals a crucial domain on mSin1 involved in Akt phosphorylation
  19. 539
    “…Currently, it is not clear whether inflammatory M1 or anti-inflammatory M2 predominate among the resident macrophages in the synovium. …”
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    TLR2 stimulation impairs anti-inflammatory activity of M2-like macrophages, generating a chimeric M1/M2 phenotype
  20. 540
    “…SARS-associated coronavirus (SCoV) M protein plays a key role in viral assembly and budding. …”
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    siRNAs targeting terminal sequences of the SARS-associated coronavirus membrane gene inhibit M protein expression through degradation of M mRNA
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