|1.||Samson, Leona D: 4 articles (11/2014 - 12/2003)|
|2.||Calvo, Jennifer A: 2 articles (11/2014 - 01/2009)|
|3.||Shah, Dharini: 2 articles (03/2010 - 01/2009)|
|4.||Guo, Haiwei H: 2 articles (03/2010 - 12/2003)|
|5.||Loeb, Lawrence A: 2 articles (03/2010 - 12/2003)|
|6.||Jhun, Iny: 1 article (11/2014)|
|7.||Muthupalani, Sureshkumar: 1 article (11/2014)|
|8.||Ayata, Cenk: 1 article (11/2014)|
|9.||Mazumder, Aprotim: 1 article (11/2014)|
|10.||Abolhassani, Nona: 1 article (11/2014)|
|1.||Type 1 Diabetes Mellitus (Autoimmune Diabetes)
02/01/2007 - "In the present work, we have extended previous studies in which mice deficient in the repair of N3-methyladenine adducts, 3-methyladenine DNA glycosylase (alkyladenine DNA glycosylase [Aag]) null mice, were reported to be resistant to the direct cytotoxic effect of STZ, but later developed autoimmune diabetes (J. "
03/26/2010 - "Frameshift mutagenesis and microsatellite instability induced by human alkyladenine DNA glycosylase."
12/01/2003 - "Here we examined tissues from noncancerous colons of ulcerative colitis patients to determine (a) the activity of two base excision-repair enzymes, AAG, the major 3-methyladenine DNA glycosylase, and APE1, the major apurinic site endonuclease; and (b) the prevalence of microsatellite instability (MSI). "
12/01/2003 - "A new report links inflammation in UC with increases in the DNA repair enzymes 3-methyladenine DNA glycosylase and apurinic/apyrimidinic endonuclease, and, paradoxically, with increased MSI. "
11/11/2014 - "Base excision repair (BER) is initiated by DNA glycosylases and is crucial in repairing RONS-induced DNA damage; the alkyladenine DNA glycosylase (Aag/Mpg) excises several DNA base lesions induced by the inflammation-associated RONS release that accompanies ischemia reperfusion (I/R). "
|4.||Hepatocellular Carcinoma (Hepatoma)
05/15/1991 - "The derived amino acid sequence of the human 3-meAde-DNA glycosylase has 85% sequence identity with the 3-meAde-DNA glycosylase from rat hepatoma cells."
04/01/1993 - "The inducibility of two DNA repair proteins, the O6-methylguanine-DNA-methyltransferase (MGMT) and the N3-methyladenine-DNA-glycosylase (ANPG), was studied by measuring the protein activities and the transcription of the MGMT and ANPG genes in a human hepatoma cell line (LICH cells). "
|5.||Xeroderma Pigmentosum (Kaposi's Disease)
|2.||DNA Glycosylases (DNA Glycosylase)
|3.||DNA (Deoxyribonucleic Acid)
|6.||DNA Repair Enzymes
|8.||Proteins (Proteins, Gene)