[1]
Huggett J, Dheda K, Bustin S, Zumla A. Real-time RT-PCR normalisation ; strategies
and considerations. 2005;279–84.
[2]
Kozera B, Rapacz M. Reference genes in real-time PCR. J Appl Genet. 2013;54(4):391–406.
[3]
Bustin SA, Benes V, Garson JA, Hellemans J, Huggett J, Kubista M, et al. The MIQE
Guidelines : M inimum I nformation for Publication of Q uantitative Real-Time PCR
E xperiments SUMMARY : 2009;622:611–22.
[4]
Thellin O, Zorzi W, Lakaye B, Borman B De, Coumans B. Housekeeping genes as internal
standards : use and limits. 1999;75:291–5.
[5]
Connell GCO, Treadway MB, Petrone AB, Tennant CS, Lucke-wold N, Chantler PD, et al.
Leukocyte Dynamics Influence Reference Gene Stability in Whole Blood : Data-Driven
qRT-PCR Normalization Is a Robust Alternative for Measurement of Transcriptional Biomarkers.
2017;346–56.
[6]
Li M, Rao M, Chen K, Zhou J, Song J. left and right ventricles. Gene [Internet]. Elsevier;
2017;620(February):30–5.
[7]
Bamias G, Goukos D, Laoudi E, Balla IG. Comparative Study of Candidate Housekeeping
Genes for Quanti fi cation of Target Gene Messenger RNA Expression by Real-Time PCR
in Patients with In fl ammatory Bowel Disease. 2013;19(13).
[8]
Arenas-hernandez M, Vega-sanchez R. Housekeeping gene expression stability in reproductive
tissues after mitogen stimulation. BMC Res Notes [Internet]. BMC Research Notes; 2013;6(1):1.
Available from: BMC Research Notes
[9]
Almeida TA, Quispe-ricalde A, Montes F, Oca D, Foronda P, Hernández MM. Gynecologic
Oncology A high-throughput open-array qPCR gene panel to identify housekeeping genes
suitable for myometrium and leiomyoma expression analysis. Gynecol Oncol [Internet].
Elsevier Inc.; 2014; Available from: http://dx.doi.org/10.1016/j.ygyno.2014.04.012
[10]
Paula A, Aline S, Damo F, Tania B, Furlanetto W. Validation of Reference Genes for
Normalizing Gene Expression in Real-Time Quantitative Reverse Transcription PCR in
Human Thyroid Cells in Primary Culture Treated with Progesterone and Estradiol. 2013;278–82.
[11]
Kaszubowska L, Karsznia S, Damska M, Foerster J. Journal of Immunological Methods.
2015
[12]
Li YI, Xiang GUIM, Liu LINLIN, Liu C, Liu FEI, Jiang DN, et al. Assessment of endogenous
reference gene suitability for serum exosomal microRNA expression analysis in liver
carcinoma resection studies. 2015;4683–91.
[13]
Caracausi M, Piovesan A, Antonaros F, Strippoli P, Vitale L, Pelleri MC. Systematic
identification of human housekeeping genes possibly useful as references in gene expression
studies. 2017;2397–410.
[14]
Campos RP De, Schultz IC, Mello PDA, Davies S, Gasparin MS, Paula A, et al. Cervical
cancer stem like cells: Systematic review and identification of reference genes for
gene expression †. 2017. 1-32 p.
[15]
Wierzbicki PM, Klacz J, Rybarczyk A, Slebioda T. Identification of a suitable qPCR
reference gene in metastatic clear cell renal cell carcinoma. 2014;12473–87.
[16]
Romani C, Calza S, Todeschini P, Tassi RA, Zanotti L, Bandiera E, et al. Identification
of Optimal Reference Genes for Gene Expression Normalization in a Wide Cohort of Endometrioid
Endometrial Carcinoma Tissues. 2014;1–16.
[17]
Noriega NC, Kohama SG, Urbanski HF. Microarray analysis of relative gene expression
stability for selection of internal reference genes in the rhesus macaque brain. 2010
[18]
Vandesompele J, Preter K De, Poppe B, Roy N Van, Paepe A De. Accurate normalization
of real-time quantitative RT -PCR data by geometric averaging of multiple internal
control genes. 2002;1–12.
[19]
Andersen CL, Jensen JL, Ørntoft TF. Normalization of Real-Time Quantitative Reverse
Transcription-PCR Data : A Model-Based Variance Estimation Approach to Identify Genes
Suited for Normalization , Applied to Bladder and Colon Cancer Data Sets. 2004;5245–50.
[20]
Pfaffl MW, Tichopad A, Prgomet C, Neuvians TP. Determination of stable housekeeping
genes , differentially regulated target genes and sample integrity : BestKeeper –
Excel-based tool using pair-wise correlations. 2004;509–15.
[21]
Beer L, Mlitz V, Gschwandtner M, Berger T, Narzt M, Gruber F, et al. Bioinformatics
approach for choosing the correct reference genes when studying gene expression in
human keratinocytes. 2015;(7):742–7.
[22]
Bahr SM, Borgschulte T, Kayser KJ, Lin N. Using Microarray Technology to Select Housekeeping
Genes in Chinese Hamster Ovary Cells. 2009;104(5):1041–6.
[23]
Thomas D, Finan C, Newport MJ, Jones S. DNA entropy reveals a signi fi cant difference
in complexity between housekeeping and tissue speci fi c gene promoters. Comput Biol
Chem [Internet]. Elsevier Ltd; 2015;58:19–24. Available from: http://dx.doi.org/10.1016/j.compbiolchem.2015.05.001
[24]
Yim AK, Wong JW, Ku Y, Qin H. Using RNA-sequencingData to Evaluate Reference Genes
Suitable for Gene Expression Studies in Soybean. 2015;1–15.
[25]
Carmona R, Arroyo M, José M, Quesada J, Seoane P, Zafra A. Automated identification
of reference genes based on RNA seq data. Biomed Eng Online. BioMed Central; 2017;16(s1):11–33.
[26]
Hoang VLT, Tom LN, Quek X, Tan J, Payne EJ, Lin LL, et al. RNA-sequencingreveals more
consistent reference genes for gene expression studies in human non-melanoma skin
cancers. 2017;1–15.
[27]
Spiegelaere W De, Dern-wieloch J, Weigel R, Schumacher V, Vandekerckhove L, Fink C.
Reference Gene Validation for RT-qPCR , a Note on Different Available Software Packages.
2015;1–13.
[28]
Lallemant B, Evrard A, Combescure C, Chapuis H, Chambon G, Raynal C, et al. Reference
gene selection for head and neck squamous cell carcinoma gene expression studies.
2009;10:1–10.
[29]
Yigin AK, Cora T, Acar H, Kurar E, Kayis SA, Colpan B, et al. Selection of reliable
reference genes for qRT-PCR analysis on head and neck squamous cell carcinomas . 2018;28(5):2014–8.
[30] Song W, Li Y, Ren M, Wang D, Li Y, Zhang T, et al. Validation of reference
genes for the normalization of qRT-PCR expression studies in head and neck squamous
cell carcinoma cell lines treated by different chemotherapy drugs. 2018;11(3):2430–7.
[31]
Rentoft M, Hultin S, Coates PJ, Laurell G, Nylander K. Tubulin α -6 chain is a stably
expressed reference gene in archival samples of normal oral tissue and oral squamous
cell carcinoma. 2010;419–23.
[32]
Faibish D, Suzuki M, Bartlett JD, Forsyth T. HHS Public Access. 2017;33–42.
[33]
Martin JL. Validation of Reference Genes for Oral Cancer Detection Panels in a Prospective
Blinded Cohort. 2016;1–7.
[34]
Song W, Zhang WH, Zhang H, Li Y, Zhang Y, Yin W, et al. Cellular and Molecular Biology
in oral squamous cell carcinoma cell line treated by 5 kinds of chemotherapy drugs.
2016;62(13):29–34.
[35]
Palve V, Pareek M, Krishnan NM, Siddappa G, Suresh A, Kuriakose MA. A minimal set
of internal control genes for gene expression studies in head and neck squamous cell
carcinoma. 2018;1–12.
[37]
Cancer T, Line C. HHS Public Access. 2012;483(7391):603–7.
[40]
Ambatipudi S, Gerstung M, Pandey M, Samant T. NIH Public Access. 2013;51(2):161–73.
[41]
Bhosale PG, Cristea S, Ambatipudi S, Desai RS, Kumar R, Patil A, et al. Tr a n s l
a t i o n a l O n c o l o g y Chromosomal Alterations and Gene Expression Changes
Associated with the Progression of Leukoplakia to Advanced Gingivobuccal Cancer. Transl
Oncol [Internet]. The Authors; 2017;10(3):396–409. Available from: http://dx.doi.org/10.1016/j.tranon.2017.03.008
[42]
Moncton U De, Brunswick N, Hung TL, Nam V. The Mean and Median Absolute Deviations.
2001;7177(01).
[43]
Society IB. Finding Groups in Data : An Introduction to Cluster Analysis . by L .
Kaufman ; P . J . Rousseuw Review by : J . E . Gentle. 2014;47(2).
[44]
Rousseeuw PJ. Silhouettes : a graphical aid to the interpretation and validation of
cluster analysis. 1987;20:53–65.
[46]
Govindan SV, Kulsum S, Pandian RS, Das D, Seshadri M, Jr WH, et al. Establishment
and characterization of triple drug resistant head and neck squamous cell carcinoma
cell lines. 2015;3025–32.
[47]
Rio DC, Jr MA, Hannon GJ, Nilsen TW. Purification of RNA Using TRIzol ( TRI Reagent
). 2019;2010(6):1–4.
[49]
Xie F, Xiao P, Chen D. miRDeepFinder : a miRNA analysis tool for deep sequencing of
plant small RNAs. 2012;75–84.
[50]
Hydroxylase RNA. Expanding Role of the Jumonji C Domain as an. 2010;285(45):34503–7.
[51]
Montecino N, Soto X, Guzma L, Klattenhoff C, Mellstrom B, Romo X, et al. Human Brain
Synembryn Interacts With Gs a and Gq a and Is Translocated to the Plasma Membrane
in Response to Isoproterenol and Carbachol. 2003;157(January):151–7.
[52]
Godi A, Campli A Di, Konstantakopoulos A, Tullio G Di, Alessi DR, Kular GS, et al.
FAPPs control Golgi-to-cell-surface membrane traffic by binding to ARF and PtdIns
( 4 ) P. 2004;6(5).
[53]
Yu H, Tardivo L, Tam S, Weiner E, Gebreab F, Fan C, et al. Next-generation sequencing
to generate interactome datasets. 2011;8(6):13–7.
[54]
Manuscript A. NIH Public Access. 2015;159(5):1212–26.
[55] Maeda Y, Ide T, Koike M, Uchiyama Y, Kinoshita T. ARTICLES GPHR is a novel
anion channel critical for acidification and functions of the Golgi apparatus. 2008;10(10).
[56] Dotto G, Hospitalier C, Vaudois U, Hospital MG. HHS Public Access. 2018;3(3):181–97.