Monica Hollstein
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    Explore the profile of Monica Hollstein including associated specialties, affiliations and a list of published articles.
          
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          Snapshot
              Articles
              42
            
            
              Citations
              3625
            
            
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          Related Specialties
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          Published In
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  Recent Articles
          1.
        
    
    Fearnley G, Latham A, Hollstein M, Odell A, Ponnambalam S
  
  
    Cell Signal
    . 2019 Nov;
          66:109481.
    
    PMID: 31760171
  
  
          Cells respond to soluble and membrane-bound factors to activate signalling cascades that control cell proliferation and cell death. Vascular endothelial growth factor A (VEGF-A) is a soluble ligand that modulates...
      
2.
        
    
    Zhivagui M, Ng A, Ardin M, Churchwell M, Pandey M, Renard C, et al.
  
  
    Genome Res
    . 2019 Mar;
          29(4):521-531.
    
    PMID: 30846532
  
  
          Humans are frequently exposed to acrylamide, a probable human carcinogen found in commonplace sources such as most heated starchy foods or tobacco smoke. Prior evidence has shown that acrylamide causes...
      
3.
        
    
    Huang M, Yu W, Teoh W, Ardin M, Jusakul A, Ng A, et al.
  
  
    Genome Res
    . 2017 Jul;
          27(9):1475-1486.
    
    PMID: 28739859
  
  
          Aflatoxin B1 (AFB1) is a mutagen and IARC (International Agency for Research on Cancer) Group 1 carcinogen that causes hepatocellular carcinoma (HCC). Here, we present the first whole-genome data on...
      
4.
        
    
    Olivier M, Weninger A, Ardin M, Huskova H, Castells X, Vallee M, et al.
  
  
    Sci Rep
    . 2017 Jan;
          7:40898.
    
    PMID: 28091586
  
  
          No abstract available.
      
5.
        
    
    Kucab J, Hollstein M, Arlt V, Phillips D
  
  
    Int J Cancer
    . 2016 Nov;
          140(4):877-887.
    
    PMID: 27813088
  
  
          TP53 mutations occur in half of all human tumours. Mutagen-induced or spontaneous TP53 mutagenesis can be studied in vitro using the human TP53 knock-in (Hupki) mouse embryo fibroblast (HUF) immortalisation...
      
6.
        
    
    Bouaoun L, Sonkin D, Ardin M, Hollstein M, Byrnes G, Zavadil J, et al.
  
  
    Hum Mutat
    . 2016 Jun;
          37(9):865-76.
    
    PMID: 27328919
  
  
          TP53 gene mutations are one of the most frequent somatic events in cancer. The IARC TP53 Database (http://p53.iarc.fr) is a popular resource that compiles occurrence and phenotype data on TP53...
      
7.
        
    
    Jennis M, Kung C, Basu S, Budina-Kolomets A, Leu J, Khaku S, et al.
  
  
    Genes Dev
    . 2016 Apr;
          30(8):918-30.
    
    PMID: 27034505
  
  
          A nonsynonymous single-nucleotide polymorphism at codon 47 in TP53 exists in African-descent populations (P47S, rs1800371; referred to here as S47). Here we report that, in human cell lines and a...
      
8.
        
    
    Nik-Zainal S, Kucab J, Morganella S, Glodzik D, Alexandrov L, Arlt V, et al.
  
  
    Mutagenesis
    . 2015 Oct;
          30(6):763-70.
    
    PMID: 26443852
  
  
          Whole genome sequencing of human tumours has revealed distinct patterns of mutation that hint at the causative origins of cancer. Experimental investigations of the mutations and mutation spectra induced by...
      
9.
        
    
    Krais A, Muhlbauer K, Kucab J, Chinbuah H, Cornelius M, Wei Q, et al.
  
  
    Toxicol In Vitro
    . 2014 Sep;
          29(1):34-43.
    
    PMID: 25230394
  
  
          We compared mouse embryonic stem (ES) cells and fibroblasts (MEFs) for their ability to metabolically activate the environmental carcinogens benzo[a]pyrene (BaP), 3-nitrobenzanthrone (3-NBA) and aristolochic acid I (AAI), measuring DNA...
      
10.
        
    
    Olivier M, Weninger A, Ardin M, Huskova H, Castells X, Vallee M, et al.
  
  
    Sci Rep
    . 2014 Mar;
          4:4482.
    
    PMID: 24670820
  
  
          Experimental models that recapitulate mutational landscapes of human cancers are needed to decipher the rapidly expanding data on human somatic mutations. We demonstrate that mutation patterns in immortalised cell lines...