2012
DOI: 10.1007/s10059-012-0001-x
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Proteomic Profiling of Differentially Expressed Proteins from Bax inhibitor-1 Knockout and Wild Type Mice

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Cited by 6 publications
(7 citation statements)
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“…From the unique set of genes detected by CANOVA (Table 3 ), a few were reported to be relevant to kidney cancer/disease: FAH, MCM3 and UGT1A9. A defect in FAH results in the accumulation of FAA that can lead to oxidative stress and severe liver and kidney disease [ 32 , 33 ]. The MCM3 gene was found to be overexpressed in various human cancers, including kidney cancer [ 34 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…From the unique set of genes detected by CANOVA (Table 3 ), a few were reported to be relevant to kidney cancer/disease: FAH, MCM3 and UGT1A9. A defect in FAH results in the accumulation of FAA that can lead to oxidative stress and severe liver and kidney disease [ 32 , 33 ]. The MCM3 gene was found to be overexpressed in various human cancers, including kidney cancer [ 34 ].…”
Section: Resultsmentioning
confidence: 99%
“…1 and Table 3 ), which other methods could not easily find. These three genes were also reported to be involved in the kidney cancer development process in the literature [ 32 36 ].…”
Section: Discussionmentioning
confidence: 99%
“…A defect in FAH results in the accumulation of FAA that can lead The bold means the first place result of all methods compared "~" means about or approximately to oxidative stress and severe liver and kidney disease [32,33]. The MCM3 gene was found to be overexpressed in various human cancers, including kidney cancer [34].…”
Section: Results From the Kidney Cancer Studymentioning
confidence: 99%
“…1 and Table 3), which other methods could not easily find. These three genes were also reported to be involved in the kidney cancer development process in the literature [32][33][34][35][36].…”
Section: Discussionmentioning
confidence: 99%
“…Although seemingly ubiquitous, the endogenous expression of BI‐1 may differ among tissues or cell types and at different stages of development, leading to various cell‐type and time‐specific roles. While nonexhaustive, protein profiling by two‐dimensional electrophoresis and mass spectrometry from liver, brain, heart, lung, and kidney tissue samples identified altered differential protein expressions of GRP75, peroxiredoxin 6, fumarylacetoacetate hydrolase, selenium‐binding protein 2, phosphatidylethanolamine‐binding protein 1, and ferritin light chain 1 in tissues from BI‐1 − / − compared to BI‐1 + / + mice, leaving clues about BI‐1 function in those organs . Despite this interest, few researchers have addressed the implication of BI‐1 in disease.…”
Section: Implication Of Bi‐1 In Diseasementioning
confidence: 99%